Gemcitabine plus sirolimus for relapsed and progressing osteosarcoma patients after standard chemotherapy: a

J Martin-Broto1,2, A Redondo3, C Valverde4

  • 1Medical Oncology Department, Hospital Universitario Virgen del Rocío, Sevilla.

Abstract

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.

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