Sarkaria Jann N, Ballman Karla V, Kizilbash Sani H, Sulman Erik P, Giannini Caterina, Friday Bret B, Butowski Nicholas A, Mohile Nimish A, Piccioni David E, Battiste James D, Drappatz Jan, Campian Jian L, Mashru Sandeep, Jaeckle Kurt A, O'Brien Barbara J, Dixon Jesse G, Kabat Brian F, Laack Nadia L, Hu Leland S, Kaufmann Timothy, Kumthekar Priya, Ellingson Benjamin M, Anderson S Keith, Galanis Evanthia
Mayo Clinic, Rochester, Minnesota.
New York University Grossman School of Medicine, New York, New York.
JAMA Oncol. 2024 Dec 1;10(12):1637-1644. doi: 10.1001/jamaoncol.2024.4361.
The prognosis for patients with glioblastoma is poor following standard therapy with surgical resection, radiation, temozolomide, and tumor-treating fields.
To evaluate the combination of veliparib and temozolomide in glioblastoma based on preclinical data demonstrating significant chemosensitizing effects of the polyadenosine diphosphate-ribose polymerase 1/2 inhibitor veliparib when combined with temozolomide.
DESIGN, SETTING, AND PARTICIPANTS: Patients with newly diagnosed glioblastoma with MGMT promoter hypermethylation who had completed concomitant radiation and temozolomide were enrolled between December 15, 2014, and December 15, 2018, in this Alliance for Clinical Trials in Oncology trial. The data for this analysis were locked on April 21, 2023.
Patients were randomized and treated with standard adjuvant temozolomide (150-200 mg/m2 orally, days 1-5) combined with either placebo or veliparib (40 mg orally, twice daily, days 1-7) for 6 cycles.
The primary end point for the phase 3 portion of the trial was overall survival (OS).
There were 322 patients randomized during the phase 2 accrual period and an additional 125 patients randomized to complete the phase 3 accrual, for a total of 447 patients in the final phase 3 analysis. The median (range) age for patients was 60 (20-85) years and 190 patients (42.5%) were female. The median OS was 24.8 months (90% CI, 22.6-27.7) for the placebo arm and 28.1 months (90% CI, 24.3-33.3) for the veliparib arm (P = .17). The difference in survival did not meet the prespecified efficacy end point. However, there was a separation of the survival curves that favored the veliparib arm over 24 to 48 months of follow-up. The experimental combination was well tolerated with an acceptable elevation in grade 3 or 4 hematologic toxic effects.
This trial found that adding veliparib to adjuvant temozolomide did not significantly extend OS in patients with newly diagnosed, MGMT-hypermethylated glioblastoma.
ClinicalTrials.gov Identifier: NCT02152982.
胶质母细胞瘤患者接受手术切除、放疗、替莫唑胺和肿瘤电场治疗等标准治疗后的预后较差。
基于临床前数据评估维利帕尼与替莫唑胺联合治疗胶质母细胞瘤的效果,该数据表明聚腺苷二磷酸核糖聚合酶1/2抑制剂维利帕尼与替莫唑胺联合使用时具有显著的化学增敏作用。
设计、地点和参与者:2014年12月15日至2018年12月15日期间,在这项肿瘤临床试验联盟试验中纳入了新诊断的MGMT启动子高甲基化的胶质母细胞瘤患者,这些患者已完成同步放疗和替莫唑胺治疗。该分析的数据于2023年4月21日锁定。
患者被随机分组,并接受标准辅助替莫唑胺(口服150 - 200 mg/m²,第1 - 5天)联合安慰剂或维利帕尼(口服40 mg,每日两次,第1 - 7天)治疗6个周期。
该试验3期部分的主要终点是总生存期(OS)。
在2期入组期间有322例患者被随机分组,另外125例患者被随机分组以完成3期入组,最终3期分析共有447例患者。患者的中位(范围)年龄为60(20 - 85)岁,190例患者(42.5%)为女性。安慰剂组的中位OS为24.8个月(90%CI,22.6 - 27.7),维利帕尼组为28.1个月(90%CI,24.3 - 33.3)(P = 0.17)。生存差异未达到预先设定的疗效终点。然而,在24至48个月的随访中,生存曲线出现分离,维利帕尼组更具优势。该实验性联合治疗耐受性良好,3级或4级血液学毒性有可接受的升高。
该试验发现,在新诊断的MGMT高甲基化胶质母细胞瘤患者中,在辅助替莫唑胺治疗中添加维利帕尼并不能显著延长总生存期。
ClinicalTrials.gov标识符:NCT02152982。