Key result
Aldoxorubicin demonstrated a progression-free survival advantage in patients with leiomyosarcoma and liposarcoma in preliminary phase 3 trials, with minimal cardiac toxicity.
Why the study?
Does aldoxorubicin improve outcomes and reduce cardiac toxicity in patients with advanced soft tissue sarcoma?
Does aldoxorubicin improve outcomes and reduce cardiac toxicity in patients with advanced soft tissue sarcoma?
Aldoxorubicin is a promising doxorubicin derivative for advanced soft tissue sarcoma that may offer a progression-free survival advantage with reduced cardiotoxicity.
Aldoxorubicin may reduce cardiotoxicity versus doxorubicin in advanced STS; leaves open its role pending further phase 3 confirmation in L-sarcomas.
Intoduction: Soft tissue sarcomas (STS) encompass a group of rare tumors arising from mesenchymal tissue. Traditionally, anthracycline-based chemotherapy, with doxorubicin, is the main treatment for advanced STS. Areas covered: Aldoxorubicin is a doxorubicin derivative containing a carboxylic hydrazone and serves as a prodrug of doxorubicin. It covalently binds to albumin in the blood until reaching the acidic tumor environment, which dissolves the hydrazone linker, thus releasing doxorubicin into the tissue. In this review paper, we analyze the pharmacokinetics, current phase I, phase II, and phase III trials, as well as adverse effect profile of aldoxorubicin in patients with advanced STS. Expert opinion: Aldoxorubicin represents a promising drug for treatment of sarcomas. The drug has minimal cardiac toxicity, which represents a significant advantage to doxorubicin. Preliminary phase 3 study results demonstrate PFS advantage in patients with leiomyosarcoma and liposarcoma. However, more studies are needed to establish the role of aldoxorubicin in sarcoma treatment.
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Sachdev et al. (2017) conducted a review in Advanced soft tissue sarcoma. Aldoxorubicin was evaluated. Aldoxorubicin demonstrated a progression-free survival advantage in patients with leiomyosarcoma and liposarcoma in preliminary phase 3 trials, with minimal cardiac toxicity.
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