Renal toxicity in children undergoing total body irradiation for bone marrow transplant

被引:37
作者
Esiashvili, Natia [1 ]
Chiang, Kuang-Yueh [2 ]
Hasselle, Michael D. [3 ]
Bryant, Cynthia [4 ]
Riffenburgh, Robert H. [5 ]
Paulino, Arnold C. [6 ]
机构
[1] Emory Univ, Sch Med, Dept Radiat Oncol, Atlanta, GA 30322 USA
[2] Childrens Healthcare Atlanta, Atlanta, GA USA
[3] Univ Chicago, Dept Radiat Oncol, Chicago, IL 60637 USA
[4] Keyserling Canc Ctr, Port Royal, SC USA
[5] Naval Med Ctr, San Diego, CA USA
[6] Baylor Coll Med, Dept Radiat Oncol, Houston, TX 77030 USA
关键词
Total body irradiation; Renal toxicity; HEMOLYTIC UREMIC SYNDROME; LONG-TERM SURVIVORS; RADIATION NEPHRITIS; ACUTE-LEUKEMIA; DYSFUNCTION; NEPHROPATHY; INSUFFICIENCY; CYCLOPHOSPHAMIDE; CHILDHOOD; FAILURE;
D O I
10.1016/j.radonc.2008.09.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Contribution of total body irradiation (TBI) to renal toxicity in children undergoing the bone marrow transplant (BMT) remains controversial. We report our institutional retrospective study that evaluates the frequency Of acute and chronic renal dysfunction in children after using total body irradiation (TBI) conditioning regimens. Materials and methods: Between 1995 and 2003, 60 children with hematological malignancies underwent TBI as part Of a conditioning regimen before allogeneic BMT. Patients received 4-14 Gy at 1.75-2 Gy/fraction in six-eight fractions. Lung shielding was used in all patients to limit lung dose to less than 10 Gy: renal shielding was not utilized. All patients had baseline renal function assessment and renal dysfunction post-BM was mainly evaluated oil the basis of persistent serum creatinine elevation at acute (0-90 days) and chronic (>90 days) intervals after completion of BMT. Results: Acute renal dysfunction (ARD) was documented in 27 patients (45%); the majority had concurrent diagnosis of veno-occlusive disease (VOD) OF graft-versus-host disease (GVHD) and other potential Causes (sepsis. antibiotic). The risk for delayed renal dysfunction (DRD) at 1 year approached 25% for surviving patients. The ARD was strongly linked with the Fisk of the DRD. There was no statistically significant relationship between ARD, DRD and underlying diagnosis, GVHD, VOD or TBI doses with both univariate and multivariate analyses. The younger age (<5 years) had significantly increased risk for the development of ARD (p = 0.011). Conclusion: Our analysis validates high incidence of renal dysfunction in the pediatric BMT population. In contrast to other reports we did not find total body irradiation dose to be a risk factor for renal dysfunction. Future prospective Studies are needed to assess risk factors and interventions for this serious toxicity in children following allogeneic BM. (C) 2008 Elsevier Ireland Ltd. All rights reserved. Radiotherapy and Oncology 90 (2009) 242-246
引用
收藏
页码:242 / 246
页数:5
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