Blockade of the programmed death ligand 1 (PD-L1) as potential therapy for anaplastic thyroid cancer
PD-L1
Adult
Aged, 80 and over
Male
Antibodies, Monoclonal
Anaplastic thyroid cancer
Middle Aged
Thyroid Carcinoma, Anaplastic
B7-H1 Antigen
3. Good health
Mice
03 medical and health sciences
Antineoplastic Agents, Immunological
Treatment Outcome
0302 clinical medicine
Cell Line, Tumor
PD-1
Animals
Humans
PD-L1, PD-1, Anaplastic thyroid cancer, Immunotherapy
Female
Immunotherapy
Thyroid Neoplasms
Aged
DOI:
10.1007/s12020-019-01865-5
Publication Date:
2019-02-14T01:00:08Z
AUTHORS (8)
ABSTRACT
Anaplastic thyroid carcinoma (ATC) is a rare, highly aggressive form of thyroid cancer (TC) characterized by an aggressive behavior and poor prognosis, resulting in patients' death within a year. Standard treatments, such as chemo and radiotherapy, as well as tyrosine kinase inhibitors, are ineffective for ATC treatment. Cancer immunotherapy is one of the most promising research area in oncology. The PD-1/PD-L1 axis is of particular interest, in light of promising data showing a restoration of host immunity against tumors, with the prospect of long-lasting remissions.In this study, we evaluated PD-L1 expression in a large series of TCs (20 cases) showing a progressive dedifferentiation of the thyroid tumor from well differentiated TC to ATC, employing two different antibodies [R&D Systems and VENTANA PD-L1 (SP263) Rabbit Monoclonal Primary Antibody]. We also tested the anti PD-L1 mAb in an in vivo animal model.We found that approximately 70-90% of ATC cases were positive for PD-L1 whereas normal thyroid and differentiated TC were negative. Moreover, all analyzed cases presented immunopositive staining in the endothelium of vessels within or in close proximity to the tumor, while normal thyroid vessels were negative. PD-L1 mAb was also effective in inhibiting ATC growth in an in vivo model.These data suggest that immunotherapy may be a promising treatment specific for ATC suggesting the need to start with clinical TRIALs.
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CITATIONS (47)
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