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.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
15 Sep 2020
Historique:
received: 15 07 2020
revised: 04 09 2020
accepted: 08 09 2020
entrez: 18 9 2020
pubmed: 19 9 2020
medline: 25 2 2021
Statut: epublish

Résumé

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.

Identifiants

pubmed: 32942768
pii: ijms21186772
doi: 10.3390/ijms21186772
pmc: PMC7555181
pii:
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
PDCD1 protein, human 0
Programmed Cell Death 1 Receptor 0
Nivolumab 31YO63LBSN

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : undefined <span style="color:gray;font-size:10px;">undefined</span>
ID : EARLYBIOSANTHELYS
Organisme : undefined <span style="color:gray;font-size:10px;">undefined</span>
ID : EARLYBIO2017
Organisme : indefined
ID : EARLYBIOCNO
Organisme : ANRT
ID : ANRTCM
Organisme : Immune insighT
ID : EARLYBIOIST

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Auteurs

Clara Milhem (C)

INSERM, CHU-Lille, U1189-ONCO-THAI-Assisted Laser Therapy and Immunotherapy for Oncology, University of Lille, F-59000 Lille, France.
Immune Insight, Institut de Biologie de Lille, 59021 Lille, France.

Olivier Moralès (O)

INSERM, CHU-Lille, U1189-ONCO-THAI-Assisted Laser Therapy and Immunotherapy for Oncology, University of Lille, F-59000 Lille, France.
CNRS UMS 3702, Institut de Biologie de Lille, 59021 Lille, France.

Céline Ingelaere (C)

Immune Insight, Institut de Biologie de Lille, 59021 Lille, France.

David Pasquier (D)

Service de Radiothérapie, Centre Oscar Lambret, 59000 Lille, France.

Serge Mordon (S)

INSERM, CHU-Lille, U1189-ONCO-THAI-Assisted Laser Therapy and Immunotherapy for Oncology, University of Lille, F-59000 Lille, France.

Laurent Mortier (L)

Service de Dermatologie, Hôpital Huriez, 59000 Lille, France.

Xavier Mirabel (X)

Service de Radiothérapie, Centre Oscar Lambret, 59000 Lille, France.

Nadira Delhem (N)

INSERM, CHU-Lille, U1189-ONCO-THAI-Assisted Laser Therapy and Immunotherapy for Oncology, University of Lille, F-59000 Lille, France.

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Classifications MeSH