van Leeuwen F E, Klokman W J, Hagenbeek A, Noyon R, van den Belt-Dusebout A W, van Kerkhoff E H, van Heerde P, Somers R
Department of Epidemiology, Netherlands Cancer Institute, Amsterdam.
J Clin Oncol. 1994 Feb;12(2):312-25. doi: 10.1200/JCO.1994.12.2.312.
To determine risk factors for the development of second primary cancers during long-term follow-up of patients with Hodgkin's disease (HD).
We assessed the risk of second cancers (SCs) in 1939 HD patients, who were admitted to the Netherlands Cancer Institute (NKI; Amsterdam) or the Dr Daniel den Hoed Cancer Center (DDHK; Rotterdam) between 1966 and 1986. For 97% of the cohort, we obtained a medical status up to at least January 1989. The median follow-up duration of the patients was 9.2 years; for 17% of the patients, follow-up was longer than 15 years. For more than 98% of all second tumors, the diagnosis was confirmed through a pathology report.
In all, 146 patients developed a SC, compared with 41.9 cases expected on the basis of incidence rates in the general population (relative risk [RR], 3.5; 95% confidence interval [CI], 2.9 to 4.1). The mean 20-year actuarial risk of all SCs was 20% (95% CI, 17% to 24%). Significantly increased RRs were observed for leukemia (RR, 34.7; 95% CI, 23.6 to 49.3), non-Hodgkin's lymphoma (NHL) (RR, 20.6; 95% CI, 13.1 to 30.9), lung cancer (RR, 3.7; 95% CI, 2.5 to 5.3), all gastrointestinal cancers combined (RR, 2.0; 95% CI, 1.2 to 3.1), all urogenital cancers combined (RR, 2.4; 95% CI, 1.4 to 3.7), melanoma (RR, 4.9; 95% CI, 1.6 to 11.3), and soft tissue sarcoma (RR, 8.8; 95% CI, 1.8 to 25.8). As compared with the general population, the cohort experienced an excess of 63 cancer cases per 10,000 person-years. Cox-model analysis indicated the following as significant risk factors for developing leukemia: first-year treatment with chemotherapy (CT), follow-up treatment with CT, age at diagnosis of HD greater than 40 years, splenectomy, and advanced stage. Patients treated with CT in the 1980s had a substantially lower risk of leukemia than patients treated in the 1970s (10-year actuarial risks of 2.1% and 6.4%, respectively; P = .07). Significant risk factors for NHL were older age, male sex, and combined modality treatment as compared with either modality alone. Risk of lung cancer was strongly related to radiotherapy (RT), while an additional role of CT could not be demonstrated. After more than 15 years of follow-up, women treated with mantle-field irradiation before age 20 years had a greater than forty-fold increased risk of breast cancer (P < .001).
While the long-term consequences of HD treatment as administered in the 1960s and 1970s are still evolving, it is promising that patients who received the new treatment regimens introduced in the 1980s have a much lower leukemia risk than patients treated in earlier years. Beginning 10 years after initial RT, the follow-up program of women who received mantle-field irradiation before age 30 years should routinely include breast palpation and yearly mammography.
确定霍奇金淋巴瘤(HD)患者长期随访期间发生第二原发性癌症的风险因素。
我们评估了1939例HD患者发生第二癌症(SCs)的风险,这些患者于1966年至1986年间被收治于荷兰癌症研究所(NKI;阿姆斯特丹)或丹尼尔·登霍德癌症中心(DDHK;鹿特丹)。对于97%的队列,我们获取了截至至少1989年1月的医疗状况。患者的中位随访时间为9.2年;17%的患者随访时间超过15年。超过98%的所有第二肿瘤通过病理报告确诊。
总共146例患者发生了SC,而根据一般人群发病率预期为41.9例(相对风险[RR],3.5;95%置信区间[CI],2.9至4.1)。所有SCs的平均20年精算风险为20%(95%CI,17%至24%)。观察到白血病(RR,34.7;95%CI,23.6至49.3)、非霍奇金淋巴瘤(NHL)(RR,20.6;95%CI,13.1至30.9)、肺癌(RR,3.7;95%CI,2.5至5.3)、所有胃肠道癌症合并(RR,2.0;95%CI,1.2至3.1)、所有泌尿生殖系统癌症合并(RR,2.4;95%CI,1.4至3.7)、黑色素瘤(RR,4.9;95%CI,1.6至11.3)和软组织肉瘤(RR,8.8;95%CI,1.8至25.8)的RR显著增加。与一般人群相比,该队列每10000人年额外发生63例癌症。Cox模型分析表明,以下因素是发生白血病的显著风险因素:化疗(CT)第一年治疗、CT后续治疗、HD诊断时年龄大于40岁、脾切除术和晚期。20世纪80年代接受CT治疗的患者发生白血病的风险明显低于20世纪70年代接受治疗者(10年精算风险分别为2.1%和6.4%;P = 0.07)。NHL的显著风险因素是年龄较大、男性以及与单一治疗方式相比的综合治疗方式。肺癌风险与放疗(RT)密切相关,而未证明CT有额外作用。随访超过15年后,20岁前接受斗篷野照射的女性患乳腺癌的风险增加了40多倍(P < 0.001)。
虽然20世纪60年代和70年代实施HD治疗的长期后果仍在演变,但有希望的是,接受20世纪80年代引入的新治疗方案的患者发生白血病的风险比早年接受治疗的患者低得多。在首次RT后10年开始,30岁前接受斗篷野照射的女性的随访计划应常规包括乳房触诊和每年的乳房X线摄影。