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Associations of PD-L1, PD-L2, and HLA class I expression with responses to immunotherapy in patients with advanced sarcoma: post hoc analysis of a phase 1/2 trial.
Miwa, S; Nojima, T; Alomesen, A A; Ikeda, H; Yamamoto, N; Nishida, H; Hayashi, K; Takeuchi, A; Igarashi, K; Higuchi, T; Yonezawa, H; Araki, Y; Morinaga, S; Asano, Y; Tsuchiya, H.
Affiliation
  • Miwa S; Department of Orthopedic Surgery, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8640, Japan. smiwa001@yahoo.co.jp.
  • Nojima T; Department of Pathology, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan.
  • Alomesen AA; Department of Pathology, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan.
  • Ikeda H; Department of Pathology, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan.
  • Yamamoto N; Department of Orthopedic Surgery, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8640, Japan.
  • Nishida H; Department of Orthopedic Surgery, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8640, Japan.
  • Hayashi K; Department of Orthopedic Surgery, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8640, Japan.
  • Takeuchi A; Department of Orthopedic Surgery, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8640, Japan.
  • Igarashi K; Department of Orthopedic Surgery, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8640, Japan.
  • Higuchi T; Department of Orthopedic Surgery, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8640, Japan.
  • Yonezawa H; Department of Orthopedic Surgery, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8640, Japan.
  • Araki Y; Department of Orthopedic Surgery, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8640, Japan.
  • Morinaga S; Department of Orthopedic Surgery, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8640, Japan.
  • Asano Y; Department of Orthopedic Surgery, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8640, Japan.
  • Tsuchiya H; Department of Orthopedic Surgery, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8640, Japan.
Clin Transl Oncol ; 23(8): 1620-1629, 2021 Aug.
Article in En | MEDLINE | ID: mdl-33635466
BACKGROUND: Although immunotherapy is thought to be a promising cancer treatment, most patients do not respond to immunotherapy. In this post hoc analysis of a phase 1/2 study, associations of programmed death ligand 1 (PD-L1), PD-L2, and HLA class I expressions with responses to dendritic cells (DCs)-based immunotherapy were investigated in patients with advanced sarcoma. METHODS: This study enrolled 35 patients with metastatic and/or recurrent sarcomas who underwent DC-based immunotherapy. The associations of PD-L1, PD-L2, and HLA class I expressions in tumor specimens, which were resected before immunotherapy, with immune responses (increases of IFN-γ and IL-12) and oncological outcomes were evaluated. RESULTS: Patients who were PD-L2 (+) showed lower increases of IFN-γ and IL-12 after DC-based immunotherapy than patients who were PD-L2 (-). The disease control (partial response or stable disease) rates of patients who were PD-L1 (+) and PD-L1 (-) were 0% and 22%, respectively. Disease control rates of patients who were PD-L2 (+) and PD-L2 (-) were 13% and 22%, respectively. Patients who were PD-L1 (+) tumors had significantly poorer overall survival compared with patients who were PD-L1 (-). No associations of HLA class I expression with the immune response or oncological outcomes were observed. CONCLUSIONS: This study suggests that PD-L1 and PD-L2 are promising biomarkers of DC-based immunotherapy, and that addition of immune checkpoint inhibitors to DC-based immunotherapy may improve the outcomes of DC-based immunotherapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sarcoma / Histocompatibility Antigens Class I / B7-H1 Antigen / Programmed Cell Death 1 Ligand 2 Protein / Immunotherapy Type of study: Risk_factors_studies Limits: Adult / Female / Humans / Male Language: En Journal: Clin Transl Oncol Year: 2021 Document type: Article Affiliation country: Japan Country of publication: Italy

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sarcoma / Histocompatibility Antigens Class I / B7-H1 Antigen / Programmed Cell Death 1 Ligand 2 Protein / Immunotherapy Type of study: Risk_factors_studies Limits: Adult / Female / Humans / Male Language: En Journal: Clin Transl Oncol Year: 2021 Document type: Article Affiliation country: Japan Country of publication: Italy