1. Basamak NSCLC'de (küçük hücreli dışı akciğer kanseri / non-small cell lung cancer) MET Uyumluluğu ve Gen Profillemesi Çalışması (Genomet)

Sade dilde özet

Bu çalışma, birinci basamak tedavi görecek küçük hücreli dışı akciğer kanserinde (non-small cell lung cancer, NSCLC) MET testleri arasındaki uyumu ve gen profillemesini incelemektedir. NGS testi, MET IHC (immünohistokimya) testi ile PD-L1 ve Her2 testlerinin yapıldığı çalışmaya; 18 yaş ve üzerinde olan, ameliyatla çıkarılamayan lokal ileri (Evre IIIB/IIIC) ya da metastatik/tekrarlayan (Evre IV) NSCLC hastaları katılabilmektedir. Çalışma faz uygulanmayan bir çalışma olarak yürütülmektedir ve halen katılımcı almaktadır.

Yukarıdaki özet, resmî kaydın sade dile aktarılmış halidir. Orijinal İngilizce başlık referans için gösterilir.

Deney bilgileri

Faz

Faz dışı

Durum

Katılımcı alıyor

Sponsor

AstraZeneca

Müdahale

NGS testing, MET IHC testing, PD-L1 and Her2 testing

Başlangıç

02.06.2026

Tahmini bitiş

31.03.2027

Ülkeler

China

İlgili genler

Merkezler

• Beijing, China
• Shanghai, China

Uygunluk kriterleri

Kriterler ClinicalTrials.gov kaydından orijinal İngilizce haliyle alınmıştır. Uygunluk kararını yalnızca deneyi yürüten ekip verebilir.

Inclusion Criteria:

Participants are eligible to be included in the study only if all of the following criteria apply:

Age

1. Participant must be ≥ 18 at the time of signing the informed consent. Type of Participant and Disease Characteristics
2. Participants who are in accordance with the Eighth Edition of TNM Staging of Lung Cancer by the International Association for the Study of Lung Cancer and American Joint Committee on Cancer, histologically or cytologically confirmed unresectable locally advanced (Stage ⅢB/ⅢC), metastatic or recurrent (Stage IV) NSCLC.
3. Willing to provide adequate tissue sample:

1Biopsy tissue must be collected after confirmation of unresectable locally advanced (Stage IIIB/IIIC), metastatic, or recurrent (Stage IV) NSCLC diagnosis, and before initiation of any antitumor therapy. The biopsy specimens require at least 16 FFPE slides.

or 2Surgical specimens only for patients with recurrent disease who either received no adjuvant therapy, or received only adjuvant chemotherapy and recurrence occurred \>6 months after completing chemotherapy. The surgical specimens require at least 13 FFPE slides (surgical specimens obtained within 2 years before ICF signing).

Informed Consent 4.Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the ICF and in this protocol.

5.Provision of signed and dated, written informed consent form prior to any mandatory study-specific procedures, sampling, and analyses.

Exclusion Criteria:

Medical Conditions

1. Currently having other malignant tumors, or having other infiltrating malignant tumors in the past 5 years. Stage I malignant tumor after radical treatment for at least 3 years, except those considered by investigators to have a small possibility of recurrence. Participants with radically treated carcinoma in situ (non-infiltrating), papillary thyroid carcinoma and skin cancer other than malignant melanoma can be enrolled.
2. Prior radiotherapy or systemic therapy for unresectable locally advanced (Stage IIIB/IIIC) or metastatic/recurrent (Stage IV) NSCLC, except patients initiating first-line therapy for this specific disease stage within 1 month before ICF signing.