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Radiation Therapy in Treating Patients With Stage I Non-Small Cell Lung Cancer And Lung Dysfunction

Phase 1
Completed
Conditions
Lung Cancer
Interventions
Radiation: accelerated conformational radiotherapy
Registration Number
NCT00009789
Lead Sponsor
Alliance for Clinical Trials in Oncology
Brief Summary

RATIONALE: Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue.

PURPOSE: Phase I trial to study the effectiveness of specialized high-dose radiation therapy in treating patients who have stage I non-small cell lung cancer and lung dysfunction.

Detailed Description

OBJECTIVES:

* Determine the maximum tolerated course of accelerated 3-dimensional conformal radiotherapy in patients with stage I non-small cell lung cancer with pulmonary dysfunction.

* Determine the short-term and long-term toxicity of this regimen in these patients.

* Determine local tumor control, failure-free survival, and overall survival in patients treated with this regimen.

* Determine the effect of radiotherapy dose volume relationships and pre-treatment pulmonary function studies on the incidence of pulmonary toxicity in these patients.

OUTLINE: This is a dose-escalation, multicenter study.

Patients receive accelerated 3-dimensional (3-D) conformal radiotherapy daily 5 days a week for 3.5-6 weeks.

Cohorts of 8 patients receive escalating fractions of accelerated 3-D conformal radiotherapy until the maximum tolerated course is determined. The maximum tolerated course is defined as the course at which no more than 2 patients develop at least grade 3 dose-limiting toxicity and no more than 1 patient develops at least grade 4 dose-limiting toxicity.

Patients are followed at 3 weeks, 6 weeks, 3 months, every 3 months for 2 years, and then every 6 months for 3 years.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
39
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Radiotherapyaccelerated conformational radiotherapyPatients receive accelerated 3-dimensional (3-D) conformal radiotherapy daily 5 days a week for 3.5-6 weeks. Cohorts of 8 patients receive escalating fractions of accelerated 3-D conformal radiotherapy until the maximum tolerated course is determined. The maximum tolerated course is defined as the course at which no more than 2 patients develop at least grade 3 dose-limiting toxicity and no more than 1 patient develops at least grade 4 dose-limiting toxicity. Patients are followed at 3 weeks, 6 weeks, 3 months, every 3 months for 2 years, and then every 6 months for 3 years.
Primary Outcome Measures
NameTimeMethod
Overall survivalUp to 5 years
Failure-free survivalUp to 5 years
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (20)

Memorial Cancer Institute at Memorial Regional Hospital

🇺🇸

Hollywood, Florida, United States

St. Joseph's Hospital Health Center - Syracuse

🇺🇸

Syracuse, New York, United States

Arthur G. James Cancer Hospital and Solove Research Institute at Ohio State University

🇺🇸

Columbus, Ohio, United States

University of Chicago Cancer Research Center

🇺🇸

Chicago, Illinois, United States

Fairview University Medical Center - University Campus

🇺🇸

Minneapolis, Minnesota, United States

Comprehensive Cancer Center at Wake Forest University

🇺🇸

Winston-Salem, North Carolina, United States

Michael & Dianne Bienes Comprehensive Cancer Center at Holy Cross Hospital

🇺🇸

Fort Lauderdale, Florida, United States

CCOP - Mount Sinai Medical Center

🇺🇸

Miami Beach, Florida, United States

Ella Milbank Foshay Cancer Center at Jupiter Medical Center

🇺🇸

Jupiter, Florida, United States

UNMC Eppley Cancer Center at the University of Nebraska Medical Center

🇺🇸

Omaha, Nebraska, United States

Saint Francis Cancer Treatment Center at Saint Francis Memorial Health Center

🇺🇸

Grand Island, Nebraska, United States

Great Plains Regional Medical Center

🇺🇸

North Platte, Nebraska, United States

Oswego Hospital

🇺🇸

Oswego, New York, United States

CCOP - Syracuse Hematology-Oncology Associates of Central New York, P.C.

🇺🇸

Syracuse, New York, United States

SUNY Upstate Medical University Hospital

🇺🇸

Syracuse, New York, United States

Veterans Affairs Medical Center - Buffalo

🇺🇸

Buffalo, New York, United States

Blumenthal Cancer Center at Carolinas Medical Center

🇺🇸

Charlotte, North Carolina, United States

Wayne Memorial Hospital, Incorporated

🇺🇸

Goldsboro, North Carolina, United States

Western Pennsylvania Cancer Institute at Western Pennsylvania Hospital

🇺🇸

Pittsburgh, Pennsylvania, United States

Saint Luke's Hospital

🇺🇸

Chesterfield, Missouri, United States

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