Dietrich P Y, Henry-Amar M, Cosset J M, Bodis S, Bosq J, Hayat M
Department of Medical Oncology, Institut Gustave Roussy, Villejuif, France.
Blood. 1994 Aug 15;84(4):1209-15.
Second primary cancers are a serious late occurrence for patients surviving Hodgkin's disease (HD). In addition to previously described risk factors such as age, gender, clinical stage, and treatment modalities, splenectomy was found to correlate with an increase in risk for secondary acute leukemia. We assumed that splenic irradiation inducing functional hyposplenia and splenectomy could have similar consequences on second cancer risk. We studied a series of 892 continuously disease-free HD adult patients treated at a single institution between 1960 and 1984. The risk of second cancer was analyzed (1) relative to the general population and (2) between risk subgroups using the Cox proportional hazards model. Fifty-six patients developed a second cancer (8 acute leukemias, 3 myelodysplastic syndromes, 8 non-Hodgkin's lymphomas, and 37 solid tumors; basal cell and in situ cervix carcinomas were excluded). The 15-year cumulative incidence rate (with 95% confidence limits) was 13.2% (9.3% to 17.2%). Relative to the general population incidence data, the risk of second cancer was multiplied by 4.68 (3.51 to 6.12; P < .001); it was multiplied by 2.80 (1.63 to 4.48; P < .001) in patients whose spleen was not treated and multiplied by 6.87 (4.81 to 9.51; P < .001) in splenectomized patients or patients whose spleen was irradiated. Multivariate regression analysis that controlled for confounding variables (age, gender, clinical stage, extent of radiation therapy, and chemotherapy regimen) showed that, in addition to age above 40 years (relative risk [RR] = 3.72; P < .001), combination of MOPP chemotherapy and regional irradiation (RR = 4.99; P = .015) and combination of MOPP chemotherapy and extended irradiation (RR = 10.86; P < .001), splenic irradiation (RR = 3.67; P = .003), and splenectomy (RR = 2.54; P = .018) also significantly correlated with an increased risk. The results of this hospital-based registry study strongly suggest that splenic irradiation and splenectomy might increase the risk for treatment-related second cancer. These findings, if confirmed, have to be considered in future HD treatment policies.
对于霍奇金淋巴瘤(HD)幸存者而言,第二原发性癌症是一种严重的晚期发病情况。除了先前描述的风险因素,如年龄、性别、临床分期和治疗方式外,还发现脾切除术与继发性急性白血病风险增加相关。我们推测,导致功能性脾功能减退的脾区照射和脾切除术可能对第二癌症风险产生类似影响。我们研究了1960年至1984年间在单一机构接受治疗的892例持续无病的HD成年患者。使用Cox比例风险模型分析了第二癌症的风险:(1)相对于一般人群;(2)在风险亚组之间。56例患者发生了第二癌症(8例急性白血病、3例骨髓增生异常综合征、8例非霍奇金淋巴瘤和37例实体瘤;基底细胞癌和原位宫颈癌被排除)。15年累积发病率(95%置信区间)为13.2%(9.3%至17.2%)。相对于一般人群发病率数据,第二癌症风险乘以4.68(3.51至6.12;P <.001);脾脏未接受治疗的患者风险乘以2.80(1.63至4.48;P <.001),脾切除患者或脾脏接受照射的患者风险乘以6.87(4.81至9.51;P <.001)。控制混杂变量(年龄、性别、临床分期、放疗范围和化疗方案)的多变量回归分析表明,除了40岁以上(相对风险[RR]=3.72;P <.001)、MOPP化疗与区域照射联合(RR = 4.99;P =.015)以及MOPP化疗与扩大照射联合(RR = 10.86;P <.001)外,脾区照射(RR = 3.67;P =.003)和脾切除术(RR = 2.54;P =.018)也与风险增加显著相关。这项基于医院登记研究的结果强烈表明,脾区照射和脾切除术可能会增加与治疗相关的第二癌症风险。如果这些发现得到证实,在未来的HD治疗策略中必须予以考虑。