Incidence of pneumonitis/interstitial lung disease induced by HER2-targeting therapy for HER2-positive metastatic breast cancer.


Journal

Breast cancer research and treatment
ISSN: 1573-7217
Titre abrégé: Breast Cancer Res Treat
Pays: Netherlands
ID NLM: 8111104

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 18 05 2020
accepted: 13 06 2020
pubmed: 28 6 2020
medline: 13 2 2021
entrez: 28 6 2020
Statut: ppublish

Résumé

Anti-human epidermal growth factor receptor 2 (HER2) therapies are associated with interstitial lung disease (ILD), also referred to as pneumonitis. In this literature review, we describe the incidence of ILD among patients with HER2-positive metastatic breast cancer (MBC) receiving anti-HER2 therapies, and we describe existing recommendations for monitoring and managing drug-induced ILD among these patients. We searched PubMed and Embase to identify clinical trials and postmarket observational studies that investigated anti-HER2 therapies for HER2-positive MBC, reported on ILD, and were published during January 1, 2009 to July 15, 2019. Articles were screened by two researchers; data were extracted from the full-text articles. The 18 articles selected for this review assessed 9,886 patients who received trastuzumab (8 articles), lapatinib (4 articles), trastuzumab emtansine (3 articles), trastuzumab deruxtecan (2 articles), or trastuzumab duocarmazine (1 article). The overall incidence of all-grade ILD was 2.4% (n = 234), with 66.7% (n = 156) occurring as grade 1-2 events, 0.5% grade 3-4 (n = 54; incidence), and 0.2% grade 5 (n = 16; incidence). The highest ILD incidence (21.4%) was among patients receiving trastuzumab combined with everolimus and paclitaxel. Ten studies indicated that ILD events were managed via dose interruption, dose reduction, or treatment discontinuation; two studies included detailed guidelines on managing drug-induced ILD. ILD is a well-described adverse drug reaction associated with several anti-HER2 drugs. Published ILD management guidelines are available for few anti-HER2 treatment regimens; however, guidance for monitoring for anti-HER2 drug-induced ILD is lacking.

Identifiants

pubmed: 32591987
doi: 10.1007/s10549-020-05754-8
pii: 10.1007/s10549-020-05754-8
pmc: PMC7376509
doi:

Substances chimiques

Immunoconjugates 0
Lapatinib 0VUA21238F
trastuzumab deruxtecan 5384HK7574
Everolimus 9HW64Q8G6G
ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1
Trastuzumab P188ANX8CK
Paclitaxel P88XT4IS4D
Ado-Trastuzumab Emtansine SE2KH7T06F
trastuzumab duocarmazine XCR2BZ80N7
Camptothecin XT3Z54Z28A

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

23-39

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Auteurs

Michelle D Hackshaw (MD)

Daiichi Sankyo, Inc., 211 Mount Airy, 1A-453, Basking Ridge, NJ, 07920, USA. mhackshawel@dsi.com.

Heather E Danysh (HE)

RTI Health Solutions, Waltham, MA, USA.

Jasmeet Singh (J)

Daiichi Sankyo, Inc., 211 Mount Airy, 1A-453, Basking Ridge, NJ, 07920, USA.

Mary E Ritchey (ME)

RTI Health Solutions, Research Triangle Park, NC, USA.

Amy Ladner (A)

RTI Health Solutions, Research Triangle Park, NC, USA.

Corina Taitt (C)

Daiichi Sankyo, Inc., 211 Mount Airy, 1A-453, Basking Ridge, NJ, 07920, USA.

D Ross Camidge (DR)

University Colorado, Aurora, CO, USA.

Hiroji Iwata (H)

Aichi Cancer Center, Nagoya, Japan.

Charles A Powell (CA)

Mount Sinai Hospital, New York, NY, USA.

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Classifications MeSH