Cargando…

Risk factors for interstitial lung disease induced by gemcitabine plus albumin-bound paclitaxel therapy in pancreatic ductal adenocarcinoma patients

BACKGROUND: Gemcitabine plus nab-paclitaxel (GnP) therapy is used for unresectable pancreatic ductal adenocarcinoma, but may cause interstitial lung disease (ILD) as a serious side effect. However, the risk factors for ILD in patients receiving GnP therapy are not well established. Here, we retrospe...

Descripción completa

Detalles Bibliográficos
Autores principales: Ueda, Rikako, Yamamoto, Naho, Hori, Yuki, Yoshida, Kouji, Ohtsubo, Koushiro, Terashima, Takeshi, Shimada, Tsutomu, Sai, Yoshimichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809002/
https://www.ncbi.nlm.nih.gov/pubmed/35105386
http://dx.doi.org/10.1186/s40780-021-00236-5
_version_ 1784643931477114880
author Ueda, Rikako
Yamamoto, Naho
Hori, Yuki
Yoshida, Kouji
Ohtsubo, Koushiro
Terashima, Takeshi
Shimada, Tsutomu
Sai, Yoshimichi
author_facet Ueda, Rikako
Yamamoto, Naho
Hori, Yuki
Yoshida, Kouji
Ohtsubo, Koushiro
Terashima, Takeshi
Shimada, Tsutomu
Sai, Yoshimichi
author_sort Ueda, Rikako
collection PubMed
description BACKGROUND: Gemcitabine plus nab-paclitaxel (GnP) therapy is used for unresectable pancreatic ductal adenocarcinoma, but may cause interstitial lung disease (ILD) as a serious side effect. However, the risk factors for ILD in patients receiving GnP therapy are not well established. Here, we retrospectively investigated the incidence of GnP-induced ILD in pancreatic ductal adenocarcinoma patients, and the risk factors. METHODS: We investigated the patients’ background, laboratory data, previous treatment history, concomitant medications, number of doses of GnP, cumulative dosage and administration period, and occurrence of side effects. RESULTS: Of the 105 patients included in this study, ILD occurred in 10 (9.5%). Patients with ILD had a significantly higher frequency of concomitant treatment with Kampo medicines, especially goshajinkigan, which is considered to help prevent chemotherapy-induced peripheral neuropathy (CIPN) (odds ratio: 11.5, 95% confidence interval: 2.67–49.38). No significant differences were observed in other clinical characteristics. Notably, the severity of CIPN in patients who used goshajinkigan for prevention was not significantly different from that in patients who did not use goshajinkigan in this study. CONCLUSIONS: These results suggest that administration of goshajinkigan to patients receiving GnP therapy for prevention of CIPN may need to be reconsidered.
format Online
Article
Text
id pubmed-8809002
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-88090022022-02-03 Risk factors for interstitial lung disease induced by gemcitabine plus albumin-bound paclitaxel therapy in pancreatic ductal adenocarcinoma patients Ueda, Rikako Yamamoto, Naho Hori, Yuki Yoshida, Kouji Ohtsubo, Koushiro Terashima, Takeshi Shimada, Tsutomu Sai, Yoshimichi J Pharm Health Care Sci Research Article BACKGROUND: Gemcitabine plus nab-paclitaxel (GnP) therapy is used for unresectable pancreatic ductal adenocarcinoma, but may cause interstitial lung disease (ILD) as a serious side effect. However, the risk factors for ILD in patients receiving GnP therapy are not well established. Here, we retrospectively investigated the incidence of GnP-induced ILD in pancreatic ductal adenocarcinoma patients, and the risk factors. METHODS: We investigated the patients’ background, laboratory data, previous treatment history, concomitant medications, number of doses of GnP, cumulative dosage and administration period, and occurrence of side effects. RESULTS: Of the 105 patients included in this study, ILD occurred in 10 (9.5%). Patients with ILD had a significantly higher frequency of concomitant treatment with Kampo medicines, especially goshajinkigan, which is considered to help prevent chemotherapy-induced peripheral neuropathy (CIPN) (odds ratio: 11.5, 95% confidence interval: 2.67–49.38). No significant differences were observed in other clinical characteristics. Notably, the severity of CIPN in patients who used goshajinkigan for prevention was not significantly different from that in patients who did not use goshajinkigan in this study. CONCLUSIONS: These results suggest that administration of goshajinkigan to patients receiving GnP therapy for prevention of CIPN may need to be reconsidered. BioMed Central 2022-02-02 /pmc/articles/PMC8809002/ /pubmed/35105386 http://dx.doi.org/10.1186/s40780-021-00236-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Ueda, Rikako
Yamamoto, Naho
Hori, Yuki
Yoshida, Kouji
Ohtsubo, Koushiro
Terashima, Takeshi
Shimada, Tsutomu
Sai, Yoshimichi
Risk factors for interstitial lung disease induced by gemcitabine plus albumin-bound paclitaxel therapy in pancreatic ductal adenocarcinoma patients
title Risk factors for interstitial lung disease induced by gemcitabine plus albumin-bound paclitaxel therapy in pancreatic ductal adenocarcinoma patients
title_full Risk factors for interstitial lung disease induced by gemcitabine plus albumin-bound paclitaxel therapy in pancreatic ductal adenocarcinoma patients
title_fullStr Risk factors for interstitial lung disease induced by gemcitabine plus albumin-bound paclitaxel therapy in pancreatic ductal adenocarcinoma patients
title_full_unstemmed Risk factors for interstitial lung disease induced by gemcitabine plus albumin-bound paclitaxel therapy in pancreatic ductal adenocarcinoma patients
title_short Risk factors for interstitial lung disease induced by gemcitabine plus albumin-bound paclitaxel therapy in pancreatic ductal adenocarcinoma patients
title_sort risk factors for interstitial lung disease induced by gemcitabine plus albumin-bound paclitaxel therapy in pancreatic ductal adenocarcinoma patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809002/
https://www.ncbi.nlm.nih.gov/pubmed/35105386
http://dx.doi.org/10.1186/s40780-021-00236-5
work_keys_str_mv AT uedarikako riskfactorsforinterstitiallungdiseaseinducedbygemcitabineplusalbuminboundpaclitaxeltherapyinpancreaticductaladenocarcinomapatients
AT yamamotonaho riskfactorsforinterstitiallungdiseaseinducedbygemcitabineplusalbuminboundpaclitaxeltherapyinpancreaticductaladenocarcinomapatients
AT horiyuki riskfactorsforinterstitiallungdiseaseinducedbygemcitabineplusalbuminboundpaclitaxeltherapyinpancreaticductaladenocarcinomapatients
AT yoshidakouji riskfactorsforinterstitiallungdiseaseinducedbygemcitabineplusalbuminboundpaclitaxeltherapyinpancreaticductaladenocarcinomapatients
AT ohtsubokoushiro riskfactorsforinterstitiallungdiseaseinducedbygemcitabineplusalbuminboundpaclitaxeltherapyinpancreaticductaladenocarcinomapatients
AT terashimatakeshi riskfactorsforinterstitiallungdiseaseinducedbygemcitabineplusalbuminboundpaclitaxeltherapyinpancreaticductaladenocarcinomapatients
AT shimadatsutomu riskfactorsforinterstitiallungdiseaseinducedbygemcitabineplusalbuminboundpaclitaxeltherapyinpancreaticductaladenocarcinomapatients
AT saiyoshimichi riskfactorsforinterstitiallungdiseaseinducedbygemcitabineplusalbuminboundpaclitaxeltherapyinpancreaticductaladenocarcinomapatients