
Release date: 2026-01-23 17:54:50 Article From: Lucius Laos Recommended: 10
Lorlatinib is a third-generation anaplastic lymphoma kinase (ALK)/c-ros oncogene 1 (ROS1) tyrosine kinase inhibitor, primarily indicated for the treatment of ALK-positive locally advanced or metastatic non-small cell lung cancer (NSCLC).
Its indications cover the following two categories of patients:
First-line therapy: For ALK-positive metastatic NSCLC patients who have not received prior ALK inhibitor treatment. It prolongs survival by inhibiting tumor growth and metastasis.
Second-line and subsequent therapy: For ALK-positive NSCLC patients whose disease has progressed or who have developed resistance after treatment with other ALK inhibitors (e.g., crizotinib, alectinib, etc.). It can overcome certain drug-resistant mutations.
Patients with brain metastases: Lorlatinib can penetrate the blood-brain barrier and exerts significant efficacy in ALK-positive NSCLC patients complicated with brain metastases.
Patients with specific gene mutations: Applicable to tumors caused by ALK gene fusions (e.g., EML4-ALK) or other ALK-related variants, which must be confirmed by genetic testing.
Strictly follow medical advice: Lorlatinib is a prescription drug. Dosage should be adjusted based on the patient's genetic test results, medical history and tolerance. Do not administer the drug without medical supervision.
Side effect management: Common side effects include hypercholesterolemia, edema and peripheral neuropathy. Regular monitoring and proper management under medical guidance are required.
Contraindicated populations: Patients with hypersensitivity to any component of the drug or severe hepatic insufficiency should use this drug with caution.
If meeting the above-mentioned indications, it is recommended that an individualized treatment plan be formulated after evaluation by an oncologist. Regular re-examinations should be conducted during treatment to monitor efficacy and adverse reactions.
On November 21, 2025, the U.S. Food and Drug Administration (FDA) approved the regimen of pembrolizu···【more】
Recommended:662025-17-12
Lung cancer is the most rapidly increasing malignant tumor with the fastest increasing morbidity and···【more】
Recommended:3652024-09-07
On December 12, 2025, the U.S. Food and Drug Administration (FDA) approved niraparib in combination ···【more】
Recommended:602025-15-12
The U.S. Food and Drug Administration (FDA) announced today that it has approved Omisirge (omidubice···【more】
Recommended:792025-10-12
On December 4, 2025, the U.S. Food and Drug Administration (FDA) approved lisocabtagene maraleucel (···【more】
Recommended:742025-08-12
On December 3, 2025, the U.S. Food and Drug Administration (FDA) granted full approval to pirtobruti···【more】
Recommended:942025-04-12
Primary analysis data from the randomized, double-blind, placebo-controlled phase III HER2CLIMB-02 s···【more】
Recommended:892025-01-12
The Cure SMA Foundation, a global leading non-profit organization dedicated to spinal muscular atrop···【more】
Recommended:922025-27-11

Lucius Pharmaceutical Co., Ltd., was established in 2020 in Vientiane, the capital of Laos. It aims to offer safe, effective, and affordable medicines globally. With a factory spanning 25,000 square meters, the company manufactures 200+ generic drugs in diverse therapeutic fields.
Address:No.26 Thongmang village, Xaythany district, Vientiane Capital, Laos
E-mail:laoslucius@gmail.com
Whatsapp: