Nivolumab in pretreated pleural mesothelioma: Results from an observational real-world study of patients treated within the AIFA 5% Fund.

IF 2 4区 医学 Q3 ONCOLOGY Tumori Pub Date : 2024-06-01 Epub Date: 2024-02-19 DOI:10.1177/03008916241229287
Luigi Cerbone, Sara Delfanti, Stefania Crivellari, Antonina Maria De Angelis, Laura Mazzeo, Claudia Proto, Mario Occhipinti, Giuseppe Lo Russo, Chiara Dellepiane, Federica Biello, Irene Alabiso, Francesco Verderame, Roberta Gauna, Irene De Simone, Federica Cuppone, Sandra Petraglia, Giulia Pasello, Giovanni Luca Ceresoli, Marina Chiara Garassino, Valter Torri, Federica Grosso
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Abstract

Background: Pleural mesothelioma is a rare cancer with a dismal prognosis and few therapeutic options, especially in the pretreated setting. Immunotherapy with checkpoint inhibitors as single agents yielded interesting results in refractory pleural mesothelioma, achieving a response rate between 10-20%, median progression-free survival of 2-5 months and median overall survival of 7-13 months.

Patients and methods: A retrospective, multi-institutional study of pleural mesothelioma patients treated with nivolumab in second and further line was performed. The endpoints of the study are response rate, disease control rate, progression free survival and overall survival.

Results: Sixty-five patients with pleural mesothelioma treated with nivolumab in second and further line were enrolled at seven Italian institutions. The response rate was 8%, disease control rate was 37%, median progression free survival was 5.7 months (95% CI: 2.9-9.0) and median overall survival was 11.1 (95% CI 6.2-19.9) months. A higher neutrophils and neutrophils to lymphocytes ratio at baseline were associated with worse prognosis.

Conclusion: Nivolumab as a single agent is fairly active in a cohort of unselected pretreated pleural mesothelioma patients. Further investigations on clinical and translational factors are needed to define which patient might benefit most from nivolumab treatment in pleural mesothelioma.

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Nivolumab治疗预处理胸膜间皮瘤:在 AIFA 5% 基金范围内接受治疗的患者的真实世界观察研究结果。
背景:胸膜间皮瘤是一种罕见的癌症,其预后很差,治疗方案很少,尤其是在预处理的情况下。以检查点抑制剂为单药的免疫疗法在难治性胸膜间皮瘤中取得了令人感兴趣的结果,反应率在10%-20%之间,中位无进展生存期为2-5个月,中位总生存期为7-13个月:对胸膜间皮瘤患者进行了一项多机构回顾性研究,研究对象为接受二线及二线以上nivolumab治疗的胸膜间皮瘤患者。研究终点为反应率、疾病控制率、无进展生存期和总生存期:意大利七家机构共招募了65名胸膜间皮瘤患者,对他们进行了二线和三线nivolumab治疗。应答率为8%,疾病控制率为37%,中位无进展生存期为5.7个月(95% CI:2.9-9.0),中位总生存期为11.1个月(95% CI:6.2-19.9)。基线中性粒细胞和中性粒细胞与淋巴细胞比值越高,预后越差:结论:Nivolumab作为一种单药,在未经选择的预处理胸膜间皮瘤患者队列中具有相当的活性。需要进一步研究临床和转化因素,以确定哪些胸膜间皮瘤患者可从尼伐单抗治疗中获益最多。
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来源期刊
Tumori
Tumori 医学-肿瘤学
CiteScore
3.50
自引率
0.00%
发文量
58
审稿时长
6 months
期刊介绍: Tumori Journal covers all aspects of cancer science and clinical practice with a strong focus on prevention, translational medicine and clinically relevant reports. We invite the publication of randomized trials and reports on large, consecutive patient series that investigate the real impact of new techniques, drugs and devices inday-to-day clinical practice.
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