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Clinical Trials/NCT06115239
NCT06115239
Not yet recruiting
Not Applicable

Evaluation of Changes in Quality of Life in Patients With Non-small Cell Lung Carcinoma Undergoing Lung Resection Before and After Receiving Adjuvant Treatment Using the EORTC-LC29 Questionnaire

University of Salamanca1 site in 1 country200 target enrollmentMay 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Carcinoma, Non-Small-Cell Lung
Sponsor
University of Salamanca
Enrollment
200
Locations
1
Primary Endpoint
Quality of life before and after adjuvant treatment in patients undergoing pulmonary resection
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

The goal of this prospective, observational study is to measure and analyze the effect of adjuvant treatment over the quality of life and recovery of patients undergoing pulmonary resection because of non-small cells lung cancer using the EORTC-LC29 questionnaire. The main question it aims to answer is:

Whether adjuvant systemic treatment affect or not the postoperative QOL of a NSCLC patient that underwent lung resection

Participants will fulfill two questionnaires (EORTC-LC29 and Hospital Anxiety and Depression Scale) in different stages of their treatment.

Detailed Description

Despite being surgery the preferred radical treatment of NSCLC in early stages, unforseen N2 disease, larger tumors or bad prognosis histological or molecular findings of the tumor will benefit of receiving adjuvant treatment. As an adjuvant treatment, postoperative platinum-based chemotherapy has demonstrated its efficacy in increasing survival rates and reducing recurrence rates. Postoperative radiotherapy (RT) is limited due to decreased lung tolerance following surgery and conflicting results. It is clear that lung cancer significantly impacts the quality of life of patients. According to the Lung Cancer Europe (LuCE) association, a survey conducted in 2021 with 515 patients revealed that 91.2% experienced limitations in their daily lives. Fatigue, sleep problems, cognitive difficulties, and significant reductions in physical activity were the main areas where patients reported the most complications. In addition to the inherent complications of cancer, we must consider the complications associated with surgery and systemic treatment. Module LC29 is an update of the previous module published by the European Organisation for Research and Treatment of Cancer (EORTC), providing a more current perspective on lung cancer. This latest module retains 12 out of the 13 items from LC13 and adds 17 new items, which gather information on the side effects of medical and targeted therapies, as well as emotional problems. Furthermore, it includes 5 specific questions related to lung surgery. This multidisciplinary approach currently makes the LC29 questionnaire the most comprehensive tool for studying the quality of life of lung cancer patients.

Registry
clinicaltrials.gov
Start Date
May 2024
End Date
January 2026
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Pablo Fernandez Salvador

Principal Investigator

University of Salamanca

Eligibility Criteria

Inclusion Criteria

  • Age: 50-85 years old
  • Patients with any histological type of non-small-cell lung cancer in clinical stage T1C N0M0 or greater
  • Patients that understand the purpose of the study, accept collaborate and sign the informed consent.

Exclusion Criteria

  • Patients not receiving adjuvant treatment due to complications, bad quality of life or express rejection at any moment of the curse of the process.
  • Patients who cannot complete the previous questionnaires to assess their quality of life

Outcomes

Primary Outcomes

Quality of life before and after adjuvant treatment in patients undergoing pulmonary resection

Time Frame: Pre-surgery, seven days after surgery, before the first dose of adjuvant treatment, 2 days after the first dose of adjuvant treatment, 2 days after finishing the whole cycle of adjuvant treatment

For quality of life assessment, patients will be asked to complete the Quality of Life Questionnaire Module LC29 (QLQ-LC29) of the European Organization for Research and Treatment of Cancer (EORTC).

Secondary Outcomes

  • Effect of complications from adjuvant treatment on the surgical items of the EORTC-LC29(Before the first dose of adjuvant treatment, 2 days after the first dose of adjuvant treatment, 2 days after finishing the whole cycle of adjuvant treatment)
  • Adjuvant chemotherapy/immunotherapy treatment regimen significantly decreases the quality of life(Before the first cycle of adjuvant treatment, 2 days after the first dose of adjuvant treatment, 2 days after finishing the whole cycle of adjuvant treatment)
  • Level of anxiety/depression in patients undergoing lung resection before and after receiving the first cycle of adjuvant treatment(Before the first dose of adjuvant treatment, 2 days after the first dose of adjuvant treatment, 2 days after finishing the whole cycle of adjuvant treatment)
  • Correlation between the type of surgical approach performed and postoperative quality of life(Before surgery, seven days after surgery)
  • Correlation between the occurrence of postoperative complications and a longer hospital stay(Before surgery, seven days after surgery, before the first dose of adjuvant treatment)
  • Effect of Performance Status (PS) and pre-adjuvant treatment ECOG on the quality of life after receiving the first cycle of any treatment modality.(Before the first dose of adjuvant treatment, 2 days after the first dose of adjuvant treatment, 2 days after finishing the whole cycle of adjuvant treatment)
  • Correlation between the type of surgical procedure performed and postoperative quality of life(Before surgery, seven days after surgery)
  • Correlation between the presence of Chronic Obstructive Pulmonary Disease (COPD) and postoperative quality of life(Before surgery, seven days after surgery, before the first dose of adjuvant treatment, 2 days after the first dose of adjuvant treatment, 2 days after finishing the whole cycle of adjuvant treatment)

Study Sites (1)

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