Division of Hematology-Oncology, Perelman Center for Advanced Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Department of Pharmacy, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Am J Hematol. 2023 Aug;98(8):1254-1264. doi: 10.1002/ajh.26991. Epub 2023 Jun 19.
Intensive chemotherapy with cytarabine and anthracycline (7&3) remains the standard therapy for patients medically fit for induction, but the assessment of fitness remains controversial. Venetoclax and hypomethylating agent (ven/HMA) combination therapy has improved outcomes in unfit patients but no prospective study has assessed ven/HMA versus 7&3 as initial therapy in older, fit patients. Given no studies and expectation of ven/HMA use in patients outside of trial criteria, we evaluated retrospective outcomes among newly diagnosed patients. A nationwide electronic health record (EHR)-derived database and the University of Pennsylvania EHR identified 312 patients receiving 7&3 and 488 receiving ven/HMA who were 60-75 years old without history of organ failure. Ven/HMA patients were older and more likely to have secondary AML, adverse cytogenetics, and adverse mutations. Median overall survival (OS) for patients receiving intensive chemotherapy was 22 versus 10 months for ven/HMA (HR 0.53, 95% CI 0.40-0.60). Controlling for measured baseline characteristic imbalances reduced survival advantage by half (HR 0.71, 95% CI 0.53-0.94). A sub-group of patients with equipoise, likelihood at least 30%-70% of receiving either treatment, had similar OS outcomes (HR 1.10, 95% CI 0.75-1.6). Regarding safety outcomes, 60-day mortality was higher for ven/HMA (15% vs. 6% at 60 days) despite higher documented infections and febrile neutropenia for 7&3. In this multicenter real-word dataset, patients selected for intensive chemotherapy had superior OS but a large group had similar outcomes with ven/HMA. Prospective randomized studies, controlling for both measured and unmeasured confounders, must confirm this outcome.
含阿糖胞苷和蒽环类药物的强化化疗(7&3)仍然是适合诱导治疗的患者的标准治疗方法,但对于适合度的评估仍存在争议。维奈克拉和低甲基化剂(ven/HMA)联合治疗已改善了不适合患者的预后,但尚无前瞻性研究评估 ven/HMA 与 7&3 作为老年、适合患者的初始治疗。鉴于没有研究且预计 ven/HMA 将在试验标准之外的患者中使用,我们评估了新诊断患者的回顾性结局。全国性电子病历(EHR)衍生数据库和宾夕法尼亚大学 EHR 确定了 312 例接受 7&3 治疗和 488 例接受 ven/HMA 治疗的 60-75 岁且无器官衰竭病史的患者。ven/HMA 患者年龄更大,更有可能患有继发性 AML、不良细胞遗传学和不良突变。接受强化化疗的患者中位总生存期(OS)为 22 个月,而接受 ven/HMA 的患者为 10 个月(HR 0.53,95%CI 0.40-0.60)。控制基线特征的测量不平衡后,生存优势减少了一半(HR 0.71,95%CI 0.53-0.94)。在具有平衡、至少 30%-70%接受两种治疗可能性的患者亚组中,OS 结局相似(HR 1.10,95%CI 0.75-1.6)。关于安全性结局,ven/HMA 的 60 天死亡率更高(60 天分别为 15%和 6%),尽管 7&3 的记录感染和发热性中性粒细胞减少症更多。在这个多中心真实世界数据集,选择接受强化化疗的患者具有更好的 OS,但很大一部分患者的 ven/HMA 结局相似。需要前瞻性随机研究,控制已测量和未测量的混杂因素,以证实这一结果。