Condition: Cervical Cancer · Sponsor: Sichuan Cancer Hospital and Research Institute
The main objective of this study is to determine whether neoadjuvant chemotherapy combined with slulimumab sequential concurrent chemoradiotherapy versus concurrent chemoradiotherapy for locally advanced cervical cancer could improve progression-free survival rates. Women in the experimental arm will receive neoadjuvant chemotherapy (cisplatin plus paclitaxel) combined with slulimumab every 21 days during 2 cycles followed by concurrent chemoradiation therapy. Women in the control arm will receive concurrent chemoradiation therapy alone. 286 patients will be recruited during 2 years, with 3 years of follow up period.
This description comes directly from the study's public registry record.
Guonan Zhang · 86-13881866599 · zhanggn@hotmail.com
Hong Liu · 86-13693447854 · liuhaotian12@163.com
Always discuss trial participation with your own doctor first.
| Sicchuan cancer hospital | Chengdu, Sichuan, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05173272