Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1784575236647157760 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8474494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT choudhurynouraj responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT schneiderjaimel responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT patiltejas responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT zhuviolaw responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT goldmandebraa responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT yangsooryum responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT falconchristinaj responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT doandrew responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT nieyunan responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT plodkowskiandrewj responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT chaftjamiee responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT digumarthysubbar responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT rekhtmannatasha responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT arcilamariae responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT iasonosalexia responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT ousaihongi responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT linjessicaj responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers AT drilonalexander responsetoimmunecheckpointinhibitionasmonotherapyorincombinationwithchemotherapyinmetastaticros1rearrangedlungcancers |