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Response to Immune Checkpoint Inhibition as Monotherapy or in Combination With Chemotherapy in Metastatic ROS1-Rearranged Lung Cancers

INTRODUCTION: ROS1 fusions are oncogenic drivers in 1% to 3% of NSCLCs. The activity of immune checkpoint inhibitor (ICI) monotherapy or in combination with chemotherapy (chemotherapy with ICI [chemo-ICI]) in these tumors and their immunophenotype have not been systematically described. METHODS: In...

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Autores principales: Choudhury, Noura J., Schneider, Jaime L., Patil, Tejas, Zhu, Viola W., Goldman, Debra A., Yang, Soo-Ryum, Falcon, Christina J., Do, Andrew, Nie, Yunan, Plodkowski, Andrew J., Chaft, Jamie E., Digumarthy, Subba R., Rekhtman, Natasha, Arcila, Maria E., Iasonos, Alexia, Ou, Sai-Hong I., Lin, Jessica J., Drilon, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474494/
https://www.ncbi.nlm.nih.gov/pubmed/34590036
http://dx.doi.org/10.1016/j.jtocrr.2021.100187
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author Choudhury, Noura J.
Schneider, Jaime L.
Patil, Tejas
Zhu, Viola W.
Goldman, Debra A.
Yang, Soo-Ryum
Falcon, Christina J.
Do, Andrew
Nie, Yunan
Plodkowski, Andrew J.
Chaft, Jamie E.
Digumarthy, Subba R.
Rekhtman, Natasha
Arcila, Maria E.
Iasonos, Alexia
Ou, Sai-Hong I.
Lin, Jessica J.
Drilon, Alexander
author_facet Choudhury, Noura J.
Schneider, Jaime L.
Patil, Tejas
Zhu, Viola W.
Goldman, Debra A.
Yang, Soo-Ryum
Falcon, Christina J.
Do, Andrew
Nie, Yunan
Plodkowski, Andrew J.
Chaft, Jamie E.
Digumarthy, Subba R.
Rekhtman, Natasha
Arcila, Maria E.
Iasonos, Alexia
Ou, Sai-Hong I.
Lin, Jessica J.
Drilon, Alexander
author_sort Choudhury, Noura J.
collection PubMed
description INTRODUCTION: ROS1 fusions are oncogenic drivers in 1% to 3% of NSCLCs. The activity of immune checkpoint inhibitor (ICI) monotherapy or in combination with chemotherapy (chemotherapy with ICI [chemo-ICI]) in these tumors and their immunophenotype have not been systematically described. METHODS: In this multi-institutional retrospective study, tumor programmed death-ligand 1 (PD-L1) expression and tumor mutational burden (TMB) were evaluated in patients with ROS1-rearranged NSCLC. Time-to-treatment discontinuation (TTD) and objective response rate (ORR) (Response Evaluation Criteria in Solid Tumors [RECIST] version 1.1) were calculated for patients treated with ICI or chemo-ICI in the metastatic setting. RESULTS: A total of 184 patients were identified. Among 146 assessable cases, PD-L1 expression was less than 1% in 60 (41%), 1% to 49% in 35 (24%), and greater than or equal to 50% in 51 tumors (35%). Of 100 (92%) TMB-assessable tumors, 92 had less than 10 mutations per megabase. TMB was significantly lower for ROS1-rearranged tumors (n = 97) compared with tumors with EGFR (n = 1250) or KRAS alterations (n = 1653) and all other NSCLC tumors (n = 2753) evaluated with Memorial Sloan Kettering-Integrated Mutation Profiling of Actionable Cancer Targets (median TMB = 2.6 versus 3.5, 7.0, and 6.1 mutations per megabase, p < 0.001). Among patients treated with ICI, median TTD was 2.1 months (95% confidence interval [CI]: 1.0–4.2 mo; n = 28) and ORR 13% (2 of 16 RECIST-assessable; 95% CI: 2%–38%). Among patients treated with chemo-ICI, median TTD was 10 months (95% CI: 4.7–14.1 mo; n = 11) and ORR 83% (5 of 6 RECIST-assessable; 95% CI: 36%–100%). There was no difference in PD-L1 expression (p = 0.91) or TMB (p = 0.83) between responders and nonresponders. CONCLUSIONS: Most ROS1-rearranged NSCLCs have low PD-L1 expression and TMB. The activity of ICI in these tumors is modest. In contrast, chemo-ICI can achieve meaningful activity.
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spelling pubmed-84744942021-09-28 Response to Immune Checkpoint Inhibition as Monotherapy or in Combination With Chemotherapy in Metastatic ROS1-Rearranged Lung Cancers Choudhury, Noura J. Schneider, Jaime L. Patil, Tejas Zhu, Viola W. Goldman, Debra A. Yang, Soo-Ryum Falcon, Christina J. Do, Andrew Nie, Yunan Plodkowski, Andrew J. Chaft, Jamie E. Digumarthy, Subba R. Rekhtman, Natasha Arcila, Maria E. Iasonos, Alexia Ou, Sai-Hong I. Lin, Jessica J. Drilon, Alexander JTO Clin Res Rep Original Article INTRODUCTION: ROS1 fusions are oncogenic drivers in 1% to 3% of NSCLCs. The activity of immune checkpoint inhibitor (ICI) monotherapy or in combination with chemotherapy (chemotherapy with ICI [chemo-ICI]) in these tumors and their immunophenotype have not been systematically described. METHODS: In this multi-institutional retrospective study, tumor programmed death-ligand 1 (PD-L1) expression and tumor mutational burden (TMB) were evaluated in patients with ROS1-rearranged NSCLC. Time-to-treatment discontinuation (TTD) and objective response rate (ORR) (Response Evaluation Criteria in Solid Tumors [RECIST] version 1.1) were calculated for patients treated with ICI or chemo-ICI in the metastatic setting. RESULTS: A total of 184 patients were identified. Among 146 assessable cases, PD-L1 expression was less than 1% in 60 (41%), 1% to 49% in 35 (24%), and greater than or equal to 50% in 51 tumors (35%). Of 100 (92%) TMB-assessable tumors, 92 had less than 10 mutations per megabase. TMB was significantly lower for ROS1-rearranged tumors (n = 97) compared with tumors with EGFR (n = 1250) or KRAS alterations (n = 1653) and all other NSCLC tumors (n = 2753) evaluated with Memorial Sloan Kettering-Integrated Mutation Profiling of Actionable Cancer Targets (median TMB = 2.6 versus 3.5, 7.0, and 6.1 mutations per megabase, p < 0.001). Among patients treated with ICI, median TTD was 2.1 months (95% confidence interval [CI]: 1.0–4.2 mo; n = 28) and ORR 13% (2 of 16 RECIST-assessable; 95% CI: 2%–38%). Among patients treated with chemo-ICI, median TTD was 10 months (95% CI: 4.7–14.1 mo; n = 11) and ORR 83% (5 of 6 RECIST-assessable; 95% CI: 36%–100%). There was no difference in PD-L1 expression (p = 0.91) or TMB (p = 0.83) between responders and nonresponders. CONCLUSIONS: Most ROS1-rearranged NSCLCs have low PD-L1 expression and TMB. The activity of ICI in these tumors is modest. In contrast, chemo-ICI can achieve meaningful activity. Elsevier 2021-05-18 /pmc/articles/PMC8474494/ /pubmed/34590036 http://dx.doi.org/10.1016/j.jtocrr.2021.100187 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Choudhury, Noura J.
Schneider, Jaime L.
Patil, Tejas
Zhu, Viola W.
Goldman, Debra A.
Yang, Soo-Ryum
Falcon, Christina J.
Do, Andrew
Nie, Yunan
Plodkowski, Andrew J.
Chaft, Jamie E.
Digumarthy, Subba R.
Rekhtman, Natasha
Arcila, Maria E.
Iasonos, Alexia
Ou, Sai-Hong I.
Lin, Jessica J.
Drilon, Alexander
Response to Immune Checkpoint Inhibition as Monotherapy or in Combination With Chemotherapy in Metastatic ROS1-Rearranged Lung Cancers
title Response to Immune Checkpoint Inhibition as Monotherapy or in Combination With Chemotherapy in Metastatic ROS1-Rearranged Lung Cancers
title_full Response to Immune Checkpoint Inhibition as Monotherapy or in Combination With Chemotherapy in Metastatic ROS1-Rearranged Lung Cancers
title_fullStr Response to Immune Checkpoint Inhibition as Monotherapy or in Combination With Chemotherapy in Metastatic ROS1-Rearranged Lung Cancers
title_full_unstemmed Response to Immune Checkpoint Inhibition as Monotherapy or in Combination With Chemotherapy in Metastatic ROS1-Rearranged Lung Cancers
title_short Response to Immune Checkpoint Inhibition as Monotherapy or in Combination With Chemotherapy in Metastatic ROS1-Rearranged Lung Cancers
title_sort response to immune checkpoint inhibition as monotherapy or in combination with chemotherapy in metastatic ros1-rearranged lung cancers
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474494/
https://www.ncbi.nlm.nih.gov/pubmed/34590036
http://dx.doi.org/10.1016/j.jtocrr.2021.100187
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