Literature DB >> 33537238

Role of Preoperative Chemoradiotherapy in Clinical Stage II/III Rectal Cancer Patients Undergoing Total Mesorectal Excision: A Retrospective Propensity Score Analysis.

Jii Bum Lee1, Han Sang Kim1, Ahrong Ham2, Jee Suk Chang3, Sang Jun Shin1, Seung-Hoon Beom1, Woong Sub Koom3, Taeil Kim4, Yoon Dae Han5, Dai Hoon Han5, Hyuk Hur5, Byung Soh Min5, Kang Young Lee5, Nam Kyu Kim5, Yu Rang Park6, Joon Seok Lim7, Joong Bae Ahn1.   

Abstract

BACKGROUND: Although the current standard preoperative chemoradiotherapy (PCRT) for stage II/III rectal cancer decreases the risk of local recurrence, it does not improve survival and increases the likelihood of preoperative overtreatment, especially in patients without circumferential resection margin (CRM) involvement.
METHODS: Stage II/III rectal cancer without CRM involvement and lateral lymph node metastasis was radiologically defined by preoperative magnetic resonance imaging (MRI). Patients who received PCRT followed by total mesorectal excision (TME) (PCRT group) and upfront surgery (US) with TME (US group) between 2010 and 2016 were analyzed. We derived cohorts of PCRT group versus US group using propensity-score matching for stage, age, and distance from the anal verge. Three-year relapse-free survival rate, disease-free survival (DFS), and overall survival (OS) were compared between the two groups.
RESULTS: A total of 202 patients were analyzed after propensity score matching. There were no differences in baseline characteristics. The median follow-up duration was 62 months (interquartile range, 46-87). There was no difference in the 3-year disease-free survival rate between the PCRT and US groups (83 vs. 88%, respectively; p=0.326). Likewise, there was no significant difference in the 3-year OS (89 vs. 91%, respectively; p=0.466). The 3-year locoregional recurrence rates (3 vs. 2% with US, p=0.667) and distant metastasis rates (16 vs. 11%, p=0.428) were not significantly different between the two groups. Time to completion of curative treatment was significantly shorter in the US group (132 days) than in the PCRT group (225 days) (p<0.001).
CONCLUSION: Using MRI-guided selection for better risk stratification, US without neoadjuvant therapy can be considered in early stage patients with good prognosis. PCRT may not be required for all stage II/III rectal cancer patients, especially for the MRI-proven intermediate-risk group (cT1-2/N1, cT3N0) without CRM involvement and lateral lymph node metastasis. Further prospective studies are warranted.
Copyright © 2021 Lee, Kim, Ham, Chang, Shin, Beom, Koom, Kim, Han, Han, Hur, Min, Lee, Kim, Park, Lim and Ahn.

Entities:  

Keywords:  chemoradiotherapy; rectal cancer; stage II/III; total mesorectal excision; upfront surgery

Year:  2021        PMID: 33537238      PMCID: PMC7848147          DOI: 10.3389/fonc.2020.609313

Source DB:  PubMed          Journal:  Front Oncol        ISSN: 2234-943X            Impact factor:   6.244


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4.  Perfusion MRI for the prediction of treatment response after preoperative chemoradiotherapy in locally advanced rectal cancer.

Authors:  Joon Seok Lim; Daehong Kim; Song-Ee Baek; Sungmin Myoung; Junjeong Choi; Sang Joon Shin; Myeong-Jin Kim; Nam Kyu Kim; Jinsuk Suh; Ki Whang Kim; Ki Chang Keum
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Journal:  J Natl Compr Canc Netw       Date:  2018-07       Impact factor: 11.908

Review 8.  The multidisciplinary management of rectal cancer.

Authors:  Deborah S Keller; Mariana Berho; Rodrigo O Perez; Steven D Wexner; Manish Chand
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2020-03-12       Impact factor: 46.802

9.  Long-term outcomes of surgery alone versus surgery following preoperative chemoradiotherapy for early T3 rectal cancer: A propensity score analysis.

Authors:  Seung Hyun Cho; Gyu-Seog Choi; Gab Chul Kim; An Na Seo; Hye Jung Kim; Won Hwa Kim; Kyung-Min Shin; So Mi Lee; Hunkyu Ryeom; See Hyung Kim
Journal:  Medicine (Baltimore)       Date:  2017-03       Impact factor: 1.889

10.  Upfront radical surgery with total mesorectal excision followed by adjuvant FOLFOX chemotherapy for locally advanced rectal cancer (TME-FOLFOX): an open-label, multicenter, phase II randomized controlled trial.

Authors:  Jii Bum Lee; Han Sang Kim; Inkyung Jung; Sang Joon Shin; Seung Hoon Beom; Jee Suk Chang; Woong Sub Koom; Tae Il Kim; Hyuk Hur; Byung Soh Min; Nam Kyu Kim; Sohee Park; Seung-Yong Jeong; Jeong-Heum Baek; Seon Hahn Kim; Joon Seok Lim; Kang Young Lee; Joong Bae Ahn
Journal:  Trials       Date:  2020-04-07       Impact factor: 2.279

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Review 1.  Surgical Treatment of Low-Lying Rectal Cancer: Updates.

Authors:  Cristopher Varela; Nam Kyu Kim
Journal:  Ann Coloproctol       Date:  2021-12-22
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