Ng Andrea K, Bernardo M Patricia, Weller Edie, Backstrand Kendall H, Silver Barbara, Marcus Karen C, Tarbell Nancy J, Friedberg Jonathan, Canellos George P, Mauch Peter M
Department of Radiation Oncology, Brigham and Women's Hospital/Dana-Farber Cancer Institute, Boston, MA, USA.
J Clin Oncol. 2002 Apr 15;20(8):2101-8. doi: 10.1200/JCO.2002.08.021.
To analyze the long-term survival and the pattern and timing of excess mortality in patients with early-stage Hodgkin's disease.
Between 1969 and 1997, 1,080 patients age 50 or younger were treated for clinical stage IA to IIB Hodgkin's disease. Overall survival was determined, and prognostic factors were assessed. Relative risk and absolute excess risk (AR) of mortality were calculated for the entire cohort and by prognostic groups (on the basis of B symptoms, mediastinal status, and number of sites, modified from the European Organization for Research and Treatment of Cancer).
The median follow-up was 12 years. The 15- and 20-year Kaplan-Meier survival estimates were 84% and 78%, respectively. Cox proportional hazards models showed that number of involved sites (P =.006), mediastinal status (P =.02), and histology (P =.02) were independent predictors of death from all causes. The AR of mortality in patients with a favorable prognosis increased over time, whereas for those with an unfavorable prognosis, the AR peaked in the first 5 years, predominantly from Hodgkin's disease. The relative risk of mortality from all causes, causes other than Hodgkin's disease, second tumors, and cardiac disease remained significantly elevated more than 20 years after treatment.
Patients treated for early-stage Hodgkin's disease have a sustained excess mortality risk despite good control of the disease. Treatment reduction efforts in patients with early-stage, favorable-prognosis disease should continue, but for patients with an unfavorable prognosis, modified treatment may not be advisable. The excess mortality noted beyond two decades underscores the importance of long-term follow-up care in patients treated for Hodgkin's disease.
分析早期霍奇金病患者的长期生存情况以及额外死亡的模式和时间。
1969年至1997年间,1080例年龄50岁及以下的患者接受了临床ⅠA期至ⅡB期霍奇金病的治疗。确定总生存率,并评估预后因素。计算了整个队列以及按预后分组(基于B症状、纵隔状态和受累部位数量,参照欧洲癌症研究与治疗组织进行修改)的死亡相对风险和绝对超额风险(AR)。
中位随访时间为12年。15年和20年的Kaplan-Meier生存估计分别为84%和78%。Cox比例风险模型显示,受累部位数量(P = 0.006)、纵隔状态(P = 0.02)和组织学类型(P = 0.02)是全因死亡的独立预测因素。预后良好的患者的死亡AR随时间增加,而预后不良的患者,AR在最初5年达到峰值,主要死于霍奇金病。治疗后20多年,全因死亡、霍奇金病以外原因死亡、二次肿瘤和心脏病的相对风险仍显著升高。
尽管疾病得到良好控制,但接受早期霍奇金病治疗的患者仍有持续的额外死亡风险。对于早期、预后良好的疾病患者,应继续努力减少治疗,但对于预后不良的患者,可能不宜采用改良治疗。二十多年后出现的额外死亡凸显了霍奇金病患者长期随访护理的重要性。