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Real-world evidence of lorlatinib therapy in Taiwanese patients with advanced anaplastic lymphoma kinase-positive non-small cell lung cancer.
Shih, Jin-Yuan; Luo, Yung-Hung; Chang, Gee-Chen; Chang, John Wen-Cheng; Wang, Chin-Chou; Yang, Tsung-Ying; Fang, Wei-Tse; Shau, Wen-Yi.
Affiliation
  • Shih JY; Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan. Electronic address: jyshih@ntu.edu.tw.
  • Luo YH; Taipei Veterans General Hospital, Taipei, Taiwan.
  • Chang GC; School of Medicine, and Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan; Division of Pulmonary Medicine, Department of Internal Medicine, Chung Shan Medical University Hospital, Taichung, Taiwan; Institute of Biomedical Sciences, National Chung Hsing University, Taichung, Taiw
  • Chang JW; Chang Gung Memorial Hospital- Linko, Taoyuan, Taiwan.
  • Wang CC; Divisions of Pulmonary & Critical Care Medicine, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan; Chang Gung University College of Medicine, Kaohsiung, Taiwan.
  • Yang TY; Taichung Veterans General Hospital, Taichung, Taiwan.
  • Fang WT; Pfizer, Taiwan.
  • Shau WY; Pfizer, Taiwan.
J Formos Med Assoc ; 123(8): 875-881, 2024 Aug.
Article in En | MEDLINE | ID: mdl-38195317
ABSTRACT

BACKGROUND:

Lorlatinib is a brain-penetrant, third-generation anaplastic lymphoma kinase (ALK) inhibitor indicated for ALK-positive metastatic non-small cell lung cancer (NSCLC). In a global phase II study, patients who experience disease progression despite prior treatment with ALK tyrosine kinase inhibitors (TKIs) was assessed. Herein, we report real-world clinical outcomes of lorlatinib-treated patients with ALK-positive advanced NSCLC who were heavily pretreated and progressed on first- and second-generation ALK-TKIs, in a Taiwanese population under the lorlatinib expanded access program (EAP).

METHODS:

This multicenter observational study examined the effectiveness and safety of ALK-positive advanced NSCLC patients that progressed from previous second-generation ALK-TKI therapy and received lorlatinib treatment subsequently. Patients who received lorlatinib treatment under EAP between Jul 2017 and Sep 2019 were eligible. Patients were followed for at least one year from the first lorlatinib treatment until study completion.

RESULTS:

Sixty-three patients were eligible for safety analysis (male 46.0 %; median age 52.8 [27.5-78.3] years; brain metastases 81.0 %). Fifty-four patients with more than one-month lorlatinib treatment were included in the effectiveness analysis. Prior to lorlatinib treatment, 10 patients (18.5 %) received one ALK-TKI, 27 (50.0 %) received two ALK-TKIs, and 17 (31.5 %) received three or more ALK-TKIs. The overall median rwPFS was 9.2 months (95 % confidence interval 5.3-21.1). The best overall response rate (n = 51) was 13.7 %, with a disease control rate of 80.4 %.

CONCLUSION:

Lorlatinib exhibits substantial activity and tolerability when used clinically in a later-line setting in a Taiwanese population with ALK-positive advanced NSCLC.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyrazoles / Carcinoma, Non-Small-Cell Lung / Lactams, Macrocyclic / Anaplastic Lymphoma Kinase / Aminopyridines / Lactams / Lung Neoplasms Type of study: Clinical_trials / Observational_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Asia Language: En Journal: J Formos Med Assoc Journal subject: MEDICINA Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyrazoles / Carcinoma, Non-Small-Cell Lung / Lactams, Macrocyclic / Anaplastic Lymphoma Kinase / Aminopyridines / Lactams / Lung Neoplasms Type of study: Clinical_trials / Observational_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Asia Language: En Journal: J Formos Med Assoc Journal subject: MEDICINA Year: 2024 Document type: Article Country of publication: