TY - JOUR
T1 - Phase II clinical trial of pazopanib for patients with unresectable or metastatic malignant peripheral nerve sheath tumors
AU - Nishida, Yoshihiro
AU - Urakawa, Hiroshi
AU - Nakayama, Robert
AU - Kobayashi, Eisuke
AU - Ozaki, Toshifumi
AU - Ae, Keisuke
AU - Matsumoto, Yoshihiro
AU - Tsuchiya, Hiroyuki
AU - Goto, Takahiro
AU - Hiraga, Hiroaki
AU - Naka, Norifumi
AU - Takahashi, Shunji
AU - Ando, Yuichi
AU - Ando, Masahiko
AU - Kuwatsuka, Yachiyo
AU - Hamada, Shunsuke
AU - Ueda, Takafumi
AU - Kawai, Akira
N1 - Funding Information:
We thank the patients who participated in our study, members of JMOG participating institutions and members to collect data (Dr K. Kikuta, Dr M. Endo, Dr J. Hasei, Dr T. Ota, Dr T. Sakai), Data and Safety Monitoring Committee (Dr H. Sugiura, Dr A. Nagano, and Dr Y. Shido), and Department of Advanced Medicine in Nagoya University Hospital (Ms F. Sugiura, and Ms M. Ito), and employees of Novartis Pharmaceuticals Corporation (Mr T. Yonezu, Ms M. Endo, Mr R. Kano, and Ms M. Machida) for their contributions to our study. We thank also Ms Y. Kawai, Ms T. Naganuma, Ms M. Yoshino for secretarial assistance. Our study is financially supported by JMOG. The operation of JMOG is financially supported by Novartis Pharmaceuticals Corporation.
Funding Information:
Yoshihiro Nishida: research funding from Zimmer‐Biomet, personal fees from Eisai Co., Ltd., Eli Lilly Japan K.K., Kaken Pharmaceutical Co. Ltd., Hisamitsu Pharmaceutical Co. Inc., Kyowa Hakko Kirin Co., Ltd., Chugai Pharmaceutical Co., Ltd., Daiici Sankyo Company Ltd, Novartis Pharma K. K., Asahi Kasei Pharma Corporation, consultant for Seikagaku corp. Akira Kawai: personal fee from Novartis Pharma K. K. Yuichi Ando: grants and personal fees from Chugai Pharmaceutical Co., Ltd., Kyowa Hakko Kirin Co., Ltd., Nippon Kayaku, Yakult Honsha, Eli Lilly Japan, Mochida Pharmaceutical, Taiho, Daiici Sankyo Company Ltd, Eisai, and personal fees from Novartis Pharma K. K., Bayer Holding, BMS, Sawai, Tsumura, Shionogi, Otsuka Holding, AstraZeneca, Roche Diagnostics, Insertion Healthcare Japan. Shunji Takahashi: grants and personal fees from Novartis Pharma K. K., Eisai, Taiho, Ono pharmaceutical. Eisuke Kobayashi: honorarium from Novartis Pharma K. K. Hiroaki Hiraga: lecture fee from Novartis Pharma K. K.
Funding Information:
We thank the patients who participated in our study, members of JMOG participating institutions and members to collect data (Dr K. Kikuta, Dr M. Endo, Dr J. Hasei, Dr T. Ota, Dr T. Sakai), Data and Safety Monitoring Committee (Dr H. Sugiura, Dr A. Nagano, and Dr Y. Shido), and Department of Advanced Medicine in Nagoya University Hospital (Ms F. Sugiura, and Ms M. Ito), and employees of Novartis Pharmaceuticals Corporation (Mr T. Yonezu, Ms M. Endo, Mr R. Kano, and Ms M. Machida) for their contributions to our study. We thank also Ms Y. Kawai, Ms T. Naganuma, Ms M. Yoshino for secretarial assistance. Our study is financially supported by JMOG. The operation of JMOG is financially supported by Novartis Pharmaceuticals Corporation.
Publisher Copyright:
© 2020 Union for International Cancer Control
PY - 2021/1/1
Y1 - 2021/1/1
N2 - Malignant peripheral nerve sheath tumor (MPNST) often does not respond well to chemotherapy and develops against a background of NF1. The purpose of our study was to examine the efficacy of pazopanib against MPNST. Our study was designed as a physician-initiated phase II clinical trial in patients with advanced MPNST. Patients were registered from 11 large hospitals. The primary endpoint was set to clarify the clinical benefit rate (CBR) at 12 weeks according to response evaluation criteria in solid tumors (RECIST). Progression-free survival (PFS), overall survival (OS) and the CBR based on modified Choi evaluation at week 12 were set as secondary endpoints along with treatment-related safety. The study enrolled 12 patients. Median age was 49 years. Seven had Grade 2 and five Grade 3 according to the FNCLCC evaluation. Median follow-up period was 10.6 months. CBR at 12 weeks was both 50.0% (RECIST and Choi). The median PFS was 5.4 months for both RECIST and Choi, and the median OS was 10.6 months. Of special interest, the median PFS was 2.9 months for patients with FNCLCC Grade 2 and 10.2 months for Grade 3 (both RECIST and Choi). Grade 4 adverse events of neutropenia and lipase elevation were noted in one patient each. The results of this pazopanib therapy were generally better than those of any of the other single molecular targeted therapies reported previously. Although accumulation of more cases remains necessary, we conclude pazopanib treatment for MPNST to be a safe and promising treatment after doxorubicin-based chemotherapy.
AB - Malignant peripheral nerve sheath tumor (MPNST) often does not respond well to chemotherapy and develops against a background of NF1. The purpose of our study was to examine the efficacy of pazopanib against MPNST. Our study was designed as a physician-initiated phase II clinical trial in patients with advanced MPNST. Patients were registered from 11 large hospitals. The primary endpoint was set to clarify the clinical benefit rate (CBR) at 12 weeks according to response evaluation criteria in solid tumors (RECIST). Progression-free survival (PFS), overall survival (OS) and the CBR based on modified Choi evaluation at week 12 were set as secondary endpoints along with treatment-related safety. The study enrolled 12 patients. Median age was 49 years. Seven had Grade 2 and five Grade 3 according to the FNCLCC evaluation. Median follow-up period was 10.6 months. CBR at 12 weeks was both 50.0% (RECIST and Choi). The median PFS was 5.4 months for both RECIST and Choi, and the median OS was 10.6 months. Of special interest, the median PFS was 2.9 months for patients with FNCLCC Grade 2 and 10.2 months for Grade 3 (both RECIST and Choi). Grade 4 adverse events of neutropenia and lipase elevation were noted in one patient each. The results of this pazopanib therapy were generally better than those of any of the other single molecular targeted therapies reported previously. Although accumulation of more cases remains necessary, we conclude pazopanib treatment for MPNST to be a safe and promising treatment after doxorubicin-based chemotherapy.
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U2 - 10.1002/ijc.33201
DO - 10.1002/ijc.33201
M3 - Article
C2 - 32638374
AN - SCOPUS:85088857928
SN - 0020-7136
VL - 148
SP - 140
EP - 149
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 1
ER -