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โ† Trials
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Feasibility Study of Tissue and Blood Collection in Oncogene-addicted and Neoadjuvantly Treated Non Small Cell Lung Cancer

Recruitingn/aAges 18 Years - anyAllRoyal Marsden NHS Foundation Trust
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In plain words

What the trial is, and whether it could suit you

This study aims to determine if it is feasible to collect samples of blood and viable lung cancer tissue in patients with either: * Stage IV mutation-driven NSCLC * Stage II-III NSCLC undergoing neoadjuvant immunotherapy prior to surgery Viable tissue has been defined by the collaborating pathology department as the presence of viable tumour cells, in accordance with recommendations from the International Association or the Study of Lung Cancer. In patients with stage IV NSCLC, obtaining adequate samples of viable tissue for advanced testing can be challenging, as sites of cancer that are accessible by biopsy are often small, and contain few viable cancer cells. If obtained, however, viable blood and tissue specimens can be utilised for genetic and other analyses aimed at identifying cancer markers that may offer prognostic information, or that may potentially lead to development of t

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria (Cohort 1): 1. Age \>/= 18. 2. Histologically confirmed locally advanced or metastatic NSCLC 3. ECOG performance score 0-2 4. Tier 1 ASCO/AMP NSCLC oncogenic variant identified through routine clinical methods, e.g. EGFR, ALK, ROS1, RET, MET, KRAS, BRAF, HER2, NTRK 5. Planned to commence targeted therapy (any line of therapy) o This includes bispecific antibodies (e.g. amivantamab), and antibody-drug conjugates (e.g. trastuzumab-deruxtecan) 6. Regular follow-up and monitoring for cancer recurrence per standard of care planned at the enrolling site 7. Provided written informed consent to participate in the study Inclusion Criteria (Cohort 2) 1. Age \>/= 18. 2. Histologically confirmed stage II/III operable NSCLC 3. Planned to undergo neoadjuvant CPI-based therapy 4. Provided written informed consent to participate in the study Exclusion Criteria: โ€ข Patient too medically unstable to commit to sampling required for the study
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What it tests

  • Not listed
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Where

1 site
The Royal Marsden NHS Foundation Trust
London, United Kingdom
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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