奥拉帕尼
DNA损伤
癌症研究
DNA修复
PARP抑制剂
前列腺癌
癌症
药理学
癌变
癌细胞
医学
生物
聚ADP核糖聚合酶
内科学
DNA
聚合酶
生物化学
作者
Antje M. Wengner,Gerhard Siemeister,Ulrich Lücking,Julien Lefranc,Lars Wortmann,Philip Lienau,Benjamin Bader,Ulf Bömer,Dieter Moosmayer,Uwe Eberspächer,Sven Golfier,Christoph A. Schatz,Simon J. Baumgart,Bernard Haendler,Pascale Lejeune,Andreas Schlicker,Franz von Nussbaum,Michael Brands,Karl Ziegelbauer,Dominik Mumberg
标识
DOI:10.1158/1535-7163.mct-19-0019
摘要
Furthermore, the combination of BAY 1895344 with the novel, nonsteroidal androgen receptor antagonist darolutamide resulted in significantly improved antitumor efficacy compared with respective single-agent treatments in hormone-dependent prostate cancer, and addition of EBRT resulted in even further enhanced antitumor efficacy. Thus, the ATR inhibitor BAY 1895344 may provide new therapeutic options for the treatment of cancers with certain DDR deficiencies in monotherapy and in combination with DNA damage-inducing or DNA repair-compromising cancer therapies by improving their efficacy.
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