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Beta-blockers combined with neoadjuvant immunochemotherapy significantly improve pathological remission in locally advanced gastric cancer: a multicenter controlled study based on hypertensive patients

Beta-blockers combined with neoadjuvant immunochemotherapy significantly improve pathological remission in locally advanced gastric cancer: a multicenter controlled study based on hypertensive patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600125565
Enrollment
Unknown
Registered
2026-05-28
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Advanced gastric cancer

Interventions

ß-blocker exposed group:None
ß-blocker unexposed group:None

Sponsors

Southern Medical University Southern Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 85 years old; 2. No gender restrictions; 3. Patients whose primary gastric lesions are pathologically diagnosed as gastric adenocarcinoma by endoscopic biopsy according to the 15th edition of the Japanese Gastric Cancer Treatment Guidelines (2017); 4. Patients who underwent gastrectomy after receiving neoadjuvant immunochemotherapy combined with immunotherapy at Nanfang Hospital of Southern Medical University and other sub-center hospitals from April 2021 to September 2025;

Exclusion criteria

Exclusion criteria: 1.Pregnant or lactating women; 2.Severe mental illness; 3.Patients with a history of chemotherapy, radiotherapy, or targeted drug therapy; 4.History of other malignant tumors within the past 5 years; 5.Patients with active infection, active or refractory autoimmune diseases, or uncontrolled systemic diseases; 6.Deemed by the researcher to be unsuitable to participate in this study;

Design outcomes

Primary

MeasureTime frame
Indicators Related to Tumor Regression in the Experimental Group;Control group tumor regression-related indicators;

Secondary

MeasureTime frame
The 3-year overall survival and relapse-free survival of patients in the experimental group;The starting time, duration, type of drug, and dosage of beta-blockers;The start time, duration, type, and dosage of antihypertensive drugs such as ACEI/ARB/CCB/diuretics; for those not taking medication, record the observation time;The 3-year overall survival and relapse-free survival of patients in the control group;

Countries

China

Contacts

Public ContactXinhua Chen

Southern Medical University Southern Hospital

xinhuachen03@163.com+86 20 6278 6379

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026