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首页> 外文期刊>Journal of Clinical Oncology >Neurotoxicity from oxaliplatin combined with weekly bolus fluorouracil and leucovorin as surgical adjuvant chemotherapy for stage II and III colon cancer: NSABP C-07.
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Neurotoxicity from oxaliplatin combined with weekly bolus fluorouracil and leucovorin as surgical adjuvant chemotherapy for stage II and III colon cancer: NSABP C-07.

机译:奥沙利铂联合每周推注氟尿嘧啶和亚叶酸作为第二和第三阶段结肠癌的手术辅助化疗的神经毒性:NSABP C-07。

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PURPOSE: The randomized, multicenter, phase III protocol C-07 compared the efficacy of adjuvant bolus fluorouracil and leucovorin (FULV) versus FULV with oxaliplatin (FLOX) in stage II or III colon cancer. Definitive analysis revealed an increase in 4-year disease-free survival from 67.0% to 73.2% in favor of FLOX. This study compares neurotoxicity between the treatments. PATIENTS AND METHODS: Neurotoxicity was recorded for all patients using standard adverse event reporting. Patients at select institutions completed a neurotoxicity questionnaire through 18 months of follow-up. RESULTS: A total of 2,492 patients enrolled onto C-07 and 400 patients enrolled onto the patient-reported substudy. Mean patient-reported neurotoxicity was higher with oxaliplatin throughout the 18 months of study (P < .0001). During therapy, patients receiving oxaliplatin experienced significantly more hand/foot toxicity (eg, "quite a bit" of cold-induced hand/foot pain 26% FLOX v 2.6% FULV) and overall weakness (eg, moderate weakness in 27.4% FLOX v 16.2% FULV). At 18 months, hand neuropathy had diminished, but patients who received oxaliplatin experienced continued foot discomfort (eg, moderate foot numbness and tingling for 22.1% FLOX v 4.6% FULV). Observer-reported neurotoxicity was low grade and primarily neurosensory rather than neuromotor. Sixty-eight percent in the FLOX group v 8% in the FULV group had neurotoxicity at their first on-treatment assessment. Time to resolution was significantly longer for those receiving oxaliplatin, and continued beyond 2 years for more than 10% in the oxaliplatin group. CONCLUSION: Oxaliplatin causes significant neurotoxicity. It is experienced primarily in the hands during therapy and in the feet during follow-up. In a minority of patients the neurotoxicity is long lasting.
机译:目的:随机,多中心,III期方案C-07比较了在II期或III期结肠癌中辅助推注氟尿嘧啶和亚叶酸钙(FULV)与FULV与奥沙利铂(FLOX)的疗效。明确的分析显示,支持FLOX的4年无病生存率从67.0%增加到73.2%。这项研究比较了治疗之间的神经毒性。患者和方法:使用标准不良事件报告记录所有患者的神经毒性。选定机构的患者通过18个月的随访完成了神经毒性问卷。结果:共有2,492名患者被纳入C-07,400名患者被纳入患者报告的子研究。在整个研究的18个月中,奥沙利铂患者报告的平均神经毒性较高(P <.0001)。在治疗期间,接受奥沙利铂治疗的患者的手/足毒性(例如,“有点”由冷引起的手/足痛26%FLOX v 2.6%FULV)明显增强,而总体虚弱(例如27.4%FLOX v中度虚弱) 16.2%FULV)。在18个月时,手部神经病已减轻,但是接受奥沙利铂治疗的患者仍出现持续的脚部不适(例如,中度麻木和刺痛感为22.1%FLOX和4.6%FULV)。观察者报告的神经毒性是低度的,主要是神经感觉而不是神经运动。在首次接受治疗时,FLOX组有68%的患者有FULV组有8%的神经毒性。对于接受奥沙利铂治疗的患者,解决问题的时间明显更长,在奥沙利铂治疗组中,超过2年的治疗持续时间超过10%。结论:奥沙利铂引起明显的神经毒性。它主要在治疗过程中手部和后续治疗中的脚部经历。在少数患者中,神经毒性是持久的。

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