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(Withdrawn by researcher) Prospective study of camrelizumab in combination with chemotherapy for the neoadjuvant treatment of resectable/potentially resectable locally advanced esophageal squamous cell carcinoma

Prospective study of camrelizumab in combination with chemotherapy for the neoadjuvant treatment of resectable/potentially resectable locally advanced esophageal squamous cell carcinoma

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070894
Enrollment
Unknown
Registered
2023-04-26
Start date
2021-12-01
Completion date
Unknown
Last updated
2023-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophageal squamous cell carcinoma

Interventions

Group A:Patients were treated with 2 cycles of the following drugs intravenously: camrelizumab (200 mg on day 1 every 3 weeks), nab-paclitaxel (260 mg/m2 on day 1 every 3 weeks), and carboplatin (area
Group B:Patients were treated with 4 cycles of the following drugs intravenously: camrelizumab (200 mg on day 1 every 3 weeks), nab-paclitaxel (260 mg/m2 on day 1 every 3 weeks), and carboplatin (area

Sponsors

People’s Hospital of Yangzhong
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Eligibility criteria for the trial included patients with pathologically confirmed esophageal squamous cell carcinoma between the age of 18 and older, with clinical stage II or III, with an Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1.

Exclusion criteria

Exclusion criteria: Patients were excluded if they had severe disease within the previous 5 years, active autoimmune disease, immunosuppressive therapy in the past two weeks, history of HIV, and esophageal perforation or hematemesis.

Design outcomes

Primary

MeasureTime frame
pathological complete response (PCR);

Secondary

MeasureTime frame
R0 resection rate;objective response rate (ORR);Disease-free survival (DFS);Overall survival (OS);Safety;

Countries

China

Contacts

Public ContactJianping Wang

People’s Hospital of Yangzhong

yangzhongwjp@163.com+86 511 8832 2460

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026