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IMAGENE trial: 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

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 check...

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Autores principales: Kato, Taigo, Matsubara, Nobuaki, Shiota, Masaki, Eto, Masatoshi, Osawa, Takahiro, Abe, Takashige, Shinohara, Nobuo, Yasumizu, Yota, Tanaka, Nobuyuki, Oya, Mototsugu, Nishimoto, Koshiro, Hayashi, Takuji, Nakayama, Masashi, Kojima, Takahiro, Namikawa, Kenjiro, Fujisawa, Takao, Okano, Susumu, Hida, Eisuke, Nakamura, Yoshiaki, Bando, Hideaki, Yoshino, Takayuki, Nonomura, Norio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9733213/
https://www.ncbi.nlm.nih.gov/pubmed/36494792
http://dx.doi.org/10.1186/s12885-022-10398-6
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author Kato, Taigo
Matsubara, Nobuaki
Shiota, Masaki
Eto, Masatoshi
Osawa, Takahiro
Abe, Takashige
Shinohara, Nobuo
Yasumizu, Yota
Tanaka, Nobuyuki
Oya, Mototsugu
Nishimoto, Koshiro
Hayashi, Takuji
Nakayama, Masashi
Kojima, Takahiro
Namikawa, Kenjiro
Fujisawa, Takao
Okano, Susumu
Hida, Eisuke
Nakamura, Yoshiaki
Bando, Hideaki
Yoshino, Takayuki
Nonomura, Norio
author_facet Kato, Taigo
Matsubara, Nobuaki
Shiota, Masaki
Eto, Masatoshi
Osawa, Takahiro
Abe, Takashige
Shinohara, Nobuo
Yasumizu, Yota
Tanaka, Nobuyuki
Oya, Mototsugu
Nishimoto, Koshiro
Hayashi, Takuji
Nakayama, Masashi
Kojima, Takahiro
Namikawa, Kenjiro
Fujisawa, Takao
Okano, Susumu
Hida, Eisuke
Nakamura, Yoshiaki
Bando, Hideaki
Yoshino, Takayuki
Nonomura, Norio
author_sort Kato, Taigo
collection PubMed
description 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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spelling pubmed-97332132022-12-10 IMAGENE trial: 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 Kato, Taigo Matsubara, Nobuaki Shiota, Masaki Eto, Masatoshi Osawa, Takahiro Abe, Takashige Shinohara, Nobuo Yasumizu, Yota Tanaka, Nobuyuki Oya, Mototsugu Nishimoto, Koshiro Hayashi, Takuji Nakayama, Masashi Kojima, Takahiro Namikawa, Kenjiro Fujisawa, Takao Okano, Susumu Hida, Eisuke Nakamura, Yoshiaki Bando, Hideaki Yoshino, Takayuki Nonomura, Norio BMC Cancer Study Protocol 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. BioMed Central 2022-12-09 /pmc/articles/PMC9733213/ /pubmed/36494792 http://dx.doi.org/10.1186/s12885-022-10398-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Study Protocol
Kato, Taigo
Matsubara, Nobuaki
Shiota, Masaki
Eto, Masatoshi
Osawa, Takahiro
Abe, Takashige
Shinohara, Nobuo
Yasumizu, Yota
Tanaka, Nobuyuki
Oya, Mototsugu
Nishimoto, Koshiro
Hayashi, Takuji
Nakayama, Masashi
Kojima, Takahiro
Namikawa, Kenjiro
Fujisawa, Takao
Okano, Susumu
Hida, Eisuke
Nakamura, Yoshiaki
Bando, Hideaki
Yoshino, Takayuki
Nonomura, Norio
IMAGENE trial: 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
title IMAGENE trial: 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
title_full IMAGENE trial: 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
title_fullStr IMAGENE trial: 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
title_full_unstemmed IMAGENE trial: 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
title_short IMAGENE trial: 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
title_sort imagene trial: 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
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9733213/
https://www.ncbi.nlm.nih.gov/pubmed/36494792
http://dx.doi.org/10.1186/s12885-022-10398-6
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