Mauch P M, Kalish L A, Marcus K C, Shulman L N, Krill E, Tarbell N J, Silver B, Weinstein H, Come S, Canellos G P, Coleman C N
Joint Center for Radiation Therapy, 50 Binney Street, Boston, MA 02115, USA.
Cancer J Sci Am. 1995 May-Jun;1(1):33-42.
Despite dramatic improvements in the survival of patients with Hodgkin's disease attributable to advances in treatment over the past 30 years, concern for the risk of treatment-related deaths has led to a number of trials to evaluate reduction of therapy. The consequences of these trials on recurrence, development of long-term complications, and survival remain unknown. We determined the causes of death in a group of patients with pathologically staged and intensively treated Hodgkin's disease who were followed for long intervals.
Between April 1969 and December 1988, 794 patients with laparotomy-staged IA to IIIB Hodgkin's disease were treated with radiation therapy alone or combined radiation therapy and chemotherapy. There were 8700 person-years of follow-up (average, 10.95 person-years/ patient). Causes of mortality were grouped into the categories Hodgkin's disease, second malignant tumors, cardiovascular, infection, and miscellaneous. Age- and gender-specific incidence rates were multiplied by corresponding person-years of observation to obtain expected numbers of events. Observed-to-expected results were calculated by type of treatment, age at treatment, sex, and time after Hodgkin's disease. Absolute (excess) risk was expressed as number of excess cases per 10,000 person-years.
Of 124 patients who died, 56 died of Hodgkin's disease, 36 of second malignant neoplasms, 15 of cardiac causes, 9 of infection, and 8 of miscellaneous causes. The 20-year actuarial survival rate for all patients in this study is 73%. Age 40 years or older, mixed cellularity/lymphocyte-depleted histologic type, and stage-III disease were adverse independent predictors of survival. The largest differences were seen by age. The 20-year actuarial rates of survival were 78%, 78%, and 46%, respectively, for patients aged 16 or less, 17 to 39, and 40 years or older at diagnosis. Hodgkin's disease diagnosed at age 40 or older was a significant risk factor for all causes of death. The use of combined chemotherapy/ radiotherapy was a significant risk factor for second tumor and infection-related mortality. The excess risk of death from all causes, including Hodgkin's disease, remained constant with time from treatment and was approximately 1.2% per year over the first 20 years. Deaths from Hodgkin's disease decreased with time from treatment, with no patients dying after 15 years. This decrease, combined with an increased excess mortality risk with time from other causes, especially second tumors, accounted for the constant excess mortality with time after Hodgkin's disease.
Hodgkin's disease followed by second tumors, cardiac events, and infections remain the major causes of death after treatment of Hodgkin's disease. Our findings suggest the importance of both maintaining a high disease-free survival and reducing long-term complications in designing treatments of Hodgkin's disease.
尽管过去30年治疗方法的进步使霍奇金病患者的生存率有了显著提高,但对治疗相关死亡风险的担忧促使开展了多项试验以评估减少治疗强度的效果。这些试验对复发、长期并发症的发生及生存的影响仍不明确。我们确定了一组经病理分期并接受强化治疗的霍奇金病患者的死亡原因,并对其进行了长期随访。
1969年4月至1988年12月期间,794例经剖腹探查分期为IA至IIIB期的霍奇金病患者接受了单纯放疗或放疗联合化疗。随访时间共计8700人年(平均每位患者10.95人年)。死亡原因分为霍奇金病、第二原发性恶性肿瘤、心血管疾病、感染及其他。将年龄和性别特异性发病率乘以相应的观察人年数,以获得预期事件数。根据治疗类型、治疗时年龄、性别及霍奇金病发病后的时间计算观察值与预期值的结果。绝对(超额)风险以每10000人年的超额病例数表示。
124例死亡患者中,56例死于霍奇金病,36例死于第二原发性恶性肿瘤,15例死于心脏疾病,9例死于感染,8例死于其他原因。本研究中所有患者的20年精算生存率为73%。40岁及以上、混合细胞型/淋巴细胞消减型组织学类型及III期疾病是生存的不良独立预测因素。年龄差异最为显著。诊断时年龄在16岁及以下、17至39岁、40岁及以上的患者,其20年精算生存率分别为78%、78%和46%。40岁及以上诊断为霍奇金病是所有死因的重要危险因素。联合化疗/放疗的使用是第二肿瘤及感染相关死亡的重要危险因素。包括霍奇金病在内的所有原因导致的超额死亡风险在治疗后的时间里保持恒定,在前20年中约为每年1.2%。死于霍奇金病的人数随治疗后的时间减少,15年后无患者死亡。这种减少,加上其他原因尤其是第二肿瘤导致的超额死亡风险随时间增加,导致霍奇金病发病后随时间的超额死亡率保持恒定。
霍奇金病后继发第二肿瘤、心脏事件及感染仍是霍奇金病治疗后主要的死亡原因。我们的研究结果表明,在设计霍奇金病治疗方案时,维持高无病生存率和减少长期并发症都很重要。