Ahn Eugene R, Mangat Pam K, Garrett-Mayer Elizabeth, Halabi Susan, Dib Elie G, Haggstrom Daniel E, Alguire Kathryn B, Calfa Carmen J, Cannon Timothy L, Crilley Pamela A, Gaba Anu G, Marr Alissa S, Sangal Ashish, Thota Ramya, Antonelli Kaitlyn R, Islam Samiha, Rygiel Andrew L, Bruinooge Suanna S, Schilsky Richard L
Cancer Treatment Centers of America, Chicago, IL.
American Society of Clinical Oncology, Alexandria, VA.
JCO Precis Oncol. 2020 Nov;4:757-766. doi: 10.1200/PO.20.00037.
The Targeted Agent and Profiling Utilization Registry (TAPUR) Study is a phase II pragmatic basket trial evaluating antitumor activity of commercially available targeted agents in patients with advanced cancer with genomic alterations known to be drug targets. Results in a cohort of patients with non-small-cell lung cancer (NSCLC) with alterations treated with palbociclib are reported.
Eligible patients were ≥ 18 years old with advanced NSCLC, no remaining standard treatment options, measurable disease, Eastern Cooperative Oncology Group performance status of 0 to 2, and adequate organ function. Patients with NSCLC with alterations and no mutations received palbociclib 125 mg orally once daily for 21 days, followed by 7 days off. Simon's two-stage design was used with a primary study end point of objective response or stable disease (SD) of at least 16 weeks in duration. Secondary end points are progression-free survival (PFS), overall survival (OS), and safety.
Twenty-nine patients were enrolled from January 2017 to June 2018; two patients were not evaluable for response but were included in safety analyses. One patient with partial response and six patients with SD were observed, for a disease control rate of 31% (90% CI, 19% to 40%). Median PFS was 8.1 weeks (95% CI, 7.1 to 16.0 weeks), and median OS was 21.6 weeks (95% CI, 14.1 to 41.1 weeks). Eleven patients had at least 1 grade 3 or 4 adverse event (AE) or serious AE (SAE) possibly related to palbociclib (most common, cytopenias). Other AEs or SAEs possibly related to the treatment included anorexia, fatigue, febrile neutropenia, hypophosphatemia, sepsis, and vomiting.
Palbociclib monotherapy demonstrated evidence of modest antitumor activity in heavily pretreated patients with NSCLC with alterations. Additional investigation is necessary to confirm efficacy and utility of palbociclib in this population.
靶向药物与特征分析利用登记(TAPUR)研究是一项II期实用型篮子试验,旨在评估市售靶向药物对已知存在基因组改变且该改变为药物靶点的晚期癌症患者的抗肿瘤活性。本文报告了一群携带特定改变的非小细胞肺癌(NSCLC)患者接受哌柏西利治疗的结果。
符合条件的患者年龄≥18岁,患有晚期NSCLC,没有剩余的标准治疗方案,有可测量的疾病,东部肿瘤协作组体能状态为0至2,且器官功能良好。携带特定改变且无特定突变的NSCLC患者口服哌柏西利125 mg,每日一次,共21天,随后休息7天。采用西蒙两阶段设计,主要研究终点为客观缓解或持续至少16周的疾病稳定(SD)。次要终点为无进展生存期(PFS)、总生存期(OS)和安全性。
2017年1月至2018年6月共纳入29例患者;2例患者无法评估缓解情况,但纳入安全性分析。观察到1例部分缓解患者和6例疾病稳定患者,疾病控制率为31%(90%CI,19%至40%)。中位PFS为8.1周(95%CI,7.1至16.0周),中位OS为21.6周(95%CI,14.1至41.1周)。11例患者发生至少1次可能与哌柏西利相关的3级或4级不良事件(AE)或严重AE(SAE)(最常见的是血细胞减少)。其他可能与治疗相关的AE或SAE包括厌食、疲劳、发热性中性粒细胞减少、低磷血症、败血症和呕吐。
哌柏西利单药治疗在携带特定改变的、经过大量前期治疗的NSCLC患者中显示出一定的抗肿瘤活性。需要进一步研究以证实哌柏西利在该人群中的疗效和实用性。