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Exploratory Study on the Combination of Bevacizumab and Anti-PD-1 Antibody for the Treatment of SMARCA4-Deficient Thoracic Tumors

Exploratory Study on the Combination of Bevacizumab and Anti-PD-1 Antibody for the Treatment of SMARCA4-Deficient Thoracic Tumors

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118967
Enrollment
Unknown
Registered
2026-02-13
Start date
2026-05-08
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

SMARCA4 deficiency/partial deficiency in chest tumors

Interventions

SMARCA4 deficient/partially deficient chest tumor patients:After the progression of the disease caused by first-line drug resistance, second-line administration of bevacizumab combined with anti-PD-1

Sponsors

Fuyang People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Enrollment age: patients aged 18-80, regardless of gender, smoking or non-smoking status. 2. Collect cases of thoracic tumors with confirmed pathological diagnosis of SMARCA4 deletion/partial deletion (patients with postoperative recurrence or stage II-IV patients who cannot undergo surgery).

Exclusion criteria

Exclusion criteria: 1.PS>2 points; 2.Exclude patients with uncontrolled diabetes, serious cardiovascular and cerebrovascular diseases or liver and kidney function damage, coagulation dysfunction and thrombosis; 3.Exclude patients with psychological or psychiatric disorders and poor compliance;

Design outcomes

Primary

MeasureTime frame
Objective Response Rate (ORR) ;Progression-Free Survival (PFS) ;Overall Survival (OS) ;Disease Control Rate (DCR);

Countries

China

Contacts

Public ContactJIANG QING

Fuyang People's Hospital

doctorjq1006@126.com+86 558 301 0307

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026