Systemic Immune Suppression Predicts Diminished Merkel Cell Carcinoma-Specific Survival Independent of Stage

被引:153
作者
Paulson, Kelly G. [1 ,2 ]
Iyer, Jayasri G. [1 ,2 ]
Blom, Astrid [1 ,2 ]
Warton, E. Margaret [3 ]
Sokil, Monica [3 ]
Yelistratova, Lola [1 ,2 ]
Schuman, Louise [4 ]
Nagase, Kotaro [1 ,2 ,5 ]
Bhatia, Shailender [1 ,2 ]
Asgari, Maryam M. [3 ]
Nghiem, Paul [1 ,2 ]
机构
[1] Univ Washington, Dept Internal Med, Div Dermatol, Seattle, WA 98109 USA
[2] Univ Washington, Dept Internal Med, Div Med Oncol, Seattle, WA 98109 USA
[3] Kaiser Permanente No Calif, Div Res, Oakland, CA USA
[4] Clin Data Syst, Fountain Valley, CA USA
[5] Saga Univ, Fac Med, Dept Internal Med, Div Dermatol, Saga 840, Japan
关键词
ORGAN TRANSPLANT RECIPIENTS; SKIN CANCERS; T-ANTIGEN; POLYOMAVIRUS; EXPRESSION; INFECTION; MELANOMA; FEATURES; MCV;
D O I
10.1038/jid.2012.388
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
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 similar to 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. Journal of Investigative Dermatology (2013) 133, 642-646; doi:10.1038/jid.2012.388; published online 29 November 2012
引用
收藏
页码:642 / 646
页数:5
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