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Tislelizumab Combined With Bevacizumab for previously untreated, PD-L1-expressing, locally advanced or metastatic non-small-cell lung cancer:a single-arm, phase 2 study.

Tislelizumab Combined With Bevacizumab for previously untreated, PD-L1-expressing, locally advanced or metastatic non-small-cell lung cancer:a single-arm, phase 2 study.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056693
Enrollment
Unknown
Registered
2022-02-10
Start date
2022-02-20
Completion date
Unknown
Last updated
2023-09-04

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

Conditions

lung cancer

Interventions

Case group:None

Sponsors

Taizhou hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Sign the informed consent form; 2. Male or female patients, age = 18 years old, when signing the informed consent form; 3. The researcher judged that he could comply with the research protocol; 4. Expected survival time = 10 months; 5. Histological or cytological examination confirms that patients with locally advanced (stage IIIB or stage IIIC) or metastatic (stage IV) non-squamous NSCLC that cannot undergo radical surgery or radiotherapy (according to the staging system of the International Anti-Cancer Union/American Cancer Federation, revised version 8), note: for patients with mixed histologic (i.e. squamous and non-squamous) tumors, if the main histological components appear to be non-squamous, they meet the requirements; 6. Have not received any anti-tumor treatment in the past; 7. According to the RECIST v1.1 standard, the expression of PD-L1 in measurable lesions is = 1%, and the samples are from previously obtained archived tumor tissues or tissues obtained from biopsy during screening; 8.ECOG PS: 0-1

Exclusion criteria

Exclusion criteria: 1. NSCLC diagnosed with EGFR sensitive mutation, ALK or ROS1 gene rearrangement; 2. During screening and before radiological imaging evaluation, active brain metastasis or leptomeningeal metastasis was confirmed by CT or MRI evaluation; 3. Untreated chronic hepatitis B patients or chronic hepatitis B virus carriers and active hepatitis C patients with HBV DNA = 500 IU/mL.

Design outcomes

Primary

MeasureTime frame
PFS rate at 6 months;

Secondary

MeasureTime frame
objective response rate;Disease Control Rate;

Countries

China

Contacts

Public ContactXu Youzu

Taizhou hospital

xuyouzu@sina.com+86 13958552363

Outcome results

None listed

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