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

Author:

Takagi Hiroaki1,Kajiura Shinya2ORCID,Hosokawa Ayumu3,Horikawa Naoki4,Terada Itsuro5,Hata Taishi6,Kobayashi Yuka7,Tsukioka Yuji5,Yabushita Kazuhisa4,Matsuo Takashi8,Yoshita Hiroki9,Ueda Akira10,Ogawa Kohei1,Ando Takayuki10,Hayashi Ryuji2,Yasuda Ichiro10

Affiliation:

1. Department of Medical Oncology Toyama Prefectural Central Hospital Toyama Japan

2. Department of Clinical Oncology University of Toyama Toyama Japan

3. Department of Clinical Oncology University of Miyazaki Hospital Miyazaki Japan

4. Department of Surgery Takaoka City Hospital Toyama Japan

5. Department of Surgery Kurobe City Hospital Toyama Japan

6. Department of Gastroenterological Surgery Kansai Rosai Hospital Amagasaki Japan

7. Department of Medical Oncology Nagaoka Chuo General Hospital Niigata Japan

8. Matsuo Family Clinic Omihachiman Japan

9. Department of Gastroenterological Medicine Toyama Nishi General Hospital Toyama Japan

10. Third Department of Internal Medicine University of Toyama Toyama Japan

Abstract

AbstractAim5‐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.MethodsIn 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/m2. 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).ResultsForty‐one non‐pretreated mCRC patients were included between April 2009 and September 2013. At an oxaliplatin dose of 500 mg/m2, 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.ConclusionShakuyakukanzoto substantially reduced oxaliplatin‐induced neurotoxicity without negatively affecting tumor response or survival in FOLFOX + BV‐treated patients with CRC.

Publisher

Wiley

Subject

Environmental Engineering

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