DaSilva Brandon, Darwin Alicia, Zhang Amy, Vyas Rutu D, Russell Kathryn, Gilbert Jason S, Tan Virginia, Feldt Susan, Johnston Hannah, Liang Emily C, DuVall Adam S, Liedtke Michaela, Stock Wendy, Cassaday Ryan D, Schwartz Marc, Leonard Jessica T, Muffly Lori S, Luskin Marlise R
Department of Medicine, Stanford University School of Medicine, Stanford, CA.
Division of Hematology Oncology, Department of Medicine, Columbia University, New York, NY.
Blood Neoplasia. 2025 May 12;2(3):100111. doi: 10.1016/j.bneo.2025.100111. eCollection 2025 Aug.
The Cancer and Leukemia Group B 10403 (C10403) trial prospectively demonstrated the safety and efficacy of administering an asparaginase-containing pediatric regimen for the treatment of adolescents and young adults (AYAs) with acute lymphoblastic leukemia. Since its implementation as standard of care, it is unknown how the C10403 regimen performs beyond the clinical trial setting. To bridge this knowledge gap, we designed a multicenter retrospective cohort study to examine the safety, efficacy, and challenges of completing C10403 in the "real world." From October 2012 through June 2020, a total of 139 patients began induction as per the C10403 regimen across 6 US academic cancer centers. The median age was 26 years (range, 17-39), 69% were male, 55% were non-Hispanic White, and 27% were Hispanic. Among them, 122 patients (88%) achieved complete remission or complete remission with incomplete count recovery (CR/CRi) with C10403, 48 (35%) completed maintenance therapy, and 47 (34%) changed postremission regimens while in CR/CRi. The 3-year event-free survival (EFS) was 66% (95% confidence interval [CI], 55-74), and the 3-year overall survival (OS) was 81% (95% CI, 74-87). Four deaths occurred while on C10403 treatment: 1 during induction; and 3 later in the treatment course. The most common grade 3 or 4 adverse events during induction included alanine aminotransferase elevation (22%) and sepsis (14%). B-cell immunophenotype (hazard ratio [HR], 2.45; 95% CI, 1.09-5.48), Philadelphia chromosome-like genetics (HR, 3.05; 95% CI, 1.25-7.44), and Hispanic ethnicity (HR, 2.00; 95% CI, 1.06-3.78) were associated with worse EFS in univariate analyses. Overall, these real-world results are comparable to those of the C10403 trial. Further improvements are needed to enhance outcomes and regimen tolerability in the AYA population.
癌症与白血病B组10403(C10403)试验前瞻性地证明了含门冬酰胺酶的儿科方案用于治疗青少年和青年成人(AYA)急性淋巴细胞白血病的安全性和有效性。自该方案作为标准治疗实施以来,C10403方案在临床试验环境之外的表现尚不清楚。为了填补这一知识空白,我们设计了一项多中心回顾性队列研究,以检查在“现实世界”中完成C10403方案的安全性、有效性和挑战。从2012年10月到2020年6月,美国6家学术癌症中心共有139例患者按照C10403方案开始诱导治疗。中位年龄为26岁(范围17 - 39岁),69%为男性,55%为非西班牙裔白人,27%为西班牙裔。其中,122例患者(88%)通过C10403方案达到完全缓解或血细胞计数未完全恢复的完全缓解(CR/CRi),48例(35%)完成维持治疗,47例(34%)在CR/CRi期间改变缓解后方案。3年无事件生存率(EFS)为66%(95%置信区间[CI],55 - 74),3年总生存率(OS)为81%(95% CI,74 - 87)。在C10403治疗期间发生了4例死亡:诱导期1例;治疗过程后期3例。诱导期最常见的3级或4级不良事件包括丙氨酸氨基转移酶升高(22%)和败血症(14%)。单因素分析中,B细胞免疫表型(风险比[HR],2.45;95% CI,1.09 - 5.48)、费城染色体样遗传学(HR,3.05;95% CI,1.25 - 7.44)和西班牙裔种族(HR,2.00;95% CI,1.06 - 3.78)与较差的EFS相关。总体而言,这些现实世界的结果与C10403试验的结果相当。需要进一步改进以提高AYA人群的治疗效果和方案耐受性。