Neoadjuvant Umbrella Trial for Patients With Unresectable Stage III NSCLC Harboring Rare Mutations.

NCT ID: NCT06563999

Last Updated: 2024-12-10

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 120 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-11-01
• Study Completion Date: 2029-11-01

Brief Summary

This umbrella trial directed by next generation sequencing (NGS) includes patients with treatment-naive unresectable stage III non-small-cell lung cancer (NSCLC). The aim of the umbrella study is to evaluate the efficacy of induction NGS-directed targeted therapies followed by surgery for stage III NSCLC patients whose tumor harbors a rare mutation.

Detailed Description

Stage III non-small-cell lung cancer (NSCLC) patients account for about one-third of newly diagnosed NSCLC, with a large population and strong heterogeneity, posing significant challenges for clinical treatment. Concurrent chemoradiotherapy plus immune checkpoint inhibitors is the recommended therapeutic approach for patients with unresectable stage III non-small cell lung cancer (NSCLC), although surgery offers the chance of cure. However, existing evidence suggests that patients with driver mutation positive NSCLC have limited benefits from immunotherapy. There is still controversy over the definition of 'unresectable', and some stage IIIA and specific stage IIIB-N2 patients may also benefit from comprehensive surgical treatment. Emerging data supports the use of targeted therapies in NSCLC patients with a rare mutation. The aim of this umbrella study is to explore the efficacy of induction next generation sequencing (NGS)-directed targeted therapies followed by surgery for unresectable stage III NSCLC patients whose tumor harbors a rare mutation (Without EGFR Sensitizing Mutations).

Conditions

Lung Cancer Stage III; Mutation

Keywords

stage III NSCLC; rare mutations; umbrella trial; neoadjuvant

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment 1-Sunvozertinib

Patients with EGFR exon20ins mutation receive Sunvozertinib 300 mg orally once a day, 28 days as one cycle for 3 cycle.

Group Type: EXPERIMENTAL

Sunvozertinib

Intervention Type: DRUG

300 mg orally once a day, 28 days as one cycle.

Treatment 2-Crizotinib

Patients with ROS1 fusion mutation receive Crizotinib 250mg orally once a day, 28 days as one cycle for 3 cycle.

Group Type: EXPERIMENTAL

Crizotinib

Intervention Type: DRUG

300 mg orally once a day, 28 days as one cycle.

Treatment 3-Pralsetinib

Patients with RET fusion mutation receive Pralsetinib 400mg orally once a day, 28 days as one cycle for 3 cycle.

Group Type: EXPERIMENTAL

Pralsetinib

Intervention Type: DRUG

400 mg orally once a day, 28 days as one cycle.

Treatment 4-Larotrectinib

Patients with NTRK fusion mutation receive Larotrectinib 100 mg orally twice daily, 28 days as one cycle for 3 cycle.

Group Type: EXPERIMENTAL

Larotrectinib

Intervention Type: DRUG

100 mg orally twice daily, 28 days as one cycle.

Treatment 5-Savolitinib

Patients with MET 14 exon mutation receive Savolitinib 600 mg or 400 mg (weight \<50 kg) orally once a day, 28 days as one cycle for 3 cycle.

Group Type: EXPERIMENTAL

Savolitinib

Intervention Type: DRUG

600 mg or 400 mg (weight \<50 kg) orally once a day, 28 days as one cycle.

Treatment 6-Pyrotinib

Patients with HER2 mutation receive Pyrotinib 400 mg orally once a day, 28 days as one cycle for 3 cycle.

Group Type: EXPERIMENTAL

Pyrotinib

Intervention Type: DRUG

400 mg orally once a day, 28 days as one cycle.

Treatment 7-Dabrafenib+Trametinib

Patients with BRAF V600E mutation receive Dabrafenib plus Trametinib, 28 days as one cycle for 3 cycle.

Group Type: EXPERIMENTAL

Dabrafenib+Trametinib

Intervention Type: DRUG

Dabrafenib 150 mg orally twice daily, 28 days as one cycle. Trametinib 150 mg orally twice daily, 28 days as one cycle.

Treatment 8-Glecirasib

Patients with KRAS G12C mutation receive Glecirasib 800 mg daily orally, 28 days as one cycle for 3 cycle.

Group Type: EXPERIMENTAL

Glecirasib

Intervention Type: DRUG

800 mg daily orally, 28 days as one cycle.

Treatment 9-Ensartinib

Patients with ALK fusion mutation receive Ensartinib 225 mg daily orally, 28 days as one cycle for 3 cycle.

Group Type: EXPERIMENTAL

Ensartinib

Intervention Type: DRUG

225 mg daily orally, 28 days as one cycle.

Interventions

Sunvozertinib

300 mg orally once a day, 28 days as one cycle.

Intervention Type: DRUG

Crizotinib

300 mg orally once a day, 28 days as one cycle.

Intervention Type: DRUG

Pralsetinib

400 mg orally once a day, 28 days as one cycle.

Intervention Type: DRUG

Larotrectinib

100 mg orally twice daily, 28 days as one cycle.

Intervention Type: DRUG

Savolitinib

600 mg or 400 mg (weight \<50 kg) orally once a day, 28 days as one cycle.

Intervention Type: DRUG

Pyrotinib

400 mg orally once a day, 28 days as one cycle.

Intervention Type: DRUG

Dabrafenib+Trametinib

Dabrafenib 150 mg orally twice daily, 28 days as one cycle. Trametinib 150 mg orally twice daily, 28 days as one cycle.

Intervention Type: DRUG

Glecirasib

800 mg daily orally, 28 days as one cycle.

Intervention Type: DRUG

Ensartinib

225 mg daily orally, 28 days as one cycle.

Intervention Type: DRUG

Other Intervention Names

DZD9008; Xalkori; GAVRETO; VITRAKVI; ORPATHYS; SHR1258; JAB-21822; X-396

Eligibility Criteria

Inclusion Criteria

• Subjects must have treatment-naive unresectable stage III NSCLC according to the AJCC 8th edition staging;
• Squamous or non-squamous NSCLC histology;
• Subjects should have a rare mutation based on NGS, including mutations of EGFR exon20ins, ROS1 fusion, RET fusion, NTRK fusion, MET 14 exon, HER2, BRAF V600E, KRAS G12C, and ALK fusion.
• Subjects should be without EGFR exon 19 deletions or exon 21 L858R activating mutation;
• Male and female, aged 18-75 years;
• Blood and specimens before and after treatment must be provided;
• Eastern Cooperative Oncology Group (ECOG) performance status of 0-1;
• Adequate hematological function: Absolute neutrophil count (ANC) ≥2.0 x 109/L, and Platelet count ≥100 x 109/L, and Hemoglobin ≥9 g/dL (may be transfused to maintain or exceed this level);
• Adequate liver function: Total bilirubin ≤ 1.5 x upper limit of normal (ULN), Aspartate aminotransferase (AST), alanine aminotransferase (ALT) ≤ 2.5 x ULN;
• Adequate renal function: Serum creatinine ≤ 1.25 x ULN, or ≥ 60 ml/min;
• Female subjects should not be pregnant or breast-feeding;
• Written informed consent provided. Being willing and able to comply with the visits, treatment plan, laboratory examinations and other study procedures scheduled in the study.

Exclusion Criteria

• Not unresectable stage III disease according to the investigator;
• Subjects with known EGFR sensitive mutations;
• Previous treatment with systemic antitumor therapy for NSCLC;
• Eye inflammation or eye infection not fully treated or conditions predisposing the subject to this.
• History of another malignancy in the last 5 years with the exception of the following: other malignancies cured by surgery alone and having a continuous disease-free interval of 5 years are permitted. Cured basal cell carcinoma of the skin and cured in situ carcinoma of the uterine cervix are permitted.
• Evidence of clinically active interstitial lung disease;
• Known history of testing positive for human immunodeficiency virus (HIV) or known acquired immunodeficiency syndrome (AIDS);
• Inability to comply with protocol or study procedures;
• Any unstable systemic disease (including active infection, active tuberculosis uncontrolled hypertension, unstable angina, congestive heart failure, myocardial infarction within the previous year, serious cardiac arrhythmia requiring medication, hepatic, renal, or metabolic disease);
• A serious concomitant systemic disorder that, in the opinion of the investigator, would compromise the patient's ability to complete the study and may confuse the study results;
• Women who are pregnant or nursing.
• Ingredients mixed with small cell lung cancer patients.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Sun Yat-sen University

OTHER

Sponsor Role: lead

Responsible Party

Si-Yu Wang

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Si-Yu Wang, MD

Role: PRINCIPAL_INVESTIGATOR

Sun Yat-sen University

Locations

Sun Yat-sen University Cancer Center

Guangzhou, Guangdong, China

Site Status: RECRUITING

Countries

China

Central Contacts

Si-Yu Wang, MD

Role: CONTACT

Phone: +86 20 87343439

Email: wangsy@sysucc.org.cn

Facility Contacts

Si-Yu Wang, Doctor

Role: primary

Other Identifiers

GASTO-10117

Identifier Type: -

Identifier Source: org_study_id