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Immune mechanisms and possible immune therapy in testicular germ cell tumours
Author(s) -
Chovanec M.,
Mardiak J.,
Mego M.
Publication year - 2019
Publication title -
andrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.947
H-Index - 43
eISSN - 2047-2927
pISSN - 2047-2919
DOI - 10.1111/andr.12656
Subject(s) - immune system , immunotherapy , immune checkpoint , medicine , malignancy , immunology , oncology
Background Testicular germ cell tumours ( GCT s) are the only universally curable solid malignancy. The long‐term cure rate of >95% is attributed to the extraordinary sensitivity to cisplatin‐based treatment but a proportion of patients die due to a progression of the chemotherapy‐refractory disease. While treatment of a variety of solid cancers was significantly improved with recent immune therapies, the immunology and immunotherapy remained underinvestigated in GCT s. Objectives In this narrative review, we summarize evidence about immune‐related mechanisms and possible immune therapies in GCT s and provide insights and implications for future research and clinical practice. Materials and methods We performed a comprehensive search of PubMed/ MEDLINE to identify original and review articles reporting on immune mechanisms and immunotherapy in GCT s. Review articles were further searched for additional original articles. Results Clear link of immune surveillance and the presence of GCT have been identified with several novel immune‐related prognostic biomarkers published recently. Several case reports, case series, and preliminary results from phase I‐ II studies are emerging to report on the efficacy of immune checkpoint inhibitors. Discussion Newly discovered immune biomarkers provide an evidence supporting the role of immune environment in the GCT biology. While these discoveries provide only an initial insight into the immunobiology, strong correlation with prognosis is evident. This provided a premise to investigate the treatment efficacy of novel immunotherapy. Some efficacy of these treatments has been reported in clinical setting; however, the results of published studies with immune checkpoint inhibitor monotherapy seem to be disappointing. Conclusion Immune‐related mechanisms and efficacy of immune checkpoint blockade in GCT s should be further investigated in preclinical and clinical studies.