Biti G, Cellai E, Magrini S M, Papi M G, Ponticelli P, Boddi V
Department of Clinical Physiopathology, University of Florence, Italy.
Int J Radiat Oncol Biol Phys. 1994 Apr 30;29(1):25-31. doi: 10.1016/0360-3016(94)90222-4.
To define the risk of having a second malignant neoplasm (ST) in different subsets of Hodgkin's disease patients and possibly to identify potentially avoidable therapeutic behaviors, linked with an increased second tumor probability.
Cumulative probability of having a ST has been calculated for the different clinical and therapeutic subgroups of a population of 1121 patients consecutively treated (1960-1988) for Hodgkin's disease. Age groups at diagnosis were as follows: < 20 years, 18%; 20-40, 48%; 41-60, 26%; > 60, 8%. Initial treatment consisted of radiation alone (67%), combined modality treatment (24%), chemotherapy alone (9%). Treatment for relapse was also coded, and the occurrence of ST was related both to initial treatment (considering relapsed patients as censored at relapse) and to the "overall" treatment burden, without censoring at relapse.
An increased ST risk has been observed in patients older at HD diagnosis. Second tumors cumulative probability rates were significantly higher in patients initially treated with chemotherapy, especially when associated with subtotal or total nodal irradiation (relative risks of 3.1 and 4.1, p = .03 and .005, respectively, when compared to involved field radiotherapy alone). The same trend was observed for second solid tumors. Acute leukemia was more frequent in patients initially given chemotherapy alone or associated with radiotherapy (p = .01), and in those treated with an increasing number of cycles (p = .004). "Salvage" chemotherapy after radiation alone at presentation does not seem to be linked with an increased risk of leukemia.
The 15-year cumulative ST probability (11%) should be evaluated in the context of the very good cure rates achieved for Hodgkin's disease. The use of chemotherapy, particularly when associated with subtotal or total nodal irradiation, entails an increased risk of second malignancies and might be inappropriate in early stage Hodgkin's disease patients.
确定霍奇金淋巴瘤患者不同亚组发生第二原发性恶性肿瘤(ST)的风险,并有可能识别与第二肿瘤发生概率增加相关的潜在可避免的治疗行为。
计算了1121例连续接受治疗(1960 - 1988年)的霍奇金淋巴瘤患者不同临床和治疗亚组发生ST的累积概率。诊断时的年龄组如下:<20岁,18%;20 - 40岁,48%;41 - 60岁,26%;>60岁,8%。初始治疗包括单纯放疗(67%)、综合治疗(24%)、单纯化疗(9%)。对复发治疗也进行了编码,ST的发生与初始治疗(将复发患者视为在复发时截尾)以及“总体”治疗负担相关,复发时不进行截尾。
在霍奇金淋巴瘤诊断时年龄较大的患者中观察到ST风险增加。初始接受化疗的患者第二肿瘤累积概率率显著更高,尤其是与次全或全淋巴结照射联合时(与单纯受累野放疗相比,相对风险分别为3.1和4.1,p分别为0.03和0.005)。第二实体瘤也观察到相同趋势。急性白血病在初始单纯接受化疗或与放疗联合的患者中更常见(p = 0.01),以及在接受周期数增加的治疗的患者中更常见(p = 0.004)。初始表现为单纯放疗后进行“挽救性”化疗似乎与白血病风险增加无关。
应在霍奇金淋巴瘤取得非常好的治愈率的背景下评估15年累积ST概率(11%)。化疗的使用,尤其是与次全或全淋巴结照射联合时,会增加第二恶性肿瘤的风险,可能不适用于早期霍奇金淋巴瘤患者。