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.
anti-PD1
immune response
immunotherapy
melanoma
stereotaxic radiotherapy
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
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
Références
Science. 2011 Mar 25;331(6024):1565-70
pubmed: 21436444
Oncoimmunology. 2016 Aug 19;5(9):e1214788
pubmed: 27757312
Int Immunol. 1996 May;8(5):765-72
pubmed: 8671665
J Natl Cancer Inst. 2013 Feb 20;105(4):256-65
pubmed: 23291374
Radiol Oncol. 2010 Mar;44(1):1-12
pubmed: 22933884
J Immunol. 2009 Mar 1;182(5):2816-26
pubmed: 19234176
Expert Rev Anticancer Ther. 2020 Feb;20(2):137-145
pubmed: 31997676
JAMA. 2016 Apr 19;315(15):1600-9
pubmed: 27092830
Cancer Res. 2016 Jun 1;76(11):3122-6
pubmed: 27197163
J Dermatol. 2017 Feb;44(2):117-122
pubmed: 27510892
N Engl J Med. 2015 Jun 25;372(26):2521-32
pubmed: 25891173
Cancer Immunol Res. 2015 Apr;3(4):345-55
pubmed: 25527358
Cancer Immunol Res. 2015 Jun;3(6):610-9
pubmed: 25701325
Cell. 2011 Mar 4;144(5):646-74
pubmed: 21376230
Nat Immunol. 2002 Nov;3(11):991-8
pubmed: 12407406
Cancer Radiother. 2015 Oct;19(6-7):421-5
pubmed: 26321647
Br J Radiol. 1953 May;26(305):234-41
pubmed: 13042090
Lancet Oncol. 2014 Apr;15(4):e170-7
pubmed: 24694640
Nat Rev Cancer. 2018 May;18(5):313-322
pubmed: 29449659
Cancer Immunol Immunother. 2005 Apr;54(4):307-14
pubmed: 15599732
Proc Natl Acad Sci U S A. 2009 Feb 24;106(8):2741-6
pubmed: 19202065
J Natl Cancer Inst. 2014 Dec 12;107(1):363
pubmed: 25505237
Int J Radiat Oncol Biol Phys. 2008 Jun 1;71(2):324-5
pubmed: 18474308