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Not yet recruiting NCT06356675

A Single-arm Pilot Study of Tislelizumab Combined With Anlotinib in Patients With Advanced NSCLC With Driver-negative After Progression to Immunotherapy

Phase IV Interventional Advanced NSCLC

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Tislelizumab, Anlotinib.
Who it may be relevant to
Registry conditions: Advanced NSCLC. Basic parameters: 18 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

Immune resistance after treatment, there is no standard treatment, one of the most important and the most effective measures is immune to combination therapy。Targeted angiogenesis therapy has always been the focus of research on the treatment of NSCLC patients with progressive disease after immunotherapy. From the mechanism of action, angiogenesis and immunosuppression are interrelated processes.

Interventions

  • Drug Tislelizumab
    200mg iv D1 Q3W
  • Drug Anlotinib
    Anlotinib 12mg D1-12 Q3W

Primary outcome measures

  • objective response rate [Time frame: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 6 months]
Secondary outcome measures (4)
  • progression free survival time [Time frame: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 12 months]
  • over survival time [Time frame: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to18 months]
  • disease control rate [Time frame: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 6 months]
  • safety including any grade adverse events [Time frame: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 18 months]

Eligibility criteria

Inclusion criteria

  • voluntary participation in clinical research; Fully understand and Informed the study and sign the Informed Consent Form (ICF); Be willing to follow and be able to complete all trial procedures;
  • age of 18-75 years old (including boundary value), regardless of gender;
  • Pathologically confirmed locally advanced, metastatic non-small cell lung cancer (NSCLC), including squamous non-small cell lung cancer and non-squamous non-small cell lung cancer. Patients with non-squamous non-small cell lung cancer should exclude known EGFR mutation or ALK gene rearrangement.
  • patients with resistance to first-line PD-(L)1 inhibitors combined with chemotherapy;
  • patients with tumor response of CR/PR/SD after at least one first-line immunotherapy;
  • Subjects' ECOG PS score was 0-1 (including boundary value);
  • Patients had to have ≥1 measurable lesion (according to RECIST1.1 criteria).
  • predicted survival time ≥6 months;

Exclusion criteria

  • Frontline treatment with anlotinib, anti-angiogenic macromolecular monoclonal antibody or other small molecule TKI drugs;
  • central lung cancer with large blood vessel invasion;
  • patients with any signs or history of bleeding that may affect treatment according to the investigator's judgment; Patients with bleeding events ≥CTCAE grade 3, unhealed wounds, ulcers, or fractures within 4 weeks before the first dose of study drug;
  • hemoptysis > 50ml/d;
  • inability to swallow capsules or diseases that significantly affect gastrointestinal function, such as malabsorption syndrome, gastric or small bowel resection, bariatric surgery, inflammatory bowel disease, partial or complete intestinal obstruction;
  • Poorly controlled hypertension (defined as systolic blood pressure >150 mmHg and/or diastolic blood pressure >100 mmHg)
  • other known malignant tumors that are developing or require active treatment;
  • Currently participating or has participated in the clinical research of other drugs;
  • interstitial lung disease or (non-infectious) pneumonia requiring steroid therapy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06356675 · A single-arm pilot

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗