Osimertinib for patients with poor performance status and EGFR T790M mutation-positive advanced non-small cell lung cancer: a phase II clinical trial.


Journal

Investigational new drugs
ISSN: 1573-0646
Titre abrégé: Invest New Drugs
Pays: United States
ID NLM: 8309330

Informations de publication

Date de publication:
12 2020
Historique:
received: 26 03 2020
accepted: 29 04 2020
pubmed: 20 5 2020
medline: 11 9 2021
entrez: 20 5 2020
Statut: ppublish

Résumé

Osimertinib is a molecularly targeted agent used to treat non-small cell lung cancer (NSCLC) patients with an epidermal growth factor receptor (EGFR) T790M mutation. However, its efficacy and safety profile when patients have poor performance status (PS) is unknown. Therefore, we conducted an open-label, multi-center, single-arm phase II study to evaluate its efficacy and safety in EGFR T790M mutation-positive NSCLC patients with Eastern Cooperative Oncology Group PS scores of between 2 and 4. Patients received 80 mg of osimertinib once daily. Our primary endpoint was progression-free survival. Eighteen patients were enrolled between June 2017 and November 2018. The median age was 77 years (range: 55-85 years). Ten, six, and two patients had PS scores of 2, 3, and 4, respectively. All patients had adenocarcinoma with common EGFR mutations and had been treated with first- or second-generation EGFR- tyrosine kinase inhibitors previously. The overall median progression-free survival was 7.0 months (90% confidence interval: 5.5-8.9 months). The overall response rate and median overall survival were 53% and 12.7 months, respectively. Moreover, improved PS scores were observed in 72% of the patients. Although the incidence of grade 3 adverse events was low, with no grade 4 or 5 events observed, three patients required treatment cessation due to the development of interstitial lung disease. Osimertinib therapy could be beneficial for EGFR T790M mutation-positive advanced NSCLC patients with poor PS. This trial was registered with the Japan Registry of Clinical Trials on March 12, 2019 (trial no. jRCT1041180081).

Identifiants

pubmed: 32424780
doi: 10.1007/s10637-020-00943-0
pii: 10.1007/s10637-020-00943-0
doi:

Substances chimiques

Acrylamides 0
Aniline Compounds 0
Antineoplastic Agents 0
Protein Kinase Inhibitors 0
osimertinib 3C06JJ0Z2O
EGFR protein, human EC 2.7.10.1
ErbB Receptors EC 2.7.10.1

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1854-1861

Références

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Auteurs

Kazuhisa Nakashima (K)

Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan. kazuhin@med.shimane-u.ac.jp.
Department of Internal Medicine, Division of Medical Oncology & Respiratory Medicine, Shimane University Faculty of Medicine, 89-1 Enya-cho, Izumo, Shimane, Japan. kazuhin@med.shimane-u.ac.jp.

Yuichi Ozawa (Y)

Internal Medicine III, Wakayama Medical University, Wakayama, Japan.

Haruko Daga (H)

Department of Medical Oncology, Osaka City General Hospital, Osaka, Japan.

Hisao Imai (H)

Division of Respiratory Medicine, Gunma Prefectural Cancer Center, Ota, Gunma, Japan.

Motohiro Tamiya (M)

Department of Thoracic Oncology, Osaka International Cancer Institute, Osaka, Japan.

Takaaki Tokito (T)

Department of Medicine, Division of Respirology, Neurology, and Rheumatology, Kurume University School of Medicine, Fukuoka, Japan.

Takahisa Kawamura (T)

Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.

Hiroaki Akamatsu (H)

Internal Medicine III, Wakayama Medical University, Wakayama, Japan.

Yuko Tsuboguchi (Y)

Department of Medical Oncology, Osaka City General Hospital, Osaka, Japan.

Toshiaki Takahashi (T)

Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.

Nobuyuki Yamamoto (N)

Internal Medicine III, Wakayama Medical University, Wakayama, Japan.

Keita Mori (K)

Clinical Research Center, Shizuoka Cancer Center, Shizuoka, Japan.

Haruyasu Murakami (H)

Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.

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