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Vandana G. Abramson

Researcher at Vanderbilt University

Publications -  141
Citations -  5675

Vandana G. Abramson is an academic researcher from Vanderbilt University. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 32, co-authored 122 publications receiving 3972 citations. Previous affiliations of Vandana G. Abramson include University of Pennsylvania & The Breast Cancer Research Foundation.

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Tucatinib, Trastuzumab, and Capecitabine for HER2-Positive Metastatic Breast Cancer.

TL;DR: In heavily pretreated patients with HER2-positive metastatic breast cancer, including those with brain metastases, adding tucatinib to trastuzumab and capecitabine resulted in better progression-free survival and overall survival outcomes than adding placebo.
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Sacituzumab Govitecan-hziy in Refractory Metastatic Triple-Negative Breast Cancer.

TL;DR: It is shown that sacituzumab govitecan‐hziy was associated with durable objective responses in patients with heavily pretreated metastatic triple‐negative breast cancer and was also associated with clinical benefit rate and overall survival.
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Phase I, Dose-Escalation Trial of the Oral Cyclin-Dependent Kinase 4/6 Inhibitor PD 0332991, Administered Using a 21-Day Schedule in Patients with Advanced Cancer

TL;DR: PD 0332991 warrants phase II testing at 125 mg once daily, at which dose neutropenia was the sole significant toxicity, and was shown to be proportional to exposure using an Emax model.
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Intracranial efficacy and survival with tucatinib plus trastuzumab and capecitabine for previously treated HER2-positive breast cancer with brain metastases in the HER2CLIMB trial

TL;DR: In patients with HER2-positive breast cancer with BMs, the addition of tucatinib to trastuzumab and capecitabine doubled ORR-IC, reduced risk of intracranial progression or death by two thirds, and reduced riskof death by nearly half.
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Subtyping of triple-negative breast cancer: Implications for therapy

TL;DR: In this review, the authors discuss recent developments in subtyping TNBC and the current and upcoming therapeutic strategies being explored in an attempt to target TNBC.