Clinical and Immunologic Features of Germline Pathogenic Variant-Positive Patients with Melanoma

被引:0
|
作者
Shen, Alan [1 ]
Arbesman, Michelle [2 ]
Lodha, Roshan [1 ]
Rayman, Patricia [3 ]
Bungo, Brandon [2 ]
Ni, Ying [4 ]
Chan, Timothy [4 ]
Gastman, Brian [4 ,5 ]
Ko, Jennifer [3 ,4 ,5 ]
Diaz-Montero, C. Marcela [3 ,4 ]
Arbesman, Joshua [5 ]
Funchain, Pauline [2 ,6 ]
机构
[1] Case Western Reserve Univ, Lerner Coll Med, Cleveland Clin, Cleveland, OH USA
[2] Cleveland Clin, Taussig Canc Inst, Cleveland, OH USA
[3] Cleveland Clin, Immuno Monitoring Lab, Cleveland, OH USA
[4] Cleveland Clin, Ctr Precis Immunotherapy, Cleveland, OH USA
[5] Cleveland Clin, Dept Dermatol & Plast Surg, Cleveland, OH USA
[6] Cleveland Clin, Taussig Canc Inst, 9500 Euclid Ave, Cleveland, OH 44195 USA
关键词
SURVIVAL; CANCER; WOMEN; MUTATIONS; PROGNOSIS; MUCOSAL; BRCA2; CELLS; RISK;
D O I
10.1158/1078-0432.CCR-23-1964
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Malignant melanoma represents the most lethal skin cancer with germline predispositions thought to comprise 10% to 15% of all melanoma cases. No studies to date examine the immunologic features that may differentiate survival differences between germline pathogenic variant (gPV)-positive patients with melanoma from gPV-negative patients with melanoma.Experimental Design: Adult patients with melanoma and clinical characteristics suggesting hereditary predisposition to cancer were prospectively recruited to undergo germline testing and flow cytometric analysis of peripheral immune suppressor cells.Results: In this cohort, gPV-positive patients (n = 72) had a significantly improved melanoma-specific survival (MSS) compared with gPV-negative patients (n = 411; HRadj, 0.32; 95% CI, 0.13-0.82; P = 0.01). These survival improvements among gPV-positive patients were most apparent among cutaneous melanoma subtypes (HRadj, 0.12; 95% CI, 0.016-0.86; P = 0.03) and numerically improved in later-stage (IIB-IV) patients (HRadj, 0.34; 95% CI, 0.10-1.11; P = 0.06). Further, gPV-positive patients had a significantly lower level of total circulating PMN-MDSC compared with gPV-negative patients (P = 0.01), which was most apparent in those diagnosed with later stages (IIB-IV) of melanoma (P = 0.009). Finally, a significant upregulation of inflammatory transcriptome signatures in later-stage gPV-positive patients (n = 21) was observed in comparison with gPV-negative patients (n = 173) in the cutaneous melanoma cohort (SKCM) of The Cancer Genome Atlas (TCGA).Conclusions: gPV-positive patients with melanoma exhibit improved MSS in addition to reduced peripheral PMN-MDSC and an enhanced inflammatory microenvironment.
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收藏
页码:564 / 574
页数:11
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