Ensartinib in Combination With Bevacizumab in ALK-positive NSCLC Patients With TP53 Mutation

• Status: Not yet recruiting
• Trial end date: 2026-12-01
• Target enrollment: 0
• Participant gender: All

Summary

This is a prospective, single-arm, multicenter, phase II study to investigate the efficacy and safety of Ensartinib plus Bevacizumab in metastatic anaplastic lymphoma kinase (ALK)-rearranged Non-Small Cell Lung Cancer (NSCLC) with TP53 mutation.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Sun Yat-sen University
• Collaborators: First Affiliated Hospital of Wenzhou Medical University; Handan Central Hospital; Harbin Medical University; Hebei Medical University Fourth Hospital; Huai'an First People's Hospital; Jiangsu Cancer Institute & Hospital; Liaoning Cancer Hospital & Institute; Second Affiliated Hospital, School of Medicine, Zhejiang University; Shenyang Chest Hospital; The First Affiliated Hospital of Soochow University; The First Affiliated Hospital with Nanjing Medical University; Wuhan Union Hospital, China
• Treatments: Bevacizumab; Ensartinib

Criteria

Inclusion Criteria:

• Histologically or cytologically confirmed advanced (stage IIIB) or metastatic (stage IV) NSCLC;

• ALK positive with TP53 mutation was confirmed by tissue samples or blood in each center; TP53 mutation detection needs to be confirmed by NGS. ALK positive can be detected by NGS,IHC,RT-PCR and FISH;

• Age ≥ 18 years old;

• ALK-TKI-naive patients, and allowed to have received at most one previous chemotherapy;

• ECOG Performance status (PS) score is 0-2;

• Karnofsky Performance Status of ≥70;

• Subjects with CNS metastases are only eligible if the CNS metastases are adequately treated with radiotherapy and/or surgery and subjects are neurologically returned to baseline (except for residual signs or symptoms related to the CNS treatment) for at least 1 week prior to randomization.

A.Patients receiving radiotherapy or radiosurgery with a dose exceeding 30 Gy will have 3 weeks for neurological stabilization before randomization.

B.This exception does not include carcinomatous meningitis which is excluded regardless of clinical stability.

• Life expectancy of at least 12 weeks;

• Able to swallow oral drugs;

• It has certain organ system functions, defined as follows:

A. Absolute neutrophil count (ANC) ≥1.5 x 109/L B. Platelets ≥100 x 109/L C. hemoglobin ≥9 g per deciliter (≥90g per liter) note that blood transfusions are permitted to achieve the required hemoglobin level.

D. Total bilirubin ≤1.5 times upper limit of normal (ULN) E. In the absence of liver metastases, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤2.5×ULN; In case of liver metastasis, ≤5×ULN.

F. Creatinine ≤1.5 x ULN. If ≥ 1.5 × ULN and creatinine clearance value calculated by Cockcroft-Gault method ≥ 50 mL/min (0.83 mL/s), patients were still eligible for inclusion.

• Female subjects of reproductive age must undergo a negative serum pregnancy test within 3 days before the start of the study medication and be willing to use a medically approved highly effective contraceptive measure (e.g., intrauterine device, contraceptive pill, or condom) during the study and within 3 months after the last administration of the study medication; Male subjects with a female partner of reproductive age should be surgically sterilized or agree to use an effective method of contraception during the study period and for 3 months after the last study dose.

• Willing and able to follow the test and follow-up procedures.

• Be able to understand the nature of the trial and complete the signing of written informed consent.

Exclusion Criteria:

• Only ALK positive or TP53 mutation;

• Patients who have received any previous ALK-TKI treatment;

• Subjects with known EGFR mutations which are sensitive to available targeted inhibitor therapy (including, but not limited to, deletions in exon 19 and exon 21 [L858R] substitution mutations) are excluded. All subjects with non-squamous histology must have been tested locally for EGFR mutation status; use of an FDA-approved test is strongly encouraged (EGFR mutation testing may be performed during the Screening Period, Non-squamous subjects with unknown or indeterminate EGFR status may not be included);

• Subjects with untreated CNS metastases are excluded;

• Subjects with previous malignancies (except non-melanoma skin cancers, and the following in situ cancers: bladder, gastric, colon, cervical/dysplasia, melanoma, or breast) are excluded unless a complete remission was achieved at least 2 years prior to study entry and no additional therapy is required or anticipated to be required during the study period;

• Active hepatitis B (serum HBV DNA≥104 copies /ml[i.e. 20,000 IU/ml]), positive for hepatitis C virus antibody, HIV antibody, and treponema pallidum antibody;

• Women of childbearing age who had a positive serum pregnancy test 7 days before the start of treatment, women who were pregnant or lactating, or male and female subjects who did not take effective contraceptive measures or planned to have children during the whole treatment period and 3 months after the end of treatment;

• Patients who have used any of the following drugs within 14 days before the first dose or need to combine them during treatment: drugs at risk for prolonged QTc and/or torsive-tip ventricular tachycardia; CYP3A strong inhibitor or strong inducer;

• Major surgery or immunotherapy was performed within 4 weeks before the first dose; He received radiotherapy within 2 weeks before the first dose.

• Imaging (CT or MRI) showed that the tumor invaded the great blood vessels or it was judged that the tumor was very likely to invade the important blood vessels and cause fatal massive bleeding during the subsequent study

• Previous interstitial lung disease, drug-induced interstitial disease, or any clinically documented active interstitial lung disease; CT scan at baseline revealed the presence of idiopathic pulmonary fibrosis

• Other severe, acute, or chronic medical conditions, including uncontrolled diabetes or medical or psychiatric disorders or laboratory abnormalities, that, in the opinion of the investigator, may increase the risk associated with study participation or may interfere with the interpretation of the study results;

• Other circumstances deemed inappropriate by the investigator for participation in the trial.