Pneumonitis associated with Trastuzumab emtansine in a patient with metastatic breast cancer.


Journal

Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners
ISSN: 1477-092X
Titre abrégé: J Oncol Pharm Pract
Pays: England
ID NLM: 9511372

Informations de publication

Date de publication:
Apr 2022
Historique:
pubmed: 23 12 2021
medline: 27 4 2022
entrez: 22 12 2021
Statut: ppublish

Résumé

Trastuzumab emtansine (TDM-1) is an antibody-drug conjugate effective in human epidermal growth factor receptor-2 - expressing advanced breast cancer. Pulmonary complications of TDM-1 are rarely reported. TDM-1-associated interstitial lung disease is referred to as pneumonitis. A 47-year-old female patient who underwent modified radical mastectomy and axillary lymph node dissection operations due to a palpable mass in the right breast and axillary region. The patient who had received multiple chemotherapy was last receiving TDM-1 treatment. Fatigue, dyspnea, and tachypnea were detected for the first time on 20 days after the 6 In our case, we first considered metastasis, pneumonia and fungal infection based on radiological findings, but the lack of response to the treatments and the results of the investigations suggested drug-induced pneumonia and steroid treatment was started. Our case had a complete radiological recovery and complete response to sterod therapy. In such cases, it is important to first exclude infections and metastasis. In cases of drug-induced pneumonia, the first treatment option is systemic corticosteroids and generally responded well. Unlike other cases of interstitial pneumonia, lung imaging of our case was resembling a metastasis, pneumonia and fungal infection. With increasing use of TDM-1, we will have more experience in both efficacy and complications of TDM-1. Although TDM-1 is a well-tolerated drug, clinicians should be aware of rare pulmonary complications and prepared to respond appropriately.

Identifiants

pubmed: 34935553
doi: 10.1177/10781552211066073
doi:

Substances chimiques

Maytansine 14083FR882
Receptor, ErbB-2 EC 2.7.10.1
Trastuzumab P188ANX8CK
Ado-Trastuzumab Emtansine SE2KH7T06F

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

740-745

Auteurs

Muzaffer Uğraklı (M)

Department of Medical Oncology, 64222Necmettin Erbakan University School of Medicine, Konya, Turkey.

Murat Araz (M)

Department of Medical Oncology, 64222Necmettin Erbakan University School of Medicine, Konya, Turkey.

Aykut Demirkıran (A)

Department of Medical Oncology, 64222Necmettin Erbakan University School of Medicine, Konya, Turkey.

Ahmet Faruk Çelik (AF)

Department of Internal Medicine, 427826Necmettin Erbakan University School of Medicine, Konya, Turkey.

Melek Karakurt Eryılmaz (M)

Department of Medical Oncology, 64222Necmettin Erbakan University School of Medicine, Konya, Turkey.

Mustafa Karaağaç (M)

Department of Medical Oncology, 64222Necmettin Erbakan University School of Medicine, Konya, Turkey.

Mehmet Artaç (M)

Department of Medical Oncology, 64222Necmettin Erbakan University School of Medicine, Konya, Turkey.

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Classifications MeSH