奥沙利铂诱导的晚期结直肠癌患者周围神经病变与羟考酮控释镇痛治疗的生存差异相关

M. Nagashima, Ayako Hiranuma, T. Oshiro, Yu Sato, Tomoaki Kitahara, T. Nabekura, Y. Moriyama, Motoaki Arai, M. Ando, Kengo Kadoya, Ayami Sato, K. Kawamitsu, R. Takagi, T. Urita, Y. Yoshida, Hiroshi Tanaka, S. Okazumi
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引用次数: 0

摘要

奥沙利铂是一种以铂为基础的细胞毒性化疗药物,通常联合使用;作为FOLFOX方案的一部分,用于治疗晚期结直肠癌(CRC)患者。然而,奥沙利铂产生明显的化疗诱导的周围神经病变(CIPN),这是治疗的潜在剂量限制副作用。奥沙利铂诱导的周围神经病变(OIPN)的预防和治疗方案尚未建立。先前,我们报道了控释氧可酮(CR氧可酮)减轻OIPN的疼痛,并延长了晚期CRC患者的FOLFOX治疗。我们进一步研究了CR羟考酮治疗OIPN的疗效及其与患者生存时间的关系。这是一项对晚期结直肠癌患者的回顾性分析。本研究共纳入64例III期或IV期结直肠癌患者。所有患者均接受手术切除原发性结直肠癌,并接受治疗目的FOLFOX化疗。在FOLFOX治疗期间给予CR羟考酮治疗的患者定义为氧合组(29例),未给予CR羟考酮治疗的患者定义为非氧合组(35例)。使用Kaplan-Meier法计算生存时间,以确定氧合组和非氧合组患者之间的差异。OXY组患者的生存期相对于非OXY组患者(中位生存期,58个月对36个月;P = 0.06)。早期给予CR羟考酮治疗OIPN可能对晚期结直肠癌患者更好的FOLFOX化疗依从性、更好的生活质量和更长的生存期相对有效。*通讯:长岛诚,东宝大学樱花医疗中心外科,日本,樱花,下清水564-1,日本,樱花,285-8741,电话:+81-43-462-8811,传真:+81-43-463-1456,电子邮件:nagashima@sakura.med。toho-u.ac.jp
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Survival difference associated with controlled-release oxycodone analgesic therapy for oxaliplatin-induced peripheral neuropathy in advanced colorectal cancer patients
Oxaliplatin is a platinum-based cytotoxic chemotherapeutic agent, and is usually used in combination; as part of the FOLFOX regimen, to treat advanced colorectal cancer (CRC) patients. However, oxaliplatin produces significant chemotherapy-induced peripheral neuropathy (CIPN), a potential dose-limiting side effect of treatment. Preventive and therapeutic protocol for oxaliplatin-induced peripheral neuropathy (OIPN) has not yet been established. Previously, we reported that controlled-release oxycodone (CR oxycodone) attenuated the pain of OIPN and extended FOLFOX therapy in advanced CRC patients. We further investigated the efficacy of CR oxycodone for OIPN and its association with patients’ survival time. This was a retrospective analysis of advanced CRC patients. A total of 64 patients with stage III or IV CRC were included in this study. All patients underwent surgery to extirpate the primary CRC and received curative-intent FOLFOX chemotherapy. Patients who were administered CR oxycodone during the FOLFOX therapy period were defined as the OXY group (29 cases), and those who did not receive CR oxycodone treatment were defined as the non-OXY group (35 cases). Survival time was calculated using the Kaplan-Meier method to determine differences between patients in the OXY and the non-OXY groups. Patients in the OXY group had relatively longer survival than those in the non-OXY group (median survival, 58 months vs. 36 months; P=0.06). Early administration of CR oxycodone for OIPN might be relatively effective for better patient compliance with FOLFOX chemotherapy, a better QOL, and longer survival in patients with advanced CRC. *Correspondence to: Makoto Nagashima, Department of Surgery, Toho University Sakura Medical Center, 564-1 Shimoshizu, Sakura 285-8741, Japan, Tel: +81-43-462-8811, Fax: +81-43-463-1456, E-mail: nagashima@sakura.med. toho-u.ac.jp
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