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Can we eliminate neoadjuvant chemoradiotherapy in favor of neoadjuvant multiagent chemotherapy for select stage II/III rectal adenocarcinomas: Analysis of the National Cancer Data base.

作者信息

Cassidy Richard J, Liu Yuan, Patel Kirtesh, Zhong Jim, Steuer Conor E, Kooby David A, Russell Maria C, Gillespie Theresa W, Landry Jerome C

机构信息

Department of Radiation Oncology, Rollins School of Public Health, Emory University, Atlanta, Georgia.

Winship Cancer Institute, Emory University, Atlanta, Georgia.

出版信息

Cancer. 2017 Mar 1;123(5):783-793. doi: 10.1002/cncr.30410. Epub 2016 Oct 25.


DOI:10.1002/cncr.30410
PMID:27780316
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5319877/
Abstract

BACKGROUND: Stage II and III rectal cancers have been effectively treated with neoadjuvant chemoradiotherapy (NCRT) followed by definitive resection. Advancements in surgical technique and systemic therapy have prompted investigation of neoadjuvant multiagent chemotherapy (NMAC) regimens with the elimination of radiation (RT). The objective of the current study was to investigate factors that predict for the use of NCRT versus NMAC and compare outcomes using the National Cancer Data Base (NCDB) for select stage II and III rectal cancers. METHODS: In the NCDB, 21,707 patients from 2004 through 2012 with clinical T2N1 (cT2N1), cT3N0, or cT3N1 rectal cancers were identified who had received NCRT or NMAC followed by low anterior resection. Kaplan-Meier analyses, log-rank tests, and Cox-proportional hazards regression analyses were conducted along with propensity score matching analysis to reduce treatment selection bias. RESULTS: The 5-year actuarial overall survival (OS) rate was 75% for patients who received NCRT versus 67.2% for those who received NMAC (P < .01). On MVA, those who received NCRT had improved OS (hazard ratio, 0.77. P < .01), and this effect was confirmed on propensity score matching analysis (hazard ratio, 0.72; P = .01). In the same model, the following variables improved OS: age < 65 years, having private insurance, treatment at an academic center, living in an affluent zip code, a low comorbidity score, receipt of adjuvant chemotherapy, and a shorter interval before surgery (all P < .05). African Americans, men, patients with high-grade tumors, those with cT3N1 tumors, and those who underwent incomplete (R1) resection had worse OS (all P < .05). CONCLUSIONS: In this series, the elimination of neoadjuvant RT for select patients with stage II and III rectal adenocarcinoma was associated with worse OS and should not be recommended outside of a clinical trial. Cancer 2017;123:783-93. © 2016 American Cancer Society.

摘要

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引用本文的文献

[1]
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Radiat Oncol J. 2021-12

[2]
Efficacy and Feasibility of Adding Induction Chemotherapy to Neoadjuvant Chemoradiation in Locally Advanced Rectal Cancer: A Phase II Clinical Trial.

Ann Coloproctol. 2019-10

[3]
A Concise Review of Pelvic Radiation Therapy (RT) for Rectal Cancer with Synchronous Liver Metastases.

Int J Surg Oncol. 2019-4-21

[4]
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J Cancer. 2018-10-21

[5]
Correlation Between Tumor Vasculogenic Mimicry and Poor Prognosis of Human Digestive Cancer Patients: A Systematic Review and Meta-Analysis.

Pathol Oncol Res. 2018-10-25

[6]
The high pCR rate of sandwich neoadjuvant treatment in locally advanced rectal cancer may translate into a better long-term survival benefit: 5-year outcome of a Phase II clinical trial.

Cancer Manag Res. 2018-10-10

[7]
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[8]
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Ann Gastroenterol Surg. 2018-2-15

[9]
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Oncotarget. 2018-4-27

[10]
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Radiat Oncol. 2018-3-27

本文引用的文献

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Lancet Oncol. 2012-5-23

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Preoperative versus postoperative chemoradiotherapy for locally advanced rectal cancer: results of the German CAO/ARO/AIO-94 randomized phase III trial after a median follow-up of 11 years.

J Clin Oncol. 2012-4-23

[9]
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J Clin Oncol. 2010-10-12

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Ann Surg Oncol. 2010-6

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