Safety of lorlatinib in ALK-positive non-small-cell lung cancer and management of central nervous system adverse events

Author:

Kilickap Saadettin12ORCID,Ak Sertac3ORCID,Dursun Oldac U4ORCID,Sendur Mehmet AN56ORCID,Karadurmus Nuri7ORCID,Demirci Umut89ORCID

Affiliation:

1. Liv Hospital Ankara, Medical Oncology Unit, Ankara, 06680, Turkey

2. Department of Medical Oncology, Istinye University Faculty of Medicine, Istanbul, 34010, Turkey

3. Hacettepe University, Faculty of Medicine, Department of Psychiatry, Ankara, 06230, Turkey

4. Pfizer, Pfizer Oncology, Istanbul, 34394, Turkey

5. Department of Medical Oncology, Ankara Yıldırım Beyazit University, Faculty of Medicine, Ankara, 06800, Turkey

6. Ankara City Hospital, Medical Oncology Clinic, Ankara, 06800, Turkey

7. Saglik Bilimleri University, Gulhane Training & Research Hospital, Medical Oncology Department, Ankara, 06010, Turkey

8. Memorial Ankara Hospital, Medical Oncology Unit, Ankara, 06520, Turkey

9. Department of Internal Diseases, Uskudar University Medical Faculty, Istanbul, 34768, Turkey

Abstract

The use of tyrosine kinase inhibitors has made a breakthrough in the treatment of non-small-cell lung cancer (NSCLC). Recently, lorlatinib, a third-generation tyrosine kinase inhibitor, has demonstrated significant systemic and intracranial activity in both first-line and subsequent-line therapy in ALK-positive NSCLC patients. In this review, general characteristics of lorlatinib, its efficacy in the treatment of ALK-positive NSCLC patients and the safety of lorlatinib, particularly addressing central nervous system adverse events, are discussed. Management of central nervous system adverse events, which seem to be specific to lorlatinib therapy, is outlined.

Funder

Pfizer, Turkey

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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