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作 者:Qihao Wang Jianjun Ye Lei Zheng Xiang Tu Hao Zeng Yige Bao Qiang Wei
机构地区:[1]Department of Urology and Institute of Urology,West China Hospital,Sichuan University,Chengdu 610041,China [2]West China School of Medicine,Sichuan University,Chengdu 610041,China
出 处:《Holistic Integrative Oncology》2024年第1期219-230,共12页整合肿瘤学(英文)
摘 要:Poly(ADP-ribose)polymerase(PARP)inhibitor(PARPi),as a novel endocrine therapy,has been investigated in patients with metastatic castration-resistant prostate cancer(mCRPC)in recent years.Multiple large-scale clinical trials have consistently demonstrated that various PARP inhibitors,including olaparib,rucaparib,niraparib,and talazoparib,con-fer longer radiographic progression-free survival(rPFS)compared to new hormonal agents(NHA)in mCRPC patients with homologous recombination deficiency(HRD).Moreover,the incidence of grade 3 and above adverse events did not significantly increase.Additionally,when combined with androgen receptor signaling inhibitors(ARSI),olapa-rib,niraparib,and talazoparib have shown significant extension of rPFS but also an increased occurrence of serious adverse events in HRD-positive patients.Only PROpel yielded positive results among the homologous recombination repair(HRR)mutation negative population.Therefore,it remains uncertain whether ARSI-PARPi combination therapy should be considered as first-line treatment for mCRPC patients without HRR mutations.In this review article,we aim to elucidate the necessity and feasibility of combination therapy versus monotherapy specifically within the HRR mutant population while exploring its potential applicability to other non-HRR mutant subtypes.Furthermore,we conducted a comprehensive search on registered clinical trials at present to summarize the research progress of PARP inhibitors in prostate cancer patients at different disease stages.
关 键 词:Poly(ADP-ribose)polymerase inhibitors Androgen receptor signaling inhibitor Castration-resistant prostate cancer Homologous recombination repair mutation
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