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abstract
Introduction: Patients with metastatic ovarian cancer continue to experience high recurrence rates and significant morbidity from standard treatments. There is a great need for efficacious tumor-specific agents in ovarian cancer. Iniparib (BSI-201) is a targeted drug currently under investigation.
Areas covered:
The authors identified the mechanistic and clinical data available on
the role of iniparib in ovarian cancer. Iniparib was initially thought
to act via the poly-ADP ribose polymerase 1 (PARP-1) pathway, but recent
studies have shown only nonspecific interactions between the drug and
PARP proteins.
Although iniparib is only active in cancer cells, the exact mechanism of action remains unclear. Iniparib was well tolerated at all dose levels in Phase I studies of solid organ malignancies. Preliminary data from Phase II studies of iniparib for the treatment of platinum-sensitive and platinum-resistant recurrent ovarian cancer show improvement in survival compared to historic controls. There are currently no Phase III studies.
Although iniparib is only active in cancer cells, the exact mechanism of action remains unclear. Iniparib was well tolerated at all dose levels in Phase I studies of solid organ malignancies. Preliminary data from Phase II studies of iniparib for the treatment of platinum-sensitive and platinum-resistant recurrent ovarian cancer show improvement in survival compared to historic controls. There are currently no Phase III studies.
Expert opinion:
Iniparib shows promise in early clinical trials; however, understanding
the pathways of cytotoxicity will be crucial as cancer therapy becomes
increasingly individualized.
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