Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY.
Department of Pediatrics, UCSF Benioff Children's Hospital Oakland, Oakland, CA; and.
Blood Adv. 2022 Apr 26;6(8):2688-2694. doi: 10.1182/bloodadvances.2021005753.
Effective reinduction regimens are needed for children with relapsed and refractory acute myeloid leukemia (AML), as outcomes remain poor. Therapeutic options are limited in this heavily pretreated patient population, many of whom have reached lifetime recommended doses of anthracycline chemotherapy. The development of effective non-anthracycline-based salvage regimens is crucial to these patients who are at significant risk of life-threatening cardiotoxicity. We previously reported results of a phase 2 trial of a clofarabine-based regimen with topotecan, vinorelbine, and thiotepa (TVTC) in patients with relapsed acute leukemias. Here we report on an expanded bicenter cohort of 33 patients, <25 years of age, with relapsed/refractory AML treated with up to 2 cycles of the TVTC reinduction regimen from 2007 to 2018. The overall response rate, defined as complete remission or complete remission with partial recovery of platelet count, was 71.4% (95% confidence interval [CI], 41.9-91.6) for those patients in first relapse (n = 14) and 47.4% (95% CI, 24.4-71.1) for patients in second or greater relapse or with refractory disease. Responses were seen across multiple high-risk cytogenetic and molecular subtypes, with 84% of responders successfully bridged to allogeneic stem cell transplantation. The 5-year overall survival for patients in first relapse was 46.2% (95% CI, 19.1-73.3) and 50.0% (95% CI, 26.9-73.1) for patients who responded to TVTC. For pediatric and young adult patients with relapsed/refractory AML, TVTC reinduction compares favorably with currently used salvage regimens and warrants further exploration.
对于复发和难治性急性髓系白血病(AML)患儿,需要有效的再诱导治疗方案,因为此类患儿的预后仍较差。在这个经过大量预处理的患者人群中,治疗选择有限,其中许多患儿已达到推荐的蒽环类化疗药物终生剂量。对于这些发生危及生命的心脏毒性风险较高的患者来说,开发有效的非蒽环类挽救性治疗方案至关重要。我们之前报道过一项含克拉屈滨的方案联合拓扑替康、长春瑞滨和噻替派(TVTC)治疗复发急性白血病患者的 2 期临床试验结果。在此,我们报告了一项扩展的双中心队列研究结果,该研究纳入了 33 例年龄<25 岁的复发/难治性 AML 患儿,自 2007 年至 2018 年,这些患儿接受了最多 2 个周期的 TVTC 再诱导治疗。对于首次复发(n = 14)的患儿,完全缓解或完全缓解伴血小板计数部分恢复的总缓解率定义为 71.4%(95%置信区间 [CI],41.9-91.6),而对于第 2 次或多次复发或难治性疾病的患儿,该缓解率为 47.4%(95% CI,24.4-71.1)。该方案在多种高危细胞遗传学和分子亚型中均观察到缓解,84%的缓解者成功桥接至异基因造血干细胞移植。首次复发患儿的 5 年总生存率为 46.2%(95% CI,19.1-73.3),对 TVTC 有反应的患儿的 5 年总生存率为 50.0%(95% CI,26.9-73.1)。对于复发/难治性 AML 的儿科和年轻成年患者,TVTC 再诱导治疗与目前使用的挽救性治疗方案相比具有优势,值得进一步探索。