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Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

904 - Serum biomarkers during the first cycle of anti-PD-1 antibody therapies in non-small cell lung cancer

Date

20 Oct 2018

Session

Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

Presenters

Takayo Ota

Citation

Annals of Oncology (2018) 29 (suppl_8): viii400-viii441. 10.1093/annonc/mdy288

Authors

T. Ota1, T. Takeda2, T. Fukui3, Y. Nakahara3, K. Kudo4, T. Okabe5, H. Hayashi6, S. Otani3, Y. Hiyoshi3, K. Yonesaka6, T. Sugiura1, T. Suzumura7, M. Terashima1, Y. Nakano1, Y. Hasegawa1, H. Tsukuda1, K. Matsui1, N. Masuda1, M. Fukuoka1

Author affiliations

  • 1 Medical Oncology, Izumi City General Hospital, 594-0073 - Izumi/JP
  • 2 Respiratory Medicine, Uji-Tokushukai Medical Center, 611-0041 - Uji/JP
  • 3 Respiratory Medicine, Kitasato University School of Medicine, 252-0375 - Sagamihara/JP
  • 4 Medical Oncology And Respiratory Medicine, National Hospital Organization Osaka Minami Medical Center, 586-8521 - Kawachinagano/JP
  • 5 Medical Oncology, Nara Hospital Kindai University Faculty of Medicine, 630-0293 - Ikoma/JP
  • 6 Medical Oncology, Kindai University Faculty of Medicine, 589-8511 - Osaka-sayama/JP
  • 7 Clinical Oncology, Osaka City University Graduate School of Medicine, 545-8586 - Osaka/JP

Resources

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Abstract 904

Background

PD-1 blockade by anti-PD-1 antibodies restore the function of exhausted T cells and release perforin, granzyme B and cytokines which induce cytotoxic activity against tumor cells. We examined serum perforin, granzyme B and immune modulators as biomarkers of response to PD-1 blockade in non-small cell lung cancer (NSCLC) patients.

Methods

Advanced NSCLC patients treated with nivolumab or pembrolizumab were studied. Serum were collected on days 1, 2, 8 and 15 for nivolumab and on days 1, 2, 8, 15 and 22 for pembrolizumab. Concentration of perforin was determined by enzyme-linked immunosorbent assay (ELISA) and ten immune modulators, including granzyme B, were measured by a multiplex immunoassay. Best objective response was evaluated by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1. Patients were followed more than 3 months.

Results

Plasma samples were obtained from 29 patients with nivolumab and 18 patients with pembrolizumab. With nivolumab, in 57% of responding patients, there were two aspects; (i) baseline levels of perforin concentration were higher in responders than in non-responders, or (ii) a ratio of perforin concentration on day 2 to the baseline was elevated (≧1.2). With pembrolizumab, there were no significant differences in baseline concentration between responders and non-responders. If patients who passed away within 3 months were excluded, in responding patients, a ratio of perforin concentration on day 22 to the baseline were significantly higher than in non-responders (partial response vs. progressive disease, p = 0.0330). The multiplex assay was performed on a part of samples (nivolumab, n = 10 and pembrolizumab, n = 6). By the multiplex assay, two out of 10 immune modulators were detected in more than 30% of samples; CD137 and FAS ligand. The correlation between these two analytes and the response to anti-PD-1 antibodies were hard to determine.

Conclusions

From serum, most immune modulators were difficult to measure. Sequential changes in perforin levels and the efficacy by two different anti-PD-1 antibodies were dissimilar. Concentration of serum perforin during the first cycle could be used to predict response to anti-PD1 antibody therapies in advanced NSCLC patients.

Clinical trial identification

Legal entity responsible for the study

Takayo Ota.

Funding

The Osaka Medical Research Foundation for Intractable Diseases.

Editorial Acknowledgement

Disclosure

All authors have declared no conflicts of interest.

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