Systemic Therapy for Metastatic Pancreatic Cancer-Current Landscape and Future Directions

被引:0
|
作者
Netto, Daniel [1 ]
Frizziero, Melissa [1 ]
Foy, Victoria [1 ]
McNamara, Mairead G. [1 ,2 ]
Backen, Alison [1 ,2 ]
Hubner, Richard A. [1 ,2 ]
机构
[1] Christie NHS Fdn Trust, 550 Wilmslow Rd, Manchester M20 4BX, England
[2] Univ Manchester, Div Canc Sci, Oxford Rd, Manchester M13 9PL, England
关键词
pancreas; metastatic; chemotherapy; KRAS; molecular profiling; PHASE-III TRIAL; GROWTH-FACTOR RECEPTOR; DOSE-ESCALATION TRIAL; NAB-PACLITAXEL; NANOLIPOSOMAL IRINOTECAN; PEPTIDE VACCINATION; POOLED-ANALYSIS; SOLID TUMORS; GEMCITABINE; CISPLATIN;
D O I
10.3390/curroncol31090385
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pancreatic ductal adenocarcinoma (PDAC) is a significant cause of cancer-associated mortality, with a rising global incidence. A paucity of strong predictive risk factors mean screening programmes are difficult to implement. Historically, a lack of identifiable and actionable driver mutations, coupled with a relatively immunosuppressed tumour microenvironment, has led to a reliance on cytotoxic chemotherapy. The NAPOLI-3 trial has reported data supporting consideration of NALIRIFOX as a new first-line standard of care. Kirsten Rat Sarcoma Virus (KRAS) G12D mutations are present in >90% of all PDAC's; exciting breakthroughs in small molecule inhibitors targeting KRAS G12D may open new modalities of treatment, and therapies targeting multiple KRAS mutations are also in early clinical trials. Although immunotherapy strategies to date have been disappointing, combination with chemotherapy and/or small molecule inhibitors hold promise and warrant further exploration.
引用
收藏
页码:5206 / 5223
页数:18
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