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Phase II trial of CDK4/6 inhibitor palbociclib in advanced sarcoma based on mRNA expression of CDK4/ CDKN2A
Javier Martin-Broto1,2,3, Jeronimo Martinez-Garcia4, David S Moura5
1Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), 28040, Madrid, Spain. jmartin@atbsarc.org.
Abstract:
Cyclin-dependent kinases 4 and 6 (CDK4/6) inhibitors demonstrated activity in terms of progression-free survival (PFS) in advanced dedifferentiated liposarcoma (DD-LPS), a sarcoma with CDK4 amplification. CDK4 overexpression is by far more common than amplification in sarcomas and it might be a rational target for CDK inhibitors. Preclinical investigators of this study found that CDK4 overexpression, while not of CDKN2A, was the most consistent predictive factor for palbociclib efficacy in sarcomas. Advanced adult-type soft-tissue sarcoma, excluding DD-LPS, or bone sarcoma patients, progressing after at least one systemic line, whose tumors overexpressed CDK4, but not CDKN2A at baseline biopsy, were accrued in this single-arm phase II trial (EudraCT number: 2016-004039-19). With the main endpoint of a 6-month PFS rate, 40% was considered promising in this population. Palbociclib was administered orally at 125 mg/day for 21 days in 28-day cycles. A total of 214 patients with 236 CDK4/CDKN2A determinations were assessed for prescreening, archival material (141), and screening, baseline biopsy (95). There were 28 (29%) with favorable mRNA profiles from 95 screened patients at baseline. From 23 enrolled patients, 21 evaluable, the 6-month PFS rate was 29% (95% CI 9-48), and there were 6 patients out of 21 with a PFS longer than 6 months. The median PFS and overall survival were 4.2 (95% CI 3.6-4.8) and 12 (95% CI 8.7-15.4) months, respectively. Translational research showed a significant correlation between CDK4 mRNA and protein expression. Palbociclib was active in a variety of sarcoma subtypes, selected by CDK4/CDKN2A, and deserves further investigation in the sarcoma context.
Insights
Cyclin-dependent kinase 4 (CDK4) inhibitors show promise in treating advanced sarcomas. Palbociclib demonstrated activity in patients with CDK4-overexpressing tumors, suggesting CDK4 as a viable therapeutic target for sarcoma treatment.
Area of Science:
- Oncology
- Pharmacology
- Genetics
Background:
- Cyclin-dependent kinases 4 and 6 (CDK4/6) inhibitors have shown efficacy in advanced dedifferentiated liposarcoma (DD-LPS).
- CDK4 overexpression is more frequent than amplification in sarcomas, making it a potential therapeutic target.
- Preclinical data identified CDK4 overexpression, not CDKN2A, as a predictor of palbociclib efficacy in sarcomas.
Purpose of the Study:
- To evaluate the efficacy of palbociclib in advanced adult-type soft-tissue or bone sarcomas with CDK4 overexpression.
- To determine the 6-month progression-free survival (PFS) rate as the primary endpoint.
- To explore the correlation between CDK4/CDKN2A status and palbociclib response.
Main Methods:
- A single-arm, phase II clinical trial.
- Patients with advanced sarcomas (excluding DD-LPS) progressing after at least one systemic line were enrolled.
- Tumors were assessed for CDK4 and CDKN2A expression at baseline; palbociclib was administered orally at 125 mg/day for 21 days in 28-day cycles.
Main Results:
- Twenty-one patients were evaluable, with a 6-month PFS rate of 29% (95% CI 9-48).
- Six out of 21 patients achieved a PFS longer than 6 months.
- Median PFS was 4.2 months, and median overall survival was 12 months.
- Translational research confirmed a significant correlation between CDK4 mRNA and protein expression.
Conclusions:
- Palbociclib demonstrated activity in a variety of sarcoma subtypes selected by CDK4/CDKN2A status.
- CDK4 overexpression is a predictive biomarker for palbociclib efficacy in sarcomas.
- Further investigation of palbociclib in sarcoma is warranted.
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