Walker Evan J, Ko Andrew H
Division of Hematology and Oncology, Department of Medicine, University of California, San Francisco, CA 94158, USA.
Helen Diller Comprehensive Cancer Center, University of California, San Francisco, CA 94158, USA.
Cancers (Basel). 2023 Jul 18;15(14):3657. doi: 10.3390/cancers15143657.
Metastatic pancreatic ductal adenocarcinoma is typically treated with multi-agent chemotherapy until disease progression or intolerable cumulative toxicity. For patients whose disease shows ongoing control or response beyond a certain timeframe (≥3-4 months), options include pausing chemotherapy with close monitoring or de-escalating to maintenance therapy with the goal of prolonging progression-free and overall survival while preserving quality of life. There is currently no universally accepted standard of care and a relative dearth of randomized clinical trials in the maintenance setting. Conceptually, such therapy can entail continuing the least toxic components of a first-line regimen and/or introducing novel agent(s) such as the poly(ADP-ribose) polymerase inhibitor olaparib, which is presently the only approved drug for maintenance treatment and is limited to a genetically defined subset of patients. In addition to identifying new therapeutic candidates and combinations in the maintenance setting, including targeted agents and immunotherapies, future research should focus on better understanding this unique biologic niche and how treatment in the maintenance setting may be distinct from resistant/refractory disease; identifying molecular predictors for more effective pairing of specific treatments with patients most likely to benefit; and establishing patient-reported outcomes in clinical trials to ensure accurate capture of quality of life metrics.
转移性胰腺导管腺癌通常采用多药化疗,直至疾病进展或出现无法耐受的累积毒性。对于疾病在特定时间框架(≥3 - 4个月)后仍显示持续控制或缓解的患者,可选择的方案包括暂停化疗并密切监测,或降级为维持治疗,目的是延长无进展生存期和总生存期,同时保持生活质量。目前,在维持治疗方面尚无普遍接受的标准治疗方案,且随机临床试验相对较少。从概念上讲,这种治疗可能包括继续使用一线方案中毒性最小的成分和/或引入新的药物,如聚(ADP - 核糖)聚合酶抑制剂奥拉帕利,它是目前唯一获批用于维持治疗的药物,且仅限于特定基因定义的患者亚组。除了在维持治疗中识别新的治疗候选药物和联合方案,包括靶向药物和免疫疗法外,未来的研究应集中在更好地理解这个独特的生物学微环境,以及维持治疗与耐药/难治性疾病的治疗有何不同;识别分子预测指标,以便更有效地将特定治疗与最可能受益的患者进行匹配;并在临床试验中建立患者报告的结局,以确保准确获取生活质量指标。