Kaatsch Peter, Reinisch Irene, Spix Claudia, Berthold Frank, Janka-Schaub Gritta, Mergenthaler Andreas, Michaelis Jörg, Blettner Maria
German Childhood Cancer Registry, Institute of Medical Biostatistics, Epidemiology and Informatics, Johannes Gutenberg-University Mainz, Obere Zahlbacher Strasse 69, 55101 Mainz, Germany.
Cancer Causes Control. 2009 Aug;20(6):965-80. doi: 10.1007/s10552-009-9315-1. Epub 2009 Mar 5.
We report on a nested case-control study with 328 cases with second malignant neoplasm (SMN) following childhood cancer and 639 matched controls based on the German Childhood Cancer Registry. In the adjusted overall analysis, the odds ratio (OR) for SMN following any radiotherapy or chemotherapy is 2.1 [95% confidence interval (CI): 1.8-3.3] and 1.8 (95% CI: 0.98-3.1), respectively. The strongest effect is seen for alkylating agents (OR=2.0, 95% CI: 1.2-3.3). The risk of SMN after leukemia is pronounced for antimetabolites (OR=17.2, 95% CI: 1.7-177) and asparaginase (OR=4.3, 95% CI: 1.7-11.0). Following solid tumors, the greatest effect is seen for platinum derivatives (OR=4.1, 95% CI: 1.7-10.1). For anthracyclines, a decreased risk is observed (OR=0.3, 95% CI: 0.1-0.6). Secondary solid tumors are mainly associated with radiotherapy (OR=4.5, 95% CI: 2.5-8.0), especially secondary carcinomas. Secondary acute myeloid leukemia and myelodysplastic syndrome are mainly associated with alkylating agents (OR=8.5, 95% CI: 0.97-74.8), asparaginase (OR=6.8, 95% CI: 2.3-20.6), and platinum derivatives (OR=4.5, 95% CI: 1.5-13.6). The observed risks are in many instances lower than the ones published in previous studies relating to earlier treatment eras of the primary diseases. These differences may be attributed to less toxic but still effective treatment regimes but also to differences in the length of follow-up.
我们报告了一项巢式病例对照研究,该研究基于德国儿童癌症登记处,纳入了328例儿童癌症后发生第二原发性恶性肿瘤(SMN)的病例以及639例匹配对照。在调整后的总体分析中,接受任何放疗或化疗后发生SMN的比值比(OR)分别为2.1[95%置信区间(CI):1.8 - 3.3]和1.8(95%CI:0.98 - 3.1)。烷化剂的影响最为显著(OR = 2.0,95%CI:1.2 - 3.3)。白血病后发生SMN的风险在抗代谢物(OR = 17.2,95%CI:1.7 - 177)和天冬酰胺酶(OR = 4.3,95%CI:1.7 - 11.0)方面较为突出。实体瘤之后,铂类衍生物的影响最大(OR = 4.1,95%CI:1.7 - 10.1)。对于蒽环类药物,观察到风险降低(OR = 0.3,95%CI:0.1 - 0.6)。继发性实体瘤主要与放疗相关(OR = 4.5,95%CI:2.5 - 8.0),尤其是继发性癌。继发性急性髓系白血病和骨髓增生异常综合征主要与烷化剂(OR = 8.5,95%CI:0.97 - 74.8)、天冬酰胺酶(OR = 6.8,95%CI:2.3 - 20.6)和铂类衍生物(OR = 4.5,95%CI:1.5 - 13.6)相关。在许多情况下,观察到的风险低于先前关于原发性疾病早期治疗时代发表的研究中的风险。这些差异可能归因于毒性较小但仍有效的治疗方案,也可能归因于随访时间的差异。