Thoracic and cutaneous sarcoid-like reaction associated with anti-PD-1 therapy: Longitudinal monitoring of PD-1 and PD-L1 expression after stopping treatment

23Citations
Citations of this article
31Readers
Mendeley users who have this article in their library.

Abstract

Background: Immune checkpoint inhibitors (ICI) target T cell inhibitory pathways that are responsible for cancer tolerance by down-modulating immune functions. ICI have revolutionized patients care with lung cancer. Nevertheless, restoring endogenous antitumor T-cell responses can induce immune related adverse events, such as sarcoidosis. Case presentation: We report here the first case of a thoracic and cutaneous sarcoid-like reaction in a patient with a relapsing unresectable non-small cell lung cancer (NSCLC) treated with nivolumab, an anti-PD-1 mAb. The expression of PD-1 and its ligands, PD-L1 and PD-L2, was assessed by flow cytometry on peripheral blood mononuclear cells (PBMC) and compared to patients who had discontinued nivolumab therapy without having developed any immune related adverse events. PD-L1 expression was transiently increased on B cells, T cells and monocytes, whereas PD-L2 expression was not modulated. PD-1 was transiently undetectable when PD-L1 was maximal, before returning to basal level. Sarcoidosis spontaneously resolved, without corticotherapy. Conclusion: This case sheds the light on a complex regulation of PD-L1 expression in vivo on PBMC after nivolumab arrest and triggers the question of monitoring the expression of immune checkpoint on immune cells during and after treatment with ICI.

Cite

CITATION STYLE

APA

Paolini, L., Poli, C., Blanchard, S., Urban, T., Croué, A., Rousselet, M. C., … Hureaux, J. (2018). Thoracic and cutaneous sarcoid-like reaction associated with anti-PD-1 therapy: Longitudinal monitoring of PD-1 and PD-L1 expression after stopping treatment. Journal for ImmunoTherapy of Cancer, 6(1). https://doi.org/10.1186/s40425-018-0372-4

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free