Prophylactic Inhaled Steroids to Reduce Radiation Pneumonitis Frequency and Severity in Non-small Cell Lung Cancer Patients

Who is this study for? Patients with non-small cell lung cancer with inoperable locally advanced or metastatic disease
What treatments are being studied? Inhaled budesonide
Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This randomized clinical study aims to assess whether prophylactic treatment with inhaled steroids in patients with locally advanced or concomitantly treated non-small cell lung carcinoma who are candidates for combination treatment with QT/RT or IMT + QT/RT. The main questions it aims to answer are: Whether prophylactic treatment decreases the severity of NPR on CTCAE v4.0 and RTOG scales. Whether inhaled steroid use modifies the response to radiation therapy treatment compared to patients who do not receive prophylactic inhaled steroids.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Patients with non-small cell lung cancer (NSCLC) with unresectable locally advanced or metastatic disease (IIIA, IIIB or IV) of the classification tumor node, metastasis (TNM) of malignant lung tumors, 7th edition.

• NSCLC patients candidates for concomitant treatment (chemotherapy plus radiotherapy or target therapy plus radiotherapy).

• Evidence of measurable disease

• Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2, Karnofsky 70-100.

• Life expectancy of \> 4 months at the time of screening

• Patients with the ability to comply with the study and follow-up procedures.

• Patients with previous surgery less than four weeks.

• Must be willing and able to give signed informed consent and, in the opinion of the Investigator, to comply with the protocol tests and procedures.

Locations
Other Locations
Mexico
Instituto Nacional de Cancerologia
RECRUITING
Mexico City
Instituto Nacional de Enfermedades Respiratorias
ACTIVE_NOT_RECRUITING
Mexico City
Contact Information
Primary
Oscar Arrieta, MD MSc
ogarrieta@gmail.com
015556280400
Backup
Diana Flores
clinicacancerpulmonincan@gmail.com
015556280400
Time Frame
Start Date: 2018-09-01
Estimated Completion Date: 2025-12-01
Participants
Target number of participants: 72
Treatments
Experimental: QT/RT + Budesonide
Patients are receiving chemotherapy (QT) and radiotherapy (RT) plus inhaled Budesonide with space chamber at 400 mcg given twice daily initiating after the first dose of RT and continuing until pneumonitis development or 12 months completed.
No_intervention: QT/RT + No medication
Patients are receiving chemotherapy (QT) and radiotherapy (RT) without intervention therapy and followed during 12 months.
Experimental: Target drug/RT + Budesonide
Patients are receiving target therapy and radiotherapy (RT) plus inhaled Budesonide with space chamber at 400 mcg given twice daily initiating after the first dose of RT and continuing until pneumonitis development or 12 months completed.
No_intervention: Target drug/RT + No medication
Patients are receiving target treatment and radiotherapy (RT) without intervention therapy and followed during 12 months.
Sponsors
Leads: Instituto Nacional de Cancerologia de Mexico
Collaborators: Instituto Nacional de Enfermedades Respiratorias

This content was sourced from clinicaltrials.gov