Combination of High Dose Hypofractionated Radiotherapy with Anti-PD1 Single Dose Immunotherapy Leads to a Th1 Immune Activation Resulting in a Complete Clinical Response in a Melanoma Patient

被引:1
作者
Milhem, Clara [1 ,2 ]
Morales, Olivier [1 ,3 ]
Ingelaere, Celine [2 ]
Pasquier, David [4 ]
Mordon, Serge [1 ]
Mortier, Laurent [5 ]
Mirabel, Xavier [4 ]
Delhem, Nadira [1 ]
机构
[1] Univ Lille, CHU Lille, INSERM, U1189,ONCO THAI,Assisted Laser Therapy & Immunoth, F-59000 Lille, France
[2] Inst Biol Lille, Immune Insight, F-59021 Lille, France
[3] Inst Biol Lille, CNRS UMS 3702, F-59021 Lille, France
[4] Ctr Oscar Lambret, Serv Radiotherapie, F-59000 Lille, France
[5] Hop Huriez, Serv Dermatol, F-59000 Lille, France
关键词
stereotaxic radiotherapy; immunotherapy; anti-PD1; melanoma; immune response; T-CELLS; CANCER; PD-1; PEMBROLIZUMAB; ANTIGEN;
D O I
10.3390/ijms21186772
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The development of immunotherapy has recently modified the anti-tumor therapeutic arsenal; particularly, immune checkpoint inhibitors have led to a significant increase in overall survival. The current challenge is now to select good responder patients by identifying early biomarkers to propose therapeutic combinations that potentiate the efficacy of the therapy. Here we report the case of a 60-year-old man with superficial melanoma treated with high-dose hypo fractionated radiotherapy (H-SRT) combined with a single dose of anti-PD1 immunotherapy (Nivolumab) for a metastatic lymph node recurrence due to cancer progression. In this study, we present the results obtained regarding the activation of the Th1 immune response after H-SRT treatment followed by anti PD-1 therapeutic protocol. These results were correlated with clinical data to identify potential immunological biomarkers of treatment efficacy. This exceptional case report shows that a combination of H-SRT with a single dose of anti-PD1 immunotherapy may allow a better activation of the immune response in favor of a complete clinical response.
引用
收藏
页码:1 / 16
页数:16
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