search
Back to results

Hypofractionated 3-Dimensional Radiation Therapy in Treating Patients With Newly Diagnosed Stage I, Stage II, or Stage III Non-Small Cell Lung Cancer. ICORG 99-09

Primary Purpose

Lung Cancer

Status
Completed
Phase
Phase 2
Locations
Ireland
Study Type
Interventional
Intervention
hypofractionated radiation therapy
Sponsored by
Cancer Trials Ireland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lung Cancer focused on measuring stage I non-small cell lung cancer, stage II non-small cell lung cancer, stage IIIA non-small cell lung cancer, stage IIIB non-small cell lung cancer

Eligibility Criteria

undefined - 120 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

DISEASE CHARACTERISTICS:

  • Histologically or cytologically confirmed newly diagnosed non-small cell lung cancer meeting 1 of the following stage criteria:

    • Stage I or II disease

      • Medically inoperable or patient refused surgery
    • Stage IIIA or IIIB disease (no pleural effusions)
  • Radiation dose parameters must satisfy the required study dose-volume constraints

PATIENT CHARACTERISTICS:

  • Karnofsky performance status 70-100%
  • Weight loss ≤ 10% within 3 months before diagnosis
  • No other malignancy within the past 5 years, except nonmelanoma skin cancer
  • No clinically significant cardiovascular disease (e.g., hypertension [blood pressure > 150/100 mm Hg], myocardial infarction or stroke within the past 6 months, or unstable angina)

PRIOR CONCURRENT THERAPY:

  • No concurrent chemotherapy

Sites / Locations

  • Saint Luke's Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Group 1

Group 2

Group 3

Arm Description

Patients undergo hypofractionated 3-dimensional conformal radiotherapy 5 days a week for 24 fractions (total of 72 Gy).

Patients undergo hypofractionated 3-dimensional conformal radiotherapy 5 days a week for 22 fractions (total of 66 Gy).

Patients undergo hypofractionated 3-dimensional conformal radiotherapy 5 days a week for 20 fractions (total of 60 Gy).

Outcomes

Primary Outcome Measures

Acute radio-induced toxicity as assessed by the RTOG/EORTC acute toxicity grading system weekly during radiotherapy
Long-term radio-induced toxicity as assessed by the long-term RTOG/EORTC and SWOG (lung) grading system every 3 months for 2 years and then every 6 months thereafter

Secondary Outcome Measures

Tumor response rate (according to WHO response criteria) as assessed by CT scan at 3 months after completion of radiotherapy
Actuarial freedom from thoracic progression rate

Full Information

First Posted
August 6, 2009
Last Updated
February 15, 2016
Sponsor
Cancer Trials Ireland
search

1. Study Identification

Unique Protocol Identification Number
NCT00955175
Brief Title
Hypofractionated 3-Dimensional Radiation Therapy in Treating Patients With Newly Diagnosed Stage I, Stage II, or Stage III Non-Small Cell Lung Cancer. ICORG 99-09
Official Title
Radiation Dose Escalation For Non-Small Cell Lung Cancer Using Hypofractionated 3-Dimensional Conformal Radiation Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Completed
Study Start Date
November 2000 (undefined)
Primary Completion Date
June 2009 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Cancer Trials Ireland

4. Oversight

5. Study Description

Brief Summary
RATIONALE: Specialized radiation therapy that delivers a high dose of radiation directly to the tumor over a shorter period of time may kill more tumor cells and cause less damage to normal tissue. PURPOSE: This phase II trial is studying the side effects of hypofractionated 3-dimensional radiation therapy and to see how well it works in treating patients with newly diagnosed stage I, stage II, or stage III non-small cell lung cancer.
Detailed Description
OBJECTIVES: Primary To evaluate the acute and long-term radio-induced toxicity (any organ) of hypofractionated 3-dimensional conformal radiotherapy in patients with newly diagnosed stage I-III non-small cell lung cancer. Secondary To assess the radiological tumor response rate at 3 months after completion of radiotherapy. To assess the actuarial freedom from thoracic progression rate. OUTLINE: Patients are stratified according to combined lung volume at 25 Gy (≤ 30% vs > 30%). Patients are assigned to 1 of 3 treatment groups. Group 1: Patients undergo hypofractionated 3-dimensional conformal radiotherapy 5 days a week for 24 fractions (total of 72 Gy). Group 2: Patients undergo hypofractionated 3-dimensional conformal radiotherapy 5 days a week for 22 fractions (total of 66 Gy). Group 3: Patients undergo hypofractionated 3-dimensional conformal radiotherapy 5 days a week for 20 fractions (total of 60 Gy). After completion of study treatment, patients are followed up every 3 months for 2 years and then every 6 months thereafter.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Cancer
Keywords
stage I non-small cell lung cancer, stage II non-small cell lung cancer, stage IIIA non-small cell lung cancer, stage IIIB non-small cell lung cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group 1
Arm Type
Experimental
Arm Description
Patients undergo hypofractionated 3-dimensional conformal radiotherapy 5 days a week for 24 fractions (total of 72 Gy).
Arm Title
Group 2
Arm Type
Experimental
Arm Description
Patients undergo hypofractionated 3-dimensional conformal radiotherapy 5 days a week for 22 fractions (total of 66 Gy).
Arm Title
Group 3
Arm Type
Experimental
Arm Description
Patients undergo hypofractionated 3-dimensional conformal radiotherapy 5 days a week for 20 fractions (total of 60 Gy).
Intervention Type
Radiation
Intervention Name(s)
hypofractionated radiation therapy
Intervention Description
Given 5 days a week for 20, 22, or 24 fractions
Primary Outcome Measure Information:
Title
Acute radio-induced toxicity as assessed by the RTOG/EORTC acute toxicity grading system weekly during radiotherapy
Time Frame
weekly during radiotherapy
Title
Long-term radio-induced toxicity as assessed by the long-term RTOG/EORTC and SWOG (lung) grading system every 3 months for 2 years and then every 6 months thereafter
Time Frame
every 3 months for 2 years and then every 6 months thereafter
Secondary Outcome Measure Information:
Title
Tumor response rate (according to WHO response criteria) as assessed by CT scan at 3 months after completion of radiotherapy
Time Frame
at 3 months after completion of radiotherapy
Title
Actuarial freedom from thoracic progression rate
Time Frame
ongoing

10. Eligibility

Sex
All
Maximum Age & Unit of Time
120 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Histologically or cytologically confirmed newly diagnosed non-small cell lung cancer meeting 1 of the following stage criteria: Stage I or II disease Medically inoperable or patient refused surgery Stage IIIA or IIIB disease (no pleural effusions) Radiation dose parameters must satisfy the required study dose-volume constraints PATIENT CHARACTERISTICS: Karnofsky performance status 70-100% Weight loss ≤ 10% within 3 months before diagnosis No other malignancy within the past 5 years, except nonmelanoma skin cancer No clinically significant cardiovascular disease (e.g., hypertension [blood pressure > 150/100 mm Hg], myocardial infarction or stroke within the past 6 months, or unstable angina) PRIOR CONCURRENT THERAPY: No concurrent chemotherapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pierre Thirion, MD
Organizational Affiliation
Saint Luke's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Saint Luke's Hospital
City
Dublin
ZIP/Postal Code
6
Country
Ireland

12. IPD Sharing Statement

Learn more about this trial

Hypofractionated 3-Dimensional Radiation Therapy in Treating Patients With Newly Diagnosed Stage I, Stage II, or Stage III Non-Small Cell Lung Cancer. ICORG 99-09

We'll reach out to this number within 24 hrs