Potential mediators of oxaliplatin-induced peripheral neuropathy from adjuvant therapy in stage III colon cancer: Findings from CALGB (Alliance)/SWOG 80702 Journal Article


Authors: Lee, S.; Ma, C.; Shi, Q.; Kumar, P.; Couture, F.; Kuebler, P.; Krishnamurthi, S.; Lewis, D.; Tan, B.; Goldberg, R. M.; Venook, A.; Blanke, C.; O'Reilly, E. M.; Shields, A. F.; Meyerhardt, J. A.
Article Title: Potential mediators of oxaliplatin-induced peripheral neuropathy from adjuvant therapy in stage III colon cancer: Findings from CALGB (Alliance)/SWOG 80702
Abstract: PURPOSEWe sought to evaluate the independent and interactive associations of planned treatment duration, celecoxib use, physical activity, body mass index (BMI), diabetes mellitus, and vitamin B6 with oxaliplatin-induced peripheral neuropathy (OIPN) among patients with stage III colon cancer enrolled in a clinical trial.METHODSWe conducted a prospective, observational study of 2,450 patients with stage III colon cancer enrolled in the CALGB/SWOG 80702 trial, randomly assigned to 6 versus 12 cycles of adjuvant fluorouracil, leucovorin, and oxaliplatin chemotherapy with or without 3 years of celecoxib. OIPN was reported using the Common Terminology Criteria for Adverse Events (CTCAE) during and following completion of chemotherapy and the FACT/GOG-NTX-13 15-17 months after random assignment. Multivariate analyses were adjusted for baseline sociodemographic and clinical factors.RESULTSPatients assigned to 12 treatment cycles, relative to 6, were significantly more likely to experience higher-grade CTCAE- and FACT/GOG-NTX-13-reported neuropathy and longer times to resolution, while neither celecoxib nor vitamin B6 intake attenuated OIPN. Exercising ≥ 9 MET-hours per week after treatment relative to < 9 was associated with improvements in FACT/GOG-NTX-13-reported OIPN (adjusted difference in means, 1.47; 95% CI, 0.49 to 2.45; P =.003). Compared with patients with baseline BMIs < 25, those with BMIs ≥ 25 were at significantly greater risk of developing higher-grade CTCAE-reported OIPN during (adjusted odds ratio, 1.18; 95% CI, 1.00 to 1.40; P =.05) and following completion (adjusted odds ratio, 1.23; 95% CI, 1.01 to 1.50; P =.04) of oxaliplatin treatment. Patients with diabetes were significantly more likely to experience worse FACT/GOG-NTX-13-reported neuropathy relative to those without (adjusted difference in means, -2.0; 95% CI, -3.3 to -0.73; P =.002). There were no significant interactions between oxaliplatin treatment duration and any of these potentially modifiable exposures.CONCLUSIONLower physical activity, higher BMI, diabetes, and longer planned treatment duration, but not celecoxib use or vitamin B6 intake, may be associated with significantly increased OIPN severity. © American Society of Clinical Oncology.
Keywords: fluorouracil; chemotherapy, adjuvant; antineoplastic agent; prospective study; prospective studies; antineoplastic combined chemotherapy protocols; peripheral neuropathy; colonic neoplasms; folinic acid; adjuvant chemotherapy; colon tumor; oxaliplatin; leucovorin; peripheral nervous system diseases; humans; human
Journal Title: Journal of Clinical Oncology
Volume: 41
Issue: 5
ISSN: 0732-183X
Publisher: American Society of Clinical Oncology  
Date Published: 2023-02-10
Start Page: 1079
End Page: 1091
Language: English
DOI: 10.1200/jco.22.01637
PUBMED: 36367997
PROVIDER: scopus
PMCID: PMC9928634
DOI/URL:
Notes: Article -- Export Date: 1 March 2023 -- Source: Scopus
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  1. Eileen O'Reilly
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