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Published on: July 25, 2020
A retrospective analysis of two different sequences of therapy lines for advanced kidney cancer
Chiara Paglino1, Giuseppe Procopio, Roberto Sabbatini
1Medical Oncology, San Matteo University Hospital Foundation, Piazzale C. Golgi, 19, 27100 Pavia, Italy. c.porta@smatteo.pv.it.
Background/Aim:
the ideal sequence of targeted agents for advanced kidney cancer is still unknown. In the present study we assessed the clinical benefit of two different sequential approaches, namely sorafenib, an inhibitor of mammalian target of rapamycin (mTORi) and sunitinib, or sunitinib (an mTORi) and sorafenib.
Patients And Methods:
we retrospectively reviewed the outcome of 40 advanced kidney cancer patients treated with one of the two above sequences.
Results:
a total of 26 patients were treated with the sequence sorafenib-mTORi-sunitinib and 14 with the sequence sunitinib-mTORi-sorafenib. The actuarial overall median progression-free survival (PFS) in the sorafenib-mTORi-sunitinib group and in the sunitinib-mTORi-sorafenib group were 21.9 and 22.8 months, respectively (log-rank test: p=0.928). In the sorafenib-mTORi-sunitinib group, patients in first-, second- and third-line therapy experienced PFS of 11.7, 5.1 and 9.1 months, respectively, while in the sunitinib-mTORi-sorafenib group PFS was 14.4, 4.3, and 3.9 months, respectively.
Conclusion:
Our results suggest there is no significant difference between the two sequence modalities.
Insights
The sequence of targeted agents, including sorafenib and sunitinib (mammalian target of rapamycin inhibitors), does not significantly impact progression-free survival in advanced kidney cancer patients. Both sequential approaches demonstrated similar clinical benefits.
Area of Science:
- Oncology
- Pharmacology
Background:
- The optimal sequencing of targeted therapies for advanced kidney cancer remains undetermined.
- Investigating sequential administration of sorafenib and mammalian target of rapamycin inhibitors (mTORi) with sunitinib is crucial for treatment optimization.
Purpose of the Study:
- To compare the clinical efficacy of two distinct sequential treatment strategies in advanced kidney cancer.
- To evaluate the progression-free survival (PFS) associated with sorafenib-mTORi-sunitinib versus sunitinib-mTORi-sorafenib sequences.
Main Methods:
- Retrospective analysis of outcomes in 40 advanced kidney cancer patients.
- Comparison of two treatment sequences: sorafenib-mTORi-sunitinib (n=26) and sunitinib-mTORi-sorafenib (n=14).
Main Results:
- Overall median PFS was comparable between the sorafenib-mTORi-sunitinib (21.9 months) and sunitinib-mTORi-sorafenib (22.8 months) groups (p=0.928).
- First-line PFS was 11.7 months for sorafenib-mTORi-sunitinib and 14.4 months for sunitinib-mTORi-sorafenib.
- Subsequent-line PFS showed variations but did not lead to significant overall differences.
Conclusions:
- No significant difference in clinical benefit was observed between the two evaluated sequential treatment modalities for advanced kidney cancer.
- The findings suggest flexibility in sequencing sorafenib and sunitinib in combination with mTOR inhibitors.
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