Rosso P, Terracini B, Fears T R, Jankovic M, Fossati Bellani F, Arrighini A, Carli M, Cordero di Montezemolo L, Garrè M L, Guazzelli C
Division of Pediatric Oncology, University of Turin, Italy.
Int J Cancer. 1994 Nov 15;59(4):451-6. doi: 10.1002/ijc.2910590402.
To evaluate the incidence of second malignant tumors in a cohort of subjects previously treated for childhood cancer, we analyzed data from the Off-Therapy Registry (OTR) of the Italian Association of Pediatric Hematology/Oncology, which collects information on children treated for Hodgkin's disease, non-Hodgkin's lymphoma, Wilms' tumor, acute lymphoblastic leukemia (ALL) and acute non-lymphatic leukemia and who had been removed from treatment in the absence of clinical signs of disease, i.e. the off-therapy stage. Second malignant tumors (SMT), diagnosed before December 31, 1988, were identified through a special enquiry to the 36 institutions cooperating in the registry. Observed cases were compared to expected numbers estimated from age- and sex-specific incidence rates derived from the Cancer Registry of the Province of Varese. In a total of 3,310 study subjects, 27 SMTs have been registered. The Cumulative Risk (CR) of SMT was 2.9% 15 years after the end of treatment and the Standard Incidence Ratio (SIR) was 10.8. The ALL sub-cohort had the highest risk of SMT (SIR 13.6) and 9 cases of CNS tumor occurred in this group (SIR 58.9). All 9 had received prophylactic cranial radiotherapy (CRT) and 5 had been treated on one protocol, characterized by low-dose intrathecal methotrexate (IT MTX) given monthly for 2 years after CRT. The Off-Therapy Registry has unique criteria for inclusion; direct comparisons with similar studies are therefore somewhat problematic. However, our data suggest that the risk of SMT in childhood ALL cancer survivors may be greater than previously reported, and that CNS tumors are the most common SMT in this group. The administration schedule of IT MTX may be an important risk factor.
为评估曾接受儿童癌症治疗的一组受试者中第二原发性恶性肿瘤的发生率,我们分析了意大利儿科血液学/肿瘤学协会的停止治疗登记处(OTR)的数据,该登记处收集了接受霍奇金病、非霍奇金淋巴瘤、肾母细胞瘤、急性淋巴细胞白血病(ALL)和急性非淋巴细胞白血病治疗且已在无疾病临床体征情况下停止治疗(即停止治疗阶段)的儿童的信息。通过对登记处合作的36家机构进行特别调查,确定了1988年12月31日前诊断的第二原发性恶性肿瘤(SMT)。将观察到的病例与根据瓦雷泽省癌症登记处得出的年龄和性别特异性发病率估算的预期数量进行比较。在总共3310名研究对象中,已登记了27例SMT。治疗结束15年后SMT的累积风险(CR)为2.9%,标准化发病比(SIR)为10.8。ALL亚组发生SMT的风险最高(SIR为13.6),该组中有9例中枢神经系统肿瘤发生(SIR为58.9)。所有9例均接受了预防性颅脑放疗(CRT),其中5例按照一个方案进行治疗,该方案的特点是在CRT后每月给予低剂量鞘内注射甲氨蝶呤(IT MTX),持续2年。停止治疗登记处有独特的纳入标准;因此与类似研究进行直接比较存在一定问题。然而,我们的数据表明,儿童ALL癌症幸存者发生SMT的风险可能比之前报道的更高,并且中枢神经系统肿瘤是该组中最常见的SMT。IT MTX的给药方案可能是一个重要的风险因素。