日本传统汉布药shakuyakukanzoto对FOLFOX联合贝伐单抗用于转移性结直肠癌治疗的神经毒性的预防作用:单组II期研究

Hiroaki Takagi, Shinya Kajiura, Ayumu Hosokawa, Naoki Horikawa, Itsuro Terada, Taishi Hata, Yuka Kobayashi, Yuji Tsukioka, Kazuhisa Yabushita, Takashi Matsuo, Hiroki Yoshita, Akira Ueda, Kohei Ogawa, Takayuki Ando, Ryuji Hayashi, Ichiro Yasuda
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Methods In this single‐arm, open‐label, phase II clinical trial, we enrolled patients with previously untreated, histologically confirmed mCRC from six hospitals in Japan who were aged 20 years and older and had an Eastern Cooperative Oncology Group performance status of 0–1. The patients received shakuyakukanzoto 2.5 g thrice daily, orally, until disease progression and/or unacceptable toxicity was noted. The primary endpoint was the incidence of neurotoxicity following oxaliplatin administration at a dose of 500 mg/m 2 . Neurotoxicity was evaluated according to the Neurotoxicity Criteria of Debiopharm (DEB‐NTC). The trial was registered in the UMIN Clinical Trials Registry of Japan (UMIN000001853). Results Forty‐one non‐pretreated mCRC patients were included between April 2009 and September 2013. At an oxaliplatin dose of 500 mg/m 2 , neurotoxicity of DEB‐NTC grade 1–2 developed in 25.0% of patients; no patient had DEB‐NTC grade 3 neurotoxicity. The most common grade 3/4 adverse events were neutropenia (34.1%), hypertension (24.4%), and fatigue (9.8%). The response rate of the 38 patients with measurable lesions was 55.2%. The median progression‐free and overall survival was 14.9 and 35.2 months respectively. Conclusion Shakuyakukanzoto substantially reduced oxaliplatin‐induced neurotoxicity without negatively affecting tumor response or survival in FOLFOX + BV‐treated patients with CRC.","PeriodicalId":23213,"journal":{"name":"Traditional & Kampo Medicine","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Preventive effect of a traditional Japanese Kampo medicine, <i>shakuyakukanzoto</i>, against neurotoxicity of <scp>FOLFOX</scp> plus bevacizumab used for metastatic colorectal cancer management: A single‐arm phase <scp>II</scp> study\",\"authors\":\"Hiroaki Takagi, Shinya Kajiura, Ayumu Hosokawa, Naoki Horikawa, Itsuro Terada, Taishi Hata, Yuka Kobayashi, Yuji Tsukioka, Kazuhisa Yabushita, Takashi Matsuo, Hiroki Yoshita, Akira Ueda, Kohei Ogawa, Takayuki Ando, Ryuji Hayashi, Ichiro Yasuda\",\"doi\":\"10.1002/tkm2.1389\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract Aim 5‐Fluorouracil/folinic acid and oxaliplatin plus bevacizumab (FOLFOX + BV) is a standard chemotherapy regimen for metastatic colorectal cancer (mCRC). This study was aimed at evaluating the preventive effects of shakuyakukanzoto against oxaliplatin‐induced neurotoxicity associated with FOLFOX + BV administration. Methods In this single‐arm, open‐label, phase II clinical trial, we enrolled patients with previously untreated, histologically confirmed mCRC from six hospitals in Japan who were aged 20 years and older and had an Eastern Cooperative Oncology Group performance status of 0–1. The patients received shakuyakukanzoto 2.5 g thrice daily, orally, until disease progression and/or unacceptable toxicity was noted. The primary endpoint was the incidence of neurotoxicity following oxaliplatin administration at a dose of 500 mg/m 2 . Neurotoxicity was evaluated according to the Neurotoxicity Criteria of Debiopharm (DEB‐NTC). The trial was registered in the UMIN Clinical Trials Registry of Japan (UMIN000001853). Results Forty‐one non‐pretreated mCRC patients were included between April 2009 and September 2013. At an oxaliplatin dose of 500 mg/m 2 , neurotoxicity of DEB‐NTC grade 1–2 developed in 25.0% of patients; no patient had DEB‐NTC grade 3 neurotoxicity. The most common grade 3/4 adverse events were neutropenia (34.1%), hypertension (24.4%), and fatigue (9.8%). The response rate of the 38 patients with measurable lesions was 55.2%. The median progression‐free and overall survival was 14.9 and 35.2 months respectively. 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摘要

目的5‐氟尿嘧啶/亚叶酸+奥沙利铂+贝伐单抗(FOLFOX + BV)是转移性结直肠癌(mCRC)的标准化疗方案。本研究旨在评估shakuyakukanzoto对与FOLFOX + BV给药相关的奥沙利铂诱导的神经毒性的预防作用。方法:在这项单臂、开放标签、II期临床试验中,我们招募了来自日本6家医院的既往未治疗、组织学证实的mCRC患者,这些患者年龄在20岁及以上,东方肿瘤合作组(Eastern Cooperative Oncology Group)评分为0-1。患者接受每日3次,每次2.5 g,口服,直至发现疾病进展和/或不可接受的毒性。主要终点是奥沙利铂剂量为500mg / m2后神经毒性的发生率。根据Debiopharm神经毒性标准(DEB - NTC)评估神经毒性。该试验已在日本UMIN临床试验注册中心注册(UMIN000001853)。结果2009年4月至2013年9月共纳入41例未经预处理的mCRC患者。奥沙利铂剂量为500mg / m2时,25.0%的患者出现DEB - NTC 1-2级的神经毒性;没有患者发生DEB - NTC 3级神经毒性。最常见的3/4级不良事件是中性粒细胞减少(34.1%)、高血压(24.4%)和疲劳(9.8%)。38例可测量病变患者的有效率为55.2%。中位无进展生存期和总生存期分别为14.9个月和35.2个月。结论:在FOLFOX + BV治疗的结直肠癌患者中,Shakuyakukanzoto可显著降低奥沙利铂诱导的神经毒性,而不会对肿瘤反应或生存产生负面影响。
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Preventive effect of a traditional Japanese Kampo medicine, shakuyakukanzoto, against neurotoxicity of FOLFOX plus bevacizumab used for metastatic colorectal cancer management: A single‐arm phase II study
Abstract Aim 5‐Fluorouracil/folinic acid and oxaliplatin plus bevacizumab (FOLFOX + BV) is a standard chemotherapy regimen for metastatic colorectal cancer (mCRC). This study was aimed at evaluating the preventive effects of shakuyakukanzoto against oxaliplatin‐induced neurotoxicity associated with FOLFOX + BV administration. Methods In this single‐arm, open‐label, phase II clinical trial, we enrolled patients with previously untreated, histologically confirmed mCRC from six hospitals in Japan who were aged 20 years and older and had an Eastern Cooperative Oncology Group performance status of 0–1. The patients received shakuyakukanzoto 2.5 g thrice daily, orally, until disease progression and/or unacceptable toxicity was noted. The primary endpoint was the incidence of neurotoxicity following oxaliplatin administration at a dose of 500 mg/m 2 . Neurotoxicity was evaluated according to the Neurotoxicity Criteria of Debiopharm (DEB‐NTC). The trial was registered in the UMIN Clinical Trials Registry of Japan (UMIN000001853). Results Forty‐one non‐pretreated mCRC patients were included between April 2009 and September 2013. At an oxaliplatin dose of 500 mg/m 2 , neurotoxicity of DEB‐NTC grade 1–2 developed in 25.0% of patients; no patient had DEB‐NTC grade 3 neurotoxicity. The most common grade 3/4 adverse events were neutropenia (34.1%), hypertension (24.4%), and fatigue (9.8%). The response rate of the 38 patients with measurable lesions was 55.2%. The median progression‐free and overall survival was 14.9 and 35.2 months respectively. Conclusion Shakuyakukanzoto substantially reduced oxaliplatin‐induced neurotoxicity without negatively affecting tumor response or survival in FOLFOX + BV‐treated patients with CRC.
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