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Primary Retroperitoneal Lymph Node Dissection for Clinical Stage II A/B Seminomas: A Systematic Review and Meta-Analysis

ABSTRACT

Introduction

Chemotherapy and radiation therapy are considered standard treatments for stage II seminoma patients; however, these therapies are associated with long-term toxicities. Recently, retroperitoneal lymph node dissection has emerged as an alternative strategy, and the first three phase II trials were published in 2023 with promising results. The present study conducted a systematic review and meta-analysis to evaluate this surgery as an alternative treatment for stage IIA/B seminoma patients.

Purpose

Seminomas are the most common testicular tumors, often affecting young adult males. Standard treatments for stage II seminomas include chemotherapy and radiation therapy, but these therapies are associated with long-term toxicities. Thus, identifying alternative strategies is paramount. Herein, we conducted a systematic review and meta-analysis to appraise the efficacy and safety of retroperitoneal lymph node dissection (RPLND) for treating this condition.

Methods

We systematically searched the PubMed, Embase, and Cochrane databases for studies evaluating RPLND as a primary treatment for stage II A/B seminomas. Using a random-effects model, single proportion and means and pooled 2-year recurrence-free survival rates with hazard rates and 95% CI were calculated.

Results

Seven studies were included, comprising 331 males with stage II seminomas. In the pooled analysis, the recurrence rate was 17.69% (95% CI 12.31–24.75), and the 2-year RFS rate was 81% (95% CI 0.77–0.86). The complication rate was 9.16% (95% CI 6.16–13.42), the Clavien–Dindo > 2 complication rate was 8.83% (95% CI 5.76–13.31), and the retrograde ejaculation rate was 7.01% (95% CI 3.54–13.40). The median operative time was 174.68 min (95% CI 122.17–249.76 min), median blood loss was 105.91 mL (95% CI 46.89–239.22 mL), and patients with no evidence of lymph node involvement ranged from 0–16%.

Conclusions

Primary RPLNDs for treating stage IIA/B seminomas have favorable RFS rates, with low complication and recurrence rates. These findings provide evidence that this surgery is a viable alternative therapy for these patients.

Testicular Neoplasms; Seminoma; Male Germ Cell Tumor [Supplementary Concept]

INTRODUCTION

Testicular cancer accounts for approximately 1% of malignancies in males, emerging as the predominant solid tumor between the second and fourth decades of life, with an increasing incidence in the later years (11. Siegel RL, Miller KD, Fuchs HE, Jemal A. Cancer statistics, 2022. CA Cancer J Clin. 2022;72:7-33. doi: 10.3322/caac.21708., 22. Smith ZL, Werntz RP, Eggener SE. Testicular Cancer: Epidemiology, Diagnosis, and Management. Med Clin North Am. 2018;102:251-64. doi: 10.1016/j.mcna.2017.10.003.
https://doi.org/10.1016/j.mcna.2017.10.0...
). Most men with testicular cancer present a low-stage disease at the time of diagnosis [limited to the testis and retroperitoneum, clinical stages (CSs) I-IIB]. Seminomas are the most common testicular germ cell tumors (GCTs), comprising 50% of all testicular cancers. This disease predominantly affects young adult males, with the highest incidence in the fourth decade (33. Oldenburg J, Berney DM, Bokemeyer C, Climent MA, Daugaard G, Gietema JA, et al. Electronic address: clinicalguidelines@esmo.org; EURACAN. Testicular seminoma and non-seminoma: ESMO-EURACAN Clinical Practice Guideline for diagnosis, treatment and follow-up. Ann Oncol. 2022;33:362-75. doi: 10.1016/j.annonc.2022.01.002.
clinicalguidelines@esmo.org...
, 44. Oosterhuis JW, Looijenga LH. Testicular germ-cell tumours in a broader perspective. Nat Rev Cancer. 2005;5:210-22. doi: 10.1038/nrc1568.). Current guidelines recommend chemotherapy or radiation therapy as standard therapeutic modalities for CS IIA/B seminomas, defined by enlarged retroperitoneal lymph nodes of up to 5 cm (55. Patrikidou A, Cazzaniga W, Berney D, Boormans J, de Angst I, Di Nardo D, et al. European Association of Urology Guidelines on Testicular Cancer: 2023 Update. Eur Urol. 2023;84:289-301. doi: 10.1016/j.eururo.2023.04.010.
https://doi.org/10.1016/j.eururo.2023.04...
, 66. Gilligan T, Lin DW, Aggarwal R, Bagrodia A, Costa D, Davis NB, et al. Testicular Cancer, version 1. NCCN clinical practice Guidelines in oncology. J Natl Compr Canc Netw. 2023;1:MS7-MS17.). These treatments are effective, with a disease-free survival rate of up to 90%. However, these therapies are associated with long-term toxicities, diminished quality of life, and potential secondary tumor development (77. Hellesnes R, Myklebust TÅ, Fosså SD, Bremnes RM, Karlsdottir Á, Kvammen Ø, et al. Testicular Cancer in the Cisplatin Era: Causes of Death and Mortality Rates in a Population-Based Cohort. J Clin Oncol. 2021;39:3561-73. doi: 10.1200/JCO.21.00637.
https://doi.org/10.1200/JCO.21.00637...

8. Fung C, Dinh P Jr, Ardeshir-Rouhani-Fard S, Schaffer K, Fossa SD, et al. Toxicities Associated with Cisplatin-Based Chemotherapy and Radiotherapy in Long-Term Testicular Cancer Survivors. Adv Urol. 2018;2018:8671832. doi: 10.1155/2018/8671832.
https://doi.org/10.1155/2018/8671832...

9. Aziz NM. Cancer survivorship research: state of knowledge, challenges and opportunities. Acta Oncol. 2007;46:417-32. doi: 10.1080/02841860701367878.
https://doi.org/10.1080/0284186070136787...
-1010. Travis LB, Fosså SD, Schonfeld SJ, McMaster ML, Lynch CF, Storm H, et al. Second cancers among 40,576 testicular cancer patients: focus on long-term survivors. J Natl Cancer Inst. 2005;97:1354-65. doi: 10.1093/jnci/dji278.
https://doi.org/10.1093/jnci/dji278...
).

Recently, retroperitoneal lymph node dissection (RPLND), which is well-defined as the primary treatment for non-seminomatous testicular cancer, has emerged as an alternative strategy in CS IIA/B seminomas (55. Patrikidou A, Cazzaniga W, Berney D, Boormans J, de Angst I, Di Nardo D, et al. European Association of Urology Guidelines on Testicular Cancer: 2023 Update. Eur Urol. 2023;84:289-301. doi: 10.1016/j.eururo.2023.04.010.
https://doi.org/10.1016/j.eururo.2023.04...
, 66. Gilligan T, Lin DW, Aggarwal R, Bagrodia A, Costa D, Davis NB, et al. Testicular Cancer, version 1. NCCN clinical practice Guidelines in oncology. J Natl Compr Canc Netw. 2023;1:MS7-MS17.). Despite promising results observed with RPLND in these cases, the current evidence remains insufficient to make definitive recommendations regarding its suitability and effectiveness as a treatment option. Therefore, we performed a systematic review and meta-analysis to evaluate RPLND as an alternative option for patients with CS IIA/B seminomas.

MATERIALS AND METHODS

A systematic review and meta-analysis were performed and reported following the Cochrane Collaboration Handbook for Systematic Reviews of Interventions and the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) Statement guidelines (1111. Higgins J, Thomas J, editors. Cochrane handbook for systematic reviews of interventions. 2nd ed. Hoboken, NJ. Wiley-Blackwell. 2019; pp., 1212. Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 2021;372:n71. doi: 10.1136/bmj.n71.
https://doi.org/10.1136/bmj.n71...
). The prospective protocol was registered in the International Prospective Register of Systematic Reviews (PROSPERO; ID CRD42023483103).

Data source and search strategy

We systematically searched PubMed (MEDLINE), Embase, and the Cochrane Central Register of Controlled Trials from inception to February 04, 2024. The search terms included “seminoma” and “retroperitoneal lymphadenectomy”. After removing duplicates, two authors (B.V.L.A.M. and M.R.S.) screened the titles and abstracts and independently assessed full-text articles for inclusion based on prespecified criteria. Discrepancies were resolved in a discussion panel with the senior author. Moreover, we utilized a snowballing technique to search for additional eligible studies by reviewing the references from articles identified in the original search.

Eligibility criteria

We considered studies eligible for inclusion if they were prospective or retrospective, enrolled patients diagnosed with CS IIA/B testicular seminoma, evaluated primary RPLND, and presented data regarding any of the prespecified endpoints of interest. Exclusion criteria included no outcomes of interest, CS I, IIC, or higher seminomas, and/or failing to specify the CS of the seminomas. Additionally, cohorts or case series with fewer than ten patients were excluded from the pooled analysis due to the high possibility of selection bias (1313. Turner RM, Bird SM, Higgins JP. The impact of study size on meta-analyses: examination of underpowered studies in Cochrane reviews. PLoS One. 2013;8(3):e59202. doi: 10.1371/journal.pone.0059202.
https://doi.org/10.1371/journal.pone.005...
).

Data extraction

Two authors (B.V.L.A.M. and G.V.G.) independently extracted the data for each study using a standardized document to collect the following characteristics: inclusion and exclusion criteria, follow-up period, baseline characteristics, CS, surgical approach, dissection templates, pathologic nodal stage, upstaging, endpoint data, and endpoint definitions. Baseline characteristics were reported as the median and interquartile range for continuous variables and proportion for binary variables.

Endpoints

Our prespecified primary endpoints were the 2-year recurrence-free survival (RFS) rate, the recurrence rate, and the complication rate according to the Clavien–Dindo (CD) classification (1414. Dindo D, Demartines N, Clavien PA. Classification of surgical complications: a new proposal with evaluation in a cohort of 6336 patients and results of a survey. Ann Surg. 2004;240:205-13. doi: 10.1097/01.sla.0000133083.54934.ae.
https://doi.org/10.1097/01.sla.000013308...
). Our secondary outcomes included the retrograde ejaculation rate, complications CD grade > 2, operative time (minutes), estimated blood loss (mL), and length of hospital stay (days).

Quality assessment

We used the Cochrane Collaboration tool Risk Of Bias In Non-randomized Studies - of Interventions (ROBINS-I) for the quality assessment of individual studies, according to the recommendations from the Cochrane Handbook for Systematic Reviews of Interventions (1111. Higgins J, Thomas J, editors. Cochrane handbook for systematic reviews of interventions. 2nd ed. Hoboken, NJ. Wiley-Blackwell. 2019; pp., 1515. Sterne JA, Hernán MA, Reeves BC, Savovic J, Berkman ND, Viswanathan M, et al. ROBINS-I: a tool for assessing risk of bias in non-randomised studies of interventions. BMJ. 2016;355:i4919. doi: 10.1136/bmj.i4919.
https://doi.org/10.1136/bmj.i4919...
). Each trial underwent a risk of bias score evaluation, indicating whether there was a serious, moderate, low, or unclear risk of bias across five domains: confounding, selection of participants, classification of interventions, deviations from intended interventions, missing data, measurement of outcomes, and selection of reported results. The two authors independently conducted the assessments (M.M.L. and B.V.L.A.M.), and consensus resolved disagreements.

Statistical analysis

We summarized single proportions (metaprop) and single means (metamean) using an inverse-variance random-effects model, reporting overall proportion and mean with a 95% confidence interval (CI) as a measure of effect size (1616. Balduzzi S, Rücker G, Schwarzer G. How to perform a meta-analysis with R: a practical tutorial. Evid Based Ment Health. 2019;22:153-60. doi: 10.1136/ebmental-2019-300117.
https://doi.org/10.1136/ebmental-2019-30...
). The exact or Clopper-Pearson method was used to establish 95% CIs for proportion from the selected individual studies (1717. Newcombe RG. Two-sided confidence intervals for the single proportion: comparison of seven methods. Stat Med. 1998;17:857-72. doi: 10.1002/(sici)1097-0258(19980430)17:8<857::aid-sim777>3.0.co;2-e.
https://doi.org/10.1002/(sici)1097-0258(...
). We applied the logit transformation (“PLOGIT”) and log transformation (“MLN”) to normalize the results before calculating the pooled proportion and means, respectively (1616. Balduzzi S, Rücker G, Schwarzer G. How to perform a meta-analysis with R: a practical tutorial. Evid Based Ment Health. 2019;22:153-60. doi: 10.1136/ebmental-2019-300117.
https://doi.org/10.1136/ebmental-2019-30...
, 1818. Wang N. Conducting meta-analyses of proportions in R. J Behav Data Sci [Internet]. 2023;3. Available at. <https://jbds.isdsa.org/jbds/article/view/60>
https://jbds.isdsa.org/jbds/article/view...
). In cases of continuous endpoints, which are reported only as medians (interquartile ranges), we estimated corresponding means ± standard deviations by applying the Wan and Luo method (1919. Wan X, Wang W, Liu J, Tong T. Estimating the sample mean and standard deviation from the sample size, median, range and/or interquartile range. BMC Med Res Methodol. 2014;14:135. doi: 10.1186/1471-2288-14-135.
https://doi.org/10.1186/1471-2288-14-135...
, 2020. Luo D, Wan X, Liu J, Tong T. Optimally estimating the sample mean from the sample size, median, mid-range, and/or mid-quartile range. Stat Methods Med Res. 2018;27:1785-805. doi: 10.1177/0962280216669183.
https://doi.org/10.1177/0962280216669183...
). Furthermore, we pooled the 2-year RFS rates (metagen) using an inverse-variance random-effects model with hazard rates (i.e., RFS) and a 95% CI (1616. Balduzzi S, Rücker G, Schwarzer G. How to perform a meta-analysis with R: a practical tutorial. Evid Based Ment Health. 2019;22:153-60. doi: 10.1136/ebmental-2019-300117.
https://doi.org/10.1136/ebmental-2019-30...
). The restricted maximum likelihood estimator was used to calculate heterogeneity variance τ2.

The RFS rates and 95% CIs from the published Kaplan–Meier (KM) curves were estimated using the highly accurate method of Liu et al. along with the Shiny application to extract raw data coordinates and reconstruct the individual patient data (IPD) from published KM curves (2121. Liu N, Zhou Y, Lee JJ. IPDfromKM: reconstruct individual patient data from published Kaplan-Meier survival curves. BMC Med Res Methodol. 2021;21:111. doi: 10.1186/s12874-021-01308-8.
https://doi.org/10.1186/s12874-021-01308...
). We also performed a leave-one-out sensitivity analysis for the 2-year RFS rate by iteratively omitting one study at a time to ensure the results were not dependent on a single study. We used R version 4.2.3 (The R Foundation for Statistical Computing, MO, USA) and the extension package “meta” for all calculations and graphics (1616. Balduzzi S, Rücker G, Schwarzer G. How to perform a meta-analysis with R: a practical tutorial. Evid Based Ment Health. 2019;22:153-60. doi: 10.1136/ebmental-2019-300117.
https://doi.org/10.1136/ebmental-2019-30...
).

RESULTS

Study selection and characteristics

Our initial search yielded 5,816 potential articles (Figure-1). After removing duplicates, twenty-five articles were retrieved and reviewed in full for possible inclusion. Seven studies were ultimately included in the pooled analysis (22–28). Four studies were prospective trials (three phase 2 clinical trials), and three were retrospective. The main characteristics of the included studies are presented in Table-1.

Figure 1
- PRISMA flow diagram of study screening and selection.

Table 1
Main characteristics of the included studies.

The seven studies included 331 male patients diagnosed with CS IIA/B pure testicular seminomas and underwent RPLND in centers across North America, Canada, and Europe. Among the studies providing detailed information about the CS of the patients at the time of RPLND, 110 (33.2%) were classified as CS IIA, and 51 (15.4%) patients were CS IIB. In one study, 16 patients (35%) received adjuvant treatment in addition to surgery based on pathological findings. Thus, for the pooled analysis of the RFS and recurrence rate, we only considered the data of the patients who underwent RPLND followed by surveillance (2626. Matulewicz RS, Benfante N, Funt SA, Feldman DR, Carver B, Doudt A, et al. Primary Retroperitoneal Lymph Node Dissection for Seminoma Metastatic to the Retroperitoneum. J Urol. 2024;211:80-9. doi: 10.1097/JU.0000000000003697.
https://doi.org/10.1097/JU.0000000000003...
). Additionally, three studies reported upstaging rates ranging from 30–44% (2222. Daneshmand S, Cary C, Masterson T, Einhorn L, Adra N, Boorjian SA, et al. Surgery in Early Metastatic Seminoma: A Phase II Trial of Retroperitoneal Lymph Node Dissection for Testicular Seminoma With Limited Retroperitoneal Lymphadenopathy. J Clin Oncol. 2023;41:3009-18. doi: 10.1200/JCO.22.00624.
https://doi.org/10.1200/JCO.22.00624...
, 2525. Ladi-Seyedian S, Alsyouf M, Hu B, Cary C, Masterson T, Einhorn L, et al. Mp33-18 surgical and oncologic outcomes of surgery in early metastatic seminoma: Multi-institutional retrospective study. [Internet]. J Urol. 2023;209(Supplement 4). Available at. <https://www.auajournals.org/doi/10.1097/JU.0000000000003266.18>
https://www.auajournals.org/doi/10.1097/...
, 2626. Matulewicz RS, Benfante N, Funt SA, Feldman DR, Carver B, Doudt A, et al. Primary Retroperitoneal Lymph Node Dissection for Seminoma Metastatic to the Retroperitoneum. J Urol. 2024;211:80-9. doi: 10.1097/JU.0000000000003697.
https://doi.org/10.1097/JU.0000000000003...
).

The median age of patients was 37 years (range: 34–42.6 years), and the follow-up ranged from 17–79 months. The median size of the clinical lymph nodes was 1.86 cm (range: 1.6–2.3 cm), with one study restricting their inclusion criteria to patients with retroperitoneal adenopathy measuring up to 3 cm (2222. Daneshmand S, Cary C, Masterson T, Einhorn L, Adra N, Boorjian SA, et al. Surgery in Early Metastatic Seminoma: A Phase II Trial of Retroperitoneal Lymph Node Dissection for Testicular Seminoma With Limited Retroperitoneal Lymphadenopathy. J Clin Oncol. 2023;41:3009-18. doi: 10.1200/JCO.22.00624.
https://doi.org/10.1200/JCO.22.00624...
). Despite variations in surgical management templates across the studies, the prevailing approach involved modified ipsilateral RPLND, employing either an open or robotic surgical approach, while the decision to adopt a bilateral template rested at the surgeon’s discretion. A bilateral full-template was performed routinely in one study, with pelvic lymph node dissection for patients with enlarged pelvic lymph nodes (2626. Matulewicz RS, Benfante N, Funt SA, Feldman DR, Carver B, Doudt A, et al. Primary Retroperitoneal Lymph Node Dissection for Seminoma Metastatic to the Retroperitoneum. J Urol. 2024;211:80-9. doi: 10.1097/JU.0000000000003697.
https://doi.org/10.1097/JU.0000000000003...
). The clinical and surgical baseline characteristics of the included patients are presented in Table-2.

Table 2
Individual characteristics of the included studies.

Overall analysis

Recurrence rates across studies ranged from 8.2–30.8%. In the pooled analysis, the recurrence rate was 17.69% (95% CI 12.31–24.75; I2=44%; Figure-2A). Four studies reported a 2-year RFS rate, while in one study, it was derived from IPD reconstructed from the KM curve, which ranged from 72–83% (2525. Ladi-Seyedian S, Alsyouf M, Hu B, Cary C, Masterson T, Einhorn L, et al. Mp33-18 surgical and oncologic outcomes of surgery in early metastatic seminoma: Multi-institutional retrospective study. [Internet]. J Urol. 2023;209(Supplement 4). Available at. <https://www.auajournals.org/doi/10.1097/JU.0000000000003266.18>
https://www.auajournals.org/doi/10.1097/...
). The pooled 2-year RFS was 81% (95% CI 0.77–0.86; I2=0%; Figure-2B).

Figure 2
- Meta-analysis of primary endpoints after primary RPLND in patients with CS IIA/B testicular seminoma.

Five studies reported a total of 23 complications after RPLND, with rates ranging from 7.27–13.33%. In the pooled analysis, RPLND was associated with a complication rate of 9.16% (95% CI 6.16–13.42; I2=0%; Figure-2C). Of these, 20 were classified as CD grade > 2. The pooled complication rate for CD grade > 2 was 8.83% (95% CI 5.76–13.31; I2=0%; Figure-3A).

Figure 3
Meta-analysis of secondary endpoints after primary RPLND in patients with CS IIA/B testicular seminoma.

The nerve-sparing procedure ranged from 71–100%, and three studies reported retrograde ejaculation rates ranging from 5.45–10%. The pooled retrograde ejaculation rate was 7.01% (95% CI 3.54–13.40; I2=0%; Figure-3B).

Among the included trials, the mean operative time was 174.68 minutes (95% CI 122.17–249.76 minutes; I2=98%; Figure-3C), the mean blood loss was 105.91 mL (95% CI 46.89–239.22 mL; I2=96%; Figure-3D), and the median hospital stay was 4.62 days (95% CI 3.17–6.73 days; I2=95%; Figure-3E).

Sensitivity analysis

The recurrence rate was the only primary outcome presenting elevated between-study heterogeneity (I2=44%). Consequently, a subgroup analysis was conducted by pooling the data exclusively from prospective trials, revealing a recurrence rate of 16.76% (95% CI, 8.80–29.58; Supplementary Figure-1A APPENDIX). Nevertheless, the observed heterogeneity remained elevated (I2=66%). Leave-one-out sensitivity analysis for the 2-year RFS rate revealed that no single study significantly influenced the heterogeneity or the overall pooled result (Supplementary Figure-1B).

Quality assessment

Supplementary Figure-2 APPENDIX summarizes the individual risk of bias assessments of studies performed according to the Cochrane Collaboration’s tool ROBINS-I. Four studies were rated as “low risk” of bias, and three were “moderate risk” due to their potential to introduce confounding factors and bias in patient selection. Moreover, their retrospective design may influence the determination of patient exclusion criteria based on specific findings such as outcomes, comorbidities, laboratory results, and treatment history (2525. Ladi-Seyedian S, Alsyouf M, Hu B, Cary C, Masterson T, Einhorn L, et al. Mp33-18 surgical and oncologic outcomes of surgery in early metastatic seminoma: Multi-institutional retrospective study. [Internet]. J Urol. 2023;209(Supplement 4). Available at. <https://www.auajournals.org/doi/10.1097/JU.0000000000003266.18>
https://www.auajournals.org/doi/10.1097/...
, 2626. Matulewicz RS, Benfante N, Funt SA, Feldman DR, Carver B, Doudt A, et al. Primary Retroperitoneal Lymph Node Dissection for Seminoma Metastatic to the Retroperitoneum. J Urol. 2024;211:80-9. doi: 10.1097/JU.0000000000003697.
https://doi.org/10.1097/JU.0000000000003...
, 2828. Warszawski N, Schmücking M. Relapses in early-stage testicular seminoma: radiation therapy versus retroperitoneal lymphadenectomy. Scand J Urol Nephrol. 1997;31:355-9. doi: 10.3109/00365599709030619.
https://doi.org/10.3109/0036559970903061...
).

DISCUSSION

In this systematic review and single-arm meta-analysis comprising seven studies and 331 non-overlapping patients, we comprehensively evaluated RPLND as a first-line therapy for CS IIA/B seminomas. Our main findings were that the recurrence rate was 17.69% (95% CI 12.31–24.75), the 2-year RFS was 81% (95% CI 0.77–0.86), and the complication rate was 9.16% (95% CI 6.16–13.42).

Currently, para-aortic and pelvic radiation therapy or systemic chemotherapy is the standard treatment option for CS IIA/B seminomas, resulting in high rates of cancer-specific survival (> 97%) and low relapse rates, ranging from 9–24% in these tumors (2929. von Amsberg G, Hamilton R, Papachristofilou A. Clinical Stage IIA-IIC Seminoma: Radiation Therapy versus Systemic Chemotherapy versus Retroperitoneal Lymph Node Dissection. Oncol Res Treat. 2018;41:360-3. doi: 10.1159/000489408.
https://doi.org/10.1159/000489408...
, 3030. Garcia-del-Muro X, Maroto P, Gumà J, Sastre J, López Brea M, Arranz JA, et al. Chemotherapy as an alternative to radiotherapy in the treatment of stage IIA and IIB testicular seminoma: a Spanish Germ Cell Cancer Group Study. J Clin Oncol. 2008;26:5416-21. doi: 10.1200/JCO.2007.15.9103.
https://doi.org/10.1200/JCO.2007.15.9103...
). While chemotherapy (either with three cycles of bleomycin, etoposide, and cisplatin or four cycles of etoposide and cisplatin) is the preferred regimen in CS IIC, in CS IIA/B, both treatment modalities seem to be equally effective. Direct comparative studies between chemotherapy and radiation therapy are scarce and primarily confined to retrospective analyses. Although none of these studies have demonstrated significant differences in survival rates, a noticeable trend in relapse was observed in patients diagnosed with CS IIB who underwent radiation therapy (3030. Garcia-del-Muro X, Maroto P, Gumà J, Sastre J, López Brea M, Arranz JA, et al. Chemotherapy as an alternative to radiotherapy in the treatment of stage IIA and IIB testicular seminoma: a Spanish Germ Cell Cancer Group Study. J Clin Oncol. 2008;26:5416-21. doi: 10.1200/JCO.2007.15.9103.
https://doi.org/10.1200/JCO.2007.15.9103...
3232. Heinzelbecker J, Schmidt S, Lackner J, Busch J, Bokemeyer C, Classen J, et al. Therapy of clinical stage IIA and IIB seminoma: a systematic review. World J Urol. 2022;40:2829-41. doi: 10.1007/s00345-021-03873-5.
https://doi.org/10.1007/s00345-021-03873...
).

However, both treatments are associated with immediate and long-term side effects, including cardiovascular disease, metabolic disorders, endocrine disorders, hypogonadism, infertility, and secondary hematological or solid tumors (88. Fung C, Dinh P Jr, Ardeshir-Rouhani-Fard S, Schaffer K, Fossa SD, et al. Toxicities Associated with Cisplatin-Based Chemotherapy and Radiotherapy in Long-Term Testicular Cancer Survivors. Adv Urol. 2018;2018:8671832. doi: 10.1155/2018/8671832.
https://doi.org/10.1155/2018/8671832...
, 3333. Haugnes HS, Bosl GJ, Boer H, Gietema JA, Brydøy M, Oldenburg J, et al. Long-term and late effects of germ cell testicular cancer treatment and implications for follow-up. J Clin Oncol. 2012;30:3752-63. doi: 10.1200/JCO.2012.43.4431.
https://doi.org/10.1200/JCO.2012.43.4431...
). Therefore, the primary goal in managing patients with testicular GCTs is to minimize the long-term toxicity associated with treatment while preserving therapeutic efficacy. Studies have explored de-escalation strategies, such as reducing radiation fields, combining radiation therapy with one cycle of carboplatin, and de-escalating systemic chemotherapy regimens (34–36). Furthermore, earlier database reviews reported a 5-year overall survival of 92% in patients who underwent primary RPLND in this setting, underscoring this surgery as a feasible therapeutic option (3737. Tabakin AL, Shinder BM, Kim S, Rivera-Nunez Z, Polotti CF, Modi PK, et al. Retroperitoneal Lymph Node Dissection as Primary Treatment for Men With Testicular Seminoma: Utilization and Survival Analysis Using the National Cancer Data Base, 2004-2014. Clin Genitourin Cancer. 2020;18:e194-e201. doi: 10.1016/j.clgc.2019.10.018.
https://doi.org/10.1016/j.clgc.2019.10.0...
).

The recurrence rate of primary RPLND for CS IIA/B seminomas was 17.69% (95% CI 12.31–24.75), while the 2-year RFS was 81% (95% CI 0.77–0.86). When compared with the standard recommended treatments, the reported relapse rates of radiation therapy ranged from 9–24%, while the 5-year RFS in CS IIA and IIB are 92% and 90%, respectively (3838. Classen J, Schmidberger H, Meisner C, Souchon R, Sautter-Bihl ML, Sauer R, et al. Radiotherapy for stages IIA/B testicular seminoma: final report of a prospective multicenter clinical trial. J Clin Oncol. 2003;21:1101-6. doi: 10.1200/JCO.2003.06.065.
https://doi.org/10.1200/JCO.2003.06.065...
, 3939. Chung PW, Gospodarowicz MK, Panzarella T, Jewett MA, Sturgeon JF, Tew-George B, et al. Stage II testicular seminoma: patterns of recurrence and outcome of treatment. Eur Urol. 2004;45:754-59; discussion 759-60. doi: 10.1016/j.eururo.2004.01.020.
https://doi.org/10.1016/j.eururo.2004.01...
). Although a few studies have reported outcomes on chemotherapy regimens for CS IIA/B seminomas, the recurrence rates were 0%, and the 5-year RFS was 100% (4040. Tandstad T, Smaaland R, Solberg A, Bremnes RM, Langberg CW, Laurell A, et al. Management of seminomatous testicular cancer: a binational prospective population-based study from the Swedish norwegian testicular cancer study group. J Clin Oncol. 2011;29:719-25. doi: 10.1200/JCO.2010.30.1044.
https://doi.org/10.1200/JCO.2010.30.1044...
, 4141. Kollmannsberger C, Tyldesley S, Moore C, Chi KN, Murray N, Daneshmand S, et al Evolution in management of testicular seminoma: population-based outcomes with selective utilization of active therapies. Ann Oncol. 2011;22:808-14. doi: 10.1093/annonc/mdq466.
https://doi.org/10.1093/annonc/mdq466...
).

The elevated RFS rate indicates that these patients who underwent RPLND were free from adverse events associated with chemotherapy or radiation therapy at a 2-year follow-up. Furthermore, even those who experienced recurrence were still successfully treated with standard therapies. For example, in the SEMS trial, among 12 patients who experienced a recurrence, ten were treated with chemotherapy, and two underwent additional surgery (2222. Daneshmand S, Cary C, Masterson T, Einhorn L, Adra N, Boorjian SA, et al. Surgery in Early Metastatic Seminoma: A Phase II Trial of Retroperitoneal Lymph Node Dissection for Testicular Seminoma With Limited Retroperitoneal Lymphadenopathy. J Clin Oncol. 2023;41:3009-18. doi: 10.1200/JCO.22.00624.
https://doi.org/10.1200/JCO.22.00624...
). In the COTRIMS trial, three patients (10%) developed an outfield relapse at 4, 6, and 9 months postoperatively and were salvaged by systemic chemotherapy (2323. Heidenreich A, Paffenholz P, Hartmann F, Seelemeyer F, Pfister D. Retroperitoneal Lymph Node Dissection in Clinical Stage IIA/B Metastatic Seminoma: Results of the COlogne Trial of Retroperitoneal Lymphadenectomy In Metastatic Seminoma (COTRIMS). Eur Urol Oncol. 2024;7:122-7. doi: 10.1016/j.euo.2023.06.004.). In the PRIMETEST trial, the median time to relapse was 6 months, and all these patients were successfully treated with systemic chemotherapy (2424. Hiester A, Che Y, Lusch A, Kuß O, Niegisch G, Lorch A, et al. Phase 2 Single-arm Trial of Primary Retroperitoneal Lymph Node Dissection in Patients with Seminomatous Testicular Germ Cell Tumors with Clinical Stage IIA/B (PRIMETEST). Eur Urol. 2023;84:25-31. doi: 10.1016/j.eururo.2022.10.021.). Additionally, Matulewicz et al. reported four relapses in the surveillance group after RPLND, all of which were treated with chemotherapy, with no retroperitoneal relapses observed (2626. Matulewicz RS, Benfante N, Funt SA, Feldman DR, Carver B, Doudt A, et al. Primary Retroperitoneal Lymph Node Dissection for Seminoma Metastatic to the Retroperitoneum. J Urol. 2024;211:80-9. doi: 10.1097/JU.0000000000003697.
https://doi.org/10.1097/JU.0000000000003...
).

Importantly, the RPLND template differed across the studies. Most patients underwent modified ipsilateral RPLND (Table-1), based on mapping studies of retroperitoneal metastasis, aiming to limit the extent of dissection in anatomic regions thought to be at a decreased risk of metastatic dissemination and to avoid ejaculatory dysfunction. The RPLND template is directly related to testis lymphatic drainage. The right-sided testicular drainage included the interaortocaval lymph nodes, followed by the precaval and paracaval nodes, whereas left-sided drainage included the left para-aortic and preaortic lymph nodes (4242. Weinstein MH. Lymphatic Drainage of the Testes. In: Testis Cancer, Rowland RG, Eds. WB, editors. Atlas of the Urologic Clinics of North America. 1999. pp.). The retroperitoneal dissemination contralateral to the testis compromised by the tumor is more common with right-sided tumors than in left-sided tumors and is usually associated with large-volume disease (4343. Sogani PC. Evolution of the management of stage I nonseminomatous germ-cell tumors of the testis. Urol Clin North Am. 1991;18:561-73.). The standard bilateral RPLND template limits are the ureters (lateral), bifurcation of iliac vessels (inferior) and renal hilum (superior). Recent data suggests that modified ipsilateral RPLND might underestimate the risk of contralateral retroperitoneal metastases in almost 32% of the patients (4444. Mano R, Di Natale R, Sheinfeld J. Current controversies on the role of retroperitoneal lymphadenectomy for testicular cancer. Urol Oncol. 2019;37:209-18. doi: 10.1016/j.urolonc.2018.09.009.
https://doi.org/10.1016/j.urolonc.2018.0...
).

In CS I, the main risk factors for relapse are testicular tumor size and stromal invasion of the rete testis (4545. Warde P, Specht L, Horwich A, Oliver T, Panzarella T, Gospodarowicz M, et al. Prognostic factors for relapse in stage I seminoma managed by surveillance: a pooled analysis. J Clin Oncol. 2002;20:4448-52. doi: 10.1200/JCO.2002.01.038.
https://doi.org/10.1200/JCO.2002.01.038...
). The risk of relapse in unselected CS I patients varies between 12–20% at five years, with 17% in the largest series (4646. Groll RJ, Warde P, Jewett MA. A comprehensive systematic review of testicular germ cell tumor surveillance. Crit Rev Oncol Hematol. 2007;64:182-97. doi: 10.1016/j.critrevonc.2007.04.014.
https://doi.org/10.1016/j.critrevonc.200...
). The absence of both factors indicates a low risk of recurrence of around 6% (4747. Aparicio J, Germà JR, García del Muro X, Maroto P, Arranz JA, Sáenz A, et al. Risk-adapted management for patients with clinical stage I seminoma: the Second Spanish Germ Cell Cancer Cooperative Group study. J Clin Oncol. 2005;23:8717-23. doi: 10.1200/JCO.2005.01.9810.
https://doi.org/10.1200/JCO.2005.01.9810...
). Recurrences, when present, occur mainly in the retroperitoneum during the first two years (4848. Nayan M, Jewett MA, Hosni A, Anson-Cartwright L, Bedard PL, Moore M, et al. Conditional Risk of Relapse in Surveillance for Clinical Stage I Testicular Cancer. Eur Urol. 2017;71:120-7. doi: 10.1016/j.eururo.2016.07.013.). Among the studies included in this meta-analysis, only one performed a bilateral RPLND and had no retroperitoneal recurrence (2626. Matulewicz RS, Benfante N, Funt SA, Feldman DR, Carver B, Doudt A, et al. Primary Retroperitoneal Lymph Node Dissection for Seminoma Metastatic to the Retroperitoneum. J Urol. 2024;211:80-9. doi: 10.1097/JU.0000000000003697.
https://doi.org/10.1097/JU.0000000000003...
). Therefore, considering the characteristics of the primary tumor, improving risk stratification and performing subgroup analyses could better individualize the RPLND template that needs to be performed.

The rate of patients with no evidence of regional lymph node involvement (N0) ranged from 0–16%. This range is consistent with rates observed in RPLND for non-seminoma tumors, where surgery has been the standard treatment modality for numerous years (4444. Mano R, Di Natale R, Sheinfeld J. Current controversies on the role of retroperitoneal lymphadenectomy for testicular cancer. Urol Oncol. 2019;37:209-18. doi: 10.1016/j.urolonc.2018.09.009.
https://doi.org/10.1016/j.urolonc.2018.0...
). The definitive pathology is a benefit exclusively attainable through surgery. Consequently, over the past several decades, patients with N0 status may have been subjected to overtreatment with primary radiation therapy or chemotherapy, potentially leading to unnecessary acute and long-term toxicity and requiring long-term follow-up. This situation underscores the necessity for refinement in pre-imaging techniques and the development and routine use of molecular serum markers. For example, measuring miR371, the most promising biomarker, levels could aid in distinguishing metastatic and non-metastatic diseases, thereby preventing unnecessary treatments (4949. Nestler T, Schoch J, Belge G, Dieckmann KP. MicroRNA-371a-3p-The Novel Serum Biomarker in Testicular Germ Cell Tumors. Cancers (Basel). 2023;15:3944. doi: 10.3390/cancers15153944.
https://doi.org/10.3390/cancers15153944...
).

Conversely, surgical interventions are susceptible to perioperative complications. Our study revealed an overall complication rate of 9.16%, with 8.83% classified as CD grade > 2, exhibiting no heterogeneity across the various studies. Heister et al. observed one patient with a post-operative ileus that required revision surgery, two with pulmonary embolisms and one with lymphocele requiring drainage (2424. Hiester A, Che Y, Lusch A, Kuß O, Niegisch G, Lorch A, et al. Phase 2 Single-arm Trial of Primary Retroperitoneal Lymph Node Dissection in Patients with Seminomatous Testicular Germ Cell Tumors with Clinical Stage IIA/B (PRIMETEST). Eur Urol. 2023;84:25-31. doi: 10.1016/j.eururo.2022.10.021.). Matulewicz et al. reported two patients with chylous ascites requiring bedside paracentesis, two with infections that resolved with oral antibiotics, and one with wound breakdown resolved with conservative treatment (2626. Matulewicz RS, Benfante N, Funt SA, Feldman DR, Carver B, Doudt A, et al. Primary Retroperitoneal Lymph Node Dissection for Seminoma Metastatic to the Retroperitoneum. J Urol. 2024;211:80-9. doi: 10.1097/JU.0000000000003697.
https://doi.org/10.1097/JU.0000000000003...
). Daneshmand et al. described four patients with complications: one with incision ulceration, one with ileus, one with ileus and pulmonary embolism and one with chylos ascites (2222. Daneshmand S, Cary C, Masterson T, Einhorn L, Adra N, Boorjian SA, et al. Surgery in Early Metastatic Seminoma: A Phase II Trial of Retroperitoneal Lymph Node Dissection for Testicular Seminoma With Limited Retroperitoneal Lymphadenopathy. J Clin Oncol. 2023;41:3009-18. doi: 10.1200/JCO.22.00624.
https://doi.org/10.1200/JCO.22.00624...
). Ladi-Seyedian et al. observed seven (7.5%) complications, including ileus, incision ulceration, pulmonary embolism and chylous ascites (2525. Ladi-Seyedian S, Alsyouf M, Hu B, Cary C, Masterson T, Einhorn L, et al. Mp33-18 surgical and oncologic outcomes of surgery in early metastatic seminoma: Multi-institutional retrospective study. [Internet]. J Urol. 2023;209(Supplement 4). Available at. <https://www.auajournals.org/doi/10.1097/JU.0000000000003266.18>
https://www.auajournals.org/doi/10.1097/...
). Heidenreich et al. reported four complications: two retroperitoneal lymphoceles, one ileus and one chylos ascites, but did not provide the resolution of these complications (2323. Heidenreich A, Paffenholz P, Hartmann F, Seelemeyer F, Pfister D. Retroperitoneal Lymph Node Dissection in Clinical Stage IIA/B Metastatic Seminoma: Results of the COlogne Trial of Retroperitoneal Lymphadenectomy In Metastatic Seminoma (COTRIMS). Eur Urol Oncol. 2024;7:122-7. doi: 10.1016/j.euo.2023.06.004.). In contrast, Thor et al. did not specify the complications encountered by seven patients (2727. Thor A, Gerdtsson A, Almas B, Halvorsen D, Cedermark GC, Neegaard H, et al. MP33-04 the early results of the swenoteca (swedish norwegian testicular cancer group) introduction of primary retroperitoneal lymph node dissection (rplnd) in seminoma stage IIA-IIB ≤ 3cm. [Internet]. J Urol. 2023;209(Supplement 4). Available at. <https://www.auajournals.org/doi/10.1097/JU.0000000000003266.04>
https://www.auajournals.org/doi/10.1097/...
).

It is well-established that post-chemotherapy RPLND is a more challenging procedure attributed to desmoplastic reaction, with complication rates reaching 24.7% (5050. Mosharafa AA, Foster RS, Leibovich BC, Bihrle R, Johnson C, Donohue JP. Is post-chemotherapy resection of seminomatous elements associated with higher acute morbidity? J Urol. 2003;169:2126-8. doi: 10.1097/01.ju.0000060121.33899.4b.
https://doi.org/10.1097/01.ju.0000060121...
). Early initiation of surgery during the management of CS II seminomas may mitigate the morbidity linked to RPLND in patients with residual masses following chemotherapy. Indeed, evidence supports the safety of this approach when performed using minimally invasive techniques (5151. Santos VE, Fornazieri L, Brazão ES Jr, Pinto PR Neto, da Costa WH, Zequi SC. Primary laparoscopic RPLND for pure seminona metastasis: feasibility of supine and lateral approaches. Int Braz J Urol. 2023;49:269-70. doi: 10.1590/S1677-5538.IBJU.2022.0370.
https://doi.org/10.1590/S1677-5538.IBJU....
). Moreover, a limited number of long-term complications of RPLND were reported in the studies, including issues such as incisional hernia, ejaculatory dysfunction, ureteral obstruction, or intestinal obstruction. Notably, these low complication rates observed are associated with an increased number of procedures performed in those centers. This result highlights the importance and preference of such RPLND-specialized centers to ensure treatment efficacy and patient safety.

Nerve-sparing surgery was performed on most patients in the studies, with rates ranging from 71–100%. It should be pointed out that a 7% retrograde ejaculation rate was observed, which may affect men’s pleasure. Furthermore, infertility has been recognized as a significant concern for survivors of testicular cancer, especially considering its elevated incidence among young men (5252. Conduit C, Hutchinson AD, Leonard M, O ‘Haire S, Moody M, Thomas B, et al. An exploration of testicular cancer survivors’ experience of ejaculatory dysfunction following retroperitoneal lymph node dissection-a sub-study of the PREPARE clinical trial. J Cancer Surviv. 2023 Nov 20. doi: 10.1007/s11764-023-01489-9. Epub ahead of print.
https://doi.org/10.1007/s11764-023-01489...
). Both hypogonadism and infertility stand as potential adverse events associated with radiation therapy and chemotherapy (88. Fung C, Dinh P Jr, Ardeshir-Rouhani-Fard S, Schaffer K, Fossa SD, et al. Toxicities Associated with Cisplatin-Based Chemotherapy and Radiotherapy in Long-Term Testicular Cancer Survivors. Adv Urol. 2018;2018:8671832. doi: 10.1155/2018/8671832.
https://doi.org/10.1155/2018/8671832...
, 3333. Haugnes HS, Bosl GJ, Boer H, Gietema JA, Brydøy M, Oldenburg J, et al. Long-term and late effects of germ cell testicular cancer treatment and implications for follow-up. J Clin Oncol. 2012;30:3752-63. doi: 10.1200/JCO.2012.43.4431.
https://doi.org/10.1200/JCO.2012.43.4431...
). In this context, nerve-sparing primary RPLND holds an advantage by providing definitive staging with low rates of ejaculatory disorders (5353. Carver BS, Serio AM, Bajorin D, Motzer RJ, Stasi J, Bosl GJ, et al. Improved clinical outcome in recent years for men with metastatic nonseminomatous germ cell tumors. J Clin Oncol. 2007;25:5603-8. doi: 10.1200/JCO.2007.13.6283.
https://doi.org/10.1200/JCO.2007.13.6283...
). However, it has been associated with higher rates of in-field recurrence and complications. Therefore, it should be performed by experienced surgeons (5454. Heidenreich A, Albers P, Hartmann M, Kliesch S, Kohrmann KU, Krege S, et al. Complications of primary nerve sparing retroperitoneal lymph node dissection for clinical stage I nonseminomatous germ cell tumors of the testis: experience of the German Testicular Cancer Study Group. J Urol. 2003;169:1710-4. doi: 10.1097/01.ju.0000060960.18092.54.
https://doi.org/10.1097/01.ju.0000060960...
).

The included studies’ main limitations are the limited follow-up and long-term oncologic data, which are essential for consolidating progression-free survival rates. Additionally, the surgical template and inclusion criteria varied among the studies. Given the well-established association between disease volume and an increased recurrence rate, these variations may explain the elevated between-study heterogeneity observed in this outcome. However, consistent results were found in the leave-one-out sensitivity analysis. Finally, there is a paucity of prospective randomized controlled trials comparing upfront RPLND with radiation therapy or chemotherapy.

Although a recently published meta-analysis has already evaluated RPLND for CS II seminomas, our study has some key advantages. First, we included three additional studies, adding 200 patients not considered in the prior meta-analysis (25–27). Second, Parizi et al. included two studies with overlapping populations, double-counting individuals in the evidence synthesis (2222. Daneshmand S, Cary C, Masterson T, Einhorn L, Adra N, Boorjian SA, et al. Surgery in Early Metastatic Seminoma: A Phase II Trial of Retroperitoneal Lymph Node Dissection for Testicular Seminoma With Limited Retroperitoneal Lymphadenopathy. J Clin Oncol. 2023;41:3009-18. doi: 10.1200/JCO.22.00624.
https://doi.org/10.1200/JCO.22.00624...
, 5555. Kardoust Parizi M, Margulis V, Bagrodia A, Bekku K, Klemm J, Matsukawa A, et al. Primary retroperitoneal lymph node dissection for clinical stage II seminoma: A systematic review and meta-analysis of safety and oncological effectiveness. Urol Oncol. 2024;42:102-9. doi: 10.1016/j.urolonc.2024.01.014., 5656. Tachibana I, Alabd A, Tong Y, Piroozi A, Mahmoud M, Kern SQ, et al. Primary Retroperitoneal Lymph Node Dissection for Stage II Seminoma: Is Surgery the New Path Forward? J Clin Oncol. 2023;41:3930-8. doi: 10.1200/JCO.22.01822.
https://doi.org/10.1200/JCO.22.01822...
, 5757. Hussein H, Nevill CR, Mefen A, Abrams KR, Bujkiewicz S, Sutton AJ, et al. Publisher Correction: Double-counting of populations in evidence synthesis in public health: a call for awareness and future methodological development. BMC Public Health. 2022 ;22:2301. doi: 10.1186/s12889-022-14741-1. Erratum for: BMC Public Health. 2022 Sep 27;22(1):1827.
https://doi.org/10.1186/s12889-022-14741...
). Third, we pooled the 2-year RFS rates estimated from the published KM curves. Fourth, additional endpoints, such as operative time, estimated blood loss, and hospital stay length, were analyzed. Finally, we also performed a sensitivity analysis, including a leave-one-out analysis, to ensure the robustness of our findings.

To the best of our knowledge, this study analyzed the most recent RPLND data in this context. It imparts pertinent information concerning recurrence rates and complications, illustrating the proposed procedure’s safety and advantages as the primary approach for treating CS IIA/B seminomas.

CONCLUSIONS

This single-arm meta-analysis of studies that evaluated patients who underwent RPLND to treat CS IIA/IIB seminomas demonstrated favorable RFS rates with low recurrence rates and complications. Additional studies are warranted to assess the comparative effectiveness of RPLND versus alternative strategies for treating this patient cohort and to investigate long-term and post-recurrence outcomes following RPLND.

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  • ABBREVIATIONS

    CD = Clavien–Dindo
    CI = Confidence interval
    CS = Clinical stage
    IPD = Individual patient data
    GCT = Germ cell tumor
    KM = Kaplan–Meier
    PRISMA = Preferred Reporting Items for Systematic Reviews and Meta-Analysis
    ROBINS-I = Risk of Bias in Non-randomized Studies of Interventions
    RPLND = Retroperitoneal lymph node dissection

Publication Dates

  • Publication in this collection
    02 Aug 2024
  • Date of issue
    Jul-Aug 2024

History

  • Received
    04 Mar 2024
  • Accepted
    23 Mar 2024
  • Published
    25 Apr 2024
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