Zamoiski Rachel D, Yanik Elizabeth, Gibson Todd M, Cahoon Elizabeth K, Madeleine Margaret M, Lynch Charles F, Gustafson Sally, Goodman Marc T, Skeans Melissa, Israni Ajay K, Engels Eric A, Morton Lindsay M
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Department of Health and Human Services, Bethesda, Maryland.
Department of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, Tennessee.
Cancer Res. 2017 Aug 1;77(15):4196-4203. doi: 10.1158/0008-5472.CAN-16-3291. Epub 2017 Jun 14.
Solid organ transplant recipients have increased risk for developing keratinocyte cancers, including cutaneous squamous cell carcinoma (SCC) and basal cell carcinoma (BCC), in part as a result of immunosuppressive medications administered to prevent graft rejection. In the general population, keratinocyte cancers are associated with increased risks of subsequent malignancy, however, the risk in organ transplant populations has not been evaluated. We addressed this question by linking the U.S. Scientific Registry of Transplant Recipients, which includes data on keratinocyte cancer occurrence, with 15 state cancer registries. Risk of developing malignancies after keratinocyte cancer was assessed among 118,440 Caucasian solid organ transplant recipients using multivariate Cox regression models. Cutaneous SCC occurrence ( = 6,169) was associated with 1.44-fold increased risk [95% confidence interval (CI), 1.31-1.59] for developing later malignancies. Risks were particularly elevated for non-cutaneous SCC, including those of the oral cavity/pharynx (HR, 5.60; 95% CI, 4.18-7.50) and lung (HR, 1.66; 95% CI, 1.16-2.31). Cutaneous SCC was also associated with increased risk of human papillomavirus-related cancers, including anal cancer (HR, 2.77; 95% CI, 1.29-5.96) and female genital cancers (HR, 3.43; 95% CI, 1.44-8.19). In contrast, BCC ( = 3,669) was not associated with overall risk of later malignancy (HR, 0.98; 95% CI, 0.87-1.12), including any SCC. Our results suggest that transplant recipients with cutaneous SCC, but not BCC, have an increased risk of developing other SCC. These findings somewhat differ from those for the general population and suggest a shared etiology for cutaneous SCC and other SCC in the setting of immunosuppression. Cutaneous SCC occurrence after transplantation could serve as a marker for elevated malignancy risk. .
实体器官移植受者患角质形成细胞癌的风险增加,包括皮肤鳞状细胞癌(SCC)和基底细胞癌(BCC),部分原因是为预防移植物排斥而使用的免疫抑制药物。在一般人群中,角质形成细胞癌与后续发生恶性肿瘤的风险增加相关,然而,器官移植人群中的风险尚未得到评估。我们通过将美国移植受者科学注册中心(其中包括角质形成细胞癌发生的数据)与15个州的癌症注册中心相链接来解决这个问题。我们使用多变量Cox回归模型评估了118440名白种人实体器官移植受者在患角质形成细胞癌后发生恶性肿瘤的风险。皮肤SCC的发生(n = 6169)与随后发生恶性肿瘤的风险增加1.44倍相关[95%置信区间(CI),1.31 - 1.59]。非皮肤SCC的风险尤其升高,包括口腔/咽部的SCC(风险比,5.60;95% CI,4.18 - 7.50)和肺部的SCC(风险比,1.66;95% CI,1.16 - 2.31)。皮肤SCC还与人类乳头瘤病毒相关癌症的风险增加相关,包括肛门癌(风险比,2.77;95% CI,1.29 - 5.96)和女性生殖系统癌症(风险比,3.43;95% CI,1.44 - 8.19)。相比之下,BCC(n = 3669)与后续发生恶性肿瘤的总体风险无关(风险比,0.98;95% CI,0.87 - 1.12),包括任何SCC。我们的结果表明,患有皮肤SCC而非BCC的移植受者发生其他SCC的风险增加。这些发现与一般人群的发现有所不同,并表明在免疫抑制情况下皮肤SCC和其他SCC存在共同的病因。移植后皮肤SCC的发生可作为恶性肿瘤风险升高的一个标志物。