Long-Term Neurotoxicity Effects of Oxaliplatin Added to Fluorouracil and Leucovorin as Adjuvant Therapy for Colon Cancer: Results from National Surgical Adjuvant Breast and Bowel Project Trials C-07 and LTS-01

被引:76
作者
Kidwell, Kelley M. [1 ,2 ]
Yothers, Greg [1 ,2 ]
Ganz, Patricia A. [1 ,3 ,4 ,5 ]
Land, Stephanie R. [1 ,2 ]
Ko, Clifford Y. [1 ,3 ,4 ,5 ]
Cecchini, Reena S. [1 ]
Kopec, Jacek A. [1 ,6 ]
Wolmark, Norman [1 ,7 ]
机构
[1] Natl Surg Adjuvant Breast & Bowel Project Operat, Pittsburgh, PA USA
[2] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Biostat, Pittsburgh, PA 15261 USA
[3] Univ Calif Los Angeles, Sch Med, Los Angeles, CA USA
[4] Univ Calif Los Angeles, Sch Publ Hlth, Los Angeles, CA 90024 USA
[5] Jonsson Comprehens Canc Ctr, Los Angeles, CA 90034 USA
[6] Univ British Columbia, Sch Populat & Publ Hlth, Vancouver, BC V5Z 1M9, Canada
[7] Allegheny Gen Hosp, Dept Human Oncol, Pittsburgh, PA 15212 USA
基金
美国国家卫生研究院;
关键词
colon cancer; oxaliplatin; neurotoxicity; stage II/III; randomized clinical trial; WEEKLY BOLUS FLUOROURACIL; STAGE-II; CHEMOTHERAPY; LEVAMISOLE; SURVIVORS; ONCOLOGY;
D O I
10.1002/cncr.27593
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Neurotoxicity from adjuvant treatment with oxaliplatin has been studied in patients with colorectal carcinoma in short-term studies, but, to the authors' knowledge, the current article is the first long-term assessment which reports the National Surgical Adjuvant Breast and Bowel Project (NSABP) investigation of whether excess neurotoxicity persists beyond 4 years. METHODS: As part of a colorectal cancer long-term survivor study (LTS-01), long-term neurotoxicity was assessed in 353 patients on NSABP Protocol C-07 (cross-sectional sample). Ninety-two of these patients from LTS-01 also had longitudinal data and were reassessed 5 to 8 years (median, 7 years) after random assignment (longitudinal sample). Contingency tables compared cohorts, a mixed model compared neurotoxicity between treatments over time, and a Wilcoxon rank-sum test compared neurotoxicity between treatments (cross-sectional sample). RESULTS: In the cross-sectional sample, the increase in mean total neurotoxicity scores of 1.8 with oxaliplatin was statistically significant (P = .005), but not clinically significant (a minimally important difference of 4 was reported at the long-term assessment). Patients who received oxaliplatin had increased odds of numbness and tingling in hands (odds ratio, 2.00; P = .015) and feet (odds ratio, 2.78; P < .001) versus patients who did not receive oxaliplatin. The magnitude of the oxaliplatin effect varied with time (P < .001) in the longitudinal sample, such that the oxaliplatin-treated group did not have significantly greater total neurotoxicity scores by 7 years. CONCLUSIONS: At the long-term endpoint, there was no clinically significant increase in total neurotoxicity scores for patients who received oxaliplatin, but the specific neurotoxicities of numbness and tingling of the hands and feet remained significantly elevated for oxaliplatin-treated patients. Cancer 2012. (c) 2012 American Cancer Society.
引用
收藏
页码:5614 / 5622
页数:9
相关论文
共 29 条
[1]   Oxaliplatin, fluorouracil, and leucovorin as adjuvant treatment for colon cancer [J].
Andre, T ;
Boni, C ;
Mounedji-Boudiaf, L ;
Navarro, M ;
Tabernero, J ;
Hickish, T ;
Topham, C ;
Zaninelli, M ;
Clingan, P ;
Bridgewater, J ;
Tabah-Fisch, I ;
de Gramont, A .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (23) :2343-2351
[2]   Improved Overall Survival With Oxaliplatin, Fluorouracil, and Leucovorin As Adjuvant Treatment in Stage II or III Colon Cancer in the MOSAIC Trial [J].
Andre, Thierry ;
Boni, Corrado ;
Navarro, Matilde ;
Tabernero, Josep ;
Hickish, Tamas ;
Topham, Clare ;
Bonetti, Andrea ;
Clingan, Philip ;
Bridgewater, John ;
Rivera, Fernando ;
de Gramont, Aimery .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (19) :3109-3116
[3]  
[Anonymous], ASCO GASTR CANC S OR
[4]  
[Anonymous], NCI CANC THER EV PRO
[5]  
[Anonymous], J CLIN ONCOL
[6]   American society of clinical oncology recommendations on adjuvant chemotherapy for stage II colon cancer [J].
Benson, AB ;
Schrag, D ;
Somerfield, MR ;
Cohen, AM ;
Figueredo, AT ;
Flynn, PJ ;
Krzyzanowska, MK ;
Maroun, J ;
McAllister, P ;
Van Cutsem, E ;
Brouwers, M ;
Charette, M ;
Haller, DG .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (16) :3408-3419
[7]   Pharmacogenetic Assessment of Toxicity and Outcome in Patients With Metastatic Colorectal Cancer Treated With LV5FU2, FOLFOX, and FOLFIRI: FFCD 2000-05 [J].
Boige, Valerie ;
Mendiboure, Jean ;
Pignon, Jean-Pierre ;
Loriot, Marie-Anne ;
Castaing, Marine ;
Barrois, Michel ;
Malka, David ;
Tregouet, David-Alexandre ;
Bouche, Olivier ;
Le Corre, Delphine ;
Miran, Isabelle ;
Mulot, Claire ;
Ducreux, Michel ;
Beaune, Philippe ;
Laurent-Puig, Pierre .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (15) :2556-2564
[8]   Molecular Markers of Chemotherapy Toxicity in Colorectal Cancer [J].
Braun, Michael S. ;
Seymour, Matthew T. .
CURRENT COLORECTAL CANCER REPORTS, 2011, 7 (01) :105-111
[9]   Measuring the side effects of taxane therapy in oncology - The functional assessment of cancer therapy-taxane (FACT-taxane) [J].
Cella, D ;
Peterman, A ;
Hudgens, S ;
Webster, K ;
Socinski, MA .
CANCER, 2003, 98 (04) :822-831
[10]   Cancer survivorship research: the challenge of recruiting adult long term cancer survivors from a cooperative clinical trials group [J].
Ganz, Patricia A. ;
Land, Stephanie R. ;
Antonio, Cynthia ;
Zheng, Ping ;
Yothers, Greg ;
Petersen, Laura ;
Wickerham, D. Lawrence ;
Wolmark, N. ;
Ko, Clifford Y. .
JOURNAL OF CANCER SURVIVORSHIP, 2009, 3 (03) :137-147