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Results of the use of ramucirumab in combination with paclitaxel or ramucirumab monotherapy as the second line treatment in patients with disseminated HER2-negative gastric or cardioesophageal junction adenocarcinoma: experience of N.N. Blokhin russian cancer research center of the ministry of health of Russia

Authors :
N. S. Besova
T. A. Titova
E. V. Trusilova
V. A. Gorbunova
A. A. Tryakin
O. O. Gordeeva
A. A. Rumyantsev
R. Yu. Nasyrova
L. G. Zhukova
A. V. Snegovoy
E. V. Artamonova
L. V. Manzyuk
A. A. Fedenko
Source :
Медицинский совет, Vol 0, Iss 10, Pp 34-40 (2018)
Publication Year :
2018
Publisher :
Remedium Group LLC, 2018.

Abstract

Background. Working out of the second line chemotherapy of advanced gastric adenocarcinoma is a promising approach to cancer therapy. Ramucirumab, an anti-angiogenic agent specifically targeting vascular endothelial growth factor receptor-2 (VEGFR-2). In April 2014, the FDA approved ramucirumab as a single agent or in combination with paclitaxel for treatment of advanced gastric or gastroesophageal junction adenocarcinoma that has progressed on or after prior fluoropyrimidineor platinum containing chemotherapy based on data of REGARD and RAINBOW trials.Materials and Methods: From June 2016 to 15Jan 201837 pts with advanced GC were treated with ramucirumabin the second line treatment as single agent (11 pts) or in combination with paclitaxel (26 pts) in N.N.Blokhin National medical research center of oncology.Results: edian PFS (MPFS) and median OS (MOS) was 1,8 and 7,6 mons for monotherapy group. For combination group MPFS was 4,0mons, MOS -10,6 mons. Ramucirumab had an acceptable safety profileConclusions:ur data are similar to the data of international randomized trials.

Details

Language :
Russian
ISSN :
2079701X, 26585790, and 74187953
Issue :
10
Database :
Directory of Open Access Journals
Journal :
Медицинский совет
Publication Type :
Academic Journal
Accession number :
edsdoj.04195fc596f7418795345774f13af70d
Document Type :
article
Full Text :
https://doi.org/10.21518/2079-701X-2018-10-34-40