Barton Virginia, Armeson Kent, Hampras Shalaka, Ferris Laura K, Visvanathan Kala, Rollison Dana, Alberg Anthony J
Hollings Cancer Center, Medical University of South Carolina, 68 President Street, MSC 955, Charleston, SC, 29425, USA.
Department of Public Health Sciences, Medical University of South Carolina, Charleston, SC, USA.
Arch Dermatol Res. 2017 May;309(4):243-251. doi: 10.1007/s00403-017-1724-5. Epub 2017 Mar 11.
Some reports suggest that a history of nonmelanoma skin cancer (NMSC) may be associated with increased mortality. NMSCs have very low fatality rates, but the high prevalence of NMSC elevates the importance of the possibility of associated subsequent mortality from other causes. The variable methods and findings of existing studies leave the significance of these results uncertain. To provide clarity, we conducted a systematic review to characterize the evidence on the associations of NMSC with: (1) all-cause mortality, (2) cancer-specific mortality, and (3) cancer survival. Bibliographic databases were searched through February 2016. Cohort studies published in English were included if adequate data were provided to estimate mortality ratios in patients with-versus-without NMSC. Data were abstracted from the total of eight studies from independent data sources that met inclusion criteria (n = 3 for all-cause mortality, n = 2 for cancer-specific mortality, and n = 5 for cancer survival). For all-cause mortality, a significant increased risk was observed for patients with a history of squamous cell carcinoma (SCC) (mortality ratio estimates (MR) 1.25 and 1.30), whereas no increased risk was observed for patients with a history of basal cell carcinoma (BCC) (MRs 0.96 and 0.97). Based on one study, the association with cancer-specific mortality was stronger for SCC (MR 2.17) than BCC (MR 1.15). Across multiple types of cancer both SCC and BCC tended to be associated with poorer survival from second primary malignancies. Multiple studies support an association between NMSC and fatal outcomes; the associations tend to be more potent for SCC than BCC. Additional investigation is needed to more precisely characterize these associations and elucidate potential underlying mechanisms.
一些报告表明,非黑色素瘤皮肤癌(NMSC)病史可能与死亡率增加有关。NMSC的死亡率非常低,但NMSC的高患病率凸显了其他原因导致后续相关死亡率可能性的重要性。现有研究的方法和结果各不相同,使得这些结果的意义尚不确定。为了弄清楚这一点,我们进行了一项系统综述,以描述有关NMSC与以下方面关联的证据:(1)全因死亡率,(2)癌症特异性死亡率,以及(3)癌症生存率。检索了截至2016年2月的文献数据库。如果提供了足够的数据来估计有或无NMSC患者的死亡率比,则纳入以英文发表的队列研究。数据从符合纳入标准的来自独立数据源的八项研究中提取(全因死亡率研究n = 3,癌症特异性死亡率研究n = 2,癌症生存率研究n = 5)。对于全因死亡率,观察到有鳞状细胞癌(SCC)病史的患者风险显著增加(死亡率比估计值(MR)为1.25和1.30),而有基底细胞癌(BCC)病史的患者未观察到风险增加(MR分别为0.96和0.97)。基于一项研究,SCC与癌症特异性死亡率的关联(MR 2.17)比BCC(MR 1.15)更强。在多种癌症类型中,SCC和BCC往往都与第二原发性恶性肿瘤的较差生存率相关。多项研究支持NMSC与致命结局之间存在关联;SCC的关联往往比BCC更强。需要进一步调查以更精确地描述这些关联并阐明潜在的潜在机制。