dotMD.com
✓ Translated by DotMD AI Clinical Council Source: The oncologist • Phase III Randomized Trial
Verify Primary Source: NIH PubMed PMID #41124598 ↗

Phase III Randomized Trial: Kinetics and management of adverse events associated with lorlatinib after 5 years of follow-up in the CROWN study (N = 149)

Original Paper Title: “Kinetics and management of adverse events associated with lorlatinib after 5 years of follow-up in the CROWN study”

Elena Rostova (AI Quant) Rigor Score
82 / 100
Sample Size (Participants)
N = 149
Evidence Classification
Phase III Randomized Trial
Sarah Jenkins, RN (AI Plain-English Editor) • Key Takeaways
  • After 5 years of follow-up, no new safety signals were observed. All-cause any-grade and grade 3/4 AEs occurred in 100% and 77% of patients, respectively; AEs led to lorlatinib dose reduction in 23% of patients, dose interruption in 62%, and permanent discontinuation in 11%.
  • Study Design & Sample: Phase III Randomized Trial published in The oncologist (N = 149 human participants).
  • Biostatistical Rigor Score: 82/100 audited by Elena Rostova (AI Biostatistician & openFDA Quant).

What the Study Found (In Plain English)

Published in The oncologist (2025), this phase iii randomized trial evaluating 149 human participants investigated: With 5 years of follow-up in the phase 3 CROWN study, lorlatinib showed unprecedented improvement in progression-free survival coupled with prolonged intracranial efficacy in patients with ALK-positive metastatic non-small cell lung cancer (mNSCLC). Key clinical takeaway: After 5 years of follow-up, no new safety signals were observed. All-cause any-grade and grade 3/4 AEs occurred in 100% and 77% of patients, respectively; AEs led to lorlatinib dose reduction in 23% of patients, dose interruption in 62%, and permanent discontinuation in 11%.

Dr. Lin (AI Evidence Lead): Statistical Endpoints & Numbers

Primary Endpoint & Quantitative Summary (The oncologist, 2025-10-01; N = 149; Rigor 82/100): After 5 years of follow-up, no new safety signals were observed. All-cause any-grade and grade 3/4 AEs occurred in 100% and 77% of patients, respectively; AEs led to lorlatinib dose reduction in 23% of patients, dose interruption in 62%, and permanent discontinuation in 11%.

Study Limitations & Caveats Before You Act

Clinical trials evaluate specific inclusion/exclusion cohorts under protocol-controlled conditions (Phase III Randomized Trial). Individual response, hepatic/renal clearance, CYP450 drug interactions, and baseline comorbidities vary; verify applicability with a board-certified physician before modifying any prescription or supplement regimen.

Related DotMD Clinical Hubs & Price Ledgers

Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

Ask our AI Specialists anything about PMID 41124598: Phase III Randomized Trial: Kinetics and management of adverse events associated with lorlatinib after 5 years of follow-up in the CROWN study (N = 149)

3 of 3 Free Questions Remaining