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The clinical study of Tislelizumab combined with Oxaliplatin and S-1 in the treatment of locally advanced Siewert type II esophagogastric junction adenocarcinoma

The clinical study of Tislelizumab combined with Oxaliplatin and S-1 in the treatment of locally advanced Siewert type II esophagogastric junction adenocarcinoma

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075638
Enrollment
Unknown
Registered
2023-09-11
Start date
2023-09-11
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

Siewert type II esophagogastric junction adenocarcinoma

Interventions

Test group:Tirelizumab combined with oxaliplatin and tigio neoadjuvant therapy

Sponsors

The Fourth Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Aged between 18 and 75; (2) It was pathologically confirmed as esophagogastric junction adenocarcinoma with Siewert type II (3) Clinical tumor stage: T2-4N0-3M0; (4) There is at least one measurable lesion; (5) ECOG PS score: 0-1; (6) Major organ function is normal, and baseline tests such as blood tests have no contraindications for immunotherapy and chemotherapy.

Exclusion criteria

Exclusion criteria: (1) Use of immunosuppressive drugs in the 14 days prior to administration, excluding inhaled corticosteroids or physiological doses of systemic steroids; (2) Existing active autoimmune disease or history of autoimmune disease before administration; (3) Combined with other malignant tumors; (4) Patients with active viral hepatitis B (HBV DNA = 100 IU/ml), viral hepatitis C, and need antiviral therapy during treatment; (5) Have a history of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation; (6) Persons with mental disorders; (7) HER2-positive patients; (8) Clinical assessment is not suitable for patients participating in this study.

Design outcomes

Primary

MeasureTime frame
Pathologic Complete Response;

Secondary

MeasureTime frame
MajorPathological Response;Complete tumor resection rate;Objective Response Rate;Disease-Free Survival;

Countries

China

Contacts

Public ContactTian Ziqaing

The Fourth Hospital of Hebei Medical University

tizq12@vip.163.com+86 185 3111 8000

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 29, 2026