Division of Pediatric Hematology/Oncology, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO.
Pediatric Hematology Oncology, University of California, San Francisco, San Francisco, CA.
Blood. 2024 May 16;143(20):2053-2058. doi: 10.1182/blood.2023021184.
Defining prognostic variables in T-lymphoblastic lymphoma (T-LL) remains a challenge. AALL1231 was a Children's Oncology Group phase 3 clinical trial for newly diagnosed patients with T acute lymphoblastic leukemia or T-LL, randomizing children and young adults to a modified augmented Berlin-Frankfurt-Münster backbone to receive standard therapy (arm A) or with addition of bortezomib (arm B). Optional bone marrow samples to assess minimal residual disease (MRD) at the end of induction (EOI) were collected in T-LL analyzed to assess the correlation of MRD at the EOI to event-free survival (EFS). Eighty-six (41%) of the 209 patients with T-LL accrued to this trial submitted samples for MRD assessment. Patients with MRD <0.1% (n = 75) at EOI had a superior 4-year EFS vs those with MRD ≥0.1% (n = 11) (89.0% ± 4.4% vs 63.6% ± 17.2%; P = .025). Overall survival did not significantly differ between the 2 groups. Cox regression for EFS using arm A as a reference demonstrated that MRD EOI ≥0.1% was associated with a greater risk of inferior outcome (hazard ratio, 3.73; 95% confidence interval, 1.12-12.40; P = .032), which was independent of treatment arm assignment. Consideration to incorporate MRD at EOI into future trials will help establish its value in defining risk groups. CT# NCT02112916.
在 T 淋巴细胞淋巴瘤(T-LL)中确定预后变量仍然是一个挑战。AALL1231 是一项儿童肿瘤学组的 3 期临床试验,针对新诊断的 T 急性淋巴细胞白血病或 T-LL 患者,将儿童和年轻成年人随机分配到改良的增强柏林-法兰克福-明斯特方案中,接受标准治疗(A 组)或硼替佐米(B 组)。在诱导结束时(EOI)收集了可选的骨髓样本以评估微小残留病(MRD),并对 T-LL 进行了分析,以评估 EOI 时的 MRD 与无事件生存(EFS)的相关性。在这项试验中,有 209 例 T-LL 患者入组,其中 86 例(41%)提交了用于 MRD 评估的样本。在 EOI 时 MRD<0.1%(n=75)的患者与 MRD≥0.1%(n=11)的患者相比,4 年 EFS 更好(89.0%±4.4%比 63.6%±17.2%;P=0.025)。两组的总生存率没有显著差异。使用 A 组作为参考的 EFS Cox 回归表明,EOI 时的 MRD≥0.1%与预后较差的风险增加相关(危险比,3.73;95%置信区间,1.12-12.40;P=0.032),这独立于治疗臂的分配。考虑将 EOI 时的 MRD 纳入未来的试验将有助于确定其在确定风险组中的价值。CT# NCT02112916。