Neoadjuvant chemoradiation does not improve outcomes for patients undergoing resection for upper rectal cancer: A US Rectal Cancer Consortium analysis.

Authors

null

Caroline Medin

Emory University, Atlanta, GA;

Caroline Medin , Adriana C. Gamboa , Emilie Warren , Scott E. Regenbogen , Samantha Hendren , Jennifer Holder-Murray , Matthew Kalady , Aslam Ejaz , Alexander Hawkins , Matthew Silviera , Shishir K. Maithel , Glen C. Balch

Organizations

Emory University, Atlanta, GA; , University of Michigan, Ann Arbor, MI; , Division of Colon and Rectal Surgery, Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA; , Ohio State University Wexner Medical Center, Columbus, OH; , The Ohio State University Wexner Medical Center, Columbus, OH; , Vanderbilt Univ. Medical Center, Nashville, TN; , Section of Colon & Rectal Surgery, Department of Surgery, Washington University School of Medicine, St. Louis, MO; , Winship Cancer Institue, Emory University, Atlanta, GA; , Division of Colon & Rectal Surgery, Department of Surgery, Emory University, Atlanta, GA;

Research Funding

Other
Katz Foundation

Background: The use of neoadjuvant chemoradiation (NCRT) for upper rectal cancer remains controversial. Our aim was to determine whether NCRT was associated with improved outcomes. Methods: The US Rectal Cancer Consortium was queried for patients who underwent resection of non-metastatic upper rectal cancer (≥12cm from anal verge) from 2007-2017. Primary outcomes were recurrence-free (RFS) and overall survival (OS). Secondary outcomes were postoperative complications. Results: 193 pts met inclusion criteria; 100 (52%) did not receive NCRT and 93 (48%) did. Median age was similar between groups (non-NCRT: 62 yrs; NCRT: 57 yrs; p=0.71). Patients in each group had similar gender and pathological stage (non-NCRT: 22% stage I, 32% stage II, 36% stage III; NCRT: 21% stage I, 23% stage II, 33% stage III; p=0.143). Median follow-up was 31 months (non-NCRT) and 34 months (NCRT). On Kaplan-Meier analysis, NCRT was not associated with improved RFS compared to non-NCRT (3-year RFS 85% vs. 80%; p=0.34) or OS (3-year OS 88% vs. 90%; p=0.49). This finding persisted on multivariable cox regression. R0 resection rate was similar between groups at 99% (non-NCRT) and 97% (NCRT; p=0.27). Anastomotic leak occurred in 11% of both cohorts. Creation of a diverting loop ileostomy (DLI) was nearly 3 times higher in NCRT (82%) versus non-NCRT patients (29%; p<0.001). Conclusions: Among patients with non-metastatic upper rectal cancer, NCRT did not improve survival or recurrence rates, but was associated with a nearly threefold higher DLI rate. Although NCRT is a mainstay of treatment for lower rectal cancer, our results do not support its use in upper rectal cancer.

Multivariable cox regression: recurrence-free and overall survival.

UnivariateMultivariable
Recurrence-Free Survivalp-valueHR (95% CI)p-valueHR (95% CI)
Neoadjuvant Chemoradiation (ref: none)
Given0.370.73 (0.36, 1.46)0.5050.74 (0.31, 1.77)
Margin Status (ref: R0)
R1 or R20.0049.38 (2.08, 42.27)0.00212.56 (2.44, 64.66)
Functional Status (ref: independent)
Dependent0.00112.06 (2.73, 53.27)0.00113.51 (2.76, 66.17)
Lymphovascular Invasion (ref: absent)
Present0.0232.46 (1.13, 5.34)0.0342.5 (1.07, 5.81)
UnivariateMultivariable
Overall Survivalp-valueHR (95% CI)p-valueHR (95% CI)
Neoadjuvant Chemoradiation (ref: none)
Given0.4951.3 (0.61, 2.78)0.4211.4 (0.6, 3.1)
Margin Status (ref: R0)
R1 or R2<.00114.7 (3.1, 69.8)0.0296 (1.2, 30.1)
pN Stage (ref: N0)
N10.0382.5 (1.1, 6.1)0.0512.5 (1, 6.2)
N20.0193.43 (1.2, 9.6)0.0383.1 (1.1, 9.1)
Gender (ref: female)
Male0.0123.9 (1.3, 11.3)0.0253.5 (1.2, 10.2)

HR: hazard ratio; CI: confidence interval.

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Abstract Details

Meeting

2023 ASCO Gastrointestinal Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session C: Cancers of the Colon, Rectum, and Anus

Track

Colorectal Cancer,Anal Cancer

Sub Track

Therapeutics

Citation

J Clin Oncol 41, 2023 (suppl 4; abstr 143)

DOI

10.1200/JCO.2023.41.4_suppl.143

Abstract #

143

Poster Bd #

H2

Abstract Disclosures

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