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E-Poster Display

1001P - PD1midKLRG1+Tbethigh effector memory T in the peripheral blood correlates with tumor response to combined therapy with lenvatinib and anti-PD-1 antibodies in unresectable hepatocellular carcinoma

Date

17 Sep 2020

Session

E-Poster Display

Topics

Tumour Site

Hepatobiliary Cancers

Presenters

Huichuan Sun

Citation

Annals of Oncology (2020) 31 (suppl_4): S629-S644. 10.1016/annonc/annonc278

Authors

H. Sun, C. Huang, X. Zhu, Y. Shen, N. Ge, Y. Chen, C. Tan, J. Zhou, J. Fan

Author affiliations

  • Liver Cancer Institute, Zhongshan Hospital - Fudan University, 200032 - Shanghai/CN

Resources

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Abstract 1001P

Background

Combination therapy of anti-angiogenic therapy and anti-PD-1antibody had shown promising anti-tumor effects for advanced hepatocellular carcinoma (HCC) in clinical trials. Despite the remarkable effect of combined therapy with lenvatinib and anti-PD-1 antibodies in HCC, most patients do not respond to the combination therapy, or develop resistance. Predicting tumor responses to the combination therapy is an important unmet need.

Methods

Patients with advanced unresectable HCC received Lenvatinib 8 mg/d regardless of patient body weight and anti-PD-1 antibody either q2wk (nivolumab or camrelizumab) or q3wk (pembrolizumab, sintilimab or toripalimab). Patients who completed at least one efficacy and safety assessment were eligible for this study. High-dimensional single-cell mass cytometry (CyTOF) and a bioinformatics pipeline for the in-depth characterization of the immune cell subsets was used to identify T cell subsets in the peripheral blood of patients before the treatment.

Results

From May 2019 to Dec. 2019, we recruited 15 patients. All the patients are assessable for efficacy. Two patients achieved complete response (CR), 7 patients achieved partial response (PR), and 6 patients achieved progressing disease (PD) per mRECIST. CyTOF identified 36 meta-clusters contained all of the major immune cell populations such as T cells, B cells, NK cells, DC cells and momocytes with a panel of 42 antibodies. Moreover, we delineated an PD1midKLRG1+Tbethigh effector memory T cell phenotype that was significantly more abundant in responders (CR or PR, n=9) to combined therapy compared with non-responders (n=6) (PD, P < 0.05).

Conclusions

PD1midKLRG1+Tbethigh effector memory T cell in the peripheral blood may be a useful biomarker for predicting tumor response to the combination therapy in HCC.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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