Abstract
Prognostic factors for local recurrence in patients with rectal cancer submitted to neoadjuvant chemoradiotherapy and total mesorectal excision.
Background:
The standard curative treatment for locally advanced rectal cancer of the middle and lower thirds is long-course chemoradiotherapy followed by total mesorectal excision.
Purpose:
To evaluate the prognostic factors associated with local recurrence in patients with rectal cancer submitted to neoadjuvant chemoradiotherapy and total mesorectal excision.
Methods:
Retrospective study including patients with rectal cancer T3–4N0M0 or T (any)N + M0 located within 10 cm from the anal border, or patients with T2N0M0 located within 5 cm, treated by long course chemoradio-therapy followed by total mesorectal excision with curative intent. Clinical, demographic, radiologic, surgical, and anatomopathological data were collected. Local recurrence was estimated using the Kaplan-Meier function, and risk was estimated according to each characteristic using univariate and multivariate analyses.
Results:
270 patients were included, 57.8% male and mean age 61.7 (30‒88) years. At initial staging, 6.7% of patients were stage I, 21.5% stage II, and 71.8% stage III. Open surgery was performed in 65.2%, with sphincter preservation in 78.1%. Mortality within 30 postoperative days was 0.7%. After 49.4 (0.5‒86.1) months of median follow-up, overall and local recurrences were 26.3% and 5.9%. On multivariate analyses, local recurrence was associated with involvement of the mesorectal fascia on restaging MRI (HR = 9.11, p = 0.001) and with pathologic involvement of radial surgical margin (HR = 8.19, p < 0.001).
Conclusion:
Local recurrence of rectal cancer treated with long-course chemoradiation and total mesorectal excision is low and is associated with pathologic involvement of the radial surgical margin and can be predicted on restaging MRI.
Keywords:
Rectal cancer; Chemoradiotherapy; Neoadjuvant therapy; Total mesorectal excision; Prognosis; Survival
HIGHLIGHTS
Rectal cancer recurrence occurs predominantly in distant organs.
Local recurrence of rectal cancer could be predicted on restaging MRI.
Rectal cancer recurrence of patients treated with long course chemoradiation and total mesorectal excision is low and is associated with pathologic involvement of the radial surgical margin.
Background
Since the introduction of a multidisciplinary approach for the treatment of primary locally advanced middle and lower rectal cancer based on improvement in radiological imaging, Chemoradiation Therapy (CRT), and Total Mesorectal Excision (TME), a significant improvement has been accomplished on oncologic outcomes.11 Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2018;68(6):394–424., 22 Glynne-Jones R, Wyrwicz L, Tiret E, Brown G, Rödel C, Cervantes A, et al. Rectal cancer: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol 2017;28(suppl_4):iv22–40. However, 2.4%‒10% of patients will develop local failure.33 Taylor FG, Quirke P, Heald RJ, Moran B, Blomqvist L, Swift I, et al. MERCURY study group. Preoperative high-resolution magnetic resonance imaging can identify good prognosis stage I, II, and III rectal cancer best managed by surgery alone: a prospective, multicenter, European study. Ann Surg. 2011;253(4):711–9., 44 Smith NJ, Shihab O, Arnaout A, Swift RI, Brown G. MRI for detection of extramural vascular invasion in rectal cancer. AJR Am J Roentgenol 2008;191(5):1517–22., 55 Patel UB, Taylor F, Blomqvist L, George C, Evans H, Tekkis P, et al. Magnetic resonance imaging-detected tumor response for locally advanced rectal cancer predicts survival outcomes: MERCURY experience. J Clin Oncol 2011;29(28):3753–60., 66 Chandramohan A, Siddiqi UM, Mittal R, Eapen A, Jesudason MR, Ram TS, et al. Diffusion weighted imaging improves diagnostic ability of MRI for determining complete response to neoadjuvant therapy in locally advanced rectal cancer. Eur J Radiol Open 2020;7:100223., 77 Beets-Tan RG, Beets GL. MRI for assessing and predicting response to neoadjuvant treatment in rectal cancer. Nat Rev Gastroenterol Hepatol 2014;11(8):480–8.
Rectal cancer prognoses can be particularly affected by other factors beyond AJCC TNM stage,88 Amin MB, Greene FL, Edge SB, Compton CC, Gershenwald JE, Brookland RK, et al. The eighth edition AJCC cancer staging manual: continuing to build a bridge from a population-based to a more “personalized” approach to cancer staging. CA Cancer J Clin 2017;67(2):93–9., 99 Weiser MR. AJCC. p 1454, 8th Edition Colorectal Cancer, 25. Ann Surg Oncol; 2018. p. 1454–5. such as tumor response to neoadjuvant treatment, involvement of Circumferential Resection Margin (CRM), involvement of the intersphincteric plane, presence of Extramural
Venous Invasion (EMVI), lateral pelvic lymph nodes, and presence of mucinous component.1010 Bailey CE, Hu CY, You YN, Bednarski BK, Rodriguez-Bigas MA, Skibber JM, et al. Increasing disparities in the age-related incidences of colon and rectal cancers in the United States, 1975-2010. JAMA Surg 2015;150(1):17–22., 1111 Quirke P, Steele R, Monson J, Grieve R, Khanna S, Couture J, et al. MRC CR07/NCICCTG CO16 trial investigators; NCRI colorectal cancer study group. Effect of the plane of surgery achieved on local recurrence in patients with operable rectal cancer: a prospective study using data from the MRC CR07 and NCIC-CTG CO16 randomised clinical trial. Lancet 2009;373(9666):821–8., 1212 Guillem JG, Chessin DB, Shia J, Suriawinata A, Riedel E, Moore HG, et al. A prospective pathologic analysis using whole-mount sections of rectal cancer following preoperative combined modality therapy: implications for sphincter preservation. Ann Surg 2007;245(1):88–93. In particular, a positive CRM is associated with increased risk for Local Recurrence (LR) (5-year local recurrence: HR = 3.50; p < 0.05;1212 Guillem JG, Chessin DB, Shia J, Suriawinata A, Riedel E, Moore HG, et al. A prospective pathologic analysis using whole-mount sections of rectal cancer following preoperative combined modality therapy: implications for sphincter preservation. Ann Surg 2007;245(1):88–93., 1313 Kapiteijn E, Marijnen CA, Nagtegaal ID, Putter H, Steup WH, Wiggers T, et al. Dutch colorectal cancer group. Preoperative radiotherapy combined with total mesorectal excision for resectable rectal cancer. N Engl J Med 2001;345(9):638–46., 1414 Weiser MR, Quah HM, Shia J, Guillem JG, Paty PB, Temple LK, et al. Sphincter preservation in low rectal cancer is facilitated by preoperative chemoradiation and inter-sphincteric dissection. Ann Surg 2009;249(2):236–42. CRM involvement increases the likelihood of LR after (TME) by more than 4-times.1515 Sauer R, Becker H, Hohenberger W, Rodel C, Wittekind C, Fietkau R, et al. German rectal cancer study group. Preoperative versus postoperative chemoradiotherapy for rectal cancer. N Engl J Med 2004;351(17):1731–40. Therefore, TME should typically be performed as a part of a low anterior resection or Abdomino-perineal Resection (APR). A 2-cm distal mural margin is usually adequate for distal rectal cancers when combined with TME. For tumors located at or below the mesorectal margin, a 1 cm distal mural margin can be acceptable only for those who have achieved a good response to CRT.1616 Guillem JG, Chessin DB, Shia J, Suriawinata A, Riedel E, Moore HG, et al. A prospective pathologic analysis using whole-mount sections of rectal cancer following preoperative combined modality therapy: implications for sphincter preservation. Ann Surg 2007;245(1):88–93.
Despite all these concerns, high-volume centers still present some local failures even after specialized multidisciplinary care. The aim of this study is to identify the prognostic factors associated with local recurrence in patients with rectal cancer submitted to neoadjuvant chemora-diotherapy and total mesorectal excision in a single institution.
Methods
This retrospective study was approved by the Institutional Board Review of the studied institution (9,076,078). It included consecutive patients with a biopsy-proven rectal adenocarcinoma located within 10 cm from the anal verge, stage T3–4N0M0 or T(any)N + M0, and patients with T2N0 of the distal rectum (0‒5 cm from the anal verge, because of the risk of needing an APR) from a prospectively collected database of the studied institution where a randomized trial was set to assess non-inferiority of the non-operative management compared to immediate surgical resection with TME in patients with Clinical Complete Response (cCR) after neoadjuvant CRT (NCT02052921)1717 Nahas SC, Nahas CS, Marques CF, Ribeiro Jr U, Cotti GC, Imperiale AR, et al. Pathologic complete response in rectal cancer: can we detect it? Lessons learned from a proposed randomized trial of watch-and-wait treatment of rectal cancer. Dis Colon Rectum 2016;59(4):255–63. from October 2011 to November 2015. Clinical complete response was defined as an absence of tumor simultaneously on three exams: digital rectal examination, colonoscopy and high-resolution MRI. Non-operative management was offered only for cCR patients. Nearly complete responders were not eligible for non-operative management. Patients with synchronous colorectal cancer or other non-colorectal cancers, rectal cancer in the setting of inflammatory bowel disease or familial adenomatous polyposis, significant delay (> 8 weeks after restaging) on performing surgery, palliative resections and patients with previous chemotherapy or radiotherapy were excluded. Patients with cCR randomized for nonoperative management were also excluded.
Patients with cCR randomized for operative management were operated in the same manner as patients who did not achieve cCR.
A total of 309 consecutive patients with primary rectal adenocarcinoma without metastatic disease were treated at the studied institution. Data from 39 patients were excluded for the following reasons: 16 for significant delays in performing surgery, 15 for interruption of CRT related to toxicity, four for being selected for non-operative treatment according to another study at the institution (NCT02052921),1717 Nahas SC, Nahas CS, Marques CF, Ribeiro Jr U, Cotti GC, Imperiale AR, et al. Pathologic complete response in rectal cancer: can we detect it? Lessons learned from a proposed randomized trial of watch-and-wait treatment of rectal cancer. Dis Colon Rectum 2016;59(4):255–63. three due to lack of preoperative MRI, and one case due to the palliative nature of the surgery due to a change in disease staging intraoperatively (Fig. 1).
Patients were staged and re-staged by the same colorectal surgeon and clinical oncologist by digital exam, colonoscopy, pelvic high-definition MRI, thorax and abdominal CT scans. The total dose of pelvic radiation was 5040 Gy given in 30 sessions (180 Gy/day, only on weekdays, along 5.6 weeks) All patients received 5-FU based chemotherapy with leucovorin by IV bolus on days 1 to 5, concomitant with radiation in weeks 1 and 5. Re-stage occurred 8 weeks after completion of CRT. Staging and restaging high-resolution MRI and CT scans were evaluated by only two radiologists who were specifically dedicated to this task. The radiologist who has seen the staging exam also reviewed the restaging exam not blinded to the pretreatment stage.
The MRI Tumor Response Grade (TRG) was adopted as described elsewhere.33 Taylor FG, Quirke P, Heald RJ, Moran B, Blomqvist L, Swift I, et al. MERCURY study group. Preoperative high-resolution magnetic resonance imaging can identify good prognosis stage I, II, and III rectal cancer best managed by surgery alone: a prospective, multicenter, European study. Ann Surg. 2011;253(4):711–9. Clinical suspicion of lateral pelvic sidewall node was primarily based on lymph node size (short axis > 0.7 cm for internal iliac or obturatory node on staging MRI, short axis > 0.6 and > 0.4 respectively for obturator and internal iliac nodes on restaging MRI).
All patients who did not achieve a cCR were submitted to TME. Surgeries were performed two weeks after restaging. All surgical procedures were performed at the studied institution by one of four surgeons who had previous training in rectal cancer surgery. All patients underwent curative or potentially curative TME, with high ligation of the inferior mesenteric artery. Resection of adjacent organs was performed en bloc with the rectum when firm adhesions or macroscopic tumor invasion were present. The decision to perform an APR was based on oncological factors (risk of involvement of distal margin), and/or sphincter invasion. All surgical specimens were staged according to the American Joint Committee on Cancer guidelines. After surgery, all patients were assessed by digital exam, proctoscopy, and CEA level, every 3 months in the first three years, and every 6 months in the 4th and 5th years thereafter. Pelvic high-definition MRI, and CT scans of thorax and abdomen were performed every 4 months in the first year, and then every 6 months. A colonoscopy was performed once a year.
The following data were collected:
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a) Gender, age, body mass index.
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b) Staging MRI characteristics: T stage (mri T2 vs. mri T3/4), N stage (mriN- vs. mriN+), MF, mucinous component, EMVI, intersphincteric plane, lateral pelvic lymph nodes, and TRG (good response TRG 1‒3 vs. poor response TRG 4, 5).
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c) Surgical data: surgical access (open versus laparoscopic), sphincter preservation, en bloc resection of adjacent organs.
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d) Surgical specimen characteristics: T-stage, N stage, lymphovascular invasion, perineural invasion, pathologic response (complete vs. incomplete), lymph node yield (< 12 vs. ≥ 12), involvement of distal and/or circumferential margin, mesorectum integrity (complete/nearly complete vs. incomplete).
By reviewing the electronic medical record, it was assessed whether there was local or systemic tumor recurrence, with a specific description of the affected site or organ. The starting point for the analyses of survival and recurrence was the day of surgery. The diagnosis of recurrence was confirmed according to the presence of radiological findings and/or clinical evolution and/or elevation of tumor markers, or through histological confirmation (biopsy or surgical resection). LR was defined as any type of recurrence (tumor, lymph node, peritoneal implant) at any pelvic site, whether in the anastomosis, perineum, perirectal tissues, genitourinary tract (bladder, prostate, seminal vesicle, ureter, vaginal wall), pre-sacral region, sacrum, coccyx, lateral pelvic walls, obturator or internal iliac lateral pelvic lymph nodes.
Statistical analysis
The qualitative characteristics evaluated in all patients were described using absolute and relative frequencies.
The LR was evaluated using the Kaplan-Meier function and compared the time according to the characteristics of interest using log-rank tests. The risks of recurrence were estimated according to each characteristic evaluated using a bivariate Cox regression with the respective 95% Confidence Intervals Multiple Cox regression was performed including the variables that had a lower descriptive level than 0.10 (p < 0.10) in the bivariate tests, keeping in the final model only the jointly significant variables, using the stepwise backward method with entry and exit criteria at 5%.
The software IBM-SPSS for Windows version 20.0 was used to carry out the analyzes and the software Microsoft Excel 2003 was used to tabulate the data. The tests were performed with a significance level of 5%.
Results
Of the 270 patients included in the study, 156 (57.8%) were male and the mean age was 61.7 (30‒88) years. As for initial staging, 18 (6.7%) patients were stage I (T2N0), 58 (21.5%) were stage II, and 194 (71.8%) were stage III. Most surgeries were performed via open access 176 (65.2%), sphincter was preserved in 211 (78.1%) cases, and en bloc resection of adjacent organs was necessary in 34 (12.6%) patients (eight cases of partial resection of the vagina, seven of the uterus, seven of the seminal vesicles, five of the uterus combined with the vagina, four of the prostate associated with the bladder, and three of the uterus associated with the ureter).
The involvement of surgical margins in the anatomopathological evaluation of the specimens occurred in 14 (5.2%) cases (13 cases radial, one case of radial and distal involvement; therefore, were all included as “radial margin involvement” in the statistical analysis). The average number of LN yield was 22.9.
Lateral pelvic lymph node dissection was performed in 18 cases and positive involvement was confirmed in the anatomopathological evaluation in 5 of them.
Detailed clinical and radiological characteristics are presented in Table 1, while the characteristics of the surgical procedures and the anatomopathological evaluation of the surgical specimens are described in Table 2.
Characteristics of surgical procedures and anatomopathological evaluation of surgical specimens of the 270 patients.
After a median follow-up time of 49.4 (0.5‒86.1) months, there were 65 (24.1%) deaths, 35 (13%) due to the disease and 30 (11.1%) due to other causes.
A total of 71 (26.3%) patients had general recurrence (local and/or systemic), 16 (5.9%) cases of LR, and 59 (21.9%) cases of systemic relapse (four patients had LR and systemic).
LR occurred in the anterior pelvic compartment in five cases (four in the vagina and one in the prostate/bladder), in the anastomotic or perianastomotic region in four cases, in the lateral compartments in four cases (internal iliac lymph node chain) and in the posterior region (pre sacral) in three cases.
On univariate analyses, stage ymriT3/4, ymriEMVI+, ymriMF+, non-preservation of the sphincter, presence of perineural invasion and involvement radial margin (p < 0.05) were associated with local recurrence (Tables 3 and 4). However, on multivariate analyses, only ymriMF + and involvement of the radial margin in the surgical specimen were associated with local recurrence (Table 5).
Univariate analysis for local recurrence according to demographic and radiological characteristics.
Univariate analysis for local recurrence according to surgical and specimen characteristics.
The 59 patients with systemic recurrence occurred in the following sites: exclusively pulmonary in 31 cases, exclusively hepatic in 16, exclusively cerebral in two, exclusively peritoneal in two, exclusively mediastinal in one, and combined (more than one site) in seven cases (hepatic + lung in four cases, bone + lung in one case, lung + brain in one case, and liver + brain in one case). In total, the most affected sites were the lungs (37 cases/62.7%) and liver (21 cases/35.6%). The mean overall DFS estimate was 65.8 months (95% CI 61.9-69.8 months).
Surgical-related mortality occurred in 4 (1.5%) patients: two cases due to colorectal anastomosis leakage (despite protective ileostomy) evolving with secondary complications and death on the 27th PO day and 36th PO day, respectively; one case of acute myocardial infarction on the 1st PO day, progressing to renal failure and death after 63 days of hospitalization; and one case of urinary anastomosis fistula associated with abdominal wound complications in a patient submitted to TME and en bloc prostatectomy that evolved to death on the 44th PO day.
Discussion
This study demonstrated that the oncological results obtained at the studied institution were adequate, with emphasis on the low LR rate (5.9%) compatible with what is reported in the literature (2.4%‒10%).33 Taylor FG, Quirke P, Heald RJ, Moran B, Blomqvist L, Swift I, et al. MERCURY study group. Preoperative high-resolution magnetic resonance imaging can identify good prognosis stage I, II, and III rectal cancer best managed by surgery alone: a prospective, multicenter, European study. Ann Surg. 2011;253(4):711–9., 44 Smith NJ, Shihab O, Arnaout A, Swift RI, Brown G. MRI for detection of extramural vascular invasion in rectal cancer. AJR Am J Roentgenol 2008;191(5):1517–22., 55 Patel UB, Taylor F, Blomqvist L, George C, Evans H, Tekkis P, et al. Magnetic resonance imaging-detected tumor response for locally advanced rectal cancer predicts survival outcomes: MERCURY experience. J Clin Oncol 2011;29(28):3753–60., 66 Chandramohan A, Siddiqi UM, Mittal R, Eapen A, Jesudason MR, Ram TS, et al. Diffusion weighted imaging improves diagnostic ability of MRI for determining complete response to neoadjuvant therapy in locally advanced rectal cancer. Eur J Radiol Open 2020;7:100223., 77 Beets-Tan RG, Beets GL. MRI for assessing and predicting response to neoadjuvant treatment in rectal cancer. Nat Rev Gastroenterol Hepatol 2014;11(8):480–8. The relapse of patients in this study was predominantly systemic (21.9%), with the lungs (62.7%) and liver (35.6%) being the main sites affected, in line with the literature data.1818 Krdzalic J, Maas M, Gollub MJ, Beets-Tan RG. Guidelines for MR imaging in rectal cancer: Europe versus United States. Abdom Radiol (NY). 2019;44(1):3498–507., 1919 Lambregts DM, Boellaard TN. Beets-Tan RG. response evaluation after neoadjuvant treatment for rectal cancer using modern MR imaging: a pictorial review. Insights Imag 2019;10(1):15., 2020 Mandard AM, Dalibard F, Mandard JC, Marnay J, Henry-Amar M, Petiot JF, et al. Pathologic assessment of tumor regression after preoperative chemoradiotherapy of esophageal carcinoma. Clinicopathol Correl Cancer 1994;73(11):2680–6., 2121 Miller ED, Robb BW, Cummings OW, Johnstone PA. The effects of preoperative chemoradiotherapy on lymph node sampling in rectal cancer. Dis Colon Rectum 2012;55(9):1002–7.
As for local recurrences, it is worth remembering that 4 of the 16 cases (25%) occurred in the internal iliac lymph nodes, which cannot be attributed to inappropriate TME. Lateral pelvic lymphadenectomy is still a controversial subject, but it has been gaining strength in recent years.
Estimated Kaplan-Meier function of local recurrence probability according to surgical radial margin involvement.
While its routine performance is not recommended in the US, some Japanese centers have been performing it prophylactically to treat patients with lower rectal cancer without the use of radiotherapy.2222 Fujita S, Mizusawa J, Kanemitsu Y, Ito M, Kinugasa Y, Komori K, et al. Colorectal cancer study group of Japan clinical oncology group. Mesorectal excision with or without lateral lymph node dissection for clinical stage II/III lower rectal cancer (JCOG0212): a multicenter, randomized controlled, noninferiority trial. Ann Surg 2017;266(2):201–7. Although the feasibility of lateral lymphadenectomy after CRT in Western patients with higher BMI has been demonstrated recently, there are some concerns about its morbidity and doubts about its benefits.2323 Malakorn S, Ouchi A, Sammour T, Bednarski BK, Chang GJ. Robotic lateral pelvic lymph node dissection after neoadjuvant chemoradiation: view from the west. Dis Colon Rectum 2018;61(9):1119–20.
As for the staging of the patients in this series, it is noteworthy that most patients were advanced on admission (71.9% stage III), which still reflects the difficulty of early diagnosis and/or difficulty in obtaining a quick referral and specialized care for patients with rectal cancer in the Unified Health System of the studied country.
Regarding the evaluation of MRI characteristics in the staging and restaging of patients, it is noteworthy that the mriT and mriN stages were not associated with a worse prognosis for patients in the current study, in contrast to the five-year survival estimates according to the AJCC TNM classification.11 Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2018;68(6):394–424. A possible explanation could be the large disproportion in the number of patients with stages rmT3/4 (80.7%) and rmN+ (71.9%) in this sample.
As for the importance of evaluating MF by MRI, the MERCURY study clearly demonstrated worse 5-year survival in the group of patients with compromised MF (42.2% vs. 62.2%) and was the only prognostic factor proven to be associated with worse OS, DFS and LR in the multivariate analysis.2424 Battersby NJ, How P, Moran B, Stelzner S, West NP, Branagan G, et al. MERCURY II study group. Prospective validation of a low rectal cancer magnetic resonance imaging staging system and development of a local recurrence risk stratification model: the MERCURY II study. Ann Surg 2016;263(4):751–60., 2525 McGlone ER, Shah V, Lowdell C, Blunt D, Cohen P, Dawson PM. Circumferential resection margins of rectal tumours post-radiotherapy: how can MRI aid surgical planning? Tech Coloproctol 2014;18(10):937–43. In the present study, the authors also observed MF involvement as a predictor of LR.
Regarding the presence of EMVI on MRI, although the authors did not find a direct independent association with a worse prognosis in the studied sample, it has been identified as a relevant factor in the literature. In a study by Yu et al.,2626 Yu SK, Chand M, Tait DM, Brown G. Magnetic resonance imaging defined mucinous rectal carcinoma is an independent imaging biomarker for poor prognosis and poor response to preoperative chemoradiotherapy. Eur J Cancer 2014;50(5):920–7. 78% of patients who had evidence of EMVI on their staging MRI were significantly less likely to respond to neoadjuvant CRT (HR = 2.5). However, neoadjuvant CRT was able to change the EMVI status from positive to negative after CRT was shown to be associated with better 3-year DFS (88%) when compared to those who remained positive (46%, p < 0.0001). Smith et al.2727 Smith NJ, Shihab O, Arnaout A, Swift RI, Brown G. MRI for detection of extramural vascular invasion in rectal cancer. AJR Am J Roentgenol 2008;191(5):1517–22. demonstrated that the 3-year DFS was 35% for mriEMVI-positive patients compared to 74.1% for mriEMVI-negative patients.
Another important study by the MERCURY Group[5] demonstrated that involvement of the intersphincteric plane assessed by MRI, as well as positive CRM, extramural invasion greater than 5 mm, and the presence of EMVI were recognized as the worst risk factors for LR. It suggests that patients with stage T3 without these conditions regardless of the suspicion of lymph node disease in the MRI evaluation, can be surgically treated without neoadjuvant therapy. In the present study, all patients, even those without these risk factors, were treated with neoadjuvant CRT. However, in this series involvement of the intersphincteric plane both on MRI before and after CRT was not associated with a worse prognosis for recurrence.
Sphincter preservation was possible in 78% of these patients, although it was not an independent prognostic factor. In the literature, variable results regarding recurrence rates for APR have been reported. Data from the National Surgical Adjuvant Breast and Bowel Project (NSABP) R-01 revealed a 5% LR rate for patients undergoing an APR.2828 Ganz PA, Day R, Costantino J. Compliance with quality-of-life data collection in the national surgical adjuvant breast and bowel project (NSABP) breast cancer prevention trial. Stat Med 1998;17(5–7):613–22. A retrospective analysis of 14 studies identified positive CRM in 10% of APR samples compared to 5% of LAR samples.2929 Mohan HM, Evans MD, Larkin JO, Beynon J, Winter DC. Multivisceral resection in colorectal cancer: a systematic review. Ann Surg Oncol 2013;20(9):2929–36. Among these patients, LR rates were high (20% vs. 11%) and 5-year survival was worse (59% vs. 70%) in patients with APR compared to those with LAR. However, it is assumed that the tumors of patients undergoing APR tend to be lower and more locally advanced at the time of the operation. Over the past decade, the improvement of extrasphincteric APR has led to a reduction in the involvement of radial surgical margin and LR. A Dutch study with wider APR resections proved equivalent data of CRM involvement when compared to LAR in 190 patients.3030 Marr R, Birbeck K, Garvican J, Macklin CP, Tiffin NJ, Parsons WJ, et al. The modern abdominoperineal excision: the next challenge after total mesorectal excision. Ann Surg 2005;242(1):74–82.
Although it was necessary in only 12% of the cases, the combined en-bloc resection of other organs also did not confer a worse prognosis on the patients, despite presuming that these were cases of larger and more invasive tumors. However, it is known from the literature that the major oncological determinant of LR is obtaining an R0 resection,3131 Nahas CS, Nahas SC, Ribeiro-Junior U, Bustamante-Lopez L, Marques CFS, Pinto RA et al. Prognostic factors affecting outcomes in multivisceral en bloc resection for colorectal cancer. Clinics 2017;72(5):258–64., 3232 Mañas MJ, Espín E, López-Cano M, Vallribera F, Armengol-Carrasco M. Multivisceral resection for locally advanced rectal cancer: prognostic factors influencing outcome. Scand J Surg 2015;104(3):154–60. which was possible in 82.3% of these cases of multivisceral en-bloc resection.
The present study has some limitations. The first is its retrospective nature, with no review of MRI imaging reports or anatomopathological evaluation of surgical specimens. Another aspect previously discussed was the non-uniformity in the indication of lateral pelvic lymphadenectomy, although the oncological benefits of this procedure are still under debate in the literature. Finally, the authors know that several tissue or serum molecular biomarkers, such as research on circulating tumor cells, research on specific gene expression profiles, expression of proteins such as the epidermal growth factor receptor and vascular endothelial growth factor, research on mutations and DNA mutilations, among others, have been widely studied in terms of their ability to predict prognosis and response to chemoradiotherapy treatment, although they were not considered in the current study due to the limited availability in this service.
Conclusions
Local recurrence of rectal cancer treated with long-course chemoradiation and total mesorectal excision is low and is associated with pathologic involvement of the radial surgical margin and can be predicted on restaging MRI.
References
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1Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2018;68(6):394–424.
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2Glynne-Jones R, Wyrwicz L, Tiret E, Brown G, Rödel C, Cervantes A, et al. Rectal cancer: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol 2017;28(suppl_4):iv22–40.
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3Taylor FG, Quirke P, Heald RJ, Moran B, Blomqvist L, Swift I, et al. MERCURY study group. Preoperative high-resolution magnetic resonance imaging can identify good prognosis stage I, II, and III rectal cancer best managed by surgery alone: a prospective, multicenter, European study. Ann Surg. 2011;253(4):711–9.
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4Smith NJ, Shihab O, Arnaout A, Swift RI, Brown G. MRI for detection of extramural vascular invasion in rectal cancer. AJR Am J Roentgenol 2008;191(5):1517–22.
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5Patel UB, Taylor F, Blomqvist L, George C, Evans H, Tekkis P, et al. Magnetic resonance imaging-detected tumor response for locally advanced rectal cancer predicts survival outcomes: MERCURY experience. J Clin Oncol 2011;29(28):3753–60.
-
6Chandramohan A, Siddiqi UM, Mittal R, Eapen A, Jesudason MR, Ram TS, et al. Diffusion weighted imaging improves diagnostic ability of MRI for determining complete response to neoadjuvant therapy in locally advanced rectal cancer. Eur J Radiol Open 2020;7:100223.
-
7Beets-Tan RG, Beets GL. MRI for assessing and predicting response to neoadjuvant treatment in rectal cancer. Nat Rev Gastroenterol Hepatol 2014;11(8):480–8.
-
8Amin MB, Greene FL, Edge SB, Compton CC, Gershenwald JE, Brookland RK, et al. The eighth edition AJCC cancer staging manual: continuing to build a bridge from a population-based to a more “personalized” approach to cancer staging. CA Cancer J Clin 2017;67(2):93–9.
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9Weiser MR. AJCC. p 1454, 8th Edition Colorectal Cancer, 25. Ann Surg Oncol; 2018. p. 1454–5.
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10Bailey CE, Hu CY, You YN, Bednarski BK, Rodriguez-Bigas MA, Skibber JM, et al. Increasing disparities in the age-related incidences of colon and rectal cancers in the United States, 1975-2010. JAMA Surg 2015;150(1):17–22.
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11Quirke P, Steele R, Monson J, Grieve R, Khanna S, Couture J, et al. MRC CR07/NCICCTG CO16 trial investigators; NCRI colorectal cancer study group. Effect of the plane of surgery achieved on local recurrence in patients with operable rectal cancer: a prospective study using data from the MRC CR07 and NCIC-CTG CO16 randomised clinical trial. Lancet 2009;373(9666):821–8.
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Publication Dates
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Publication in this collection
16 Sept 2024 -
Date of issue
2024
History
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Received
21 Apr 2024 -
Reviewed
13 June 2024 -
Accepted
14 July 2024