Results 71 to 80 of about 1,013 (109)
Background: Lorlatinib, a 3rd-generation ALK inhibitor, significantly prolonged progression-free survival (PFS) vs crizotinib in the CROWN trial in patients with untreated ALK-positive non-small cell lung cancer (NSCLC).
Chiu, CH +19 more
core +1 more source
This large real‐world study confirms crizotinib's intracranial benefit and underscores the importance of next‐generation ROS1 inhibitors and older‐generation agents like lorlatinib—for improved patient outcomes after crizotinib resistance. ABSTRACT Intracranial efficacy of crizotinib and optimal postprogression therapies in c‐ros oncogene 1 (ROS1 ...
Zihua Zou +18 more
wiley +1 more source
ABSTRACT CRISPR‐Cas9 genome‐wide screening has been instrumental towards identifying novel targets for drug discovery in cancer research. However, much of this research has centred specifically on adult cancers, with paediatric cancers being underserviced by current research and screening.
Steven He +2 more
wiley +1 more source
Abstract 3144: Prediction of ALK mutations associated with acquired resistance to lorlatinib
Anaplastic lymphoma kinase (ALK) rearrangements are important therapeutic targets in non-small cell lung cancer. They are currently treated with the first-generation ALK inhibitor crizotnib followed by more potent, second-generation ALK inhibitors, such ...
Satoshi Yoda +5 more
core +1 more source
Inhibition of ROS1 activity with lorlatinib reversibly suppresses fertility in male mice [PDF]
Oyama Y., Shimada K., Miyata H., et al. Inhibition of ROS1 activity with lorlatinib reversibly suppresses fertility in male mice. Andrology , (2024); https://doi.org/10.1111/andr.13808.Background: Inhibition of sperm maturation in the epididymis is a ...
Miyata, Haruhiko +9 more
core +2 more sources
We report a case of ALK‐positive NSCLC in which lorlatinib was successfully administered after discontinuation of alectinib due to drug eruption. Switching to another ALK inhibitor with a distinct chemical structure and safety profile may represent a practical therapeutic option when hypersensitivity reactions prevent continuation of alectinib. Further
Shunsuke Omura +5 more
wiley +1 more source
Oral coadministration of elacridar and ritonavir enhances brain accumulation and oral availability of the novel ALK/ROS1 inhibitor lorlatinib [PDF]
Lorlatinib, a novel generation oral anaplastic lymphoma kinase (ALK) and ROS1 inhibitor with high membrane and blood-brain barrier permeability, recently received accelerated approval for treatment of ALK-rearranged non-small-cell lung cancer (NSCLC ...
Afd Chemical Biology and Drug Discovery +8 more
core +1 more source
BackgroundThe ALTA-1 L trial and EXP-3B arm of NCT01970865 trial found that both brigatinib and lorlatinib showed durable and robust responses in treating ALK-positive non-small cell lung cancer (NSCLC) patients.
Wenjie Liu +11 more
doaj +1 more source
In the present study, we developed and validated a rapid and simple liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the determination of lorlatinib in mouse serum and tissue samples, and such a method was successfully applied to ...
Wei Chen +6 more
doaj +1 more source
Abstracts submitted to the ‘EACR 2026 Congress: Innovative Cancer Science’, from 08–11 June 2026 and accepted by the Congress Organising Committee are published in this Supplement of Molecular Oncology, an affiliated journal of the European Association for Cancer Research (EACR).
wiley +1 more source

