@article{2621da9901dc4827aa4d02bdc1d137d7,
title = "Time lapse analysis of tumor response in patients with soft tissue sarcoma treated with trabectedin: A pooled analysis of two phase II clinical trials",
abstract = "The time course of the response to each drug is important to avoid inappropriate termination of treatment by misjudging tumor progression; however, little is known about soft tissue sarcoma (STS) regarding this matter. This study aimed to perform a time-lapse analysis of tumor response in patients with STS treated with trabectedin from 2 phase II clinical trials. We examined 66 patients with translocation-related sarcoma registered in 2 Japanese phase II clinical trials. All patients previously received standard therapy before the administration of trabectedin at 1.2 mg/m2 every 3 weeks. Imaging evaluation was performed according to the study protocol. The sum of the maximum diameters of the target lesions was calculated and analyzed over time. Among the 66 patients, 9 (13.6%) showed partial response (PR) to trabectedin. Histological diagnoses of these 9 responders comprised 6 myxoid liposarcoma, 2 synovial sarcoma, and a mesenchymal chondrosarcoma. The median period from treatment initiation to the first PR was 123 (range, 34-328) days. The pattern of tumor response to trabectedin showed an increasing tendency in size in the initial stage, usually followed by a size decrease with repeated administration. STS response to trabectedin was characterized as delayed and potentially persistent. Clinicians treating STS with trabectedin should know the features of the response pattern to avoid interrupting the treatment before maximal efficacy is achieved.",
keywords = "chemotherapy, clinical trial, soft tissue sarcoma",
author = "Makoto Endo and Shunji Takahashi and Nobuhito Araki and Hideshi Sugiura and Takafumi Ueda and Tsukasa Yonemoto and Mitsuru Takahashi and Hideo Morioka and Hiroaki Hiraga and Toru Hiruma and Toshiyuki Kunisada and Akihiko Matsumine and Kazato Goda and Akira Kawai",
note = "Funding Information: Makoto Endo received grant from Japan Orthopaedics and Traumatology Research Foundation Inc; personal fee from Taisho Toyama Pharmaceutical Co., Ltd., Daiichi Sankyo Company, Limited, Eli Lilly and Company, Eisai Co., Ltd., and Novartis International AG. Shunji Takahashi received grant, personal fee from Eisai, Novartis, Daiichi‐Sankyo, Taiho, MSD, Chugai, Bayer, and Astrazeneca. Nobuhito Araki and Hideshi Sugiura have no conflicts of interest. Takafumi Ueda received grant from Eisai, Takara Bio, Eli Lilly; personal fee from Daiichi‐Sankyo and Taiho Pharmaceuticals. Tsukasa Yonemoto, Mitsuru Takahashi, and Hideo Morioka have no conflicts of interest. Hiroaki Hiraga received grant from Taiho and Eli Lilly; personal fee from Daiichi Sankyo, Ono, Eisai, Nippon Kayaku, Kaken, and Novartis. Toru Hiruma, Toshiyuki Kunisada, and Akihiko Matsumine have no conflicts of interest. Kazato Goda is employed by Taiho Pharmaceutical Co., Ltd and received personal fees from Taiho Pharmaceutical Co., Ltd both during the study period and outside the submitted work. Akira Kawai received personal fee from Taiho Pharmaceutical Co. Funding Information: The phase II clinical trials were sponsored by Taiho Pharmaceutical Co., Ltd funded by The National Institute of Biomedical Innovation (Osaka, Japan) in the development of trabectedin under orphan drug designation in Japan. These phase II clinical trials data were kindly provided by Taiho Pharmaceutical Co., Ltd for this study. This analysis was supported by Taiho pharmaceutical Co., Ltd. This paper underwent English language editing by Honyaku Center Inc, which was funded by Taiho Pharmaceutical Co., Ltd. This analysis was conducted with the support of Yoshiyuki Kuriya and Masashi Shimura, and overall management of drafting the manuscript was conducted by Yuichi Fukushima?from Taiho Pharmaceutical Co., Ltd. Funding Information: The phase II clinical trials were sponsored by Taiho Pharmaceutical Co., Ltd funded by The National Institute of Biomedical Innovation (Osaka, Japan) in the development of trabectedin under orphan drug designation in Japan. These phase II clinical trials data were kindly provided by Taiho Pharmaceutical Co., Ltd for this study. This analysis was supported by Taiho pharmaceutical Co., Ltd. This paper underwent English language editing by Honyaku Center Inc, which was funded by Taiho Pharmaceutical Co., Ltd. Publisher Copyright: {\textcopyright} 2020 The Authors. Cancer Medicine published by John Wiley & Sons Ltd",
year = "2020",
month = jun,
day = "1",
doi = "10.1002/cam4.2991",
language = "English",
volume = "9",
pages = "3656--3667",
journal = "Cancer Medicine",
issn = "2045-7634",
publisher = "John Wiley and Sons Ltd",
number = "11",
}