Fabi Alessandra, Carbognin Luisa, Botticelli Andrea, Paris Ida, Fuso Paola, Savastano Maria Cristina, La Verde Nicla, Strina Carla, Pedersini Rebecca, Guarino Stefania, Curigliano Giuseppe, Criscitiello Carmen, Raffaele Mimma, Beano Alessandra, Franco Antonio, Valerio Maria Rosaria, Verderame Francesco, Fontana Andrea, Haspinger Eva Regina, Caldara Alessia, Di Leone Alba, Tortora Giampaolo, Giannarelli Diana, Scambia Giovanni
Precision Medicine Unit in Senology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Division of Gynecology Oncology, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
NPJ Breast Cancer. 2023 Sep 8;9(1):73. doi: 10.1038/s41523-023-00579-2.
The combination of atezolizumab and nab-paclitaxel is recommended in the EU as first-line treatment for PD-L1-positive metastatic triple-negative breast cancer (mTNBC), based on the results of phase III IMpassion130 trial. However, 'real-world' data on this combination are limited. The ANASTASE study (NCT05609903) collected data on atezolizumab plus nab-paclitaxel in PD-L1-positive mTNBC patients enrolled in the Italian Compassionate Use Program. A retrospective analysis was conducted in 29 Italian oncology centers among patients who completed at least one cycle of treatment. Data from 52 patients were gathered. Among them, 21.1% presented de novo stage IV; 78.8% previously received (neo)adjuvant treatment; 55.8% patients had only one site of metastasis; median number of treatment cycles was five (IQR: 3-8); objective response rate was 42.3% (95% CI: 28.9-55.7%). The median time-to-treatment discontinuation was 5 months (95% CI: 2.8-7.1); clinical benefit at 12 months was 45.8%. The median duration of response was 12.7 months (95% CI: 4.1-21.4). At a median follow-up of 20 months, the median progression-free survival was 6.3 months (95% CI: 3.9-8.7) and the median time to next treatment or death was 8.1 months (95% CI: 5.5-10.7). At 12 months and 24 months, the overall survival rates were 66.3% and 49.1%, respectively. The most common immune-related adverse events included rash (23.1%), hepatitis (11.5%), thyroiditis (11.5%) and pneumonia (9.6%). Within the ANASTASE study, patients with PD-L1-positive mTNBC treated with first-line atezolizumab plus nab-paclitaxel achieved PFS and ORR similar to those reported in the IMpassion130 study, with no unexpected adverse events.
基于III期IMpassion130试验的结果,阿替利珠单抗和白蛋白结合型紫杉醇的联合疗法在欧盟被推荐用于PD-L1阳性转移性三阴性乳腺癌(mTNBC)的一线治疗。然而,关于这种联合疗法的“真实世界”数据有限。ANASTASE研究(NCT05609903)收集了参与意大利同情用药计划的PD-L1阳性mTNBC患者使用阿替利珠单抗加白蛋白结合型紫杉醇的数据。在29个意大利肿瘤中心对至少完成一个治疗周期的患者进行了回顾性分析。收集了52例患者的数据。其中,21.1%为初发IV期;78.8%此前接受过(新)辅助治疗;55.8%的患者只有一个转移部位;治疗周期中位数为5个(四分位间距:3 - 8);客观缓解率为42.3%(95%置信区间:28.9 - 55.7%)。治疗中断的中位时间为5个月(95%置信区间:2.8 - 7.1);12个月时的临床获益率为45.8%。缓解持续时间中位数为12.7个月(95%置信区间:4.1 - 21.4)。在中位随访20个月时,无进展生存期中位数为6.3个月(95%置信区间:3.9 - 8.7),下次治疗或死亡的中位时间为8.1个月(95%置信区间:5.5 - 10.7)。在12个月和24个月时,总生存率分别为66.3%和49.1%。最常见的免疫相关不良事件包括皮疹(23.1%)、肝炎(11.5%)、甲状腺炎(11.5%)和肺炎(9.6%)。在ANASTASE研究中,一线使用阿替利珠单抗加白蛋白结合型紫杉醇治疗的PD-L1阳性mTNBC患者的无进展生存期和客观缓解率与IMpassion130研究报告的相似,且未出现意外不良事件。