TY - JOUR
T1 - IMAGENE trial
T2 - multicenter, proof-of-concept, phase II study evaluating the efficacy and safety of combination therapy of niraparib with PD-1 inhibitor in solid cancer patients with homologous recombination repair genes mutation
AU - Kato, Taigo
AU - Matsubara, Nobuaki
AU - Shiota, Masaki
AU - Eto, Masatoshi
AU - Osawa, Takahiro
AU - Abe, Takashige
AU - Shinohara, Nobuo
AU - Yasumizu, Yota
AU - Tanaka, Nobuyuki
AU - Oya, Mototsugu
AU - Nishimoto, Koshiro
AU - Hayashi, Takuji
AU - Nakayama, Masashi
AU - Kojima, Takahiro
AU - Namikawa, Kenjiro
AU - Fujisawa, Takao
AU - Okano, Susumu
AU - Hida, Eisuke
AU - Nakamura, Yoshiaki
AU - Bando, Hideaki
AU - Yoshino, Takayuki
AU - Nonomura, Norio
N1 - Funding Information:
We would like to thank all the patients and their families who participated in this trial; all the co-investigators and site personnel. We also thank the clinical trial office members in the Department of Medical Innovation, Osaka University Hospital (Yoko Kawamura, Kento Asano, and Tomoharu Dohi) and FiveRings Corporation (Harumi Sakata, Chiho Uegaki, Tatsushi Goto, and Hiroshi Miyamoto).
Funding Information:
IMAGENE trial receives financial support from the Japan Agency for Medical Research and Development (AMED; grant Number, 21ck0106656h0001). Takeda Pharmaceutical Co., Ltd. provides investigational drugs as well as financial support for the translational research. The funders had no role in the study design; in data collection, analysis, or interpretation; or in the writing of the report.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Background: Previous clinical trials have demonstrated the potential efficacy of poly (ADP-ribose) polymerase (PARP) inhibitors (PARPis) in patients with cancer involving homologous recombination repair (HRR) gene-mutation. Moreover, HRR gene-mutated cancers are effectively treated with immune checkpoint inhibitors (ICIs) with the increase in tumor mutation burden. We have proposed to conduct a multicenter, single-arm phase II trial (IMAGENE trial) for evaluating the efficacy and safety of niraparib (PARPi) plus programmed cell death-1 inhibitor combination therapy in patients with HRR gene-mutated cancers who are refractory to ICIs therapy using a next generation sequencing-based circulating tumor DNA (ctDNA) and tumor tissue analysis. Methods: Key eligibility criteria for this trial includes HRR gene-mutated tumor determined by any cancer gene tests; progression after previous ICI treatment; and Eastern Cooperative Oncology Group Performance Status ≤ 1. The primary endpoint is the confirmed objective response rate (ORR) in all patients. The secondary endpoints include the confirmed ORR in patients with HRR gene-mutation of ctDNA using the Caris Assure (CARIS, USA). The target sample size of the IMAGENE trial is 57 patients. Biomarker analyses will be performed in parallel using the Caris Assure, proteome analysis, and T cell repertoire analysis to reveal tumor immunosurveillance in peripheral blood. Expected outcome: Our trial aims to confirm the clinical benefit of PARPi plus ICI combination therapy in ICI-resistant patients. Furthermore, through translational research, our trial will shed light on which patients would benefit from the targeted combination therapy for patients with HRR gene-mutated tumor even after the failure of ICIs. Trial registration: The IMAGENE trial: jRCT, Clinical trial no.: jRCT2051210120, Registered date: November 9, 2021.
AB - Background: Previous clinical trials have demonstrated the potential efficacy of poly (ADP-ribose) polymerase (PARP) inhibitors (PARPis) in patients with cancer involving homologous recombination repair (HRR) gene-mutation. Moreover, HRR gene-mutated cancers are effectively treated with immune checkpoint inhibitors (ICIs) with the increase in tumor mutation burden. We have proposed to conduct a multicenter, single-arm phase II trial (IMAGENE trial) for evaluating the efficacy and safety of niraparib (PARPi) plus programmed cell death-1 inhibitor combination therapy in patients with HRR gene-mutated cancers who are refractory to ICIs therapy using a next generation sequencing-based circulating tumor DNA (ctDNA) and tumor tissue analysis. Methods: Key eligibility criteria for this trial includes HRR gene-mutated tumor determined by any cancer gene tests; progression after previous ICI treatment; and Eastern Cooperative Oncology Group Performance Status ≤ 1. The primary endpoint is the confirmed objective response rate (ORR) in all patients. The secondary endpoints include the confirmed ORR in patients with HRR gene-mutation of ctDNA using the Caris Assure (CARIS, USA). The target sample size of the IMAGENE trial is 57 patients. Biomarker analyses will be performed in parallel using the Caris Assure, proteome analysis, and T cell repertoire analysis to reveal tumor immunosurveillance in peripheral blood. Expected outcome: Our trial aims to confirm the clinical benefit of PARPi plus ICI combination therapy in ICI-resistant patients. Furthermore, through translational research, our trial will shed light on which patients would benefit from the targeted combination therapy for patients with HRR gene-mutated tumor even after the failure of ICIs. Trial registration: The IMAGENE trial: jRCT, Clinical trial no.: jRCT2051210120, Registered date: November 9, 2021.
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U2 - 10.1186/s12885-022-10398-6
DO - 10.1186/s12885-022-10398-6
M3 - Article
C2 - 36494792
AN - SCOPUS:85143704750
SN - 1471-2407
VL - 22
JO - BMC Cancer
JF - BMC Cancer
IS - 1
M1 - 1292
ER -