Skip to content

A Prospective, Single-institutional, Observational Cohort Study for Patterns of Adjuvant Therapy and Prognosis for Incompletely Resected NSCLC Patients

A Prospective, Single-institutional, Observational Cohort Study for Patterns of Adjuvant Therapy and Prognosis for Incompletely Resected Non-Small Cell Lung Cancer Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000032087
Enrollment
Unknown
Registered
2020-04-19
Start date
2020-05-01
Completion date
Unknown
Last updated
2020-04-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-Small Cell Lung Cancer

Interventions

Case series:radical resection of lung cancer

Sponsors

Shanghai Chest Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients receiving lung cancer surgery (lobectomy, sleeve resection, pneumonectomy) with radical intention from May 1, 2020 to April 30, 2021 in our hospital; 2. Patients with non-small cell lung cancer confirmed by surgical pathology. If the disease is in pathologic complete remission after neoadjuvant therapy, cytopathology or histopathology must be confirmed as non-small cell lung cancer before operation; 3. Patients with incomplete resection (R1 or R2) indicated by surgical pathology, or incomplete resection indicated by surgical records, intraoperative judgment of surgeons, the first postoperative chest CT, or lymph node dissection failing to meet the requirements of at least three mediastinum stations, or patients with positive lymph nodes in the highest station confirmed by pathology; 4. Patients without supraclavicular lymph nodes metastasis or distant metastasis according to preoperative examinations; 5. Patients surviving at least 30 days after operation; 6. Within 90 days after operation, patients need to have post-operative baseline examination, at least chest CT (enhanced or not) and abdominal B-ultrasound; If no examination of brain is applied before surgery, brain MR/CT with contrast is needed within 90 days after surgery and need no signs of metastasis, plain scans can be considered for patients who do not tolerate contrast media; 7. The operation must be carried out in our hospital; Examinations and neoadjuvant/adjuvant therapy can be carried out in other hospitals, and there must be at least a paper report and discharge summary (if hospitalized); 8. Patients willing to sign an informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with pathologically confirmed mixture of small cell components by preoperative biopsy or surgical pathology; 2. Patients with cancer history within 5 years before the operation; 3. Patients with any lung surgical history (benign or malignant) before the lung cancer operation.

Design outcomes

Primary

MeasureTime frame
Patterns of failure;2-year loco-regional recurrence free survival;

Secondary

MeasureTime frame
5-year overall survival;Toxicity;Quality of life;

Countries

China

Contacts

Public ContactXiaolong Fu

Shanghai Chest Hospital

xlfu1964@hotmail.com+86 13651635103

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026