Real-world treatment outcomes of immune checkpoint inhibitors used off-label in oncology: A comprehensive cancer institution experience.

IF 2.9 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pharmacology Research & Perspectives Pub Date : 2024-02-01 DOI:10.1002/prp2.1167
Sandra Fontanals, Anna Esteve, Andrea González, Cristina Ibáñez, Ricard Mesía, Ana Clopés
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Abstract

Off-label use (OLU) is quite common in oncology due to the complexity of cancer and the time-consuming regulatory process. However, outcomes of OLU in cancer treatment remain unclear. This study aimed to evaluate the overall survival (OS), event-free survival (EFS), duration of treatment (DOT), and reason for treatment discontinuation in patients receiving immune checkpoint inhibitors (ICI) as OLU for solid tumors from 2011 to 2020. The study collected data on 356 episodes (353 patients), with a median age of 64.4 years, 36.2% women, and 14.6% ECOG ≥ 2. Median OS was 15.7 (11.9-18.7) months, and median EFS was 5.4 (3.8-6.6) months. Men, patients with metastatic disease or ECOG-PS higher than 1, had worse survival outcomes. The findings derived from this study provide valuable information regarding the real-world use of ICI-OLU and contributes to enhancing the decision-making process for individuals with cancer. Further research on immunotherapy outcomes of OLU in cancer is needed.

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免疫检查点抑制剂在肿瘤学中标示外使用的实际治疗效果:综合癌症机构的经验。
由于癌症的复杂性和耗时的监管过程,标签外使用(OLU)在肿瘤学中十分常见。然而,OLU 在癌症治疗中的效果仍不明确。本研究旨在评估2011年至2020年期间接受免疫检查点抑制剂(ICI)作为OLU治疗实体瘤患者的总生存期(OS)、无事件生存期(EFS)、治疗持续时间(DOT)和治疗中止原因。该研究收集了356次发病(353名患者)的数据,中位年龄为64.4岁,36.2%为女性,14.6% ECOG≥2。中位 OS 为 15.7(11.9-18.7)个月,中位 EFS 为 5.4(3.8-6.6)个月。男性、患有转移性疾病或ECOG-PS高于1的患者生存率较低。这项研究的结果为ICI-OLU在现实世界中的应用提供了有价值的信息,有助于加强癌症患者的决策过程。我们需要对癌症患者使用 OLU 进行免疫治疗的结果进行进一步研究。
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来源期刊
Pharmacology Research & Perspectives
Pharmacology Research & Perspectives Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
5.30
自引率
3.80%
发文量
120
审稿时长
20 weeks
期刊介绍: PR&P is jointly published by the American Society for Pharmacology and Experimental Therapeutics (ASPET), the British Pharmacological Society (BPS), and Wiley. PR&P is a bi-monthly open access journal that publishes a range of article types, including: target validation (preclinical papers that show a hypothesis is incorrect or papers on drugs that have failed in early clinical development); drug discovery reviews (strategy, hypotheses, and data resulting in a successful therapeutic drug); frontiers in translational medicine (drug and target validation for an unmet therapeutic need); pharmacological hypotheses (reviews that are oriented to inform a novel hypothesis); and replication studies (work that refutes key findings [failed replication] and work that validates key findings). PR&P publishes papers submitted directly to the journal and those referred from the journals of ASPET and the BPS
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