Neoadjuvant Therapy in Cervical Cancer

Recruiting N/A Interventional Study
Uterine Cervical Neoplasms
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 70
Sex
Female
Study type
Interventional
Purpose
Treatment
Participants needed
48 (estimated)
Sponsor
Qilu Hospital of Shandong University · Other
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About This Trial
In the comprehensive dataset of clinical diagnoses and treatments for cervical cancer in China, 49.8% of patients with stage IB3 and IIA2 receive surgical intervention following neoadjuvant chemotherapy. This indicates a pressing need to optimize neoadjuvant chemotherapy regimens for locally advanced cervical cancer. While paclitaxel combined with cisplatin is the conventional approach, 9.8% to 30…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Clinical diagnosis of cervical squamous cell carcinoma * HER-2 positive Exclusion Criteria: * Cervical adenocarcinoma
Contacts

Hualei Bu

86-0531-82169269

buhualei@email.sdu.edu.cn

CONTACT