Related Experiment Video
Updated: Sep 23, 2026

Establishment and Characterization of Three Afatinib-resistant Lung Adenocarcinoma PC-9 Cell Lines Developed with Increasing Doses of Afatinib
Published on: June 26, 2019
Imatinib in small cell lung cancer
Jean-Charles Soria1, Bruce E Johnson, Thierry Le Chevalier
1Division of Medicine, Gustave Roussy Institute, 39 rue Camille Desmoulins, 94805, Villejuif, France. tle-che@igr.fr
Purpose:
To evaluate the clinical efficacy of Imatinib Mesylate in untreated or sensitive relapsed small cell lung carcinoma patients. Secondary endpoints included assessment of the safety and tolerance of Imatinib, and an analysis of KIT expression in tumor samples.
Patients And Methods:
Patients with previously untreated small cell lung cancer (SCLC) or with a sensitive relapse (one prior regimen with a sustained response for over 60 days) were eligible. Imatinib was delivered at 600 mg on a daily basis. Response was evaluated at 6 weeks using SWOG criteria.
Results:
As planned in the study design, a total of 19 patients were included in the trial (9 chemonaive patients with extensive disease and 10 sensitive relapse SCLC patients). No objective responses were observed with most previously untreated patients staying on study for less than 30 days. The median time to progression was 1 and 1.2 month in the untreated and sensitive relapse groups, respectively. Only 4 out of 19 tumor samples (21%) stained for KIT by means of immunohistochemistry.
Conclusions:
No evidence of antitumor activity was observed in this small phase II trial including 19 SCLC patients treated with Imatinib Mesylate. KIT positivity in tumor samples appeared to be far less common than anticipated (21 vs. 70%). Future trials should include a screening procedure to evaluate KIT expression in SCLC samples. A better evaluation of KIT contribution to SCLC tumor progression needs to be achieved.
Insights
Imatinib Mesylate showed no antitumor activity in small cell lung cancer (SCLC) patients. KIT expression was lower than expected, suggesting it may not be a reliable target for SCLC treatment.
Area of Science:
- Oncology
- Medical Oncology
Background:
- Small cell lung cancer (SCLC) is an aggressive malignancy with limited treatment options.
- Imatinib Mesylate is a tyrosine kinase inhibitor with demonstrated efficacy in certain cancers.
- The role of KIT expression in SCLC pathogenesis and treatment response requires further investigation.
Purpose of the Study:
- To assess the clinical efficacy of Imatinib Mesylate in patients with untreated or sensitive relapsed SCLC.
- To evaluate the safety and tolerance of Imatinib Mesylate in this patient population.
- To analyze KIT protein expression in SCLC tumor samples.
Main Methods:
- A Phase II clinical trial was conducted involving 19 SCLC patients (9 treatment-naive, 10 sensitive relapse).
- Patients received Imatinib Mesylate at a dose of 600 mg daily.
- Tumor samples were analyzed for KIT expression using immunohistochemistry; response was assessed using SWOG criteria.
Main Results:
- No objective responses were observed in any patient treated with Imatinib Mesylate.
- Median time to progression was short, at 1 month for treatment-naive and 1.2 months for sensitive relapse groups.
- KIT expression was detected in only 21% of tumor samples, significantly lower than the anticipated 70%.
Conclusions:
- Imatinib Mesylate demonstrated no significant antitumor activity in this SCLC cohort.
- The low incidence of KIT positivity suggests limited utility of Imatinib Mesylate targeting KIT in SCLC.
- Future SCLC trials should incorporate KIT expression screening and explore other therapeutic strategies.
Related Concept Videos
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Combination Therapies and Personalized Medicine
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
Inhibition of Cdk Activity
Drugs that Stabilize Microtubules
