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系统免疫抑制预测 Merkel 细胞癌特异性生存降低,与分期无关。

Systemic immune suppression predicts diminished Merkel cell carcinoma-specific survival independent of stage.

机构信息

Divisions of Dermatology and Medical Oncology, Department of Internal Medicine, University of Washington, Seattle, Washington, USA.

Division of Research, Kaiser Permanente Northern California, Oakland, California, USA.

出版信息

J Invest Dermatol. 2013 Mar;133(3):642-646. doi: 10.1038/jid.2012.388. Epub 2012 Nov 29.

Abstract

Merkel cell carcinoma (MCC) is an aggressive cutaneous malignancy linked to a contributory virus (Merkel cell polyomavirus). Multiple epidemiologic studies have established an increased incidence of MCC among persons with systemic immune suppression. Several forms of immune suppression are associated with increased MCC incidence, including hematologic malignancies, HIV/AIDS, and immunosuppressive medications for autoimmune disease or transplant. Indeed, immune-suppressed individuals represent ∼10% of MCC patients, a significant overrepresentation relative to the general population. We hypothesized that immune-suppressed patients may have a poorer MCC-specific prognosis and examined a cohort of 471 patients with a combined follow-up of 1,427 years (median 2.1 years). Immune-suppressed patients (n=41) demonstrated reduced MCC-specific survival (40% at 3 years) compared with patients with no known systemic immune suppression (n=430; 74% MCC-specific survival at 3 years). By competing risk regression analysis, immune suppression was a stage-independent predictor of worsened MCC-specific survival (hazard ratio 3.8, P<0.01). Thus, immune-suppressed individuals have both an increased chance of developing MCC and poorer MCC-specific survival. It may be appropriate to follow these higher-risk individuals more closely, and, when clinically feasible, there may be a benefit of diminishing iatrogenic systemic immune suppression.

摘要

默克尔细胞癌(Merkel cell carcinoma,MCC)是一种与一种辅助病毒(默克尔细胞多瘤病毒)相关的侵袭性皮肤恶性肿瘤。多项流行病学研究已经确定,系统性免疫抑制人群中 MCC 的发病率增加。多种形式的免疫抑制与 MCC 发病率增加有关,包括血液系统恶性肿瘤、HIV/AIDS 以及用于自身免疫性疾病或移植的免疫抑制药物。事实上,免疫抑制个体占 MCC 患者的约 10%,相对于一般人群,这一比例显著偏高。我们假设免疫抑制患者可能具有更差的 MCC 特异性预后,并对 471 例患者进行了一项队列研究,总随访时间为 1427 年(中位数为 2.1 年)。与无已知系统性免疫抑制的患者(n=430)相比,免疫抑制患者(n=41)的 MCC 特异性生存率降低(3 年时为 40%)。通过竞争风险回归分析,免疫抑制是 MCC 特异性生存率恶化的独立预测因素(风险比 3.8,P<0.01)。因此,免疫抑制个体既更有可能患上 MCC,又具有更差的 MCC 特异性生存率。对这些高风险个体进行更密切的随访可能是恰当的,并且在临床上可行的情况下,减少医源性系统性免疫抑制可能有益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6db/3570636/0ed7b0117321/nihms408859f1.jpg

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