Cargando…

Organ-specific immune checkpoint inhibitor treatment in lung cancer: a systematic review and meta-analysis

OBJECTIVES: Based on the acknowledged organ-specific immune microenvironment, little is known regarding the efficacy of immunotherapy in patients with lung cancer according to metastatic sites. This meta-analysis aimed to explore the efficacy of immune checkpoint inhibitors (ICIs) vs chemotherapy in...

Descripción completa

Detalles Bibliográficos
Autores principales: Yu, Shufei, Zhang, Shuyang, Xu, Haiyan, Yang, Guangjian, Xu, Fei, Yang, Liang, Chen, Duo, An, Guangyu, Wang, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030562/
https://www.ncbi.nlm.nih.gov/pubmed/36931679
http://dx.doi.org/10.1136/bmjopen-2021-059457
_version_ 1784910402883158016
author Yu, Shufei
Zhang, Shuyang
Xu, Haiyan
Yang, Guangjian
Xu, Fei
Yang, Liang
Chen, Duo
An, Guangyu
Wang, Yan
author_facet Yu, Shufei
Zhang, Shuyang
Xu, Haiyan
Yang, Guangjian
Xu, Fei
Yang, Liang
Chen, Duo
An, Guangyu
Wang, Yan
author_sort Yu, Shufei
collection PubMed
description OBJECTIVES: Based on the acknowledged organ-specific immune microenvironment, little is known regarding the efficacy of immunotherapy in patients with lung cancer according to metastatic sites. This meta-analysis aimed to explore the efficacy of immune checkpoint inhibitors (ICIs) vs chemotherapy in patients with lung cancer with liver metastases (LM) or brain metastases (BM). DESIGN: Meta-analysis and systematic review. DATA SOURCES: We systematically searched in electronic databases (PubMed, EMBASE, Cochrane Library and Web of Science), up to 31 January 2022. We also reviewed the abstracts from major international conferences. Eligibility criteria were randomised controlled phase II or III trials reporting the overall survival (OS) or progression-free survival (PFS) of LM or BM subsets. DATA EXTRACTION AND SYNTHESIS: Hazard ratios (HRs) with 95% CIs for OS and PFS were extracted and aggregated using a random-effects model. RESULTS: Twenty-four randomised controlled trials with available outcomes for patients with BMs or LMs were identified. A total of 1124 patients with BM and 2077 patients with LM were included in the analysis. The pooled OS HR of patients with LMs was 0.83 (95% CI 0.72 to 0.95), and that of patients without LM 0.73 (95% CI 0.69 to 0.79). LM was associated with less benefits from ICIs. In patients with BM treated with ICIs, the pooled OS HR compared with the control arms was 0.71 (95% CI 0.53 to 0.94). Subgroup analyses by histology suggested that only patients with non-small cell lung cancer (NSCLC) with BM could gain benefit from ICIs (HR 0.53, 95% CI 0.41 to 0.68). BM negatively influenced efficacy of immunotherapy in patients with small cell lung cancer. CONCLUSIONS: Our results showed immunotherapy demonstrated efficacy in patients with lung cancer with LM and BM, survival benefits dominantly favoured patients with NSCLC. Patients with lung cancer with LM obtained less benefits from ICIs than those without. Therefore, organ-specific immunotherapeutic approaches should be considered. PROSPERO REGISTRATION NUMBER: CRD42020212797.
format Online
Article
Text
id pubmed-10030562
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BMJ Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-100305622023-03-23 Organ-specific immune checkpoint inhibitor treatment in lung cancer: a systematic review and meta-analysis Yu, Shufei Zhang, Shuyang Xu, Haiyan Yang, Guangjian Xu, Fei Yang, Liang Chen, Duo An, Guangyu Wang, Yan BMJ Open Oncology OBJECTIVES: Based on the acknowledged organ-specific immune microenvironment, little is known regarding the efficacy of immunotherapy in patients with lung cancer according to metastatic sites. This meta-analysis aimed to explore the efficacy of immune checkpoint inhibitors (ICIs) vs chemotherapy in patients with lung cancer with liver metastases (LM) or brain metastases (BM). DESIGN: Meta-analysis and systematic review. DATA SOURCES: We systematically searched in electronic databases (PubMed, EMBASE, Cochrane Library and Web of Science), up to 31 January 2022. We also reviewed the abstracts from major international conferences. Eligibility criteria were randomised controlled phase II or III trials reporting the overall survival (OS) or progression-free survival (PFS) of LM or BM subsets. DATA EXTRACTION AND SYNTHESIS: Hazard ratios (HRs) with 95% CIs for OS and PFS were extracted and aggregated using a random-effects model. RESULTS: Twenty-four randomised controlled trials with available outcomes for patients with BMs or LMs were identified. A total of 1124 patients with BM and 2077 patients with LM were included in the analysis. The pooled OS HR of patients with LMs was 0.83 (95% CI 0.72 to 0.95), and that of patients without LM 0.73 (95% CI 0.69 to 0.79). LM was associated with less benefits from ICIs. In patients with BM treated with ICIs, the pooled OS HR compared with the control arms was 0.71 (95% CI 0.53 to 0.94). Subgroup analyses by histology suggested that only patients with non-small cell lung cancer (NSCLC) with BM could gain benefit from ICIs (HR 0.53, 95% CI 0.41 to 0.68). BM negatively influenced efficacy of immunotherapy in patients with small cell lung cancer. CONCLUSIONS: Our results showed immunotherapy demonstrated efficacy in patients with lung cancer with LM and BM, survival benefits dominantly favoured patients with NSCLC. Patients with lung cancer with LM obtained less benefits from ICIs than those without. Therefore, organ-specific immunotherapeutic approaches should be considered. PROSPERO REGISTRATION NUMBER: CRD42020212797. BMJ Publishing Group 2023-03-17 /pmc/articles/PMC10030562/ /pubmed/36931679 http://dx.doi.org/10.1136/bmjopen-2021-059457 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Oncology
Yu, Shufei
Zhang, Shuyang
Xu, Haiyan
Yang, Guangjian
Xu, Fei
Yang, Liang
Chen, Duo
An, Guangyu
Wang, Yan
Organ-specific immune checkpoint inhibitor treatment in lung cancer: a systematic review and meta-analysis
title Organ-specific immune checkpoint inhibitor treatment in lung cancer: a systematic review and meta-analysis
title_full Organ-specific immune checkpoint inhibitor treatment in lung cancer: a systematic review and meta-analysis
title_fullStr Organ-specific immune checkpoint inhibitor treatment in lung cancer: a systematic review and meta-analysis
title_full_unstemmed Organ-specific immune checkpoint inhibitor treatment in lung cancer: a systematic review and meta-analysis
title_short Organ-specific immune checkpoint inhibitor treatment in lung cancer: a systematic review and meta-analysis
title_sort organ-specific immune checkpoint inhibitor treatment in lung cancer: a systematic review and meta-analysis
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030562/
https://www.ncbi.nlm.nih.gov/pubmed/36931679
http://dx.doi.org/10.1136/bmjopen-2021-059457
work_keys_str_mv AT yushufei organspecificimmunecheckpointinhibitortreatmentinlungcancerasystematicreviewandmetaanalysis
AT zhangshuyang organspecificimmunecheckpointinhibitortreatmentinlungcancerasystematicreviewandmetaanalysis
AT xuhaiyan organspecificimmunecheckpointinhibitortreatmentinlungcancerasystematicreviewandmetaanalysis
AT yangguangjian organspecificimmunecheckpointinhibitortreatmentinlungcancerasystematicreviewandmetaanalysis
AT xufei organspecificimmunecheckpointinhibitortreatmentinlungcancerasystematicreviewandmetaanalysis
AT yangliang organspecificimmunecheckpointinhibitortreatmentinlungcancerasystematicreviewandmetaanalysis
AT chenduo organspecificimmunecheckpointinhibitortreatmentinlungcancerasystematicreviewandmetaanalysis
AT anguangyu organspecificimmunecheckpointinhibitortreatmentinlungcancerasystematicreviewandmetaanalysis
AT wangyan organspecificimmunecheckpointinhibitortreatmentinlungcancerasystematicreviewandmetaanalysis