Gemcitabine plus sirolimus for relapsed and progressing osteosarcoma patients after standard chemotherapy: a multicenter, single-arm phase II trial of Spanish Group for Research on Sarcoma (GEIS)
J Martin-Broto1,2, A Redondo3, C Valverde4
1Medical Oncology Department, Hospital Universitario Virgen del Rocío, Sevilla.
Background:
Patients with relapsed unresectable osteosarcoma represents an unmet need, so active and safe systemic treatments are required. Fas cell surface death receptor and mammalian target of rapamycin pathways are implicated in progressing osteosarcoma, and we had preclinical and clinical experience with a scheme that targets both pathways. Therefore, we designed a phase II trial with gemcitabine plus rapamycin, to determine the efficacy and safety, in this subset of patients.
Patients And Methods:
A multicenter, single-arm phase II trial was sponsored by the Spanish Group for Research on Sarcoma. Osteosarcoma patients, relapsed or progressing after standard chemotherapy and unsuitable for metastasectomy received gemcitabine and rapamycin p.o. 5 mg/day except for the same day of gemcitabine administration, and the day before. The main end point was 4-month progression-free survival rate (PFSR), with the assumption that rates higher than 40% would be considered as an active regimen. Translational research aimed to correlate biomarkers with the clinical outcome.
Results:
Thirty-five patients were enrolled and received at least one cycle. PFSR at 4 months was 44%, and after central radiologic assessment, 2 partial responses and 14 stabilizations (48.5%) were reported from 33 assessable patients. The most frequent grade 3-4 adverse events were: neutropenia (37%), thrombocytopenia (20%), anemia (23%), and fatigue (15%); however, only three patients had febrile neutropenia. Positive protein expression of RRM1 significantly correlated with worse PFS and overall survival, while positivity of P-ERK1/2 was correlated with significant better overall survival.
Conclusion:
Gemcitabine plus sirolimus exhibits satisfactory antitumor activity and safety in this osteosarcoma population, exceeding the prespecified 40% of 4-month PFSR. The significant correlation of biomarkers with clinical outcome encourages further prospective investigation.
Insights
This study shows gemcitabine plus sirolimus is an active and safe treatment for relapsed osteosarcoma, exceeding the target 4-month progression-free survival rate. Biomarker correlations suggest further research potential.
Area of Science:
- Oncology
- Pharmacology
- Translational Research
Background:
- Relapsed unresectable osteosarcoma presents a significant unmet medical need requiring novel systemic treatments.
- The Fas and mammalian target of rapamycin (mTOR) pathways are implicated in osteosarcoma progression.
- Previous studies suggested targeting both pathways could be beneficial.
Purpose of the Study:
- To evaluate the efficacy and safety of gemcitabine plus sirolimus in patients with relapsed or progressing osteosarcoma.
- To determine if the combination therapy achieves a 4-month progression-free survival rate (PFSR) greater than 40% in this patient population.
- To explore potential correlations between biomarkers and clinical outcomes.
Main Methods:
- A multicenter, single-arm phase II clinical trial was conducted.
- Patients received oral gemcitabine and sirolimus (rapamycin).
- The primary endpoint was the 4-month PFSR, with secondary analysis of adverse events and biomarker correlations.
Main Results:
- The 4-month PFSR was 44% in 35 enrolled patients, exceeding the 40% target.
- Objective responses included 2 partial responses and 14 stabilizations (48.5%) among 33 assessable patients.
- Common grade 3-4 adverse events included neutropenia, thrombocytopenia, anemia, and fatigue, with low rates of febrile neutropenia. RRM1 expression correlated with worse outcomes, while P-ERK1/2 positivity correlated with better overall survival.
Conclusions:
- Gemcitabine plus sirolimus demonstrates satisfactory antitumor activity and an acceptable safety profile in patients with relapsed osteosarcoma.
- The combination therapy successfully exceeded the predefined efficacy endpoint.
- The identified biomarker correlations warrant further investigation in prospective studies.
Related Concept Videos
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Treatment Resistant Cancers
Rous Sarcoma Virus (RSV) and Cancer
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...
Rous Sarcoma Virus (RSV) and Cancer
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Treatment Resistent Cancers


