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The Impact of Surgical Technique on Circulating Tumor DNA in Stage I-III Non-Small Cell Lung Cancer

Sponsored by Thomas Jefferson University

About this study

This clinical trial compares the effect of pulmonary vein-first surgical technique to pulmonary artery-first surgical technique in decreasing circulating tumor cell deoxyribonucleic acid (ctDNA) in patients with stage I-III non-small cell lung cancer. Pulmonary vein first and pulmonary artery first surgical techniques are standard surgical techniques for the division of the blood vessels during lung resection surgery. Pulmonary vein-first surgical technique may reduce the risk of shedding tumor cells during surgery and influence long term overall survival.

PRIMARY OBJECTIVE: I. To determine the association between sequence of surgical resection and postoperative ctDNA levels at specified time points. SECONDARY OBJECTIVE: I. To determine the associated between sequence of surgical resection and postoperative ctDNA level and clinical oncologic outcomes. II. To assess disease-free survival and the role of circulating tumor DNA in disease recurrence in patients with resectable non-small cell lung cancer. OUTLINE: Patients are randomized to 1 of 2 groups. GROUP I: Patients undergo pulmonary vein first approach surgical procedure on day of surgery. GROUP II: Patients undergo pulmonary artery first approach surgical procedure on day of surgery. After completion of surgery, patients are followed up at day 1, day 7, days 7-28, 4 months, every…

Where this study is enrolling (4)

  • Abington Memorial Hospital

    Abington, Pennsylvania

    I'm interested
  • Asplundh Cancer Pavilion at Jefferson Health

    Willow Grove, Pennsylvania

    Call 215-481-4000

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  • Jefferson Health Northeast

    Philadelphia, Pennsylvania

    Call 215-866-8690

    This research site can be reached directly by phone. Call to ask about this study.

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  • Thomas Jefferson University Hospital

    Philadelphia, Pennsylvania

    I'm interested
Who can participate

Inclusion criteria

  • ✓Any patients 18 years of age or older with confirmed or suspected early-stage (stage I-III) NSCLC
  • ✓Eligible and scheduled for surgical anatomic lung resection (e.g. lobectomy or segmentectomy) as routine clinical care for their disease

Exclusion criteria

  • ✕Previous cancer diagnosis within 5 years (except ductal carcinoma in situ \[DCIS\] of the breast, superficial bladder cancer, non-melanoma skin primary, other malignancy that does not require treatment).
  • ✕Preoperative chemotherapy, immunotherapy, or radiation therapy
  • ✕Receipt of perioperative blood transfusion

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Trial data sourced from ClinicalTrials.gov.