Cargando…

Efficacy of anti-PD-1/PD-L1 antibodies after discontinuation due to adverse events in non-small cell lung cancer patients (HANSHIN 0316)

BACKGROUND: Immune checkpoint inhibitors (ICIs) have emerged as promising therapeutic agents in non-small cell lung cancer (NSCLC). However, the duration for which ICIs should be continued remains a clinical problem. METHODS: We examined the efficacy of anti-PD-1/PD-L1 inhibitors after the discontin...

Descripción completa

Detalles Bibliográficos
Autores principales: Tachihara, Motoko, Negoro, Shunichi, Inoue, Takako, Tamiya, Motohiro, Akazawa, Yuki, Uenami, Takeshi, Urata, Yoshiko, Hattori, Yoshihiro, Hata, Akito, Katakami, Nobuyuki, Yokota, Soichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171229/
https://www.ncbi.nlm.nih.gov/pubmed/30285770
http://dx.doi.org/10.1186/s12885-018-4819-2
_version_ 1783360755093995520
author Tachihara, Motoko
Negoro, Shunichi
Inoue, Takako
Tamiya, Motohiro
Akazawa, Yuki
Uenami, Takeshi
Urata, Yoshiko
Hattori, Yoshihiro
Hata, Akito
Katakami, Nobuyuki
Yokota, Soichiro
author_facet Tachihara, Motoko
Negoro, Shunichi
Inoue, Takako
Tamiya, Motohiro
Akazawa, Yuki
Uenami, Takeshi
Urata, Yoshiko
Hattori, Yoshihiro
Hata, Akito
Katakami, Nobuyuki
Yokota, Soichiro
author_sort Tachihara, Motoko
collection PubMed
description BACKGROUND: Immune checkpoint inhibitors (ICIs) have emerged as promising therapeutic agents in non-small cell lung cancer (NSCLC). However, the duration for which ICIs should be continued remains a clinical problem. METHODS: We examined the efficacy of anti-PD-1/PD-L1 inhibitors after the discontinuation of antibodies due to adverse events (AEs) in patients with NSCLC. This was a multicenter retrospective study that analyzed NSCLC patients who were treated with PD-1/PD-L1 inhibitors by August 2016. RESULTS: The patients with NSCLC were 18 males and 1 female at a median 67 years of age (range: 49–80 years). Eighteen of 19 patients were treated with nivolumab, one was with atezolizumab. Approximately half of AEs were interstitial pneumonia. Fourteen patients (73.7%) were treated with steroid therapy. The median number of treatment cycles was 7 (range, 1–70), and the median duration of treatment was 2.8 months (range, 1 day-32.9 months). The overall response rate with confirmation during treatment was 21.1%. The median progression-free survival (PFS) was 10.2 months (95% confidence interval [CI] = 3.2–17.1 months) and 5.6 months (95% CI = 0–12.2 months) from the initiation and the discontinuation of PD-1/PD-L1 treatment, respectively. The median PFS after discontinuation according to the confirmed response during administration was not reached for partial response (PR) and 4.9 months (95% CI, 3.7–6.0) for stable disease (SD) patients (P = 0.02). CONCLUSION: The PFS of the PR patients was completely different from that of the SD patients. The cases with PR prior to the onset of AE tended to show a durable response after the discontinuation of PD-1/PD-L1 inhibitors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-018-4819-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6171229
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-61712292018-10-10 Efficacy of anti-PD-1/PD-L1 antibodies after discontinuation due to adverse events in non-small cell lung cancer patients (HANSHIN 0316) Tachihara, Motoko Negoro, Shunichi Inoue, Takako Tamiya, Motohiro Akazawa, Yuki Uenami, Takeshi Urata, Yoshiko Hattori, Yoshihiro Hata, Akito Katakami, Nobuyuki Yokota, Soichiro BMC Cancer Research Article BACKGROUND: Immune checkpoint inhibitors (ICIs) have emerged as promising therapeutic agents in non-small cell lung cancer (NSCLC). However, the duration for which ICIs should be continued remains a clinical problem. METHODS: We examined the efficacy of anti-PD-1/PD-L1 inhibitors after the discontinuation of antibodies due to adverse events (AEs) in patients with NSCLC. This was a multicenter retrospective study that analyzed NSCLC patients who were treated with PD-1/PD-L1 inhibitors by August 2016. RESULTS: The patients with NSCLC were 18 males and 1 female at a median 67 years of age (range: 49–80 years). Eighteen of 19 patients were treated with nivolumab, one was with atezolizumab. Approximately half of AEs were interstitial pneumonia. Fourteen patients (73.7%) were treated with steroid therapy. The median number of treatment cycles was 7 (range, 1–70), and the median duration of treatment was 2.8 months (range, 1 day-32.9 months). The overall response rate with confirmation during treatment was 21.1%. The median progression-free survival (PFS) was 10.2 months (95% confidence interval [CI] = 3.2–17.1 months) and 5.6 months (95% CI = 0–12.2 months) from the initiation and the discontinuation of PD-1/PD-L1 treatment, respectively. The median PFS after discontinuation according to the confirmed response during administration was not reached for partial response (PR) and 4.9 months (95% CI, 3.7–6.0) for stable disease (SD) patients (P = 0.02). CONCLUSION: The PFS of the PR patients was completely different from that of the SD patients. The cases with PR prior to the onset of AE tended to show a durable response after the discontinuation of PD-1/PD-L1 inhibitors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-018-4819-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-03 /pmc/articles/PMC6171229/ /pubmed/30285770 http://dx.doi.org/10.1186/s12885-018-4819-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Tachihara, Motoko
Negoro, Shunichi
Inoue, Takako
Tamiya, Motohiro
Akazawa, Yuki
Uenami, Takeshi
Urata, Yoshiko
Hattori, Yoshihiro
Hata, Akito
Katakami, Nobuyuki
Yokota, Soichiro
Efficacy of anti-PD-1/PD-L1 antibodies after discontinuation due to adverse events in non-small cell lung cancer patients (HANSHIN 0316)
title Efficacy of anti-PD-1/PD-L1 antibodies after discontinuation due to adverse events in non-small cell lung cancer patients (HANSHIN 0316)
title_full Efficacy of anti-PD-1/PD-L1 antibodies after discontinuation due to adverse events in non-small cell lung cancer patients (HANSHIN 0316)
title_fullStr Efficacy of anti-PD-1/PD-L1 antibodies after discontinuation due to adverse events in non-small cell lung cancer patients (HANSHIN 0316)
title_full_unstemmed Efficacy of anti-PD-1/PD-L1 antibodies after discontinuation due to adverse events in non-small cell lung cancer patients (HANSHIN 0316)
title_short Efficacy of anti-PD-1/PD-L1 antibodies after discontinuation due to adverse events in non-small cell lung cancer patients (HANSHIN 0316)
title_sort efficacy of anti-pd-1/pd-l1 antibodies after discontinuation due to adverse events in non-small cell lung cancer patients (hanshin 0316)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171229/
https://www.ncbi.nlm.nih.gov/pubmed/30285770
http://dx.doi.org/10.1186/s12885-018-4819-2
work_keys_str_mv AT tachiharamotoko efficacyofantipd1pdl1antibodiesafterdiscontinuationduetoadverseeventsinnonsmallcelllungcancerpatientshanshin0316
AT negoroshunichi efficacyofantipd1pdl1antibodiesafterdiscontinuationduetoadverseeventsinnonsmallcelllungcancerpatientshanshin0316
AT inouetakako efficacyofantipd1pdl1antibodiesafterdiscontinuationduetoadverseeventsinnonsmallcelllungcancerpatientshanshin0316
AT tamiyamotohiro efficacyofantipd1pdl1antibodiesafterdiscontinuationduetoadverseeventsinnonsmallcelllungcancerpatientshanshin0316
AT akazawayuki efficacyofantipd1pdl1antibodiesafterdiscontinuationduetoadverseeventsinnonsmallcelllungcancerpatientshanshin0316
AT uenamitakeshi efficacyofantipd1pdl1antibodiesafterdiscontinuationduetoadverseeventsinnonsmallcelllungcancerpatientshanshin0316
AT uratayoshiko efficacyofantipd1pdl1antibodiesafterdiscontinuationduetoadverseeventsinnonsmallcelllungcancerpatientshanshin0316
AT hattoriyoshihiro efficacyofantipd1pdl1antibodiesafterdiscontinuationduetoadverseeventsinnonsmallcelllungcancerpatientshanshin0316
AT hataakito efficacyofantipd1pdl1antibodiesafterdiscontinuationduetoadverseeventsinnonsmallcelllungcancerpatientshanshin0316
AT katakaminobuyuki efficacyofantipd1pdl1antibodiesafterdiscontinuationduetoadverseeventsinnonsmallcelllungcancerpatientshanshin0316
AT yokotasoichiro efficacyofantipd1pdl1antibodiesafterdiscontinuationduetoadverseeventsinnonsmallcelllungcancerpatientshanshin0316