Division of Hematology and Oncology, Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Cancer Res Treat. 2022 Oct;54(4):1230-1239. doi: 10.4143/crt.2021.1011. Epub 2021 Dec 17.
Approximately 30%-40% of pediatric acute myeloid leukemia (AML) patients relapse. In this study, we analyzed the outcome and prognostic factors of relapsed AML patients who had previously received first-line therapy at our institution.
The study group consisted of 50 patients who had been diagnosed with AML from April 2009 to December 2018, and then showed first relapse. Thirty-two of the patients (64%) had previously received allogeneic hematopoietic stem cell transplantation (HSCT) in first complete remission (CR).
Forty-five of the patients (90%) received intensive chemotherapy upon diagnosis of relapse, and 76% (34/45) of these patients achieved a second CR. Estimated 5-year overall survival for these 45 patients was 44.9%±7.6%. Time from diagnosis to relapse, extramedullary involvement (EMI) at diagnosis, core binding factor AML, and complex karyotype were significant prognostic factors; in multivariate study, both time from diagnosis to relapse and EMI at diagnosis proved significant. There was no difference in 5-year disease-free survival between patients previously treated with chemotherapy only and those who received HSCT in first CR (52.4%±14.9% vs. 52.6%±11.5%). Of the 19 patients who achieved second CR after previous allogeneic HSCT in first CR and subsequent relapse, 11 were treated with chemotherapy only, and seven survive disease-free.
Intensive therapy allowed for long-term survival in 40%-50% of patients, and 50% of patients who achieved second CR, regardless of prior treatment modalities in first CR. Intensive treatment may allow for salvage of a significant portion of patients with relapsed pediatric AML.
约 30%-40%的儿科急性髓系白血病(AML)患者会复发。本研究分析了在我院接受一线治疗后复发的 AML 患者的结局和预后因素。
研究组包括 50 例 2009 年 4 月至 2018 年 12 月诊断为 AML 并首次复发的患者。其中 32 例(64%)患者在首次完全缓解(CR)时已接受异基因造血干细胞移植(HSCT)。
45 例(90%)患者在复发时接受了强化化疗,其中 76%(34/45)的患者获得了第二次 CR。这 45 例患者的 5 年总生存率为 44.9%±7.6%。从诊断到复发的时间、诊断时的髓外累及(EMI)、核心结合因子 AML 和复杂核型是显著的预后因素;在多变量研究中,从诊断到复发的时间和诊断时的 EMI 均具有显著意义。仅接受化疗治疗的患者与在首次 CR 时接受 HSCT 治疗的患者 5 年无病生存率无差异(52.4%±14.9% vs. 52.6%±11.5%)。在 19 例首次 CR 时接受异基因 HSCT 并随后复发后获得第二次 CR 的患者中,11 例仅接受化疗治疗,7 例无病生存。
强化治疗使 40%-50%的患者和 50%的获得第二次 CR 的患者长期生存,而无论首次 CR 中采用何种治疗方式。强化治疗可能挽救相当一部分复发的儿科 AML 患者。