Majhail Navneet S
Blood and Marrow Transplant Program, University of Minnesota, Center for International Blood and Marrow Transplant Research, Minneapolis, MN 55455, USA.
Hematology Am Soc Hematol Educ Program. 2008:142-9. doi: 10.1182/asheducation-2008.1.142.
Relapse of primary disease and occurrence of new cancers can cause significant morbidity and mortality in recipients of autologous and allogeneic hematopoietic-cell transplantation (HCT). Treatment options for relapse are generally limited and can include disease-specific chemotherapy or targeted therapy. Additional relapse-directed therapies that are available for allogeneic HCT recipients include withdrawal of immunosuppression and donor lymphocyte infusion. Selected patients can be offered a second transplant procedure. Newer strategies to eliminate minimal residual disease and, in allogeneic HCT recipients, to augment the graft-versus-tumor effect are needed for patients who are at high risk for relapse after HCT. Second cancers after HCT include post-transplant lymphoproliferative disorder, hematologic malignancies and new solid cancers. The incidence of second solid cancers continues to rise without a plateau with increasing follow up of HCT survivors. Secondary myelodysplastic syndrome and acute leukemia are almost exclusively seen in autologous HCT recipients while post-transplant lymphoproliferative disorders complicate recipients of allogeneic HCT. Appropriate screening evaluations should be performed in HCT survivors to facilitate early detection and treatment of second cancers.
原发性疾病复发和新发癌症可导致自体和异基因造血细胞移植(HCT)受者出现显著的发病率和死亡率。复发的治疗选择通常有限,可包括针对特定疾病的化疗或靶向治疗。异基因HCT受者可用的其他针对复发的治疗方法包括停用免疫抑制和输注供体淋巴细胞。部分患者可接受第二次移植手术。对于HCT后复发风险高的患者,需要新的策略来消除微小残留病,并在异基因HCT受者中增强移植物抗肿瘤效应。HCT后的第二癌症包括移植后淋巴细胞增殖性疾病、血液系统恶性肿瘤和新发实体癌。随着对HCT幸存者随访时间的增加,第二实体癌的发病率持续上升且无平台期。继发性骨髓增生异常综合征和急性白血病几乎仅见于自体HCT受者,而异基因HCT受者会出现移植后淋巴细胞增殖性疾病并发症。应对HCT幸存者进行适当的筛查评估,以便于早期发现和治疗第二癌症。