Next-generation therapies for pancreatic cancer

被引:10
|
作者
Buckley, Conor W. [1 ]
O'Reilly, Eileen M. [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, 300 East 66th St, New York, NY 10065 USA
[2] Weill Cornell Med, Dept Med, New York, NY USA
关键词
BRCA; homologous recombination repair; immune checkpoint blockade; KRAS; pancreatic adenocarcinoma; Poly-ADP ribose polymerase inhibitor; targeted therapy; tumor microenvironment; TUMOR-INFILTRATING MACROPHAGES; POSITIVE SOLID TUMORS; OPEN-LABEL; DUCTAL ADENOCARCINOMA; GERMLINE MUTATIONS; SIGNALING PATHWAYS; CIGARETTE-SMOKING; MODIFIED FOLFOX; NAB-PACLITAXEL; TARGETING KRAS;
D O I
10.1080/17474124.2024.2322648
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
IntroductionPancreas ductal adenocarcinoma (PDAC) is a frequently lethal malignancy that poses unique therapeutic challenges. The current mainstay of therapy for metastatic PDAC (mPDAC) is cytotoxic chemotherapy. NALIRIFOX (liposomal irinotecan, fluorouracil, leucovorin, oxaliplatin) is an emerging standard of care in the metastatic setting. An evolving understanding of PDAC pathogenesis is driving a shift toward targeted therapy. Olaparib, a poly-ADP-ribose polymerase (PARP) inhibitor, has regulatory approval for maintenance therapy in BRCA-mutated mPDAC along with other targeted agents receiving disease-agnostic approvals including for PDAC with rare fusions and mismatch repair deficiency. Ongoing research continues to identify and evaluate an expanding array of targeted therapies for PDAC.Areas coveredThis review provides a brief overview of standard therapies for PDAC and an emphasis on current and emerging targeted therapies.Expert opinionThere is notable potential for targeted therapies for KRAS-mutated PDAC with opportunity for meaningful benefit for a sizable portion of patients with this disease. Further, emerging approaches are focused on novel immune, tumor microenvironment, and synthetic lethality strategies.
引用
收藏
页码:55 / 72
页数:18
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