Department of Pediatrics, Institution for Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Pediatrics and Adolescent Medicine, Hong Kong Children's Hospital and Hong Kong Pediatric Hematology and Oncology Study Group (HKPHOSG), Hong Kong, China.
Br J Haematol. 2023 May;201(4):757-765. doi: 10.1111/bjh.18685. Epub 2023 Feb 10.
A significant proportion of events in paediatric acute myeloid leukaemia (AML) are caused by resistant disease (RD). We investigated clinical and biological characteristics in 66 patients with RD from 1013 children with AML registered and treated according to the NOPHO-AML 93, NOPHO-AML 2004, DB AML-01 and NOPHO-DBH AML 2012 protocols. Risk factors for RD were age10 years or older and a white-blood-cell count (WBC) of 100 × 10 /L or more at diagnosis. The five-year overall survival (OS) was 38% (95% confidence interval [CI]: 28%-52%). Of the 63 children that received salvage therapy with chemotherapy, 59% (N = 37) achieved complete remission (CR) with OS 57% (95% CI: 42%-75%) compared to 12% (95% CI: 4%-35%) for children that did not achieve CR. Giving more than two salvage chemotherapy courses did not increase CR rates. OS for all 43 patients receiving allogeneic haematopoietic stem cell transplantation (HSCT) was 49% (95% CI: 36%-66%). Those achieving CR and proceeding to HSCT had an OS of 56% (95% CI: 41%-77%, N = 30). This study showed that almost 40% of children with primary resistant AML can be cured with salvage therapy followed by HSCT. Children that did not achieve CR after two salvage courses with chemotherapy did not benefit from additional chemotherapy.
在儿童急性髓系白血病(AML)中,相当一部分事件是由耐药性疾病(RD)引起的。我们研究了根据 NOPHO-AML 93、NOPHO-AML 2004、DB AML-01 和 NOPHO-DBH AML 2012 方案登记和治疗的 1013 例 AML 儿童中 66 例 RD 患者的临床和生物学特征。RD 的危险因素是年龄 10 岁或以上,以及诊断时白细胞计数(WBC)为 100×10/L 或更高。五年总生存率(OS)为 38%(95%置信区间[CI]:28%-52%)。在接受化疗挽救治疗的 63 例儿童中,59%(N=37)获得完全缓解(CR),OS 为 57%(95%CI:42%-75%),而未获得 CR 的儿童 OS 为 12%(95%CI:4%-35%)。给予两次以上的挽救性化疗并不会增加 CR 率。所有接受异基因造血干细胞移植(HSCT)的 43 例患者的 OS 为 49%(95%CI:36%-66%)。那些获得 CR 并进行 HSCT 的患者的 OS 为 56%(95%CI:41%-77%,N=30)。这项研究表明,近 40%的原发性耐药 AML 儿童可以通过挽救性治疗联合 HSCT 治愈。接受两次挽救性化疗后未获得 CR 的儿童不会从额外的化疗中获益。