Sex differences in chemotherapy completion, toxicities, and survival in colon cancer: An analysis of 2201 patients from CALGB/SWOG 80702 (Alliance)

  • En Cheng
  • , Qian Shi
  • , Anthony F. Shields
  • , Xiaonan Xue
  • , Thomas E. Rohan
  • , Chaoyuan Kuang
  • , Ardaman P. Shergill
  • , Chao Ma
  • , Felix Couture
  • , J. Philip Kuebler
  • , Pankaj Kumar
  • , Benjamin Tan
  • , Smitha S. Krishnamurthi
  • , Kimmie Ng
  • , Eileen M. O'Reilly
  • , Justin C. Brown
  • , Jeffrey A. Meyerhardt

Research output: Contribution to journalArticlepeer-review

Abstract

Background Completing adjuvant chemotherapy and reducing toxicities are critical for maximizing survival after a colon cancer diagnosis. Sex, as a biological variable, may affect colon cancer chemotherapy completion, toxicities, and survival differently. Methods From a National Cancer Institute-sponsored trial conducted among patients with stage III colon cancer (Cancer and Leukemia Group B (Alliance)/Southwest Oncology Group 80702), we included 2201 patients receiving the standard adjuvant chemotherapy regimen of fluorouracil, leucovorin, and oxaliplatin. We calculated relative dose intensity to indicate chemotherapy completion and considered reduced relative dose intensity (values <85%) as a clinically significant deviation from standard fluorouracil, leucovorin, and oxaliplatin. Using National Cancer Institute's Common Terminology Criteria for Adverse Events, we defined severe adverse events (grade ≥3) as the occurrence of any following event, including neutrophil count decrease, nausea, platelet count decrease, hypertension, peripheral neuropathy, diarrhea, fatigue, gastritis, creatinine level increase, gastric ulcer, myocardial ischemia, and cerebral ischemia. The primary survival outcome was disease-free survival (time from enrollment to colon cancer recurrence or death from any cause), and secondary survival outcomes were recurrence-free and overall survival. Results Compared with men, women were at statistically significantly higher risks of experiencing reduced relative dose intensity (adjusted odds ratio = 1.59, 95% CI = 1.29 to 1.96; P <. 001) and severe advance events (adjusted odds ratio = 1.72, 95% CI = 1.41 to 2.11; P <. 001). Yet, women had statistically significantly better disease-free survival (adjusted hazard ratio = 0.72, 95% CI = 0.59 to 0.87; P <. 001) as well as better recurrence-free and overall survival. Conclusions Our findings suggested that women with colon cancer are more likely to have worse chemotherapy completion rates and more severe adverse events, but they have better survival. Sex as a biological variable warrants further consideration in chemotherapy administration and survivorship management after colon cancer diagnosis.

Original languageEnglish
Pages (from-to)2643-2652
Number of pages10
JournalJournal of the National Cancer Institute
Volume117
Issue number12
DOIs
StatePublished - Dec 1 2025

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