Hijiya Nobuko, Ness Kirsten K, Ribeiro Raul C, Hudson Melissa M
Division of Hematology, Oncology, and Stem Cell Transplant, Children's Memorial Hospital, and Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60614-3394, USA.
Cancer. 2009 Jan 1;115(1):23-35. doi: 10.1002/cncr.23988.
Secondary acute leukemia is a devastating complication in children and adolescents who have been treated for cancer. Secondary acute lymphoblastic leukemia (s-ALL) was rarely reported previously but can be distinguished today from recurrent primary ALL by comparison of immunoglobulin and T-cell receptor rearrangement. Secondary acute myeloid leukemia (s-AML) is much more common, and some cases actually may be second primary cancers. Treatment-related and host-related characteristics and their interactions have been identified as risk factors for s-AML. The most widely recognized treatment-related risk factors are alkylating agents and topoisomerase II inhibitors (epipodophyllotoxins and anthracyclines). The magnitude of the risk associated with these factors depends on several variables, including the administration schedule, concomitant medications, and host factors. A high cumulative dose of alkylating agents is well known to predispose to s-AML. The prevalence of alkylator-associated s-AML has diminished among pediatric oncology patients with the reduction of cumulative alkylator dose and limited use of the more leukemogenic alkylators. The best-documented topoisomerase II inhibitor-associated s-AML is s-AML associated with epipodophyllotoxins. The risk of s-AML in these cases is influenced by the schedule of drug administration and by interaction with other antineoplastic agents but is not consistently found to be related to cumulative dose. The unpredictable risk of s-AML after epipodophyllotoxin therapy may discourage the use of these agents, even in patients at a high risk of disease recurrence, although the benefit of recurrence prevention may outweigh the risk of s-AML. Studies in survivors of adult cancers suggest that, contrary to previous beliefs, the outcome of s-AML is not necessarily worse than that of de novo AML when adjusted for cytogenetic features. More studies are needed to confirm this finding in the pediatric patient population.
继发性急性白血病是接受过癌症治疗的儿童和青少年中一种严重的并发症。继发性急性淋巴细胞白血病(s-ALL)以前很少被报道,但如今可通过免疫球蛋白和T细胞受体重排的比较与复发性原发性ALL区分开来。继发性急性髓系白血病(s-AML)更为常见,实际上有些病例可能是第二原发性癌症。与治疗相关和与宿主相关的特征及其相互作用已被确定为s-AML的危险因素。最广为人知的与治疗相关的危险因素是烷化剂和拓扑异构酶II抑制剂(表鬼臼毒素和蒽环类药物)。与这些因素相关的风险程度取决于几个变量,包括给药方案、伴随用药和宿主因素。众所周知,高累积剂量的烷化剂易引发s-AML。随着累积烷化剂剂量的减少以及更具致白血病性的烷化剂使用受限,烷化剂相关s-AML在儿科肿瘤患者中的患病率有所下降。记录最完善的拓扑异构酶II抑制剂相关s-AML是与表鬼臼毒素相关的s-AML。这些病例中s-AML的风险受给药方案以及与其他抗肿瘤药物相互作用的影响,但并未始终发现与累积剂量有关。表鬼臼毒素治疗后s-AML的不可预测风险可能会阻碍这些药物的使用,即使在疾病复发风险高的患者中也是如此,尽管预防复发的益处可能超过s-AML的风险。对成年癌症幸存者的研究表明,与之前的看法相反,调整细胞遗传学特征后,s-AML的预后不一定比原发性AML更差。需要更多研究来在儿科患者群体中证实这一发现。