ClinicalTrials.gg
Status unknownNCT05394233Updated May 27, 2022

Tislelizumab +Bevacizumab+pc for Untreated EGFR+ and High PD-L1 Non-squamous NSCLC

A Phase 2 interventional study of Tislelizumab Combined With Bevacizumab and Platinum Plus Pemetrexed in Non-squamous Non-small Cell Lung Cancer and EGFR Gene Mutation, sponsored by Sichuan Cancer Hospital and Research Institute. Status unknown at 3 sites in China. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2022-05-27.

Sponsored by Sichuan Cancer Hospital and Research Institute · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified May 2022), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
18 Years to 75 Years
Sex
All
01

Study summary

A study to evaluate the efficacy and safety of tislelizumab combined with bevacizumab and platinum-based pemetrexed in the treatment of naïve patients with advanced non-squamous non-small cell lung cancer with sensitive EGFR mutations and high PD-L1 expression Prospective, open-label, single-arm phase II clinical study

Read the detailed description

A study to evaluate the efficacy and safety of tislelizumab combined with bevacizumab and platinum-based pemetrexed in the treatment of naïve patients with advanced non-squamous non-small cell lung cancer with sensitive EGFR mutations and high PD-L1 expression Prospective, open-label, single-arm phase II clinical study;

Research purposes:

Main purpose: To evaluate the median progression-free rate of tislelizumab combined with bevacizumab and platinum pemetrexed in treatment-naïve advanced non-small cell lung cancer patients with sensitive EGFR mutations and high PD-L1 expression Survival (middle progression free survival, mPFS)

Secondary purpose:

  • Evaluation of objective response rate (ORR) according to RECIST version 1.1;
  • Evaluation of disease control rate (DCR) according to RECIST version 1.1;
  • Assess overall survival (OS);
  • Assess Duration of Response (DOR);
  • Evaluate the safety of the treatment using NCI-CTCAE v5;

Exploratory Purpose:

  • Assess potential predictive biomarkers.
02

Conditions studied

  • Non-squamous Non-small Cell Lung Cancer
  • EGFR Gene Mutation
03

In context

Carcinoma, Non-Small-Cell Lung

7,620 studies on the registry are indexed under Carcinoma, Non-Small-Cell Lung; 1,838 are open to participants now.

This study's planned enrollment of 20 is below the median of 62 across 6,019 interventional studies indexed under Carcinoma, Non-Small-Cell Lung.

Browse Carcinoma, Non-Small-Cell Lung studies →

Lead sponsor

Sichuan Cancer Hospital and Research Institute is the lead sponsor of 64 studies on the registry; 33 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. ≥ 18 and ≤ 75 years of age. Signed the form prior to patient entry
  2. or pathologically confirmed non-squamous non-small cell lung cancer(NSCLC) with stage IV /III
  3. Patients with EGFR sensitive mutations: 19del and L858R who have not been treated with TKI for the first time, the patients need to provide the test results of the certified detection platform, and the expression based on tissue specimen detection is greater than 50% (PD-L1 detection clone number: SP263).
  4. A World Health Organization (WHO)/ (ECOG) Performance Status Score (PS) of 0 or 1 at the time of recruitment.
  5. Adequate organ and bone marrow function, defined as:

    • ≥9.0 g/dL
    • ≥1.5 × 109/L
    • count ≥100 × 109/L
    • Serum ≤ 1.5 × (ULN). This does not apply to patients diagnosed with Gilbert's syndrome (persistent or recurrent hyperbilirubinemia [primarily unconjugated bilirubin] without evidence of hemolysis or liver pathology), which may be allowed after consultation with a physician patients participating in the study.
    • and AST ≤2.5 × ULN
    • Measured (CL) >40 mL/min or Cockcroft-Gault calculated CL >40 mL/min (using actual body weight) Men: Creatinine clearance (mLmin⁄) = body weight (kg) x (140-age) 72 x serum creatinine (mg/dL) Female: creatinine clearance (mLmin⁄) = body weight (kg) x (140-age) 72 x serum creatinine (mg/dL) x 0.85
  6. The expected survival time of patients is ≥3 months
  7. Weight > 30 kg
  8. Have the ability to sign the informed consent form and comply with the requirements and restrictions listed in the informed consent form (ICF) and this protocol.

Exclusion criteria

Exclusion Criteria:

  1. Patients with grade ≥2 non-infectious pneumonia.
  2. History of allogeneic organ transplantation, except corneal transplantation.
  3. Active or previously documented or inflammatory diseases (including inflammatory bowel disease [eg, colitis or Crohn's disease], diverticulitis [except diverticulosis], systemic lupus erythematosus, Sarcoidosis syndrome, or Wegener syndrome [granulomatous vasculitis, Graves disease, rheumatoid arthritis, hypophysitis, uveitis, etc.]). Exceptions to this standard include:

    • Vitiligo or alopecia patients
    • Patients with hypothyroidism who are stable on hormone replacement therapy (eg, after Hashimoto's syndrome)
    • Any chronic skin disease that does not require systemic treatment
    • Patients without active disease within the past 5 years may be included in the study, but only after consultation with the study physician
    • Patients with celiac disease that can be controlled with diet alone
  4. Uncontrolled concurrent diseases, including but not limited to: persistent or active infection, symptomatic congestive heart failure, uncontrolled hypertension, unstable angina pectoris, uncontrolled arrhythmia, active ILD , Severe chronic gastrointestinal disease with diarrhea, or a psychiatric/social condition that may limit compliance with study requirements, cause a significantly increased risk of AEs, or interfere with the subject's ability to provide written .
  5. History of another primary malignant tumor, except for the following cases;

    • Malignant tumors with low potential risk of recurrence and no known active disease ≥5 years prior to first dose treated with curative intent
    • Adequately treated non-melanoma skin cancer with no evidence of disease or lentigo maligna
    • Adequately treated cervical carcinoma in situ without evidence of disease
  6. History of active primary immunodeficiency
  7. Active infection, including tuberculosis (clinical assessment, including clinical history, physical examination, radiographic findings, and tuberculosis testing consistent with local clinical practice).
  8. Known history of (HIV) infection; known active syphilis infection.
  9. Untreated active

    Hepatitis B patients who meet the following criteria are eligible for inclusion:

    - Hepatitis B virus (HBV) load was below the lower limit of detection in our hospital before the first dose, and received anti-HBV therapy throughout the study period to avoid viral reactivation.

  10. Subjects with active (HCV) infection, HCV antibody positive patients only meet the study inclusion criteria when the polymerase chain reaction of HCV RNA is negative.
  11. Active or spinal cord compression. Prior to study entry, all patients underwent MRI (preferred) or CT examination, preferably brain examination with intravenous contrast.
  12. Known allergy or reaction to any study drug or any study drug
  13. Previous exposure to immune-mediated therapy, including but not limited to: , anti-PD-L1 and anti-programmed death ligand 2 (anti-PD-L2) antibodies, except for therapeutic anti-tumor vaccines .
  14. should be vaccinated within 30 days before the first dose, and live vaccine should not be vaccinated within 30 days after the last dose.
  15. Major surgery (as defined by the investigator) within 42 days prior to the first dose.
  16. Within 14 days before administration, drugs are being used or have been used in the past. Exceptions to this standard include:

    • Intranasal, inhaled, topical , or topical steroid injections (eg, intra-articular injections)
    • Systemic corticosteroid therapy not exceeding 10 mg/day of prednisone or its physiologic equivalent
    • Steroids administered as prophylactic for hypersensitivity reactions (eg, prophylactic administration of CT scan)
  17. Pregnant or lactating female patients and fertile male or female patients are unwilling to take effective measures from screening to 6 months after the last dose.
  18. Other researchers think that it is not suitable for inclusion.
  19. Mixed cell lung cancer: non-small cell and small cell mixed lung cancer and mixed adenosquamous lung cancer dominated by squamous cell carcinoma.
  20. Non-squamous non-small cell lung cancer with hemoptysis (>50 ml/day); hemoptysis or bleeding symptoms occurred within 3 months before enrollment.
  21. Patients with brain metastases whose symptoms are not controlled after treatment.
  22. Imaging (CT/MRI) shows that the tumor lesion is less than 5 mm away from the large blood vessels, there is a central tumor that invades the local large blood vessels and is less than 2 cm away from the bronchial tree; or there is an obvious lung cavity or necrotic tumor.
  23. Arterial/venous thrombotic events that occurred within 12 months before enrollment
  24. Patients with any severe and/or uncontrolled disease (hypertension, liver cirrhosis, heart failure, etc.)
  25. Major surgical operation or severe traumatic injury, fracture or ulcer occurred within 4 weeks before enrollment
  26. Severe weight loss (greater than 10%)
  27. Abnormal coagulation function, with bleeding tendency or receiving thrombolytic or anticoagulation therapy
Terms in these criteria, in plain language(23)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Histologically or cytologically confirmed

The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).

Your pathology report is the document that shows this.

PD-1, PD-L1 and checkpoint inhibitors

PD-1, PD-L1 and CTLA-4 are proteins that act as brakes on the immune system. Checkpoint inhibitors, such as pembrolizumab or nivolumab, block them so the immune system can attack a cancer.

PD-L1 can also be measured in a tumour sample. Some scores count stained tumour cells only (TPS); others also count certain immune cells (CPS). The study names the score and the minimum it uses.

ECOG performance status

A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

Absolute neutrophil count (ANC)

The number of neutrophils, white blood cells that help fight infection, in a given amount of blood. Too few raises the risk of infection.

It is a count, not a percentage of the white cells. Limits are written in units that mean the same: ≥ 1.5 × 10⁹/L is ≥ 1,500 per mm³ (µL). Each lab has its own reference range.

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

Creatinine clearance (CrCl)

How quickly the kidneys clear creatinine, a waste product, from the blood. A study may estimate it from a blood test with age, weight and sex (often by the Cockcroft–Gault formula), or measure it using blood and urine collected over a set time. Given in mL/min; higher is better.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

Brain metastases

Cancer deposits in the brain from a cancer that started elsewhere in the body (CNS metastases include the spinal cord).

Studies differ: some leave out any brain metastases, some accept ones treated and stable for some weeks. Check what this study allows.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

Excipients

The other ingredients in a medicine besides the active drug, such as fillers, colours or preservatives.

Live vaccines

Vaccines made with a weakened form of the germ, such as measles–mumps–rubella (MMR), chickenpox and yellow fever. They can be risky when the immune system is weakened. Flu injections are not live; the nasal flu spray is.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (estimated)

Study arms

  • Experimental
    tislelizumab combined with bevacizumab and platinum plus pemetrexed

    Drug: Induction Phase: Bevacizumab: 7.5 mg/kg administered as an IV infusion on Day 1 of each 3-week cycle for 4 cycles Cisplatin 75 mg/m2 will be administered as an intravenous infusion over 2 hours every 3 weeks for 4 cycles. Pemetrexed, 500 mg/m2, intravenously, every 3 weeks for 4 cycles Maintenance phase: Tislelizumab, 200 mg IV every 3 weeks;until disease progression or intolerance Bevacizumab: 7.5 mg/kg administered as an intravenous infusion on Day 1 of each 3-week cycle;until disease progression or intolerance

    Drug: Tislelizumab Combined With Bevacizumab and Platinum Plus Pemetrexed

Interventions

  • DrugTislelizumab Combined With Bevacizumab and Platinum Plus Pemetrexed

    Drug pages: Tislelizumab · Bevacizumab · Platinum Compounds · Pemetrexed

    Bevacizumab: 7.5 mg/kg administered as an intravenous infusion on Day 1 of each 3-week cycle Cisplatin 75 mg/m2 will be administered as an intravenous infusion over 2 hours, every 3 weeks, Pemetrexed, 500 mg/m2, intravenously every 3 weeks, Tislelizumab, 200 mg IV every 3 weeks

06

What researchers measure

Primary outcomes

  1. middle progression free survival

    To evaluate the median progression-free survival (middle) of tislelizumab combined with bevacizumab and platinum-based pemetrexed in treatment-naïve advanced non-small cell lung cancer patients with sensitive EGFR mutations and high PD-L1 expression. progression free survival (mPFS)

    Time frame: Estimated about 6 months

07

Study locations

3 sites
  • Sichuan Cancer Hospital
    Chengdu, Sichuan 610041, China
  • Sichuan Cancer Hospital
    Chengdu, Sichuan 610041, China
  • Sichuan Cancer Hospital
    Chengdu, Sichuan, China
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 27, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05394233
Lead sponsor
Sichuan Cancer Hospital and Research Institute
Responsible party
Juan LI, MD (Director of standard treatment department of medical oncology, Sichuan Cancer Hospital and Research Institute) — Principal investigator
First posted
May 27, 2022
Start date
Jun 1, 2022 (estimated)
Primary completion
Dec 1, 2023 (estimated)
Completion
Jun 1, 2024 (estimated)
Last update
May 27, 2022

Study contacts

juan li
Contact
dr.lijuan@hotmail.com
+86 13880276636
juan li
study director · Sichuan Cancer Hospital Chengdu, Sichuan China

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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Studies of the drugs tested here: Tislelizumab · Bevacizumab · Platinum Compounds · Pemetrexed

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