Stereotactic Body Radiation Therapy in Treating Patients With Stage I or Stage II Non-Small Cell Lung Cancer

Lung Cancer Clinical Trial

Official title:

A Phase I/II Study of Hypofractionated Stereotactic Body Radiotherapy for Stage I/II Non-small Cell Lung Cancer Within the Central Lung Region and the Prognostic Impact of FDG Positron Emission Tomography

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT00471835
• Other study ID #: CCCWFU-62206
• Secondary ID: CDR0000543743CCC
• Status: Withdrawn
• Phase: Phase 1/Phase 2
• First received: May 8, 2007
• Last updated: January 17, 2017
• Start date: January 2007

Study information

• Verified date: June 2013
• Source: Wake Forest University Health Sciences
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Stereotactic body radiation therapy may be able to send x-rays directly to the tumor and cause less damage to normal tissue.

PURPOSE: This phase I/II trial is studying the side effects and best dose of stereotactic body radiation therapy and to see how well it works in treating patients with stage I or stage II non-small cell lung cancer.

Description:

OBJECTIVES:

Primary

• Determine the maximum tolerated dose of hypofractionated stereotactic body radiotherapy (SBRT) to the central lung region (peri-mediastinum) in patients with stage I or II non-small cell lung cancer. (Phase I)

• Determine local control and time to local progression in patients treated with this regimen. (Phase II)

• Evaluate the ability of peak standardized uptake values (SUV) for fludeoxyglucose F 18 (FDG)-PET scan, obtained shortly after SBRT (post-treatment), to predict local control and time to progression in these patients.

Secondary

• Evaluate the ability of maximum SUV for FDG-PET scan, obtained shortly after SBRT, to predict long-term local control and time to progression in these patients.

• Evaluate the ability of peak SUV and max SUV for FDG-PET scan, obtained prior to SBRT, to predict local control and time to progression in these patients.

• Determine the utility of PET/CT scan data in guiding treatment planning.

• Determine if treatment with radiotherapy involving high biological doses with limited treatment volume using these SBRT techniques achieves acceptable treatment-related toxicity.

OUTLINE: This is a phase I dose-escalation study followed by a phase II open-label study.

• Phase I: Patients undergo hypofractionated stereotactic body radiotherapy (SBRT) 3 times within a 2-week time frame.

Cohorts of 3-6 patients receive escalating doses of hypofractionated SBRT until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.

• Phase II: Patients undergo hypofractionated SBRT at the MTD as in phase I. In both phases, patients undergo fludeoxyglucose F 18-PET/CT scans at baseline and at 12-16 weeks after completion of SBRT.

After completion of study treatment, patients are followed periodically for 4 years.

PROJECTED ACCRUAL: A total of 90 patients will be accrued for this study.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 120 Years

Eligibility

DISEASE CHARACTERISTICS:

• Histologically or cytologically confirmed stage I or II non-small cell lung cancer meeting the following criteria:

• No bronchoalveolar cell carcinoma

• Maximum T2 or T3 tumor size = 5 cm

• T3 primary tumor must be limited to chest wall

• Primary tumor of any T stage must be within or touching the zone of the trachea or proximal bronchial tree, defined as a volume of 2 cm in all directions around the trachea and proximal bronchial tree (carina, right and left main bronchi, right and left upper lobe bronchi, intermedius bronchi, right middle lobe bronchus, right and left lower lobe bronchi)

• For lesions inferior to the proximal bronchial tree, the primary tumor must be within 2 cm of the esophagus

• Patients with N1 (hilar) lymph nodes positive for malignancy based on size, fludeoxyglucose F 18 (FDG)-PET scan uptake, or biopsy are eligible if the N1 lymph nodes are located such that they are contiguously within the same stereotactic radiation treatment field as the primary tumor

• Mediastinal lymph nodes must be = 1 cm and no abnormal uptake on FDG-PET scan in those areas

• Patients with > 1 cm lymph nodes or abnormal FDG-PET scan (including suspicious but non-diagnostic uptake) are eligible if directed tissue biopsy of all abnormally identified areas are negative for cancer

• No evidence of distant metastases

• Suspected M1 disease based on pre-treatment PET imaging must be biopsied

• If the biopsy is positive, the patient is ineligible

• If the biopsy is negative and representative of the lesion in question, the patient is eligible

• If the biopsy is non-diagnostic, consideration should be given to repeat biopsy

• If the repeat biopsy remains non-diagnostic or a biopsy is not feasible, then the patient is ineligible

• Technically resectable disease

• Surgery refused or patient deemed medically inoperable due to co-morbid conditions

PATIENT CHARACTERISTICS:

• Zubrod performance status 0-2

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

• No synchronous primary or invasive malignancy within the past 2 years other than non-melanomatous skin cancer

• No active systemic, pulmonary, or pericardial infection

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics

• No prior chest radiotherapy (lung or mediastinum)

• No other concurrent anticancer therapy, including other radiotherapy, radiofrequency ablation (or other antineoplastic interventional radiology techniques), chemotherapy, biological therapy, vaccine therapy, or surgery

Related Conditions & MeSH terms

• Carcinoma, Non-Small-Cell Lung
• Lung Cancer
• Lung Neoplasms

Intervention

Procedure:
• computed tomography

• positron emission tomography

Radiation:
• stereotactic body radiation therapy

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
Wake Forest University Health Sciences	National Cancer Institute (NCI)

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum tolerated dose (Phase I)
Primary	Time to progression and local control at 1 and 2 years (Phase II)
Secondary	Rate of acute and late treatment-related toxicity related to specific symptoms, including gastrointestinal, cardiac, neurologic, hemorrhagic, and pulmonary symptoms
Secondary	Toxicity
Secondary	Patterns of failure and overall survival at 2 years
Secondary	Measurement of pre-treatment and post-treatment PET scan standardized uptake values and correlation of this data with local control at 1 and 2 years