Curtis R E, Rowlings P A, Deeg H J, Shriner D A, Socíe G, Travis L B, Horowitz M M, Witherspoon R P, Hoover R N, Sobocinski K A, Fraumeni J F, Boice J D
Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892, USA.
N Engl J Med. 1997 Mar 27;336(13):897-904. doi: 10.1056/NEJM199703273361301.
The late effects of bone marrow transplantation, including cancer, need to be determined in a large population at risk.
We studied 19,229 patients who received allogeneic transplants (97.2 percent) or syngeneic transplants (2.8 percent) between 1964 and 1992 at 235 centers to evaluate the risk of the development of a new solid cancer. Risk factors relating to the patient, the transplant, and the course after transplantation were evaluated.
The transplant recipients were at significantly higher risk of new solid cancers than the general population (observed cases, 80; ratio of observed to expected cases, 2.7; P<0.001). The risk was 8.3 times higher than expected among those who survived 10 or more years after transplantation. The cumulative incidence rate was 2.2 percent (95 percent confidence interval, 1.5 to 3.0 percent) at 10 years and 6.7 percent (95 percent confidence interval, 3.7 to 9.6 percent) at 15 years. The risk was significantly elevated (P<0.05) for malignant melanoma (ratio of observed to expected cases, 5.0) and cancers of the buccal cavity (11.1), liver (7.5), brain or other parts of the central nervous system (7.6), thyroid (6.6), bone (13.4), and connective tissue (8.0). The risk was higher for recipients who were younger at the time of transplantation than for those who were older (P for trend <0.001). In multivariate analyses, higher doses of total-body irradiation were associated with a higher risk of solid cancers. Chronic graft-versus-host disease and male sex were strongly linked with an excess risk of squamous-cell cancers of the buccal cavity and skin.
Patients undergoing bone marrow transplantation have an increased risk of new solid cancers later in life. The trend toward an increased risk over time after transplantation and the greater risk among younger patients indicate the need for life-long surveillance.
骨髓移植的远期效应,包括癌症,需要在大量有风险的人群中进行确定。
我们研究了1964年至1992年间在235个中心接受同种异体移植(97.2%)或同基因移植(2.8%)的19229例患者,以评估发生新发实体癌的风险。评估了与患者、移植及移植后病程相关的危险因素。
移植受者发生新发实体癌的风险显著高于普通人群(观察到的病例数为80例;观察病例数与预期病例数之比为2.7;P<0.001)。在移植后存活10年或更长时间的患者中,该风险比预期高8.3倍。10年时的累积发病率为2.2%(95%置信区间为1.5%至3.0%),15年时为6.7%(95%置信区间为3.7%至9.6%)。恶性黑色素瘤(观察病例数与预期病例数之比为5.0)、口腔癌(11.1)、肝癌(7.5)、脑或中枢神经系统其他部位的癌症(7.6)、甲状腺癌(6.6)、骨癌(13.4)和结缔组织癌(8.0)的风险显著升高(P<0.05)。移植时年龄较小的受者的风险高于年龄较大的受者(趋势P<0.001)。在多变量分析中,更高剂量的全身照射与实体癌风险较高相关。慢性移植物抗宿主病和男性与口腔和皮肤鳞状细胞癌额外风险密切相关。
接受骨髓移植的患者在晚年发生新发实体癌的风险增加。移植后随着时间推移风险增加的趋势以及年轻患者中更高的风险表明需要进行终身监测。