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Association of inflammatory biomarkers with clinical outcomes in nivolumab-treated patients with advanced hepatocellular carcinoma.
Sangro, Bruno; Melero, Ignacio; Wadhawan, Samir; Finn, Richard S; Abou-Alfa, Ghassan K; Cheng, Ann-Lii; Yau, Thomas; Furuse, Junji; Park, Joong-Won; Boyd, Zachary; Tang, Hao Tracy; Shen, Yun; Tschaika, Marina; Neely, Jaclyn; El-Khoueiry, Anthony.
Afiliação
  • Sangro B; Clinica Universidad de Navarra-IDISNA and CIBEREHD, Pamplona, Spain. Electronic address: bsangro@unav.es.
  • Melero I; Universidad de Navarra and CIBERONC, Pamplona, Spain.
  • Wadhawan S; Bristol Myers Squibb, Princeton, NJ, USA.
  • Finn RS; University of California, Los Angeles, CA, USA.
  • Abou-Alfa GK; Memorial Sloan Kettering Cancer Center, New York, NY, USA; Weill Medical College at Cornell University, New York, NY, USA.
  • Cheng AL; National Taiwan University Hospital, Taipei, Taiwan.
  • Yau T; University of Hong Kong, Hong Kong, China.
  • Furuse J; Kyorin University Faculty of Medicine, Tokyo, Japan.
  • Park JW; National Cancer Center, Goyang, South Korea.
  • Boyd Z; Bristol Myers Squibb, Princeton, NJ, USA.
  • Tang HT; Bristol Myers Squibb, Princeton, NJ, USA.
  • Shen Y; Bristol Myers Squibb, Princeton, NJ, USA.
  • Tschaika M; Bristol Myers Squibb, Princeton, NJ, USA.
  • Neely J; Bristol Myers Squibb, Princeton, NJ, USA.
  • El-Khoueiry A; USC Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
J Hepatol ; 73(6): 1460-1469, 2020 12.
Article em En | MEDLINE | ID: mdl-32710922
BACKGROUND & AIMS: Nivolumab, a programmed death (PD)-1 (PD-1) inhibitor, led to durable responses, manageable safety, and increased survival in patients with advanced hepatocellular carcinoma (HCC). In our retrospective analysis, we studied the immunobiology and potential associations between biomarkers and outcomes with nivolumab in HCC. METHODS: Fresh and archival tumour samples from dose-escalation and dose-expansion phases of the CheckMate 040 trial were analysed by immunohistochemistry and RNA sequencing to assess several inflammatory gene expression signatures, including CD274 (PD-ligand 1 [PD-L1]), CD8A, LAG3, and STAT1. Biomarkers were assessed for association with clinical outcomes (best overall response by blinded independent central review per RECIST v1.1 and overall survival [OS]). RESULTS: Complete or partial tumour responses were observed in PD-L1-positive and PD-L1-negative patients treated with nivolumab monotherapy. Median OS was 28.1 (95% CI 18.2-n.a.) vs. 16.6 months (95% CI 14.2-20.2) for patients with tumour PD-L1 ≥1% vs. <1% (p = 0.03). Increased CD3 and CD8 showed a non-significant trend towards improved OS (both p = 0.08), and macrophage markers were not associated with OS. Tumour PD-1 and PD-L1 expression were associated with improved OS (p = 0.05 and p = 0.03, respectively). An inflammatory gene signature consisting of 4 genes was associated with improved objective response rate (p = 0.05) and OS (p = 0.01). CONCLUSIONS: PD-1 and PD-L1 expression, biomarkers of inflammation, and inflammatory gene signatures trended with improved survival and response. While further confirmation within a larger phase III trial is needed to evaluate predictive value of these biomarkers, these exploratory analyses suggest that anti-tumour immune response may play a role in the treatment benefit of nivolumab in HCC. LAY SUMMARY: Certain tests may be used to provide a picture of how a tumour is escaping the immune system, allowing it to continue to grow and create more tumours. Therapies such as nivolumab are designed to help the immune system fight the tumour. These tests may be used to determine how effective such therapies will be in the treatment of advanced liver cancer. NCT NUMBER: NCT01658878.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Carcinoma Hepatocelular / Biomarcadores Farmacológicos / Receptor de Morte Celular Programada 1 / Nivolumabe / Neoplasias Hepáticas Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: J Hepatol Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Carcinoma Hepatocelular / Biomarcadores Farmacológicos / Receptor de Morte Celular Programada 1 / Nivolumabe / Neoplasias Hepáticas Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: J Hepatol Ano de publicação: 2020 Tipo de documento: Article