Children's National Medical Center, Washington, DC 20010, USA.
Biol Blood Marrow Transplant. 2011 Dec;17(12):1783-9. doi: 10.1016/j.bbmt.2011.05.008. Epub 2011 May 20.
We describe the incidence of malignancy in patients with primary immunodeficiency disorders (PIDD) following hematopoietic cell transplantation (HCT). From the Center for International Blood and Marrow Transplant Research, 2266 PIDD patients who had undergone allogeneic HCT between 1968 and 2003 were identified. Patient, disease, and transplant factors for development of malignancy were examined and pathology reports for reported malignancies reviewed independently by a pathologist for confirmation. The incidence of malignancy was highest for Wiskott-Aldrich syndrome (3.3%), with an overall incidence of 2.3% for PIDD. Post-HCT malignancy was confirmed for 52 of 63 reported cases. Forty-five of 52 patients developed posttransplant lymphoproliferative disorders (PTLD) at a median of 3 months post-HCT. Of these, 26 had received T cell-depleted (TCD) bone marrow. Three patients who developed myelodysplastic syndrome had received TCD marrow and total body irradiation. Three patients developed a solid tumor. Patients with PIDD are at a relatively low risk of developing malignancies post-HCT compared with their historic risk of cancer. The most frequent malignancy or lymphoproliferative disorder was early-onset PTLD. As in other HCT recipients, TCD appears to correlate with PTLD development. Our results lend support to the hypothesis that immune reconstitution in PIDD following HCT leads to a decrease in cancer risk.
我们描述了原发性免疫缺陷病(PIDD)患者在接受造血细胞移植(HCT)后的恶性肿瘤发病率。从国际血液和骨髓移植研究中心确定了 1968 年至 2003 年间接受异基因 HCT 的 2266 名 PIDD 患者。检查了患者、疾病和移植因素与恶性肿瘤的发展,并由病理学家独立审查了报告的恶性肿瘤的病理报告进行确认。Wiskott-Aldrich 综合征(3.3%)的恶性肿瘤发病率最高,PIDD 的总体发病率为 2.3%。52 例报告的恶性肿瘤中有 52 例得到确认。在 HCT 后,45 例患者在 HCT 后 3 个月内发生了移植后淋巴增殖性疾病(PTLD)。其中 26 例接受了 T 细胞耗竭(TCD)骨髓。3 例发生骨髓增生异常综合征的患者接受了 TCD 骨髓和全身照射。3 例患者发生了实体瘤。与癌症的历史风险相比,PIDD 患者在 HCT 后发生恶性肿瘤的风险相对较低。最常见的恶性肿瘤或淋巴增殖性疾病是早期 PTLD。与其他 HCT 受者一样,TCD 似乎与 PTLD 的发生相关。我们的结果支持以下假设,即 HCT 后 PIDD 的免疫重建导致癌症风险降低。