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A single-arm, single-center, prospective clinical study of preoperative short-course treatment for potentially resectable locally advanced esophageal cancer

A single-arm, single-center, prospective clinical study of preoperative short-course treatment for potentially resectable locally advanced esophageal cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103362
Enrollment
Unknown
Registered
2025-05-28
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-06-02

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

Conditions

Esophageal cancer

Interventions

Single arm:Radiotherapy was intensity-modulated radiotherapy PTVDT30Gy/10F/2W, concurrent with chemotherapy and immunotherapy (D22-31).

Sponsors

Yunnan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. patients aged >=18 years and <=75 years with potentially resectable locally advanced esophageal cancer; 2. Radical treatment of esophageal cancer (including surgery, radiotherapy, chemotherapy and immunotherapy); 3. patients with pathologically confirmed esophageal cancer and pathological stage cT2N+ or cT3-4a any N thoracic or abdominal esophageal cancer; 4. PS score 0-2; 5. Women of childbearing age who are contraindicated to xenophobic treatment should use contraception for at least one month before screening, and commit to use contraception throughout the study period and continue for the specified time after the end of the study.

Exclusion criteria

Exclusion criteria: 1. patients with pathologically confirmed early esophageal cancer 2. pregnant or lactating women 3. patients with serious non-neoplastic medical complications, which may affect the implementation of radiotherapy 4. severe liver and kidney dysfunction or immune system diseases, and contraindications to chemotherapy and immunotherapy 5) a history of malignant tumors within the past 5 years (excluding previous lobular carcinoma in situ, skin basal cell carcinoma, skin carcinoma in situ, and cervical carcinoma in situ) 6) previous history of thoracic radiotherapy 7) had active collagen vasculopathy 8) distant metastasis confirmed by pathology or imaging 9) patients who refused radiotherapy

Design outcomes

Primary

MeasureTime frame
objective response rate, ORR;progression free survival, PFS;

Secondary

MeasureTime frame
Convert to operable rate;Pathological remission rate;Overall survival;

Countries

China

Contacts

Public ContactXia Yaoxiong

Yunnan Cancer Hospital

wangli20060521@126.com+86 153 9849 5669

Outcome results

None listed

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