TY - JOUR
T1 - Sex differences in chemotherapy completion, toxicities, and survival in colon cancer
T2 - An analysis of 2201 patients from CALGB/SWOG 80702 (Alliance)
AU - Cheng, En
AU - Shi, Qian
AU - Shields, Anthony F.
AU - Xue, Xiaonan
AU - Rohan, Thomas E.
AU - Kuang, Chaoyuan
AU - Shergill, Ardaman P.
AU - Ma, Chao
AU - Couture, Felix
AU - Kuebler, J. Philip
AU - Kumar, Pankaj
AU - Tan, Benjamin
AU - Krishnamurthi, Smitha S.
AU - Ng, Kimmie
AU - O'Reilly, Eileen M.
AU - Brown, Justin C.
AU - Meyerhardt, Jeffrey A.
N1 - Publisher Copyright:
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PY - 2025/12/1
Y1 - 2025/12/1
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/105024095805
U2 - 10.1093/jnci/djaf281
DO - 10.1093/jnci/djaf281
M3 - Article
C2 - 40996326
AN - SCOPUS:105024095805
SN - 0027-8874
VL - 117
SP - 2643
EP - 2652
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
IS - 12
ER -