Bitan Menachem, Ahn Kwang Woo, Millard Heather R, Pulsipher Michael A, Abdel-Azim Hisham, Auletta Jeffery J, Brown Valerie, Chan Ka Wah, Diaz Miguel Angel, Dietz Andrew, Vincent Marta González, Guilcher Gregory, Hale Gregory A, Hayashi Robert J, Keating Amy, Mehta Parinda, Myers Kasiani, Page Kristin, Prestidge Tim, Shah Nirali N, Smith Angela R, Woolfrey Ann, Thiel Elizabeth, Davies Stella M, Eapen Mary
Department of Pediatric Hematology/Oncology, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.
Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin; Division of Biostatistics, Institute for Health and Society, Medical College of Wisconsin, Milwaukee, Wisconsin.
Biol Blood Marrow Transplant. 2017 Sep;23(9):1523-1530. doi: 10.1016/j.bbmt.2017.05.011. Epub 2017 May 17.
We studied leukemia-free (LFS) and overall survival (OS) in children with acute myeloid (AML, n = 790) and acute lymphoblastic leukemia (ALL, n = 1096) who underwent transplantation between 2000 and 2010 and who survived for at least 1 year in remission after related or unrelated donor transplantation. Analysis of patient-, disease-, and transplantation characteristics and acute and chronic graft-versus-host disease (GVHD) was performed to identify factors with adverse effects on LFS and OS. These data were used to develop risk scores for survival. We did not identify any prognostic factors beyond 4 years after transplantation for AML and beyond 3 years for ALL. Risk score for survival for AML includes age, disease status at transplantation, cytogenetic risk group, and chronic GVHD. For ALL, the risk score includes age at transplantation and chronic GVHD. The 10-year probabilities of OS for AML with good (score 0, 1, or 2), intermediate (score 3), and poor risk (score 4, 5, 6, or 7) were 94%, 87%, and 68%, respectively. The 10-year probabilities of OS for ALL were 89% and 80% for good (score 0 or 1) and poor risk (score 2), respectively. Identifying children at risk for late mortality with early intervention may mitigate some excess late mortality.
我们研究了2000年至2010年间接受移植且在相关或无关供体移植后至少缓解存活1年的急性髓系白血病(AML,n = 790例)和急性淋巴细胞白血病(ALL,n = 1096例)患儿的无白血病生存期(LFS)和总生存期(OS)。对患者、疾病和移植特征以及急慢性移植物抗宿主病(GVHD)进行分析,以确定对LFS和OS有不利影响的因素。这些数据用于制定生存风险评分。我们未发现AML移植后4年以上及ALL移植后3年以上的任何预后因素。AML的生存风险评分包括年龄、移植时的疾病状态、细胞遗传学风险组和慢性GVHD。对于ALL,风险评分包括移植时的年龄和慢性GVHD。AML中低危(评分0、1或2)、中危(评分3)和高危(评分4、5、6或7)的10年OS概率分别为94%、87%和68%。ALL中低危(评分0或1)和高危(评分2)的10年OS概率分别为89%和80%。通过早期干预识别有晚期死亡风险的儿童可能会减轻一些额外的晚期死亡率。