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本文引用的文献

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Incidence and risk factors associated with development of oxalipatin-induced acute peripheral neuropathy in colorectal cancer patients.结直肠癌患者中奥沙利铂诱导的急性周围神经病变发生的发生率及相关危险因素。
J Oncol Pharm Pract. 2023 Mar;29(2):311-318. doi: 10.1177/10781552211068138. Epub 2021 Dec 17.
2
Colorectal Cancer Survivors Suffering From Sensory Chemotherapy-Induced Peripheral Neuropathy Are Not a Homogenous Group: Secondary Analysis of Patients' Profiles With Oxaliplatin-Induced Peripheral Neuropathy.患有感觉性化疗引起的周围神经病变的结直肠癌幸存者并非同质群体:奥沙利铂引起的周围神经病变患者资料的二次分析。
Front Pharmacol. 2021 Nov 4;12:744085. doi: 10.3389/fphar.2021.744085. eCollection 2021.
3
Chemotherapy-Induced Peripheral Neuropathy: Epidemiology, Pathomechanisms and Treatment.化疗引起的周围神经病变:流行病学、发病机制与治疗
Oncol Ther. 2021 Dec;9(2):385-450. doi: 10.1007/s40487-021-00168-y. Epub 2021 Oct 16.
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The Role of Neurotropic B Vitamins in Nerve Regeneration.神经滋养 B 族维生素在神经再生中的作用。
Biomed Res Int. 2021 Jul 13;2021:9968228. doi: 10.1155/2021/9968228. eCollection 2021.
5
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JAMA. 2021 Apr 6;325(13):1277-1286. doi: 10.1001/jama.2021.2454.
6
The effects of exercise on chemotherapy-induced peripheral neuropathy symptoms in cancer patients: a systematic review and meta-analysis.运动对癌症患者化疗引起的周围神经病变症状的影响:系统评价和荟萃分析。
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8
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Lancet Oncol. 2020 Dec;21(12):1620-1629. doi: 10.1016/S1470-2045(20)30527-1.
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Central Obesity is Associated With Neuropathy in the Severely Obese.中心型肥胖与重度肥胖患者的神经病变有关。
Mayo Clin Proc. 2020 Jul;95(7):1342-1353. doi: 10.1016/j.mayocp.2020.03.025.
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Neuropathy experienced by colorectal cancer patients receiving oxaliplatin: A qualitative study to validate the Functional Assessment of Cancer Therapy/Gynecologic Oncology Group-Neurotoxicity scale.接受奥沙利铂治疗的结直肠癌患者的神经病变:一项验证癌症治疗功能评估/妇科肿瘤学组神经毒性量表的定性研究。
World J Gastrointest Oncol. 2020 Feb 15;12(2):205-218. doi: 10.4251/wjgo.v12.i2.205.

奥沙利铂辅助治疗 III 期结肠癌所致周围神经病的潜在中介物:CALGB(联盟)/SWOG80702 研究结果。

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

机构信息

Yale School of Medicine, New Haven, CT.

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

出版信息

J Clin Oncol. 2023 Feb 10;41(5):1079-1091. doi: 10.1200/JCO.22.01637. Epub 2022 Nov 11.

DOI:10.1200/JCO.22.01637
PMID:36367997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9928634/
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; = .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; = .05) and following completion (adjusted odds ratio, 1.23; 95% CI, 1.01 to 1.50; = .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; = .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.

摘要

目的

我们旨在评估计划治疗持续时间、塞来昔布使用、体力活动、体重指数(BMI)、糖尿病和维生素 B6 与接受 III 期结肠癌临床试验的患者奥沙利铂诱导的周围神经病变(OIPN)之间的独立和交互关联。

方法

我们对 2450 名 III 期结肠癌患者进行了前瞻性观察性研究,这些患者参加了 CALGB/SWOG 80702 试验,随机分配至 6 或 12 个周期的辅助氟尿嘧啶、亚叶酸和奥沙利铂化疗,同时使用或不使用 3 年塞来昔布。在化疗期间和完成后,使用常见不良事件术语标准(CTCAE)报告 OIPN,并在随机分配后 15-17 个月使用 FACT/GOG-NTX-13 进行报告。多变量分析调整了基线社会人口统计学和临床因素。

结果

与 6 个周期相比,接受 12 个周期治疗的患者发生更高等级 CTCAE 和 FACT/GOG-NTX-13 报告的神经病变和更长时间恢复的可能性显著更高,而塞来昔布或维生素 B6 的摄入并没有减轻 OIPN。与治疗后每周进行 ≥ 9 MET 小时的体力活动相比,进行 < 9 MET 小时的体力活动与 FACT/GOG-NTX-13 报告的 OIPN 改善相关(调整后的平均差异,1.47;95%CI,0.49 至 2.45; =.003)。与基线 BMI<25 的患者相比,BMI≥25 的患者在接受奥沙利铂治疗期间(调整后的优势比,1.18;95%CI,1.00 至 1.40; =.05)和完成后(调整后的优势比,1.23;95%CI,1.01 至 1.50; =.04)发生更高等级 CTCAE 报告的 OIPN 的风险显著更高。与无糖尿病的患者相比,患有糖尿病的患者发生 FACT/GOG-NTX-13 报告的神经病变更差(调整后的平均差异,-2.0;95%CI,-3.3 至-0.73; =.002)。奥沙利铂治疗持续时间与这些潜在可改变的暴露之间没有显著的相互作用。

结论

体力活动较少、BMI 较高、糖尿病和计划治疗持续时间较长,但不是塞来昔布的使用或维生素 B6 的摄入,可能与 OIPN 严重程度显著增加相关。