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Spots Global Cancer Trial Database for To Evaluate the Efficacy and Safety of Afatinib for Advanced ALTRK-negative ESCC

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Trial Identification

Brief Title: To Evaluate the Efficacy and Safety of Afatinib for Advanced ALTRK-negative ESCC

Official Title: A Multicenter, Open-label, Randomized, Controlled Phase II Study to Evaluate the Efficacy and Safety of Afatinib Versus Irinotecan as a Second-line and Above Treatment for Advanced ALTRK-negative ESCC

Study ID: NCT05818982

Interventions

Afatinib
Irinotecan

Study Description

Brief Summary: This is a phase II study to evaluate the effectiveness and safety of Afininib compared to irinotecan in the 3-gene RNA sequencing (ALTRK) negative advanced esophageal squamous squamous carcinoma.

Detailed Description: Participants were assigned to either group A or group B at 2:1 randomization (block randomization). Group A received afatinib (40 mg orally/day) every 6 weeks; Group B received irinotecan (140-180mg/m2 intravenous) every 2 weeks.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Beijing Cancer Hospital, Beijing, China, Beijing, , China

First Hospital of Xiamen University Affiliated Hospital,Xiamen,China, Xiamen, , China

Xinxiang Central Hospital of Henan Province, Xinxiang, China, Xinxiang, , China

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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