Neo-/adjuvant phase III trial to compare intense dose-dense (idd) treatment with EnPC to tailored dose-dense (dt) therapy with dtEC-dtD for patients with high-risk early breast cancer: Results on pathological complete response (pCR) for patients treated within the neoadjuvant setting.

6533b833fe1ef96bd129b568

RESEARCH PRODUCT

Neo-/adjuvant phase III trial to compare intense dose-dense (idd) treatment with EnPC to tailored dose-dense (dt) therapy with dtEC-dtD for patients with high-risk early breast cancer: Results on pathological complete response (pCR) for patients treated within the neoadjuvant setting.

Jenny Furlanetto Marcus Schmidt Frederik Marmé Peter Klare Michael Untch Peter A. Fasching Volker Moebus Stefanie Noeding Andreas Schneeweiss Elmar Stickeler Sabine Schmatloch Volkmar Müller Bruno Valentin Sinn Wolfgang Janni Sibylle Loibl Toralf Reimer Gunter Von Minckwitz Ekkehart Ladda Nicole Burchardi

subject

0301 basic medicine Oncology Cancer Research medicine.medical_specialty business.industry Neo adjuvant 03 medical and health sciences Regimen 030104 developmental biology 0302 clinical medicine Oncology 030220 oncology & carcinogenesis Internal medicine medicine business Pathological Complete response Early breast cancer

description

568Background: GAIN-2 compares the effectiveness and safety of a predefined idd regimen (EnPC) vs. a dd regimen with modification of single doses depending on individual hematological and non-hemat...

year	journal	country	edition	language
2018-05-20	Journal of Clinical Oncology

https://doi.org/10.1200/jco.2018.36.15_suppl.568

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