Sex differences in chemotherapy completion and adverse events among patients with colon cancer (CALGB/SWOG 80702) (Alliance).

E En Cheng (Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, NY) Q Qian Shi A Anthony F. Shields (Karmanos Cancer Institute, Wayne State University, Detroit, MI) C Chaoyuan Kuang (Montefiore Einstein Comprehensive Cancer Center, Bronx, NY) A Ardaman Shergill (Alliance for Clinical Trials in Oncology, Chicago) C Chao Ma K Katherine A. Guthrie (Fred Hutchinson Cancer Center; and SWOG Statistics and Data Management Center, Seattle, WA) F Felix Couture J J. Phillip Kuebler (Columbus NCI Community Oncology Research Program, Columbus, OH) P Pankaj Kumar (Department of Chemistry) B Benjamin R. Tan (Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO) S Smitha S. Krishnamurthi (Cleveland Clinic, Cleveland, OH) K Kimmie Ng E Eileen M. O'Reilly (Memorial Sloan Kettering Cancer Center, New York City, NY) J Justin Brown P Philip A. Philip (Department of Oncology and Pharmacology, Wayne State University School of Medicine, Detroit, MI) J Jeffrey A. Meyerhardt

Abstract

3624 Background: Increasing chemotherapy completion and reducing chemotherapy adverse events (AE) are critical to improve survival after colon cancer diagnosis. Sex, as a biological variable, may impact chemotherapy treatment differently, and thus further investigation is needed to examine sex differences in chemotherapy completion and adverse events among patients with colon cancer. Methods: Among an NCI-sponsored trial conducted among patients with stage III colon cancer (CALGB/SWOG 80702), all patients received standard adjuvant chemotherapy FOLFOX (fluorouracil, leucovorin, and oxaliplatin). To signal chemotherapy completion, we utilized relative dose intensity (RDI) calculated as the ratio of the delivered dose intensity to planned dose intensity; and reduced RDI (RDI <85%) was considered as a clinically significant deviation from standard FOLFOX. From clinicians’ records of NCI’s Common Terminology Criteria for Adverse Events (CTCAE), we primarily focused on clinically significant AE such as neutrophils decrease, nausea, platelets decrease, hypertension, peripheral neuropathy, diarrhea, fatigue, gastritis, creatinine increase, gastric ulcer, myocardial ischemia, and cerebral ischemia; and severe AE was defined as the occurrence of any above AE with CTCAE grade ≥3. Using multivariable logistic regression that adjusted for body surface area (BSA) and other clinicopathological confounders, we estimated adjusted odds ratios (OR) for the associations of sex with reduced RDI and severe AE. Results: Of 2201 patients, mean (standard deviation [SD]) age was 60.9 (10.9) years, 1019 (46.3%) were female, 1750 (79.5%) were White, 172 (7.8%) were Hispanic, 964 (43.8%) experienced reduced RDI, and 1156 (52.5%) had severe adverse events. Compared to males, females were at significantly higher risks of experiencing reduced RDI (OR [95% CI]: 1.57 [1.27-1.93], P <0.001) and severe AE (OR [95% CI]: 1.73 [1.41-2.12], P <0.001). Conclusions: Our findings suggested females are more likely than men to experience reduced RDI and severe AE during colon cancer chemotherapy. Clinical Impact: In the era of precision medicine, sex (as a biological variable) should be considered in optimizing colon cancer chemotherapy to improve completion and reduce toxicities. Clinical trial information: NCT01150045 .

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 3624-3624
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (17)

E

En Cheng

Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, NY

Q

Qian Shi

A

Anthony F. Shields

Karmanos Cancer Institute, Wayne State University, Detroit, MI

C

Chaoyuan Kuang

Montefiore Einstein Comprehensive Cancer Center, Bronx, NY

A

Ardaman Shergill

Alliance for Clinical Trials in Oncology, Chicago

C

Chao Ma

K

Katherine A. Guthrie

Fred Hutchinson Cancer Center; and SWOG Statistics and Data Management Center, Seattle, WA

F

Felix Couture

J

J. Phillip Kuebler

Columbus NCI Community Oncology Research Program, Columbus, OH

P

Pankaj Kumar

Department of Chemistry

B

Benjamin R. Tan

Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO

S

Smitha S. Krishnamurthi

Cleveland Clinic, Cleveland, OH

K

Kimmie Ng

E

Eileen M. O'Reilly

Memorial Sloan Kettering Cancer Center, New York City, NY

J

Justin Brown

P

Philip A. Philip

Department of Oncology and Pharmacology, Wayne State University School of Medicine, Detroit, MI

J

Jeffrey A. Meyerhardt