Durable response to first-line PARP inhibition in BRCA-mutated metastatic cholangiocarcinoma: case report

被引:1
作者
Smith, Jarrod T. [1 ]
Sama, Shashank [2 ]
Florou, Vaia [2 ]
Nevala-Plagemann, Christopher [2 ]
Garrido-Laguna, Ignacio [2 ]
机构
[1] Univ Utah, Sch Med, Dept Internal Med, Salt Lake City, UT 84112 USA
[2] Univ Utah, Sch Med, Dept Internal Med, Div Oncol,Huntsman Canc Inst, 2000 Circle Hope,Room 2143, Salt Lake City, UT 84112 USA
关键词
Cholangiocarcinoma (CCA); BRCA; poly(ADP-ribose) polymerase inhibitor (PARP inhibitor); talazoparib; case report; POSITIVE SOLID TUMORS; INTRAHEPATIC CHOLANGIOCARCINOMA; OPEN-LABEL; CANCER; OLAPARIB; THERAPY; MULTICENTER; EFFICACY; SURVIVAL;
D O I
10.21037/jgo-23-425
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Cholangiocarcinoma (CCA) is an increasingly prevalent malignancy worldwide, with poor outcomes even when diagnosed at an early stage. While recent trials have shown benefit from the addition of immunotherapy to standard-of-care chemotherapy, the improvement in overall survival is modest. Multiple novel therapies for advanced CCA targeting actionable genetic alterations have been approved in recent years; BRCA1/2 mutations are identified in up to 5% of CCA patients and may be an additional target for novel treatment approaches. While BRCA mutations have been shown in clinical trials to predict response to poly(ADP-ribose) polymerase (PARP) inhibitors in several solid tumors including breast, ovarian, prostate, and pancreas, no similar large-scale trials have been published in CCA to date. We report here a durable response to PARP inhibitor monotherapy in BRCA-mutated extrahepatic CCA; to our knowledge, this is the second report of first-line PARP inhibitor monotherapy and the first reported use of the second-generation PARP inhibitor talazoparib in this setting. Case Description: We report the case of a 79-year-old man with metastatic extrahepatic CCA harboring a somatic BRCA1 mutation who declined chemotherapy and was instead treated in the first-line metastatic setting with the PARP inhibitor talazoparib; he experienced a complete radiographic response six months into treatment and has remained on talazoparib for over three years without evidence of disease recurrence. Conclusions: This case adds to a growing list of retrospective studies supporting the clinical activity of PARP inhibitors in BRCA-mutated extrahepatic CCA. However, prospective data are clearly needed prior to adoption of this strategy in clinical practice. Fortunately, multiple trials investigating novel combination therapies utilizing PARP inhibitors in CCA are underway.
引用
收藏
页码:2637 / 2643
页数:7
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