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Inavolisib and lenvatinib for PIK3CA-mutated refractory splenic angiosarcoma: a case report
Xinyue Zhao1, Chenyu Wang2, Yuping Ge2
1Department of Health Care, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Abstract:
Primary splenic angiosarcoma (PSA) is a rare vascular malignancy with a poor prognosis and limited therapeutic options. A 62-year-old man with metastatic PSA underwent splenectomy followed by first-line paclitaxel, achieving stable disease for 7 months. Disease progression manifested as hepatic and bone marrow metastases with tumor-induced hepatic failure and refractory thrombocytopenia. Sequential treatment with liposomal doxorubicin, eribulin, toripalimab, and lenvatinib failed to control the disease failed to control the disease. Genomic profiling identified a PIK3CA p.P471L missense mutation. A combination regimen of inavolisib (a selective PI3Kα inhibitor) and lenvatinib was initiated. Bilirubin levels normalized, and platelet counts recovered within 2 weeks; follow-up MRI confirmed radiological stabilization. At 16 months postdiagnosis, the patient remains alive on this regimen, though long-term durability of response has yet to be determined. To our knowledge, this is the first reported use of inavolisib in angiosarcoma. The rapid biochemical and radiological response observed in this PIK3CA-mutated PSA supports early genomic profiling to identify actionable alterations and warrants prospective evaluation of combined phosphoinositide 3-kinase and vascular endothelial growth factor pathway inhibition in refractory angiosarcoma.
Insights
A patient with advanced primary splenic angiosarcoma (PSA) and a PIK3CA mutation showed rapid improvement with inavolisib and lenvatinib. This combination therapy offers a promising new option for refractory angiosarcoma.
Area of Science:
- Oncology
- Genetics
- Vascular Biology
Background:
- Primary splenic angiosarcoma (PSA) is a rare and aggressive vascular cancer with limited treatment options and poor prognosis.
- Metastatic PSA presents significant challenges, often leading to treatment resistance and complications like hepatic failure and thrombocytopenia.
Purpose of the Study:
- To report the first use of inavolisib, a PI3Kα inhibitor, in combination with lenvatinib for treating refractory metastatic primary splenic angiosarcoma.
- To evaluate the efficacy and safety of this novel combination therapy in a patient with a specific PIK3CA mutation.
Main Methods:
- Genomic profiling of metastatic PSA identified a PIK3CA p.P471L missense mutation.
- A patient received sequential treatments including paclitaxel, liposomal doxorubicin, eribulin, toripalimab, and lenvatinib, with limited success.
- Treatment was switched to a combination regimen of inavolisib and lenvatinib.
Main Results:
- The combination of inavolisib and lenvatinib led to rapid normalization of bilirubin levels and recovery of platelet counts within two weeks.
- Follow-up MRI confirmed radiological stabilization of the disease.
- The patient remains alive and on treatment 16 months postdiagnosis, demonstrating significant clinical benefit.
Conclusions:
- This case demonstrates the potential efficacy of targeting the PI3K/AKT/mTOR pathway in PIK3CA-mutated angiosarcoma.
- Combined phosphoinositide 3-kinase and vascular endothelial growth factor pathway inhibition shows promise for refractory angiosarcoma.
- Early genomic profiling is crucial for identifying actionable mutations and guiding personalized treatment strategies in rare cancers like PSA.
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