New malignant diseases after allogeneic marrow transplantation for childhood acute leukemia

被引:254
作者
Socié, G
Curtis, RE
Deeg, HJ
Sobocinski, KA
Filipovich, AH
Travis, LB
Sullivan, KM
Rowlings, PA
Kingma, DW
Banks, PM
Travis, WD
Witherspoon, RP
Sanders, J
Jaffe, ES
Horowitz, MM
机构
[1] Hop St Louis, Serv Hematol Greffe Moelle, F-75475 Paris 10, France
[2] NCI, Pathol Lab, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
[3] NCI, Pathol Lab, Div Canc Biol & Diag, Bethesda, MD 20892 USA
[4] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
[5] Med Coll Wisconsin, Int Bone Marrow Transplant Registry, Milwaukee, WI 53226 USA
[6] Childrens Hosp, Med Ctr, Cincinnati, OH 45229 USA
[7] Carolinas Med Ctr, Charlotte, NC 28203 USA
[8] Armed Forces Inst Pathol, Washington, DC 20306 USA
关键词
D O I
10.1200/JCO.2000.18.2.348
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine the incidence of and risk factors for second malignancies after allogeneic bone mar row transplantation (BMT) far childhood leukemia. Patients and Methods: We studied a cohort of 3,182 children diagnosed with acute leukemia before the age of 17 years who received allogeneic BMT between 1964 and 1992 at 235 centers. Observed second cancers were compared with expected cancers in an age and sex-matched general population. Risks factors were evaluated using Poisson regression. Results: Twenty-five solid tumors and 20 posttransplant lymphoproliferative disorders (PTLDs) were observed compared with 1.0 case expected (P <.001), Cumulative risk of solid cancers increased sharply to 11.0% (95% confidence interval, 2.3% to 19.8%) at 15 years and was highest among children at ages younger than 5 years at transplantation. Thyroid and brain cancers (n = 14) accounted for most of the strong age trend; many of these patients received cranial irradiation before BMT, Multivariate analyses showed increased solid tumor risks associated with high-dose total-body irradiation (relative risk [RR] = 3.1) and younger age at transplantation (RR = 3.7), whereas chronic graft-versus-host disease was associated with a decreased risk (RR = 0.2). Risk factors for PTLD included chronic graft-versus-host disease (RR = 6.5), unrelated or HLA-disparate related donor (RR = 7.5), T-cell-depleted graft (RR = 4.8), and antithymocyte globulin therapy (RR = 3.1). Conclusion: Long-term survivors of BMT for childhood leukemia have an increased risk of solid cancers and PTLDs, related to both transplant therapy and treatment given before BMT. Transplant recipients, especially those given radiation, should be monitored closely for second cancers. (C) 2000 by American Society of Clinical Oncology.
引用
收藏
页码:348 / 357
页数:10
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