<?xml version='1.0' encoding='UTF-8'?><xml><records><record><source-app name="HighWire" version="7.x">Drupal-HighWire</source-app><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mosley, Mary</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Arnold, Dirk</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Active Maintenance Therapy Prolongs TFS and PFS in CRC</style></title><secondary-title><style face="normal" font="default" size="100%">MD Conference Express</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2014-10-01 00:00:00</style></date></pub-dates></dates><pages><style  face="normal" font="default" size="100%">15-15</style></pages><abstract><style  face="normal" font="default" size="100%">One of the current standards of care for the first-line therapy of metastatic colorectal cancer (mCRC) is combination chemotherapy with fluoropyrimidine (FP) and oxaliplatin (OX) plus the angiogenesis inhibitor, bevacizumab (BEV). The Phase 3 AIO KRK 0207 study [NCT00973609] showed that active maintenance therapy with FP+BEV or BEV alone, compared with no treatment, prolonged the time-to-failure of strategy and progression-free survival in patients with mCRC after induction treatment [Arnold D et al. Ann Oncol. 2014 (abstr O-0027); J Clin Oncol. 2014 (abstr 3503)].</style></abstract><number><style face="normal" font="default" size="100%">22</style></number><volume><style face="normal" font="default" size="100%">14</style></volume></record></records></xml>