Cortellini Alessio, Bersanelli Melissa, Buti Sebastiano, Gambale Elisabetta, Atzori Francesco, Zoratto Federica, Parisi Alessandro, Brocco Davide, Pireddu Annagrazia, Cannita Katia, Iacono Daniela, Migliorino Maria R, Gamucci Teresa, De Tursi Michele, Sidoni Tina, Tiseo Marcello, Michiara Maria, Papa Anselmo, Angius Gesuino, Tomao Silverio, Fargnoli Maria C, Natoli Clara, Ficorella Corrado
Medical Oncology Unit, St Salvatore Hospital, Department of Biotechnological & Applied Clinical Sciences, University of L'Aquila, Via Vetoio, 67100, L'Aquila, Italy.
Department of Biotechnological & Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
Immunotherapy. 2018 Jun;10(8):643-655. doi: 10.2217/imt-2017-0167. Epub 2018 Mar 22.
Tumors related to hereditary susceptibility seem to have an immunosensitive phenotype.
MATERIALS & METHODS: We conducted a multicenter retrospective study, to investigate if family history of cancer, multiple neoplasms and early onset of cancer could be related to clinical outcomes of anti-PD-1/PD-L1 therapy. Activity and efficacy data of 211 advanced cancer patients (kidney, non-small-cell lung cancer, melanoma, urothelium, colorectal and HeN), treated at seven Italian centers with anti-PD-1/PD-L1 agents, were analyzed.
In this preliminary report at multivariate analyses, positive family history of cancer showed a statistically significant relationship with a better objective response rate (p = 0.0024), disease control rate (p = 0.0161), median time to treatment failure (p = 0.0203) and median overall survival (p = 0.0221). Diagnosis of multiple neoplasms significantly correlates only to a better disease control rate, while interestingly non-early onset of cancer and sex (in favor of female patients) showed significant correlation with a better median overall survival (p = 0.0268 and p = 0.0272, respectively).
This pilot study seems to individuate easily available patient's features as possible predictive surrogates of clinical benefit for anti-PD-1/PD-L1 treatments. These preliminary results need to be confirmed with a greater sample size, in prospective trials with immunotherapy.
与遗传易感性相关的肿瘤似乎具有免疫敏感表型。
我们进行了一项多中心回顾性研究,以调查癌症家族史、多发肿瘤和癌症早发是否与抗PD-1/PD-L1治疗的临床结果相关。分析了在意大利七个中心接受抗PD-1/PD-L1药物治疗的211例晚期癌症患者(肾癌、非小细胞肺癌、黑色素瘤、尿路上皮癌、结直肠癌和头颈癌)的活性和疗效数据。
在这份多变量分析的初步报告中,癌症家族史阳性与更好的客观缓解率(p = 0.0024)、疾病控制率(p = 0.0161)、中位治疗失败时间(p = 0.0203)和中位总生存期(p = 0.0221)具有统计学显著相关性。多发肿瘤的诊断仅与更好的疾病控制率显著相关,而有趣的是,癌症非早发和性别(女性患者更有利)与更好的中位总生存期显著相关(分别为p = 0.0268和p = 0.0272)。
这项初步研究似乎确定了容易获得的患者特征,作为抗PD-1/PD-L1治疗临床获益的可能预测替代指标。这些初步结果需要在免疫治疗的前瞻性试验中用更大的样本量进行证实。