Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Department of Bone Marrow Transplantation, West German Cancer Center, University Hospital of Essen, Essen, Germany.
Blood Adv. 2021 Mar 23;5(6):1760-1769. doi: 10.1182/bloodadvances.2020003600.
The inclusion of mutation status improved risk stratification for newly diagnosed patients with chronic myelomonocytic leukemia (CMML). Stem cell transplantation is a potentially curative treatment option, and patient selection is critical because of relevant transplant-related morbidity and mortality. We aimed to evaluate the impact of mutation status together with clinical presentations on posttransplant outcome. Our study included 240 patients with a median follow-up of 5.5 years. A significant association with worse survival was identified for the presence of mutations in ASXL1 and/or NRAS. In multivariable analysis, ASXL1- and/or NRAS-mutated genotype (hazard ratio [HR], 1.63), marrow blasts >2% (HR, 1.70), and increasing comorbidity index (continuous HR, 1.16) were independently associated with worse survival. A prognostic score (CMML transplant score) was developed, and the following points were assigned: 4 points for an ASXL1- and/or NRAS-mutated genotype or blasts >2% and 1 point each for an increase of 1 in the comorbidity index. The CMML transplant score (range, 0-20) was predictive of survival and nonrelapse mortality (P < .001 for both). Up to 5 risk groups were identified, showing 5-year survival of 81% for a score of 0 to 1, 49% for a score of 2 to 4, 43% for a score of 5 to 7, 31% for a score of 8 to 10, and 19% for a score >10. The score retained performance after validation (concordance index, 0.68) and good accuracy after calibration. Predictions were superior compared with existing scores designed for the nontransplant setting, which resulted in significant risk reclassification. This CMML transplant score, which incorporated mutation and clinical information, was prognostic in patients specifically undergoing transplantation and may facilitate personalized counseling.
基因突变状态的纳入改善了新诊断的慢性粒单核细胞白血病(CMML)患者的风险分层。干细胞移植是一种潜在的根治性治疗选择,由于相关的移植相关发病率和死亡率,患者选择至关重要。我们旨在评估突变状态与临床表现一起对移植后结果的影响。我们的研究包括 240 名患者,中位随访时间为 5.5 年。ASXL1 和/或 NRAS 基因突变的存在与较差的生存显著相关。在多变量分析中,ASXL1 和/或 NRAS 突变基因型(危险比 [HR],1.63)、骨髓原始细胞>2%(HR,1.70)和增加的合并症指数(连续 HR,1.16)与较差的生存独立相关。开发了一种预后评分(CMML 移植评分),并分配了以下分数:ASXL1 和/或 NRAS 突变基因型或原始细胞>2%为 4 分,合并症指数增加 1 分为 1 分。CMML 移植评分(范围,0-20)可预测生存和非复发死亡率(两者均<.001)。确定了多达 5 个风险组,显示评分 0-1 的 5 年生存率为 81%,评分 2-4 的为 49%,评分 5-7 的为 43%,评分 8-10 的为 31%,评分>10 的为 19%。验证后评分保留了性能(一致性指数,0.68)和良好的校准精度。与专为非移植环境设计的现有评分相比,预测结果更优,导致风险重新分类显著。这种纳入基因突变和临床信息的 CMML 移植评分在专门接受移植的患者中具有预后价值,并可能有助于个性化咨询。