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A phase 2 basket trial of combination therapy with trastuzumab and pertuzumab in patients with solid cancers harboring human epidermal growth factor receptor 2 amplification (JUPITER trial)

Authors :
80456863
40360698
Takahashi, Kenta
Ishibashi, Eri
Kubo, Toshio
Harada, Yohei
Hayashi, Hideyuki
Kano, Masayuki
Shimizu, Yasushi
Shirota, Hidekazu
Mori, Yukiko
Muto, Manabu
Ishioka, Chikashi
Dosaka-Akita, Hirotoshi
Matsubara, Hisahiro
Nishihara, Hiroshi
Sueoka-Aragane, Naoko
Toyooka, Shinichi
Hirakawa, Akihiro
Tateishi, Ukihide
Miyake, Satoshi
Ikeda, Sadakatsu
80456863
40360698
Takahashi, Kenta
Ishibashi, Eri
Kubo, Toshio
Harada, Yohei
Hayashi, Hideyuki
Kano, Masayuki
Shimizu, Yasushi
Shirota, Hidekazu
Mori, Yukiko
Muto, Manabu
Ishioka, Chikashi
Dosaka-Akita, Hirotoshi
Matsubara, Hisahiro
Nishihara, Hiroshi
Sueoka-Aragane, Naoko
Toyooka, Shinichi
Hirakawa, Akihiro
Tateishi, Ukihide
Miyake, Satoshi
Ikeda, Sadakatsu
Publication Year :
2020

Abstract

Introduction: Human epidermal growth factor receptor 2 (HER2) gene amplification and mutations have emerged as oncogenic drivers and therapeutic targets not limited to breast and gastric cancers, but also in a variety of cancers. However, even if an actionable gene alteration is found, the incidence of HER2 amplification in these cancers is less than 5%. It is too difficult to conduct a conventional randomized, controlled trial in a rare fraction. Therefore, we have designed a organ-agnostic basket study, which covers a variety of solid cancers harboring HER2 amplification, in 1 study protocol. Methods/Design: This trial is a multicenter, single-arm, basket phase 2 study in Japan. Patients with solid cancers harboring HER2 amplification that have progressed with standard treatment, or rare cancers for which there is no standard treatment, will be eligible. Target cancers include bile duct, urothelial, uterine, ovarian, and other solid cancers where HER2 amplification is detected by comprehensive genomic profiling using next-generation sequencing technology. A total of 38 patients will be treated with combination therapy with trastuzumab and pertuzumab every 3 weeks until disease progression, unmanageable toxicity, death, or patient refusal. The primary endpoint is the objective response rate, and secondary endpoints are progression-free survival, overall survival, and duration of response. Discussion: The aim of this trial is to evaluate the safety and efficacy of combination therapy with trastuzumab and pertuzumab in patients with locally advanced or metastatic, solid cancers harboring HER2 amplification. Instead of focusing on 1 organ type, our trial design uses a basket study focusing on HER2 amplification, regardless of the site or origin of the cancer. The results of our study will advance clinical and scientific knowledge concerning the treatment of locally advanced, rare solid cancers harboring HER2 amplification, using the combination of trastuzumab and pert

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1238092863
Document Type :
Electronic Resource