Strong Response to Neoadjuvant Gemzar/Epirubicin/Abraxan

Article

A triplet of biweeklyneoadjuvant gemcitabine (Gemzar),epirubicin (Ellence), and nabpaclitaxel(Abraxane) (GEA) was "exceptionally well tolerated" andproduced a 94% overall pathologicresponse in women with locallyadvanced breast cancer.

A triplet of biweeklyneoadjuvant gemcitabine (Gemzar),epirubicin (Ellence), and nabpaclitaxel(Abraxane) (GEA) was"exceptionally well tolerated" andproduced a 94% overall pathologicresponse in women with locallyadvanced breast cancer (abstract3069). Denise A. Yardley, MD,discussed the results. The phase IIstudy enrolled 48 women with T1c–T4d and/or N0-3 disease. Most (81%)were HER2-negative. Patients receivedG at 2,000 mg/m2, E at 50 mg/m2, andA at 175 mg/m2 every 14 days for 6cycles, followed by surgery. Postoperatively,they received 4 cycles of G at2,000 mg/m2 and A at 220 mg/m2 every14 days. Patients were given G-CSFsupport on day 2 of all cycles.Pathologic responses in 35 evaluablepatients were pCR (in primary breastand lymph nodes) in 20% and pPR in74%, for an overall pRR of 94%; theremaining 6% of patients had stabledisease. The incidence of grade 3/4neutropenia was 8% and of thrombocytopeniawas 6%. The incidence ofanemia was 2%, and 2% requiredtransfusions (of platelets, RBCs). Febrileneutropenia did not occur. Only onepatient experienced a grade 4nonhematologic toxicity (fatigue). Themost common nonhematologic toxicitywas arthralgia (10.5%), followed byfatigue and hyperglycemia (6% each),and edema and thrombosis (2% each).There were no cases of grade 3/4 neuropathy.Accrual is continuing, and correlationof tumor expression of SPARCand degree of response will be reportedat a later date.

Recent Videos
Leading experts in the breast cancer field highlight the use of CDK4/6 inhibitors, antibody-drug conjugates, and other treatment modalities.
Patients with node-negative disease who are older and have comorbidities may not be suitable to receive CDK4/6 inhibitors.
An observed carryover effect with CDK4/6 inhibitors may reduce the risk of recurrence years after a patient stops treatment.
Breast oncologist Jade E. Jones, MD, says she tries to send patients with BRCA-mutant HR-positive TNBC to clinical trials that use PARP inhibitors.
Related Content