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Updated: Feb 14, 2026

Detection of Targetable Alterations in Non-small Cell Lung Cancer using Next-generation Sequencing
Published on: October 10, 2025
ROS1 rearranged nonsmall cell lung cancer and crizotinib: An Indian experience
V Noronha1, M V Chandrakanth1, A P Joshi1
1Department of Medical Oncology, Tata Memorial Hospital, Mumbai, Maharashtra, India.
Crizotinib significantly improves outcomes for patients with advanced non-small cell lung cancer (NSCLC) harboring ROS1 rearrangements. This targeted therapy demonstrates high response rates and prolonged survival, offering a valuable treatment option.
Area of Science:
- Oncology
- Genetics
- Pharmacology
Background:
- ROS1 rearrangements are driver mutations in 1-2% of non-small cell lung cancer (NSCLC).
- Crizotinib is an approved targeted therapy for ROS1-rearranged NSCLC in both treatment-naïve and pre-treated patients.
Purpose of the Study:
- To evaluate the efficacy and safety of crizotinib in patients with advanced NSCLC and ROS1 rearrangement.
- To assess treatment outcomes, including response rates, progression-free survival (PFS), and overall survival (OS).
Main Methods:
- Retrospective analysis of 11 patients with advanced NSCLC and ROS1 rearrangement.
- Evaluation of outcomes in patients treated with crizotinib versus those not exposed to the drug.
- Assessment of response rates, median PFS, median OS, and 1-year OS.
Main Results:
- Crizotinib treatment in 5 patients resulted in an 80% response rate.
- Patients receiving crizotinib had not reached median PFS and OS, compared to 2.5 months PFS and 4.2 months OS for untreated patients (p<0.05).
- Estimated 1-year OS was 80% for crizotinib-treated patients versus 18% for untreated patients.
Conclusions:
- Crizotinib is an effective treatment for ROS1-rearranged NSCLC, demonstrating significant improvements in PFS and OS.
- The drug exhibits an acceptable side effect profile in this patient population.
- Crizotinib represents a crucial therapeutic option for advanced NSCLC patients with ROS1 alterations.
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