MedPath

Interstitial Brachytherapy With or Without External-Beam Radiation Therapy in Treating Patients With Prostate Cancer

Phase 3
Completed
Conditions
Prostate Cancer
Interventions
Radiation: Brachytherapy (125/145)
Radiation: Brachytherapy (100/110)
Radiation: External Beam Radiation Therapy
Registration Number
NCT00063882
Lead Sponsor
Radiation Therapy Oncology Group
Brief Summary

RATIONALE: Radiation therapy uses high-energy x-rays and other sources to damage tumor cells. Interstitial brachytherapy uses radioactive material placed directly into or near a tumor to kill tumor cells. Combining interstitial brachytherapy with external-beam radiation therapy may kill more tumor cells. It is not yet known whether interstitial brachytherapy is more effective with or without external-beam radiation therapy in treating prostate cancer.

PURPOSE: Randomized phase III trial to compare the effectiveness of interstitial brachytherapy with or without external-beam radiation therapy in treating patients who have prostate cancer.

Detailed Description

OBJECTIVES:

* Compare the 5-year freedom from progression in patients with intermediate-risk prostate cancer treated with interstitial brachytherapy with or without external beam radiotherapy (EBRT).

* Compare biochemical (i.e., prostate-specific antigen) failure, biochemical failure by the Phoenix definition, disease-specific survival, local progression, and distant metastases in patients treated with these regimens.

* Compare morbidity and quality of life of patients treated with these regimens.

* Determine the feasibility of collecting Medicare data in a large Radiation Therapy Oncology Group (RTOG) prostate cancer clinical trial for cost effectiveness and cost utility analysis of combined treatment with interstitial brachytherapy and EBRT.

* Prospectively collect diagnostic biopsy samples from these patients for future biomarker analyses.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to disease stage (T1c vs T2a or T2b), Gleason score (≤ 6 vs 7), prostate-specific antigen (\< 10 ng/mL vs 10-20 ng/mL), and prior neoadjuvant hormonal therapy (yes vs no). Patients are randomized to 1 of 2 treatment arms.

* Arm I: Patients undergo external beam radiotherapy 5 days a week for 5 weeks. Within 2-4 weeks of radiotherapy, patients undergo interstitial brachytherapy with iodine I 125 or palladium Pd 103 seeds.

* Arm II: Patients undergo interstitial brachytherapy only, as in arm I. Quality of life is assessed at baseline, at 4, 12, and 24 months, and then annually for 3 years.

After completion of study treatment, patients are followed at 3-5 weeks, at 4, 6, 9, and 12 months, every 6 months for 4 years, and then annually thereafter.

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
588
Inclusion Criteria

Not provided

Read More
Exclusion Criteria

Not provided

Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Brachytherapy OnlyBrachytherapy (125/145)Transperineal interstitial permanent brachytherapy (125/145)
EBRT + BrachytherapyBrachytherapy (100/110)External beam radiation therapy (EBRT) and transperineal interstitial permanent brachytherapy (100/110)
EBRT + BrachytherapyExternal Beam Radiation TherapyExternal beam radiation therapy (EBRT) and transperineal interstitial permanent brachytherapy (100/110)
Primary Outcome Measures
NameTimeMethod
5-Year Freedom From Progression RateFrom randomization to 5 years

A Freedom from Progression (FFP) failure includes biochemical failure, local failure, distant failure, or death due to any cause. Patients who are failure free with less than 5 years of follow-up or who receive any secondary salvage therapy are censored. Freedom from Progression rates are estimated using the Kaplan-Meier method.

Secondary Outcome Measures
NameTimeMethod
Biochemical Failure Rate (Protocol Definition)From randomization to last follow-up. Analysis occurs after all patients have been potentially followed for 5 years. Maximum follow-up at time of analysis was 13.9 years.

Biochemical failure is defined as having 3 consecutive rises of post-treatment PSA or starting hormones after one or more elevations in post-treatment PSA but before 3 consecutive elevations are documented. The sum of the 3 consecutive rises must exceed 1 ng/mL above the nadir. If 3 consecutive PSA rises occur during the first 24 months followed by a subsequent non-hormonal induced PSA decrease, patients will not be considered PSA failures. Three consecutive rises with any of the 3 PSA values occurring more than 24 months after the implant procedure will constitute a failure. Time to biochemical is defined as time from randomization to the date of first biochemical failure, last known follow-up (censored), or death without biochemical failure (competing risk). Biochemical failure rates are estimated using the cumulative incidence method. Five year rates are reported.

Distant MetastasesFrom randomization to last follow-up. Analysis occurs after all patients have been potentially followed for 5 years. Maximum follow-up at time of analysis was 13.9 years.

Failure is defined as the appearance of any distant metastases. Time to distant metastases is defined as time from randomization to the date of first distant metastases, last known follow-up (censored), or death without distant metastases (competing risk). Distant metastases rates are estimated using the cumulative incidence method. Five year rates are reported.

Time to Late Grade 3+ Toxicities [Genitourinary (GU), Gastrointestinal (GI), and Overall]From 181 days after the start of radiation to last follow-up. Maximum follow-up at time of analysis was 13.9 years.

Late toxicities are scored according to the Radiation Therapy Oncology Group (RTOG)/European Organisation for Research and Treatment of Cancer (EORTC) Late Radiation Morbidity Scoring Scheme and will be defined as the worst severity of the toxicity occurring \> 180 days from radiation start. Grade 3+ GU/GI and overall were analyzed. RTOG/EORTC Late Radiation Morbidity Scoring Scheme assigns Grades 1 through 5 with unique clinical descriptions of severity for each toxicity based on this general guideline: Grade 1 Mild, Grade 2 Moderate, Grade 3 Severe, Grade 4 Life-threatening or disabling, Grade 5 Death related to toxicity. Time to late grade 3+ toxicity is defined as time from randomization to the date of first late grade 3+ toxicity, last known follow-up (censored), or death without late grade 3+ toxicity (competing risk). Late grade 3+ toxicity rates are estimated using the cumulative incidence method. Five year rates are reported.

Change in Total American Urological Association Symptom Index (AUA-SI) Score From Baseline to 24 MonthsBaseline and 24 months after start of radiation

The AUA-SI is a validated 7-item measure used to assess urinary symptoms. A higher score indicates more severe symptoms for the individual questions and overall total. Six questions ask about frequency of symptoms over the past month with possible responses: 0= Not at all; 1 = Less than 1 time in 5; 2 = less than half the time, 3 = About half the time, 4 = More than half the time, 5 = Almost always. An additional question asks the number of times one gets up to urinate after going to bed, with response indicating the exact number of times ranging from 0 to 5. The total score is the sum of the questions and ranges from 0 to 35. Change is calculated as follow-up timepoint score - baseline score such that a negative change reflects an improvement at the follow-up timepoint and a positive change reflects a decline at the follow-up timepoint.

Local FailureFrom randomization to last follow-up. Analysis occurs after all patients have been potentially followed for 5 years. Maximum follow-up at time of analysis was 13.9 years.

Failure is defined as progression (increase in palpable abnormality) at any time, failure of regression of the palpable tumor by two years, and redevelopment of a palpable abnormality after complete disappearance of previous abnormalities. Histologic criteria for local failure are presence of prostatic carcinoma upon biopsy and positive biopsy of the palpably normal prostate more than two years after the start of treatment. Time to local failure is defined as time from randomization to the date of first local failure, last known follow-up (censored), or death without local failure (competing risk). Local failure rates are estimated using the cumulative incidence method. Five year rates are reported.

Overall SurvivalFrom randomization to last follow-up. Analysis occurs after all patients had been on study for at least 5 years. Maximum follow-up at time of analysis was 13.9 years.

Failure is defined as death due to any cause. Overall survival time is defined as time from randomization to the date of death or last known follow-up (censored). Survival rates are estimated using the Kaplan-Meier method. Five year rates are reported.

Percentage of Patients With Acute Grade 2+ and Grade 3+ Toxicities [Genitourinary (GU), Gastrointestinal (GI), and Overall]Zero to 180 days from the start of radiation

Acute toxicities are scored according to NCI Common Toxicity Criteria (CTC) version 2.0 and will be defined as the worst severity of the toxicity occurring ≤ 180 days from start of radiation. The CTC v 2.0 assigns Grades 1 through 5 with unique clinical descriptions of severity for each toxicity based on this general guideline: Grade 1 Mild, Grade 2 Moderate, Grade 3 Severe, Grade 4 Life-threatening or disabling, Grade 5 Death related to based.

Change in Expanded Prostate Cancer Index Composite (EPIC) From Baseline to 24 MonthsBaseline and 24 months after start of radiation

The EPIC form is a 50-item, validated tool to assess disease-specific aspects of prostate cancer and its therapies and comprises of four summary domains (bowel, urinary, sexual, and hormonal function). The urinary domain summary score can be separated into 2 distinct subscales: urinary incontinence and urinary irritative. Hormonal domain was excluded as concurrent use of hormones was exclusionary and prior neoadjuvant hormone use was low. Response options for each EPIC item form a Likert scale and multi-item scale scores are transformed linearly to a 0-100 scale, with higher scores representing better health related quality of life. The change score was calculated as the value at 24 months minus the value at baseline. A negative change reflects a decline at 24 months and a positive change reflects an improvement at 24 months.

Change in European Quality of Life-5 Domains (EQ-5D) From Baseline to 4 MonthsBaseline and 4 months after start of radiation

The EQ-5D is a 2-part self-assessment questionnaire. First part is 5 items (mobility, self care, usual activities, pain/discomfort, anxiety/depression) each with 3 problem levels (1-none, 2-moderate, 3-extreme). The 5-item index score is transformed into a utility score between 0 (worst health state) and 1 (best health state). The 2nd part is a visual analogue scale (VAS) valuing current health state, measured on a 20-cm scale ranging from 0 for the worst imaginable health state to 100 for best imaginable health state, marked at 10-point intervals. The change score was calculated as the value at the follow-up timepoint minus the value at baseline. A negative change reflects a decline at the follow-up timepoint and a positive change reflects an improvement at the follow-up timepoint.

Biochemical Failure (Phoenix Definition)From randomization to last follow-up. Analysis occurs after all patients have been potentially followed for 5 years.Maximum follow-up at time of analysis was 13.9 years.

Biochemical Failure is defined as an increase of 2 ng/ml or more in PSA over the nadir PSA after 24 months from the start of treatment or the start of salvage hormones. Time to biochemical is defined as time from randomization to the date of first biochemical failure, last known follow-up (censored), or death without biochemical failure (competing risk). Biochemical failure rates are estimated using the cumulative incidence method. Five year rates are reported.

Prostate Cancer DeathFrom randomization to last follow-up. Analysis occurs after all patients have been potentially followed for 5 years. Maximum follow-up at time of analysis was 13.9 years.

Prostate cancer death is defined as death due to prostate cancer or complications of treatment or death associated with any of the following: 1) further clinical tumor progression occurring after initiation of salvage androgen suppression therapy; 2) a rise that exceeds 1.0 ng/ml in the serum PSA level on at least two consecutive occasions that occurs during or after salvage androgen suppression therapy; and 3) disease progression in the absence of any anti-tumor therapy. Time to prostate cancer death is defined as time from randomization to the date of prostate cancer death, last known follow-up (censored), or death without prostate cancer (competing risk). Prostate cancer death rates are estimated using the cumulative incidence method. Five year rates are reported.

Change in Expanded Prostate Cancer Index Composite (EPIC) From Baseline to 4 MonthsBaseline and 4 months after start of radiation

The EPIC form is a 50-item, validated tool to assess disease-specific aspects of prostate cancer and its therapies and comprises of four summary domains (bowel, urinary, sexual, and hormonal function). The urinary domain summary score can be separated into 2 distinct subscales: urinary incontinence and urinary irritative. Hormonal domain was excluded as concurrent use of hormones was exclusionary and prior neoadjuvant hormone use was low. Response options for each EPIC item form a Likert scale and multi-item scale scores are transformed linearly to a 0-100 scale, with higher scores representing better health related quality of life. The change score was calculated as the value at 4 months minus the value at baseline. A negative change reflects a decline at 4 months and a positive change reflects an improvement at 4 months.

Change in European Quality of Life-5 Domains (EQ-5D) From Baseline to 24 MonthsBaseline and 24 months after start of radiation

The EQ5D is a 2-part self-assessment questionnaire. First part is 5 items (mobility, self care, usual activities, pain/discomfort, anxiety/depression) each with 3 problem levels (1-none, 2-moderate, 3-extreme). The 5-item index score is transformed into a utility score between 0 (worst health state) and 1 (best health state). The 2nd part is a visual analogue scale (VAS) valuing current health state, measured on a 20-cm scale ranging from 0 for the worst imaginable health state to 100 for best imaginable health state, marked at 10-point intervals. The change score was calculated as the value at the follow-up timepoint minus the value at baseline. A negative change reflects a decline at the follow-up timepoint and a positive change reflects an improvement at the follow-up timepoint.

Change in Total American Urological Association Symptom Index (AUA-SI) Score From Baseline to 4 MonthsBaseline and 4 months after start of radiation

The AUA-SI is a validated 7-item measure used to assess urinary symptoms. A higher score indicates more severe symptoms for the individual questions and overall total. Six questions ask about frequency of symptoms over the past month with possible responses: 0= Not at all; 1 = Less than 1 time in 5; 2 = less than half the time, 3 = About half the time, 4 = More than half the time, 5 = Almost always. An additional question asks the number of times one gets up to urinate after going to bed, with response indicating the exact number of times ranging from 0 to 5. The total score is the sum of the questions and ranges from 0 to 35. Change is calculated as follow-up timepoint score - baseline score such that a negative change reflects an improvement at the follow-up timepoint and a positive change reflects a decline at the follow-up timepoint.

Trial Locations

Locations (169)

Contra Costa Regional Medical Center

🇺🇸

Martinez, California, United States

Kaiser Permanente Medical Center - Redwood City

🇺🇸

Redwood City, California, United States

Heartland Regional Medical Center

🇺🇸

Saint Joseph, Missouri, United States

Saint Joseph Oncology, Incorporated

🇺🇸

Saint Joseph, Missouri, United States

CCOP - Columbus

🇺🇸

Columbus, Ohio, United States

Grant Medical Center Cancer Care

🇺🇸

Columbus, Ohio, United States

Mount Carmel Health - West Hospital

🇺🇸

Columbus, Ohio, United States

Doctors Hospital at Ohio Health

🇺🇸

Columbus, Ohio, United States

Geisinger Cancer Institute at Geisinger Health

🇺🇸

Danville, Pennsylvania, United States

Fox Chase Cancer Center - Philadelphia

🇺🇸

Philadelphia, Pennsylvania, United States

Northwest Ohio Oncology Center

🇺🇸

Maumee, Ohio, United States

Cancer Care Center, Incorporated

🇺🇸

Salem, Ohio, United States

Val and Ann Browning Cancer Center at McKay-Dee Hospital Center

🇺🇸

Ogden, Utah, United States

Fredericksburg Oncology, Incorporated

🇺🇸

Fredericksburg, Virginia, United States

M. D. Anderson Cancer Center at University of Texas

🇺🇸

Houston, Texas, United States

Fox Chase Virtua Health Cancer Program at Virtua West Jersey

🇺🇸

Voorhees, New Jersey, United States

New York Methodist Hospital

🇺🇸

Brooklyn, New York, United States

Franciscan Cancer Center at St. Joseph Medical Center

🇺🇸

Tacoma, Washington, United States

CCOP - Nevada Cancer Research Foundation

🇺🇸

Las Vegas, Nevada, United States

Kaiser Permanente Medical Center - San Francisco Geary Campus

🇺🇸

San Francisco, California, United States

UCSF Helen Diller Family Comprehensive Cancer Center

🇺🇸

San Francisco, California, United States

California Pacific Medical Center - California Campus

🇺🇸

San Francisco, California, United States

Utah Cancer Specialists at UCS Cancer Center

🇺🇸

Salt Lake City, Utah, United States

LDS Hospital

🇺🇸

Salt Lake City, Utah, United States

Auburn Radiation Oncology

🇺🇸

Auburn, California, United States

Arizona Oncology Services Foundation

🇺🇸

Phoenix, Arizona, United States

Alta Bates Summit Comprehensive Cancer Center

🇺🇸

Berkeley, California, United States

Mercy Cancer Center at Mercy San Juan Medical Center

🇺🇸

Carmichael, California, United States

East Bay Radiation Oncology Center

🇺🇸

Castro Valley, California, United States

Peninsula Medical Center

🇺🇸

Burlingame, California, United States

Radiation Oncology Centers - Cameron Park

🇺🇸

Cameron Park, California, United States

Valley Medical Oncology Consultants - Castro Valley

🇺🇸

Castro Valley, California, United States

Valley Medical Oncology

🇺🇸

Fremont, California, United States

Kaiser Permanente Medical Center - Hayward

🇺🇸

Hayward, California, United States

El Camino Hospital Cancer Center

🇺🇸

Mountain View, California, United States

Sutter Health - Western Division Cancer Research Group

🇺🇸

Novato, California, United States

Alta Bates Summit Medical Center - Summit Campus

🇺🇸

Oakland, California, United States

Bay Area Breast Surgeons, Incorporated

🇺🇸

Oakland, California, United States

CCOP - Bay Area Tumor Institute

🇺🇸

Oakland, California, United States

Kaiser Permanente - Division of Research - Oakland

🇺🇸

Oakland, California, United States

Larry G Strieff MD Medical Corporation

🇺🇸

Oakland, California, United States

Tom K Lee, Incorporated

🇺🇸

Oakland, California, United States

Kaiser Permanente Medical Center - Oakland

🇺🇸

Oakland, California, United States

Kaiser Permanente Medical Center - Rancho Cordova

🇺🇸

Rancho Cordova, California, United States

Kaiser Permanente Medical Center - Richmond

🇺🇸

Richmond, California, United States

Rohnert Park Cancer Center

🇺🇸

Rohnert Park, California, United States

Radiation Oncology Center - Roseville

🇺🇸

Roseville, California, United States

Kaiser Permanente Medical Center - Roseville

🇺🇸

Roseville, California, United States

Kaiser Permanente Medical Center - Santa Teresa

🇺🇸

San Jose, California, United States

Kaiser Permanente Medical Center - Santa Rosa

🇺🇸

Santa Rosa, California, United States

Kaiser Permanente Medical Center - Santa Clara Kiely Campus

🇺🇸

Santa Clara, California, United States

Kaiser Foundation Hospital - San Rafael

🇺🇸

San Rafael, California, United States

Kaiser Permanente Medical Facility - Stockton

🇺🇸

Stockton, California, United States

Solano Radiation Oncology Center

🇺🇸

Vacaville, California, United States

Sutter Solano Medical Center

🇺🇸

Vallejo, California, United States

Saint Francis/Mount Sinai Regional Cancer Center at Saint Francis Hospital and Medical Center

🇺🇸

Hartford, Connecticut, United States

Kaiser Permanente Medical Center - Walnut Creek

🇺🇸

Walnut Creek, California, United States

CCOP - Christiana Care Health Services

🇺🇸

Newark, Delaware, United States

Sibley Memorial Hospital

🇺🇸

Washington, District of Columbia, United States

Michael and Dianne Bienes Comprehensive Cancer Center at Holy Cross Hospital

🇺🇸

Fort Lauderdale, Florida, United States

Ella Milbank Foshay Cancer Center at Jupiter Medical Center

🇺🇸

Jupiter, Florida, United States

CCOP - Mount Sinai Medical Center

🇺🇸

Miami Beach, Florida, United States

Northeast Georgia Medical Center

🇺🇸

Gainesville, Georgia, United States

Cancer Institute at St. John's Hospital

🇺🇸

Springfield, Illinois, United States

Regional Cancer Center at Memorial Medical Center

🇺🇸

Springfield, Illinois, United States

CCOP - Kansas City

🇺🇸

Prairie Village, Kansas, United States

Greenebaum Cancer Center at University of Maryland Medical Center

🇺🇸

Baltimore, Maryland, United States

St. Agnes Hospital Cancer Center

🇺🇸

Baltimore, Maryland, United States

South Suburban Oncology Center

🇺🇸

Quincy, Massachusetts, United States

Cape Cod Hospital

🇺🇸

Hyannis, Massachusetts, United States

Shields Radiation Oncology Center - Mansfield

🇺🇸

Mansfield, Massachusetts, United States

Winchester Hospital Radiation Oncology Center

🇺🇸

Winchester, Massachusetts, United States

Oakwood Cancer Center at Oakwood Hospital and Medical Center

🇺🇸

Dearborn, Michigan, United States

Hickman Cancer Center at Bixby Medical Center

🇺🇸

Adrian, Michigan, United States

Genesys Hurley Cancer Institute

🇺🇸

Flint, Michigan, United States

Hurley Medical Center

🇺🇸

Flint, Michigan, United States

St. Joseph Mercy Oakland

🇺🇸

Pontiac, Michigan, United States

Sparrow Regional Cancer Center

🇺🇸

Lansing, Michigan, United States

Foote Memorial Hospital

🇺🇸

Jackson, Michigan, United States

Mercy Regional Cancer Center at Mercy Hospital

🇺🇸

Port Huron, Michigan, United States

St. John Macomb Hospital

🇺🇸

Warren, Michigan, United States

Liberty Hospital

🇺🇸

Liberty, Missouri, United States

Siteman Cancer Center at Barnes-Jewish Hospital - Saint Louis

🇺🇸

Saint Louis, Missouri, United States

Barnes-Jewish West County Hospital

🇺🇸

Saint Louis, Missouri, United States

Kingsbury Center for Cancer Care at Cheshire Medical Center

🇺🇸

Keene, New Hampshire, United States

Siteman Cancer Center at Barnes-Jewish St. Peters Hospital - St. Peters

🇺🇸

Saint Peters, Missouri, United States

Nevada Cancer Institute

🇺🇸

Las Vegas, Nevada, United States

Fox Chase Virtua Health Cancer Program at Virtua Memorial Hospital Marlton

🇺🇸

Marlton, New Jersey, United States

Roswell Park Cancer Institute

🇺🇸

Buffalo, New York, United States

Beth Israel Medical Center - Petrie Division

🇺🇸

New York, New York, United States

Coleman Radiation Oncology Center at Carter General Hospital

🇺🇸

Morehead City, North Carolina, United States

Blumenthal Cancer Center at Carolinas Medical Center

🇺🇸

Charlotte, North Carolina, United States

CarolinaEast Cancer Care

🇺🇸

New Bern, North Carolina, United States

South Atlantic Radiation Oncology, LLC

🇺🇸

Supply, North Carolina, United States

Radiation Oncology Center

🇺🇸

Alliance, Ohio, United States

Barberton Citizens Hospital

🇺🇸

Barberton, Ohio, United States

Arthur G. James Cancer Hospital and Richard J. Solove Research Institute at Ohio State University Comprehensive Cancer Center

🇺🇸

Columbus, Ohio, United States

Adena Regional Medical Center

🇺🇸

Chillicothe, Ohio, United States

Riverside Methodist Hospital Cancer Care

🇺🇸

Columbus, Ohio, United States

Community Cancer Center

🇺🇸

Elyria, Ohio, United States

Grady Memorial Hospital

🇺🇸

Delaware, Ohio, United States

Hematology Oncology Center

🇺🇸

Elyria, Ohio, United States

Lima Memorial Hospital

🇺🇸

Lima, Ohio, United States

Strecker Cancer Center at Marietta Memorial Hospital

🇺🇸

Marietta, Ohio, United States

Licking Memorial Cancer Care Program at Licking Memorial Hospital

🇺🇸

Newark, Ohio, United States

Community Hospital of Springfield and Clark County

🇺🇸

Springfield, Ohio, United States

St. Vincent Mercy Medical Center

🇺🇸

Toledo, Ohio, United States

St. Charles Mercy Hospital

🇺🇸

Oregon, Ohio, United States

North Coast Cancer Care, Incorporated

🇺🇸

Sandusky, Ohio, United States

Flower Hospital Cancer Center

🇺🇸

Sylvania, Ohio, United States

Mercy Hospital of Tiffin

🇺🇸

Tiffin, Ohio, United States

Toledo Hospital

🇺🇸

Toledo, Ohio, United States

Medical University of Ohio Cancer Center

🇺🇸

Toledo, Ohio, United States

CCOP - Toledo Community Hospital

🇺🇸

Toledo, Ohio, United States

St. Anne Mercy Hospital

🇺🇸

Toledo, Ohio, United States

Toledo Clinic, Incorporated - Main Clinic

🇺🇸

Toledo, Ohio, United States

Genesis - Good Samaritan Hospital

🇺🇸

Zanesville, Ohio, United States

Mount Carmel St. Ann's Cancer Center

🇺🇸

Westerville, Ohio, United States

Cancer Treatment Center

🇺🇸

Wooster, Ohio, United States

Frank M. and Dorothea Henry Cancer Center at Geisinger Wyoming Valley Medical Center

🇺🇸

Wilkes-Barre, Pennsylvania, United States

McGlinn Family Regional Cancer Center at Reading Hospital and Medical Center

🇺🇸

Reading, Pennsylvania, United States

Sandra L. Maxwell Cancer Center

🇺🇸

Cedar City, Utah, United States

York Cancer Center at Apple Hill Medical Center

🇺🇸

York, Pennsylvania, United States

Logan Regional Hospital

🇺🇸

Logan, Utah, United States

Dixie Regional Medical Center - East Campus

🇺🇸

Saint George, Utah, United States

Utah Valley Regional Medical Center - Provo

🇺🇸

Provo, Utah, United States

Jon and Karen Huntsman Cancer Center at Intermountain Medical Center

🇺🇸

Murray, Utah, United States

Norris Cotton Cancer Center - North

🇺🇸

Saint Johnsbury, Vermont, United States

St. Francis Hospital

🇺🇸

Federal Way, Washington, United States

Good Samaritan Cancer Center

🇺🇸

Puyallup, Washington, United States

Columbia Saint Mary's Hospital - Ozaukee

🇺🇸

Mequon, Wisconsin, United States

MultiCare Regional Cancer Center at Tacoma General Hospital

🇺🇸

Tacoma, Washington, United States

CCOP - Northwest

🇺🇸

Tacoma, Washington, United States

All Saints Cancer Center at Wheaton Franciscan Healthcare

🇺🇸

Racine, Wisconsin, United States

West Allis Memorial Hospital

🇺🇸

West Allis, Wisconsin, United States

Princess Margaret Hospital

🇨🇦

Toronto, Ontario, Canada

California Cancer Center - Woodward Park Office

🇺🇸

Fresno, California, United States

Menorah Medical Center

🇺🇸

Overland Park, Kansas, United States

Saint Alphonsus Cancer Care Center at Saint Alphonsus Regional Medical Center

🇺🇸

Boise, Idaho, United States

Sands Cancer Center

🇺🇸

Canandaigua, New York, United States

Renown Institute for Cancer at Renown Regional Medical Center

🇺🇸

Reno, Nevada, United States

Summa Center for Cancer Care at Akron City Hospital

🇺🇸

Akron, Ohio, United States

Norris Cotton Cancer Center at Dartmouth-Hitchcock Medical Center

🇺🇸

Lebanon, New Hampshire, United States

Radiological Associates of Sacramento Medical Group, Incorporated

🇺🇸

Sacramento, California, United States

Mercy General Hospital

🇺🇸

Sacramento, California, United States

South Sacramento Cancer Center

🇺🇸

Sacramento, California, United States

South Sacramento Kaiser-Permanente Medical Center

🇺🇸

Sacramento, California, United States

Kaiser Permanente Medical Center - Sacramento

🇺🇸

Sacramento, California, United States

Hospital of Saint Raphael

🇺🇸

New Haven, Connecticut, United States

Saint Joseph Mercy Cancer Center

🇺🇸

Ann Arbor, Michigan, United States

CCOP - Michigan Cancer Research Consortium

🇺🇸

Ann Arbor, Michigan, United States

Mayo Clinic Cancer Center

🇺🇸

Rochester, Minnesota, United States

Saint Luke's Cancer Institute at Saint Luke's Hospital

🇺🇸

Kansas City, Missouri, United States

St. Joseph Medical Center

🇺🇸

Kansas City, Missouri, United States

North Kansas City Hospital

🇺🇸

Kansas City, Missouri, United States

Parvin Radiation Oncology

🇺🇸

Kansas City, Missouri, United States

Research Medical Center

🇺🇸

Kansas City, Missouri, United States

Veterans Affairs Medical Center - Richmond

🇺🇸

Richmond, Virginia, United States

Columbia-Saint Mary's Cancer Care Center

🇺🇸

Milwaukee, Wisconsin, United States

Vince Lombardi Cancer Clinic at Aurora St. Luke's Medical Center

🇺🇸

Milwaukee, Wisconsin, United States

Cross Cancer Institute at University of Alberta

🇨🇦

Edmonton, Alberta, Canada

Highland Hospital of Rochester

🇺🇸

Rochester, New York, United States

University Radiation Oncology at Parkridge Hospital

🇺🇸

Rochester, New York, United States

James P. Wilmot Cancer Center at University of Rochester Medical Center

🇺🇸

Rochester, New York, United States

Van Elslander Cancer Center at St. John Hospital and Medical Center

🇺🇸

Grosse Pointe Woods, Michigan, United States

Seton Cancer Institute at Saint Mary's - Saginaw

🇺🇸

Saginaw, Michigan, United States

St. Mary Mercy Hospital

🇺🇸

Livonia, Michigan, United States

Coastal Carolina Radiation Oncology Center

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Wilmington, North Carolina, United States

Kaiser Permanente Medical Center - South San Francisco

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South San Francisco, California, United States

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