Clinical Hematology and Bone Marrow Transplant Unit, Civil Service Hospital, Kathmandu, Nepal.
Department of Pathology, Civil Service Hospital, Kathmandu, Nepal.
JCO Glob Oncol. 2023 Jun;9:e2200408. doi: 10.1200/GO.22.00408.
Data on survival outcomes in patients with acute lymphoblastic leukemia (ALL) originating from Nepal are limited. We aim to present the real-world data on treatment outcomes of patients with de novo ALL treated with pediatric ALL-Berlin-Frankfurt-Muenster (BFM)-95 protocol in Nepal.
We used the medical records of 103 consecutive patients with ALL treated in our center from 2013 to 2016 to evaluate the overall survival (OS) and relapse-free survival (RFS) and analyzed the effects of clinicopathologic factors on survival outcomes in patients with ALL.
The 3-year OS and RFS in the entire cohort was 89.4% (95% CI, 82.1 to 96.7) and 87.3% (95% CI, 79.8 to 94.7), with a mean OS and RFS of 79.4 months (95% CI, 74.2 to 84.5) and 76.6 months (95% CI, 70.8 to 82.4), respectively. Patients with prednisone good response (PGR) showed better mean OS and RFS, whereas complete marrow response on day 33 was associated with better mean OS alone. Patients with Philadelphia (Ph)-positive ALL showed worse mean RFS compared to those with Ph-negative status. On multivariate analysis, PGR (hazard ratio [HR], 0.11; 95% CI, 0.03 to 0.49; = .004) and sagittal vein thrombosis (SVT; HR, 5.95; 95% CI, 1.30 to 27.18; = .02) were the only independent predictors of OS and RFS, respectively. Adverse events on BFM-95 protocol included SVT (4.9%), peripheral neuropathy (7.8%), myopathy (20.4%), hyperglycemia (24.3%), intestinal obstruction (7.8%), avascular necrosis of femur (6.8%), and mucositis (46%).
BFM-95 protocol appears to be a safe and effective strategy in adolescent and young adults and adult Nepalese population with ALL with a low toxicity profile.
尼泊尔有关急性淋巴细胞白血病(ALL)患者生存结果的数据有限。本研究旨在介绍尼泊尔采用儿童 ALL-Berlin-Frankfurt-Muenster(BFM)-95 方案治疗初发 ALL 患者的真实世界数据。
我们使用了 2013 年至 2016 年期间在本中心接受治疗的 103 例连续 ALL 患者的病历,评估了 ALL 患者的总生存(OS)和无复发生存(RFS),并分析了临床病理因素对 ALL 患者生存结果的影响。
整个队列的 3 年 OS 和 RFS 分别为 89.4%(95%CI,82.1 至 96.7)和 87.3%(95%CI,79.8 至 94.7),平均 OS 和 RFS 分别为 79.4 个月(95%CI,74.2 至 84.5)和 76.6 个月(95%CI,70.8 至 82.4)。泼尼松反应良好(PGR)的患者具有更好的平均 OS 和 RFS,而第 33 天完全骨髓缓解仅与更好的平均 OS 相关。费城染色体阳性(Ph+)ALL 患者的平均 RFS 较 Ph-状态患者差。多变量分析显示,PGR(风险比 [HR],0.11;95%CI,0.03 至 0.49;P=0.004)和矢状窦血栓形成(SVT;HR,5.95;95%CI,1.30 至 27.18;P=0.02)是 OS 和 RFS 的唯一独立预测因素。BFM-95 方案的不良事件包括 SVT(4.9%)、周围神经病变(7.8%)、肌病(20.4%)、高血糖(24.3%)、肠梗阻(7.8%)、股骨无菌性坏死(6.8%)和黏膜炎(46%)。
BFM-95 方案在尼泊尔青少年和年轻成人及成人 ALL 患者中似乎是一种安全有效的策略,其毒性谱较低。