18F-FDG PET/CT Evaluation of Crizotinib and Lorlatinib Therapy in Metastatic ROS-1-Positive Non-Small Cell Lung

Sébastien Dejust1, Abdenasser Moubtakir1, Alain Prevost2

  • 1From the Unité de Médecine Nucléaire.

Clinical Nuclear Medicine
|January 25, 2020
PubMed

Insights

ROS-1 positive non-small cell lung cancer (NSCLC) is rare and often develops crizotinib resistance. Lorlatinib shows promise as a second-line treatment, achieving complete tumor response in a patient with advanced NSCLC.

Area of Science:

  • Oncology
  • Pharmacology

Background:

  • ROS-1-positive non-small cell lung cancer (NSCLC) accounts for ~1% of NSCLC cases.
  • Crizotinib is the standard first-line therapy, but resistance develops frequently within a year.
  • Lorlatinib, a novel ROS-1 tyrosine kinase inhibitor, is indicated for crizotinib-resistant metastatic or locally advanced NSCLC.

Observation:

  • A case of metastatic NSCLC with ROS-1 rearrangement is presented.
  • The patient received lorlatinib as second-line therapy after crizotinib treatment failure.
  • Treatment response was evaluated using 2-[18F]fluoro-2-deoxy-D-glucose (F-FDG) Positron Emission Tomography/Computed Tomography (PET/CT).

Findings:

  • Complete tumoral response was achieved with lorlatinib treatment.
  • Tumor regression was observed within 3 months of initiating second-line lorlatinib therapy.
  • F-FDG PET/CT demonstrated significant reduction in tumor metabolic activity.

Implications:

  • Lorlatinib represents a viable and effective second-line treatment option for crizotinib-resistant ROS-1-positive NSCLC.
  • F-FDG PET/CT is a crucial tool for monitoring treatment efficacy and guiding targeted therapy in metastatic NSCLC.
  • This case highlights the potential for rapid and complete responses with novel targeted agents in rare oncogenic-driven lung cancers.