|Phase II Study of Hypofractionated Highly Conformal Radiotherapy With Helical Tomotherapy in Patients With Extracranial Oligometastases
First Published: 10/23/2007  Last Modified: 7/2/2010
Basic Trial Information
Trial Contact Information
Conformal Radiation Therapy in Treating Patients With Metastatic Cancer Outside the Brain
Basic Trial Information
|Phase II||Treatment||Completed||Over 18||NCI-07-C-0230|
NIH Clinical Center trial, NCI Web site featured trial
- To evaluate local control (defined as absence of local progression) at all treated sites of metastatic disease in patients with extracranial oligometastases treated with ablative doses of highly conformal radiotherapy delivered with helical tomotherapy.
- To evaluate local control at each treated site of metastatic disease in these patients.
- To determine median time to local progression in patients treated with this regimen.
- To evaluate interfraction and intrafraction motion with megavoltage CT imaging based on site of metastasis in these patients.
- To compare tumor growth during systemic therapy in tumors treated with targeted radiotherapy vs newly developed tumors that have not been treated with radiotherapy.
- To evaluate if treatment with hypofractionated highly conformal radiotherapy with helical tomotherapy can improve pain scores and decrease the need for analgesia in these patients.
- Pathologically confirmed cancer
- No active disease at the primary site as assessed by physical examination, clinical evaluation, or site-specific imaging
- Measurable metastatic disease meeting the following criteria:
- Four or fewer sites of extracranial lesions < 5 cm in size
- If metastatic site(s) is within the lung, the following criteria must be met:
- No more than two metastases in the proximal bronchial tree area (defined as 2 cm from the trachea or mainstem bronchi)
- DLCO > 30% predicted and FEV1 > 1.2 L (in patients with more than one metastatic site in the lungs)
- If metastatic site(s) is within 2 cm of either kidney, creatinine level must be < 1.5 times upper limit of normal (ULN)
- If metastatic site(s) is within 2 cm of the liver, bilirubin level must be < 1.5 times ULN
- Patients with metastatic disease that meets any of the following criteria are excluded:
- Proposed site(s) of treatment has been previously treated with radiotherapy
- Metastatic site(s) requires emergent treatment (e.g., spinal cord compression, cauda equina, airway compromise, or life-threatening end-organ dysfunction)
- Disease that is untreated or previously treated and progressive in the brain
- Pathologic fracture or impending pathologic fracture at the metastatic site
- Metastatic site(s) of a disease histology that is known to be sensitive to low doses of radiotherapy (e.g., pure seminoma, lymphoma, or small cell carcinoma)
- Patients in whom surgery is deemed an appropriate option as standard of care (e.g., isolated lung metastasis from sarcoma or isolated liver metastasis from colon cancer) but who refuse surgical therapy are eligible
- See Disease Characteristics
- More than 2 weeks since prior and no concurrent chemotherapy
- Prior or concurrent hormonal agents, including antiandrogens, gonadotropin-releasing hormone agonists, aromatase inhibitors, tamoxifen, or similar agents allowed
No change in systemic therapy for 6 weeks before or within 4 weeks after initiating study radiotherapy
- ECOG performance status 0-2
- Life expectancy > 12 weeks as assessed by the consulting radiation oncologist
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
- No history of lupus erythematosus or scleroderma
- No known hypersensitivity to therapeutic radiotherapy
- No other malignancy within the past 2 years except nonmelanoma skin cancer or in situ malignancies of the cervix, bladder, or head and neck
- No unrelated systemic illness that, in the judgment of the investigator, would compromise the patient’s ability to tolerate study therapy or would likely interfere with study procedures or results
- Able or likely to adhere to study treatment
6-month local control (i.e., complete response, partial response, or stable disease) at all treated sites of metastatic diseaseSecondary Outcome(s)
6-month local control at each treated site of metastatic disease
Median time to local progression
1-year local control at all treated sites of metastatic disease and at each treated site of metastatic disease
Interfraction and intrafraction motion based on site of metastasis
Alleviation of pain at sites of metastases as measured by the Brief Pain Inventory at 1 and 3 months after treatment
Comparison of tumor doubling times during systemic treatment in tumors treated with radiotherapy vs newly developed tumors that have not been treated with radiotherapy
Patients are stratified according to histology (renal cell carcinoma vs melanoma vs sarcoma vs other histologies).
Patients undergo hypofractionated highly conformal radiotherapy with helical tomotherapy once every other day over 5 days for a total of 3 fractions. Patients undergo megavoltage imaging before and after each fraction to verify the positioning of each target lesion.
Patients complete a pain assessment questionnaire at baseline and at 1 and 3 months after treatment.
After completion of study therapy, patients are followed at 1 and 3 months and then every 3 months for up to 1 year.
Trial Contact Information
Trial Lead Organizations
NCI - Center for Cancer Research
|Deborah Citrin, MD, Principal investigator|
Featured trial article
|Official Title|| ||A Phase II Study of Hypofractionated Highly Conformal Radiation with Helical Tomotherapy for Extra-Cranial Oligo|
|Trial Start Date|| ||2007-10-02|
|Trial Completion Date|| ||2010-05-06|
|Registered in ClinicalTrials.gov|| ||NCT00550654|
|Date Submitted to PDQ|| ||2007-10-02|
|Information Last Verified|| ||2009-06-07|
Note: The purpose of most clinical trials listed in this database is to test new cancer treatments, or new methods of diagnosing, screening, or preventing cancer. Because all potentially harmful side effects are not known before a trial is conducted, dose and schedule modifications may be required for participants if they develop side effects from the treatment or test. The therapy or test described in this clinical trial is intended for use by clinical oncologists in carefully structured settings, and may not prove to be more effective than standard treatment. A responsible investigator associated with this clinical trial should be consulted before using this protocol.