Potential Mediators of Oxaliplatin-Induced Peripheral Neuropathy From Adjuvant Therapy in Stage III Colon Cancer: Findings From CALGB (Alliance)/SWOG 80702

Author:

Lee Seohyuk1ORCID,Ma Chao2ORCID,Shi Qian3ORCID,Kumar Pankaj4ORCID,Couture Felix5,Kuebler Philip6,Krishnamurthi Smitha7ORCID,Lewis DeQuincy8,Tan Benjamin9,Goldberg Richard M.10ORCID,Venook Alan11ORCID,Blanke Charles12,O'Reilly Eileen M.13ORCID,Shields Anthony F.14ORCID,Meyerhardt Jeffrey A.2ORCID

Affiliation:

1. Yale School of Medicine, New Haven, CT

2. Department of Medical Oncology, Dana-Farber/Partners CancerCare, Boston, MA

3. Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, MN, USA

4. Heartland Cancer Research NCORP, Illinois CancerCare PC, Peoria, IL

5. Hôtel-Dieu de Québec, Québec City, QC, Canada

6. Columbus NCI Community Oncology Research Program, Columbus, OH

7. Cleveland Clinic, Cleveland, OH

8. Southeast Clinical Oncology Research Consortium NCORP, Cone Health Medical Group, Asheboro, NC

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

10. West Virginia University Cancer Institute, Morgantown, WV

11. University of California San Francisco, San Francisco, CA

12. Knight Cancer Institute, Oregon Health and Science University, Portland, OR

13. Memorial Sloan Kettering Cancer Center, Weill Cornell Medical Center, New York, NY

14. Karmanos Cancer Institute, Wayne State University, MI

Abstract

PURPOSE We 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. METHODS We 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. RESULTS Patients 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. CONCLUSION Lower 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.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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