Cargando…

In small cell lung cancer patients treated with RRx-001, a downregulator of CD47, decreased expression of PD-L1 on circulating tumor cells significantly correlates with clinical benefit

BACKGROUND: Small cell lung cancer (SCLC) is the most aggressive lung tumor, characterized by a rapid doubling time and the development of widespread metastases, for which immune checkpoint inhibitors have been approved to overcome T cell anergy. In light of its dismal prognosis, and lack of curativ...

Descripción completa

Detalles Bibliográficos
Autores principales: Tomita, Yusuke, Oronsky, Bryan, Abrouk, Nacer, Cabrales, Pedro, Reid, Tony R., Lee, Min-Jung, Yuno, Akira, Baker, Jonathan, Lee, Sunmin, Trepel, Jane B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867783/
https://www.ncbi.nlm.nih.gov/pubmed/33569311
http://dx.doi.org/10.21037/tlcr-20-359
_version_ 1783648341616230400
author Tomita, Yusuke
Oronsky, Bryan
Abrouk, Nacer
Cabrales, Pedro
Reid, Tony R.
Lee, Min-Jung
Yuno, Akira
Baker, Jonathan
Lee, Sunmin
Trepel, Jane B.
author_facet Tomita, Yusuke
Oronsky, Bryan
Abrouk, Nacer
Cabrales, Pedro
Reid, Tony R.
Lee, Min-Jung
Yuno, Akira
Baker, Jonathan
Lee, Sunmin
Trepel, Jane B.
author_sort Tomita, Yusuke
collection PubMed
description BACKGROUND: Small cell lung cancer (SCLC) is the most aggressive lung tumor, characterized by a rapid doubling time and the development of widespread metastases, for which immune checkpoint inhibitors have been approved to overcome T cell anergy. In light of its dismal prognosis, and lack of curative options, new therapies for extensive-disease SCLC are desperately needed. METHODS: RRx-001 is a small molecule Myc inhibitor and down-regulates CD47 expression on tumor cells. We evaluated the programmed death-ligand 1 (PD-L1) status of circulating tumor cells (CTCs) pre and post RRx-001 treatment in a phase 2 clinical trial, called QUADRUPLE THREAT, where patients with previously treated SCLC received RRx-001 in combination with a platinum doublet. The trial was registered with ClinicalTrials.gov, number NCT02489903. Fourteen patients with SCLC were analyzed to investigate the association between clinical outcome and PD-L1 expression on CTCs pre and post RRx-001. The correlation between the binary clinical outcome (clinical benefit vs. progressive disease) and the change of PD-L1 expression on CTCs after RRx-001 was analyzed using a logistic regression adjusting for baseline PD-L1 expression. RESULTS: The logistic model McFadden goodness of fit score was 0.477. The logistic model analyzing the association between decreased PD-L1 expression on CTCs after RRx-001 and response to reintroduced platinum doublet had an approximate 92.8% accuracy in its prediction of clinical benefit. The estimated receiver operating characteristic (ROC) displayed a ROC area under the curve (AUC) of 0.93 (95% confidence interval, 0.78–0.99). CONCLUSIONS: These results suggest that PD-L1 expression on CTCs decreased after RRx-001 was significantly correlated with response to reintroduced platinum-based doublet therapy. Monitoring PD-L1 expression on CTCs during RRx-001 treatment may serve as a biomarker to predict response to RRx-001-based cancer therapy.
format Online
Article
Text
id pubmed-7867783
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher AME Publishing Company
record_format MEDLINE/PubMed
spelling pubmed-78677832021-02-09 In small cell lung cancer patients treated with RRx-001, a downregulator of CD47, decreased expression of PD-L1 on circulating tumor cells significantly correlates with clinical benefit Tomita, Yusuke Oronsky, Bryan Abrouk, Nacer Cabrales, Pedro Reid, Tony R. Lee, Min-Jung Yuno, Akira Baker, Jonathan Lee, Sunmin Trepel, Jane B. Transl Lung Cancer Res Original Article BACKGROUND: Small cell lung cancer (SCLC) is the most aggressive lung tumor, characterized by a rapid doubling time and the development of widespread metastases, for which immune checkpoint inhibitors have been approved to overcome T cell anergy. In light of its dismal prognosis, and lack of curative options, new therapies for extensive-disease SCLC are desperately needed. METHODS: RRx-001 is a small molecule Myc inhibitor and down-regulates CD47 expression on tumor cells. We evaluated the programmed death-ligand 1 (PD-L1) status of circulating tumor cells (CTCs) pre and post RRx-001 treatment in a phase 2 clinical trial, called QUADRUPLE THREAT, where patients with previously treated SCLC received RRx-001 in combination with a platinum doublet. The trial was registered with ClinicalTrials.gov, number NCT02489903. Fourteen patients with SCLC were analyzed to investigate the association between clinical outcome and PD-L1 expression on CTCs pre and post RRx-001. The correlation between the binary clinical outcome (clinical benefit vs. progressive disease) and the change of PD-L1 expression on CTCs after RRx-001 was analyzed using a logistic regression adjusting for baseline PD-L1 expression. RESULTS: The logistic model McFadden goodness of fit score was 0.477. The logistic model analyzing the association between decreased PD-L1 expression on CTCs after RRx-001 and response to reintroduced platinum doublet had an approximate 92.8% accuracy in its prediction of clinical benefit. The estimated receiver operating characteristic (ROC) displayed a ROC area under the curve (AUC) of 0.93 (95% confidence interval, 0.78–0.99). CONCLUSIONS: These results suggest that PD-L1 expression on CTCs decreased after RRx-001 was significantly correlated with response to reintroduced platinum-based doublet therapy. Monitoring PD-L1 expression on CTCs during RRx-001 treatment may serve as a biomarker to predict response to RRx-001-based cancer therapy. AME Publishing Company 2021-01 /pmc/articles/PMC7867783/ /pubmed/33569311 http://dx.doi.org/10.21037/tlcr-20-359 Text en 2021 Translational Lung Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Tomita, Yusuke
Oronsky, Bryan
Abrouk, Nacer
Cabrales, Pedro
Reid, Tony R.
Lee, Min-Jung
Yuno, Akira
Baker, Jonathan
Lee, Sunmin
Trepel, Jane B.
In small cell lung cancer patients treated with RRx-001, a downregulator of CD47, decreased expression of PD-L1 on circulating tumor cells significantly correlates with clinical benefit
title In small cell lung cancer patients treated with RRx-001, a downregulator of CD47, decreased expression of PD-L1 on circulating tumor cells significantly correlates with clinical benefit
title_full In small cell lung cancer patients treated with RRx-001, a downregulator of CD47, decreased expression of PD-L1 on circulating tumor cells significantly correlates with clinical benefit
title_fullStr In small cell lung cancer patients treated with RRx-001, a downregulator of CD47, decreased expression of PD-L1 on circulating tumor cells significantly correlates with clinical benefit
title_full_unstemmed In small cell lung cancer patients treated with RRx-001, a downregulator of CD47, decreased expression of PD-L1 on circulating tumor cells significantly correlates with clinical benefit
title_short In small cell lung cancer patients treated with RRx-001, a downregulator of CD47, decreased expression of PD-L1 on circulating tumor cells significantly correlates with clinical benefit
title_sort in small cell lung cancer patients treated with rrx-001, a downregulator of cd47, decreased expression of pd-l1 on circulating tumor cells significantly correlates with clinical benefit
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867783/
https://www.ncbi.nlm.nih.gov/pubmed/33569311
http://dx.doi.org/10.21037/tlcr-20-359
work_keys_str_mv AT tomitayusuke insmallcelllungcancerpatientstreatedwithrrx001adownregulatorofcd47decreasedexpressionofpdl1oncirculatingtumorcellssignificantlycorrelateswithclinicalbenefit
AT oronskybryan insmallcelllungcancerpatientstreatedwithrrx001adownregulatorofcd47decreasedexpressionofpdl1oncirculatingtumorcellssignificantlycorrelateswithclinicalbenefit
AT abrouknacer insmallcelllungcancerpatientstreatedwithrrx001adownregulatorofcd47decreasedexpressionofpdl1oncirculatingtumorcellssignificantlycorrelateswithclinicalbenefit
AT cabralespedro insmallcelllungcancerpatientstreatedwithrrx001adownregulatorofcd47decreasedexpressionofpdl1oncirculatingtumorcellssignificantlycorrelateswithclinicalbenefit
AT reidtonyr insmallcelllungcancerpatientstreatedwithrrx001adownregulatorofcd47decreasedexpressionofpdl1oncirculatingtumorcellssignificantlycorrelateswithclinicalbenefit
AT leeminjung insmallcelllungcancerpatientstreatedwithrrx001adownregulatorofcd47decreasedexpressionofpdl1oncirculatingtumorcellssignificantlycorrelateswithclinicalbenefit
AT yunoakira insmallcelllungcancerpatientstreatedwithrrx001adownregulatorofcd47decreasedexpressionofpdl1oncirculatingtumorcellssignificantlycorrelateswithclinicalbenefit
AT bakerjonathan insmallcelllungcancerpatientstreatedwithrrx001adownregulatorofcd47decreasedexpressionofpdl1oncirculatingtumorcellssignificantlycorrelateswithclinicalbenefit
AT leesunmin insmallcelllungcancerpatientstreatedwithrrx001adownregulatorofcd47decreasedexpressionofpdl1oncirculatingtumorcellssignificantlycorrelateswithclinicalbenefit
AT trepeljaneb insmallcelllungcancerpatientstreatedwithrrx001adownregulatorofcd47decreasedexpressionofpdl1oncirculatingtumorcellssignificantlycorrelateswithclinicalbenefit