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Efficacy of BSI-201, a PARP-Inhibitor in combination with Gemcitabine/Carboplatin in Triple Negative Breast Cancer: Randomized Phase II trial Presented by Dr. Joyce O’Shaughnessey Authors: Dr. Sunil Verma Date posted: June 22nd, 2009 www.OncologyEducation.ca Background • Triple Negative (TN) disease represents the next frontier in Breast Cancer • TN disease shares key features with Basal-like and BRCA associated cancer – BRCA dysfunction – Susceptibility to DNA damaging agents • In the setting of BRCA dysfunction, the cancer cell increasingly relies on PARP for DNA repair process – This may represent an important therapeutic target www.OncologyEducation.ca Treatment A: Gemcitabine +Carboplatin R Triple Negative MBC Treatment B: Gemcitabine + Carboplatin + BSI-201 (a PARP – inhibitor) www.OncologyEducation.ca RESULTS Treatment A Treatment B p-value Response Rate (%) 16% 48% 0.002 PFS/TTP (median, mos) 3.3 m 6.9 m <0.0001 OS (median, mos) 5.7 m 9.2 m 0.0005 www.OncologyEducation.ca STUDY COMMENTARY • This is an important study as it shows that the addition of PARPinhibitors to chemotherapy improves the outcome for TN MBC • This is the first Phase II trial evaluating this class of drugs in MBC • There is a planned Phase III trial designed to evaluate BSI-201 in combination with carboplatin+gemcitabine • There are some unanswered questions related to this class of drugs: - Do PARP-Inhibitors need DNA damaging stimulus? -Will they be effective in a broader subgroup of patients? TN Non-TN - What are the long-term toxicities associated with these agents? ? Increase risk of tumorogenesis - Oral vs. IV www.OncologyEducation.ca BOTTOM LINE FOR CANADIAN MEDICAL ONCOLOGISTS • Triple Negative Breast Cancer is associated with poor prognosis and represents an aggressive phenotype of breast cancer. • Majority of TN disease is associated with basal-like profile. Furthermore, basal-like breast cancer shares a number of features associated with BRCA related cancers • TN breast cancer may particularly be sensitive to DNA damaging agents including Cisplatin and PARP inhibitors • This study suggests that PARP inhibitors are efficacious for TN MBC • While the results from this Phase II trial are impressive, there are still a number of unanswered questions and future trials evaluating PARPinhibitors will help establish the magnitude of benefit and their role for early stage and advanced TN breast cancer www.OncologyEducation.ca