Tislelizumab Plus Chemotherapy as First-Line Treatment for Advanced Squamous NSCLC With Brain Metastases

Sun Yat-sen University

Status and phase

Unknown

Phase 2

Conditions

Brain Metastases

Non-Small Cell Squamous Lung Cancer

Treatments

Drug: Tislelizumab, paclitaxel, Carboplatin

Study type

Interventional

Funder types

Other

Identifiers

NCT05207904

B2020-241

Details and patient eligibility

About

This study is a prospective, single-arm, phase II clinical study to evaluate the efficacy and safety of Tislelizumab Plus Chemotherapy in patients with squamous NSCLC with brain metastases who had not previously received systemic therapy.

Enrollment

41 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Histologically or cytologically confirmed squamous non-small cell lung cancer;
Asymptomatic brain metastases or brain metastases that are relieved by dehydration therapy and remain clinically stable for at least 2 weeks
MRI confirmed tumor parenchymal metastases, ≥ 3 brain lesions; or patients with 1-2 brain lesions but do not require local treatment or refuse local treatment. At least one measurable lesion in the brain lesion must be ≥ 5mm in diameter; patients with local meningeal metastasis are allowed, but those with extensive meningeal metastasis are not included
Patients with stable brain metastasis symptoms after stereotactic radiotherapy are allowed (the number of stereotactic radiotherapy lesions is not more than 3)
No prior systemic treatment for metastatic NSCLC
Tumor tissue biomarker detection results must meet the following conditions at the same time: （1）EGFR mutation negative.（2）ALK rearrangement negative.（3）There are sufficient tissue samples for PD-L1 detection
Aged ≥ 18 years and ≤ 75 years
ECOG (Eastern Cooperative Oncology Group) performance status ≤ 1
Life expectancy of more than 3 months
Have adequate organ function as indicated by the following laboratory values
Written informed consent before any trial-related procedures are performed

Exclusion criteria

Subjects with any of the following criteria may not be included in this study:

With mixed adenosquamous carcinoma or small cell lung cancer mainly composed of adenocarcinoma
Currently participating in interventional clinical study treatment, or have received other investigational drugs or investigational device treatment before the first dose;
Received prior therapies targeting PD-1, PD-L1, CTLA-4, cytotoxic chemotherapy or other immune checkpoints inhibitors
Received solid organ or blood system transplantation
Have active autoimmune diseases requiring systemic therapy within 2 years before the first dose
Diagnosis of immunodeficiency or systemic glucocorticoid therapy or any other form of immunosuppressive therapy within 7 days before the first dose of the study
History of non-infectious pneumonia requiring glucocorticoid therapy or current interstitial lung disease within 1 year before the first dose
Known history of human immunodeficiency virus (HIV) infection
Untreated active hepatitis B; Note: hepatitis B subjects who meet the following criteria are also eligible: a) HBV viral load must be < 1000 copies/ml before the first dose, and subjects should receive anti-HBV therapy to avoid viral reactivation throughout the study chemotherapy drug treatment b) For subjects with anti-HBc (+), HBsAg (-), anti-HBs (-), and HBV viral load (-), prophylactic anti-HBV therapy is not required, but viral reactivation needs to be closely monitored;
Subjects with active HCV infection
Pregnant and lactating women
Malignant tumors other than NSCLC within 5 years before screening, except for adequately treated cervical carcinoma in situ, basal cell or squamous cell epithelial skin cancer, local prostate cancer after radical resection, and ductal carcinoma in situ after radical resection