TY - JOUR
T1 - Results of sub-analysis of a phase 2 study on trabectedin treatment for extraskeletal myxoid chondrosarcoma and mesenchymal chondrosarcoma
AU - Morioka, Hideo
AU - Takahashi, Shunji
AU - Araki, Nobuhito
AU - Sugiura, Hideshi
AU - Ueda, Takafumi
AU - Takahashi, Mitsuru
AU - Yonemoto, Tsukasa
AU - Hiraga, Hiroaki
AU - Hiruma, Toru
AU - Kunisada, Toshiyuki
AU - Matsumine, Akihiko
AU - Susa, Michiro
AU - Nakayama, Robert
AU - Nishimoto, Kazumasa
AU - Kikuta, Kazutaka
AU - Horiuchi, Keisuke
AU - Kawai, Akira
N1 - Funding Information:
HM reports grants, personal fees, and non-financial support from Taiho Pharmaceutical, Daiichi-Sankyo Company and GSK; grants and non-financial support from Eisai; and personal fees from Novartis Pharma. ST reports grants and personal fees from Taiho Pharmaceutical, Eisai, Boehringer Ingelheim, Novartis Pharma, Bayer, Daiichi-Sankyo Company, Merck, and Astellas Pharma; grants from GSK, Chugai Pharmaceutical, Zenyaku Kogyo, Sanofi, Otsuka Pharmaceutical, Pfizer, and Japan Clinical Oncology Group; grants, personal fees, and non-financial support from AstraZeneca. NA reports grants and non-financial support from Taiho Pharmaceutical, GSK, Eisai, Japan Clinical Oncology Group, and MSD. HS reports grants, personal fees, and non-financial support from Taiho Pharmaceutical; grants and non-financial support from GSK, Eisai, and MSD. TU reports grants and non-financial support from Taiho Pharmaceutical, Eisai and MSD; grants, personal fees, and non-financial support from Daiichi-Sankyo Company and GSK. MT reports grants, personal fees, and non-financial support from Taiho Pharmaceutical. TY reports grants, personal fees, and non-financial support from Taiho Pharmaceutical. HH reports grants and non-financial support from Taiho Pharmaceutical, GSK, Eisai, and MSD; grants from Ono Pharmaceutical, Daiichi-Sankyo Company, Ministry of Health, Labour and Welfare, Center for Clinical Trials, Japan Medical Association, and National Cancer Center. TH reports grants, personal fees, and non-financial support from Taiho Pharmaceutical; personal fees from GSK. TK reports grants and non-financial support from Taiho Pharmaceutical; nonfinancial support from Japan Clinical Oncology Group. AM reports grants and non-financial support from Taiho Pharmaceutical, GSK, Eisai, MSD, and Japan Clinical Oncology Group. MS has no conflict of interest directly relevant to the content of this article. RN has no conflict of interest directly relevant to the content of this article. KN has no conflict of interest directly relevant to the content of this article. KK has no conflict of interest directly relevant to the content of this article. KH has no conflict of interest directly relevant to the content of this article. AK reports grants, personal fees, and non-financial support from Taiho Pharmaceutical, GSK, Eisai, Novartis Pharma, Merck Serono and Eli Lilly.
Funding Information:
The randomized phase 2 study was sponsored by Taiho Pharmaceutical Co., Ltd. Trabectedin was supplied by Taiho Pharmaceutical Co., Ltd. The English used in this manuscript was revised by Usaco Corporation Ltd. (Tokyo, Japan), and was funded by Taiho Pharmaceutical Co., Ltd.
Publisher Copyright:
© 2016 The Author(s).
PY - 2016/7/14
Y1 - 2016/7/14
N2 - Background: Trabectedin is reported to be particularly effective against translocation-related sarcoma. Recently, a randomized phase 2 study in patients with translocation-related sarcomas unresponsive or intolerable to standard chemotherapy was conducted, which showed clinical benefit of trabectedin compared with best supportive care(BSC). Extraskeletal myxoid chondrosarcoma (EMCS) and Mesenchymal chondrosarcoma (MCS) are very rare malignant soft tissue sarcomas, and are associated with translocations resulting in fusion genes. In addition, the previous in vivo data showed that trabectedin affect tumor necrosis and reduction in vascularization in a xenograft model of a human high-grade chondrosarcoma. The aim of the present analysis was to clarify the efficacy of trabectedin for EMCS and MCS subjects in the randomized phase 2 study. Methods: Five subjects with EMCS and MCS received trabectedin treatment in the randomized phase 2 study. Three MCS subjects were allocated to the BSC group. Objective response and progression-free survival (PFS) were assessed according to the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 by central radiology imaging review. Results: The median follow-up time of the randomized phase 2 study was 22.7months, and one subject with MCS was still receiving trabectedin treatment at the final data cutoff. The median PFS was 12.5months (95 % CI: 7.4-not reached) in the trabectedin group, while 1.0months (95 % CI: 0.3-1.0months) in MCS subjects of the BSC group. The six-month progression-free rate was 100% in the trabectedin group. One subject with MCS showed partial response, and the others in the trabectedin group showed stable disease. Overall survival of EMCS and MCS subjects was 26.4months (range, 10.4-26.4months) in the trabectedin group. At the final data cutoff, two of five subjects were still alive. Conclusions: This sub-analysis shows that trabectedin is effective for patients with EMCS and MCS compared with BSC. The efficacy results were better than previously reported data of TRS. These facts suggest that trabectedin become an important choice of treatment for patients with advanced EMCS or MCS who failed or were intolerable to standard chemotherapy. Trial registration: The randomized phase 2 study is registered with the Japan Pharmaceutical Information Center, number JapicCTI-121850(May 31, 2012).
AB - Background: Trabectedin is reported to be particularly effective against translocation-related sarcoma. Recently, a randomized phase 2 study in patients with translocation-related sarcomas unresponsive or intolerable to standard chemotherapy was conducted, which showed clinical benefit of trabectedin compared with best supportive care(BSC). Extraskeletal myxoid chondrosarcoma (EMCS) and Mesenchymal chondrosarcoma (MCS) are very rare malignant soft tissue sarcomas, and are associated with translocations resulting in fusion genes. In addition, the previous in vivo data showed that trabectedin affect tumor necrosis and reduction in vascularization in a xenograft model of a human high-grade chondrosarcoma. The aim of the present analysis was to clarify the efficacy of trabectedin for EMCS and MCS subjects in the randomized phase 2 study. Methods: Five subjects with EMCS and MCS received trabectedin treatment in the randomized phase 2 study. Three MCS subjects were allocated to the BSC group. Objective response and progression-free survival (PFS) were assessed according to the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 by central radiology imaging review. Results: The median follow-up time of the randomized phase 2 study was 22.7months, and one subject with MCS was still receiving trabectedin treatment at the final data cutoff. The median PFS was 12.5months (95 % CI: 7.4-not reached) in the trabectedin group, while 1.0months (95 % CI: 0.3-1.0months) in MCS subjects of the BSC group. The six-month progression-free rate was 100% in the trabectedin group. One subject with MCS showed partial response, and the others in the trabectedin group showed stable disease. Overall survival of EMCS and MCS subjects was 26.4months (range, 10.4-26.4months) in the trabectedin group. At the final data cutoff, two of five subjects were still alive. Conclusions: This sub-analysis shows that trabectedin is effective for patients with EMCS and MCS compared with BSC. The efficacy results were better than previously reported data of TRS. These facts suggest that trabectedin become an important choice of treatment for patients with advanced EMCS or MCS who failed or were intolerable to standard chemotherapy. Trial registration: The randomized phase 2 study is registered with the Japan Pharmaceutical Information Center, number JapicCTI-121850(May 31, 2012).
KW - Chemotherapy
KW - Extraskeletal myxoid chondrosarcoma
KW - Mesenchymal chondrosarcoma
KW - Trabectedin
KW - Translocation-related sarcoma
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U2 - 10.1186/s12885-016-2511-y
DO - 10.1186/s12885-016-2511-y
M3 - Article
C2 - 27418251
AN - SCOPUS:84987704688
SN - 1471-2407
VL - 16
JO - BMC Cancer
JF - BMC Cancer
IS - 1
M1 - 479
ER -