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  • First Published: 3/24/2006
  • Last Modified: 7/22/2011

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Phase III Randomized Study of Adjuvant Combination Chemotherapy and Hormonal Therapy Versus Adjuvant Hormonal Therapy Alone in Women With Previously Resected Axillary Node-Negative Breast Cancer With Various Levels of Risk for Recurrence (TAILORx Trial)

Alternate Title
Basic Trial Information
Objectives
Entry Criteria
Expected Enrollment
Outcomes
Outline
Related Publications
Trial Contact Information
Related Information
Registry Information

Alternate Title

Hormone Therapy With or Without Combination Chemotherapy in Treating Women Who Have Undergone Surgery for Node-Negative Breast Cancer (The TAILORx Trial)

Basic Trial Information

PhaseTypeStatusAgeSponsorProtocol IDs
Phase IIIBiomarker/Laboratory analysis, TreatmentActive18 to 75NCIECOG-PACCT-1
PACCT-1, NCT00310180

Special Category: NCI Web site featured trial, CTSU trial

Objectives

Primary

  1. Compare the disease-free survival of women with previously resected axillary-node negative breast cancer with an Oncotype DX Recurrence Score (ODRS) of 11-25 treated with adjuvant combination chemotherapy and hormonal therapy vs adjuvant hormonal therapy alone.
  2. Compare the distant recurrence-free interval, recurrence-free interval, and overall survival of patients with an ODRS of 11-25 treated with these regimens.
  3. Create a tissue and specimen bank that includes formalin-fixed, paraffin-embedded tumor specimens, tissue microarrays, plasma, and DNA obtained from peripheral blood of patients enrolled in this trial.

Secondary

  1. Determine if adjuvant hormonal therapy alone is sufficient treatment (i.e., 10-year distant disease-free survival of at least 95%) for patients with an ODRS of ≤ 10.
  2. Determine the disease-free survival, distant recurrence-free interval, recurrence-free interval, and overall survival of patients with ODRS of ≤ 10.
  3. Compare the outcomes projected at 10 years using classical pathologic information, including tumor size, hormone receptor status, and histologic grade, with those made by the Genomic Health Oncotype DX test in patients treated with these regimens.
  4. Estimate failure rates as a function of ODRS separately in patients treated with combination chemotherapy (group 2/arm II and group 3) and in patients treated with no chemotherapy (group 1 and group 2/arm I).
  5. Determine the prognostic significance of the ODRS and of the individual recurrent score gene groups (proliferation gene group, HER2 gene group, estrogen receptor gene group, invasion gene group, and other genes) in patients treated with these regimens.

Tertiary

  1. To evaluate the effects of chemotherapy and hormonal therapy vs hormonal therapy alone on perceived cognitive impairment, fatigue, fear of recurrence among pre-menopausal patients, endocrine symptoms and sexual dysfunction, and overall health-related quality of life (HRQL).
  2. To determine whether perceived cognitive impairment, fatigue, fear of recurrence, endocrine symptoms, and overall HRQL are similar for patients receiving chemotherapy plus hormonal therapy in secondary study group 2 as for those in the primary study group (arm D vs C).
  3. To determine whether perceived cognitive impairment, fatigue, fear of recurrence, endocrine symptoms, and overall HRQL are similar for patients receiving hormonal therapy alone in secondary study group 1 as for those in the primary study group (arms A vs B).
  4. To determine whether age will be inversely associated with a fear of recurrence, independent of treatment assignment.
  5. Among participants receiving hormonal treatment alone on arm A and arm B, to determine whether ODRS will be inversely correlated with fear of recurrence.

Entry Criteria

Disease Characteristics:

  • Histologically confirmed adenocarcinoma of the breast

  • Hormone receptor status: estrogen and/or progesterone receptor positive tumor

  • Her2/neu negative tumor by either fluorescent in situ hybridization (FISH) or immunohistochemistry (e.g., 0 or 1+ by DAKO Herceptest)

  • Must have undergone surgery to remove the primary tumor by either a mastectomy or local excision plus an acceptable axillary procedure (i.e., sentinel lymph node biopsy and/or axillary dissection) within the past 84 days
    • Must have adequate (i.e., ≥ 1 mm, if margin width specified) tumor-free margins of resection for invasive and ductal carcinoma in situ
      • Lobular carcinoma in situ involving the resection margins are allowed
    • Negative axillary nodes as determined by a sentinel lymph node biopsy and/or axillary dissection as defined by the American Joint Committee on Cancer sixth edition staging system

  • Tumor size 1.1-5.0 cm
    • Tumors that measure 5 mm-1.0 cm are allowed provided there are unfavorable histological features, defined as intermediate or poor nuclear and/or histologic grade or lymphovascular invasion
    • Pathologic tumor size should be used
      • If microscopic measurement is used and tumor includes ductal carcinoma in situ, the measurement should include only the invasive component of the tumor

  • Tissue specimen from the primary tumor available for diagnostic testing with Oncotype DX to determine Oncotype Recurrence Score
    • No prior Oncotype DX Assay unless patient has a recurrence score of 11-25

  • Patients who develop breast cancer while receiving a selective estrogen-receptor modulator (SERM) (e.g., tamoxifen, toremifene, or raloxifene) or an aromatase inhibitor (e.g., anastrazole, letrozole, or exemestane) for breast cancer prevention or a SERM for other indications (e.g., raloxifene for osteoporosis) are ineligible

  • No prior ipsilateral or contralateral invasive breast cancer, bilateral synchronous cancers, or prior ipsilateral or contralateral ductal carcinoma in situ

Prior/Concurrent Therapy:

  • See Disease Characteristics
  • No prior chemotherapy or radiotherapy (including MammoSite® brachytherapy radiotherapy) for this cancer
  • Prior SERM or aromatase inhibitor therapy that was administered for up to 8 weeks for this cancer is allowed
  • No concurrent radiotherapy with chemotherapy
  • Concurrent enrollment on another CTSU study allowed provided patient is already enrolled on ECOG-PACCT-1 and the treatment options in the other study are consistent with PACCT-1-specified treatment assignment (i.e., chemohormonal therapy or hormonal therapy alone)

Patient Characteristics:

  • Female only
  • Any menopausal status allowed
  • WBC count ≥ 3,500/mm3
  • Platelet count ≥ 100,000/mm3
  • Creatinine ≤ 1.5 mg/dL
  • AST ≤ 3 times upper limit of normal
  • Life expectancy ≥ 10 years
  • No chronic obstructive pulmonary disease requiring treatment
  • No chronic liver disease (e.g., cirrhosis or chronic active hepatitis)
  • No history of cerebrovascular accident
  • No history of congestive heart failure or other cardiac disease that would contradict the use of an anthracycline (e.g., doxorubicin hydrochloride or epirubicin)
  • No chronic psychiatric condition or other condition that would preclude study compliance
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective nonhormonal contraception (e.g., intrauterine device, condoms, diaphragm, abstinence)
  • No other invasive malignancies within the past 5 years except curatively treated basal cell or squamous cell carcinoma of the skin or carcinoma in situ of the cervix

Expected Enrollment

11248

A total of 11,248 patients will be accrued for this study.

Outcomes

Primary Outcome(s)

Disease-free survival
Distant recurrence-free interval
Recurrence-free interval
Overall survival
Comparison of FACT-Cog perceived cognitive impairment scores between participants on arm B and arm at 3 months

Secondary Outcome(s)

Comparison of FACT-Cog scores between arms B and C at 3, 12, 18, 24, and 36 months
Differences in FACT-Cog change scores from randomization to 3, 6, 12, 18, 24, and 36 months
Differences between arms B and C on other patient-reported outcomes measures
Differences between participants receiving hormonal treatment alone (arm B vs arm A) on patient-reported outcomes measures
Differences between participants receiving chemotherapy followed by hormonal treatment (arm C vs arm D) on patient-reported outcomes measures

Outline

This is a multicenter, partially randomized study. Patients are assigned to 1 of 3 treatment groups based on their risk of distant recurrence determined by Oncotype DX Breast Cancer Assay.

  • Group 1 (Secondary study group 1; Oncotype DX recurrence score [ODRS] < 11): Patients receive standard hormonal therapy (e.g., oral tamoxifen alone, oral aromatase inhibitor [e.g., anastrozole, letrozole, or exemestane] alone, or oral tamoxifen followed by oral aromatase inhibitor) at the discretion of the treating physician for 5 or 10 years.

  • Group 2 (Primary study group; ODRS 11-25): Patients are stratified according to tumor size (≤ 2.0 cm vs ≥ 2.1 cm), menopausal status (postmenopausal vs premenopausal vs perimenopausal), planned chemotherapy (taxane-containing [i.e., paclitaxel, docetaxel] vs nontaxane-containing), planned radiotherapy (whole breast with no boost planned vs whole breast with boost planned vs partial breast irradiation planned vs no planned radiation therapy [for patients who have had a mastectomy]) and Oncotype DX Recurrence Score (11-15 vs 16-20 vs 21-25). Patients are then randomized to receive either hormonal therapy alone or combination chemotherapy and hormonal therapy.
    • Arm I (experimental): Patients receive hormonal therapy as in group 1 at the discretion of the treating physician.

    • Arm II (standard): Patients receive standard combination chemotherapy at the discretion of the treating physician. Within 4 weeks after the last dose of chemotherapy, patients receive hormonal therapy as in group 1 at the discretion of the treating physician.

  • Group 3 (Secondary study group 2; ODRS > 25): Patients receive combination chemotherapy as in group 2, arm II followed by hormonal therapy as in group 1.

Patients in all groups who have had breast-conservation surgery are also treated with radiotherapy. Radiotherapy should begin within 4 weeks of registration for patients receiving hormonal therapy alone or within 8 weeks after completion of chemotherapy. Patients participating in NSABP and/or RTOG partial irradiation trial(s) may receive partial breast radiation.

Tissue obtained at surgery (performed prior to study entry) is examined by the Oncotype DX Recurrence Score Assay and other assays to correlate response with various biomarkers.

Patients may complete quality-of-life assessments at baseline and at 3, 6, 12, 24, and 36 months.

After completion of study treatment, patients are followed up periodically for up to 20 years.

Related Publications

Zujewski JA, Kamin L: Trial assessing individualized options for treatment for breast cancer: the TAILORx trial. Future Oncol 4 (5): 603-10, 2008.[PUBMED Abstract]

Trial Contact Information

Trial Lead Organizations

Eastern Cooperative Oncology Group

Joseph Sparano, MD, Protocol chair
Ph: 718-920-4826
Email: jsparano@montefiore.org

Southwest Oncology Group

Daniel Hayes, MD, Protocol chair
Ph: 734-615-6725; 800-865-1125
Email: hayesdf@umich.edu

Cancer and Leukemia Group B

Elizabeth Dees, MD, Protocol chair
Ph: 919-966-4431

American College of Surgeons Oncology Group

John Olson, MD, PhD, Protocol chair
Ph: 919-668-1767
Email: jaomd@duke.edu

North Central Cancer Treatment Group

Edith Perez, MD, Protocol chair
Ph: 507-284-1159
Email: perez.edith@mayo.edu

NCIC-Clinical Trials Group

Kathleen Pritchard, MD, Protocol chair
Ph: 416-480-4616
Email: kathy.pritchard@sunnybrook.ca

National Surgical Adjuvant Breast and Bowel Project

Charles Geyer, FACP, MD, Protocol chair
Ph: 412-359-8353; 866-680-0004

Trial Sites

U.S.A.
Alabama
  Mobile
 University of South Alabama Mitchell Cancer Institute
 Hung Khong
Ph: 251-460-6993
Arkansas
  Little Rock
 Arkansas Cancer Research Center at University of Arkansas for Medical Sciences
 Clinical Trial Office - Arkansas Cancer Research Center at University of Arkansas for Medical Sciences
Ph: 501-686-8274
California
  Berkeley
 Alta Bates Summit Comprehensive Cancer Center
 Clinical Trials Office - Alta Bates Summit Comprehensive Cancer Center
Ph: 510-204-3428
  Burbank
 Roy and Patricia Disney Family Cancer Center at Providence Saint Joseph Medical Center
 Clinical Trials Office - Providence Saint Joseph Medical Center - Burbank
Ph: 818-847-3220
  Burlingame
 Peninsula Medical Center
 David Irwin, MD
Ph: 510-204-1591
  La Jolla
 Scripps Cancer Center - San Diego
 Joan Kroener, MD
Ph: 858-554-8629
  Loma Linda
 Loma Linda University Cancer Institute at Loma Linda University Medical Center
 Clinical Trials Office - Loma Linda University Cancer Institute
Ph: 909-558-3375
  Los Angeles
 Jonsson Comprehensive Cancer Center at UCLA
 Clinical Trials Office - Jonsson Comprehensive Cancer Center at UCLA
Ph: 888-798-0719
 USC/Norris Comprehensive Cancer Center and Hospital
 Clinical Trials Office - USC/Norris Comprehensive Cancer Center and Hospital
Ph: 323-865-0451
  Marysville
 Tibotec Therapeutics - Division of Ortho Biotech Products, LP
 Helen Chew, MD
Ph: 916-734-3771
  Mission Hills
 Providence Holy Cross Cancer Center
 Shamel Sanani, MD
Ph: 818-365-3099
  Modesto
 Memorial Medical Center
 Clinical Trials Office - Memorial Medical Center
Ph: 209-572-7116
  Orange
 Chao Family Comprehensive Cancer Center at University of California Irvine Medical Center
 Clinical Trials Office - Chao Family Comprehensive Cancer Center
Ph: 877-UC-STUDY
  Email: ucstudy@uci.edu
  Pleasanton
 Valley Medical Oncology Consultants - Pleasanton
 Helen Chew, MD
Ph: 916-734-3771
  Sacramento
 University of California Davis Cancer Center
 Clinical Trials Office - University of California Davis Cancer Center
Ph: 916-734-3089
  San Diego
 Naval Medical Center - San Diego
 Jarrod Holmes
Ph: 619-532-7303
 Sharp Memorial Hospital Cancer Center
 Clinical Trials Office - Sharp Memorial Hospital Cancer Center
Ph: 858-939-5015
  San Francisco
 California Pacific Medical Center - California Campus
 David Irwin, MD
Ph: 510-204-1591
  San Rafael
 Sutter Health - Western Division Cancer Research Group
 David Irwin, MD
Ph: 510-204-1591
  Vallejo
 Sutter Solano Medical Center
 David Irwin, MD
Ph: 510-204-1591
Colorado
  Boulder
 Boulder Community Hospital
 Clinical Trials Office - Boulder Community Hospital
Ph: 303-938-5253
  Colorado Springs
 Penrose Cancer Center at Penrose Hospital
 Clinical Trials Office - Penrose Cancer Center
Ph: 719-776-5275
  Denver
 CCOP - Colorado Cancer Research Program
 Eduardo Pajon, MD
Ph: 303-399-8020ext2261
 Porter Adventist Hospital
 Eduardo Pajon, MD
Ph: 303-399-8020ext2261
 St. Joseph Hospital
 Eduardo Pajon, MD
Ph: 303-399-8020ext2261
  Grand Junction
 St. Mary's Regional Cancer Center at St. Mary's Hospital and Medical Center
 Eduardo Pajon, MD
Ph: 303-399-8020ext2261
  Greeley
 North Colorado Medical Center
 Eduardo Pajon, MD
Ph: 303-399-8020ext2261
  Longmont
 Hope Cancer Care Center at Longmont United Hospital
 Eduardo Pajon, MD
Ph: 303-399-8020ext2261
  Wheat Ridge
 Exempla Lutheran Medical Center
 Clinical Trials Office - Exempla Lutheran Medical Center
Ph: 303-403-3605
Connecticut
  Greenwich
 Bendheim Cancer Center at Greenwich Hospital
 Clinical Trials Office - Bendheim Cancer Center
Ph: 203-863-3698
  Hartford
 Saint Francis/Mount Sinai Regional Cancer Center at Saint Francis Hospital and Medical Center
 Philip Stella, MD
Ph: 734-712-1000
  Norwich
 Eastern Connecticut Hematology and Oncology Associates
 Dennis Slater, MD
Ph: 860-886-8362
District of Columbia
  Washington
 Walter Reed Army Medical Center
 Clinical Trials Office - Walter Reed Army Medical Center
Ph: 202-782-7840
Florida
  Fort Lauderdale
 Michael and Dianne Bienes Comprehensive Cancer Center at Holy Cross Hospital
 Clinical Trials Office - Michael and Dianne Bienes Comprehensive Cancer Center
Ph: 954-776-3239
  Gainesville
 University of Florida Shands Cancer Center
 Clinical Trials Office - University of Florida Shands Cancer Center
Ph: 888-254-7581
  Jupiter
 Ella Milbank Foshay Cancer Center at Jupiter Medical Center
 Clinical Trials Office - Ella Milbank Foshay Cancer Center
Ph: 561-745-5768
  Miami Beach
 CCOP - Mount Sinai Medical Center
 Rogerio Lilenbaum, MD
Ph: 305-535-3310
  Weston
 Cleveland Clinic Florida - Weston
 Clinical Trials Office - Cleveland Clinic Florida - Weston
Ph: 954-659-5705
Georgia
  Augusta
 Augusta Oncology Associates - Walton Way
 Alice David
Ph: 706-821-2944
Idaho
  Boise
 Saint Alphonsus Cancer Care Center at Saint Alphonsus Regional Medical Center
 Clinical Trials Office - Saint Alphonsus Cancer Care Center
Ph: 208-367-7954
Illinois
  Chicago
 John H. Stroger, Jr. Hospital of Cook County
 Thomas Lad, MD
Ph: 312-864-3200
  Elmhurst
 Elmhurst Memorial Hospital
 Robert Eisner
Ph: 630-833-1400
  Moline
 Trinity Cancer Center at Trinity Medical Center - 7th Street Campus
 Costas Constantinou, MD
Ph: 563-359-9876
  Normal
 Mid-Illinois Hematology-Oncology Associates at Community Cancer Center
 John Migas, MD
Ph: 309-451-2207
  Olympia Fields
 Saint James Hospital and Health Centers Comprehensive Cancer Institute - Olympia Fields
 Clinical Trials Office - Saint James Hospital and Health Centers Comprehensive Cancer Institute - Olympia Fields
Ph: 708-679-2217
  Rockford
 Swedish-American Regional Cancer Center
 Clinical Trials Office - Swedish-American Regional Cancer Center
Ph: 815-489-4413
Indiana
  Indianapolis
 Community Regional Cancer Care at Community Hospital East
 Sumeet Bhatia
Ph: 317-355-5347
 Community Regional Cancer Care at Community Hospital North
 Sumeet Bhatia
Ph: 317-621-4300
  Munster
 Community Hospital
 Erwin Robin, MD
Ph: 219-836-2860
Iowa
  Bettendorf
 Hematology Oncology Associates of the Quad Cities
 Shobha Chitneni, MD, MBBS
Ph: 563-355-7733
  Ottumwa
 McCreery Cancer Center at Ottumwa Regional
 Robert Behrens
Ph: 641-684-2946
  Waterloo
 Covenant Cancer Treatment Center
 Clinical Trials Office - Covenant Cancer Treatment Center
Ph: 319-272-2070
Louisiana
  Alexandria
 Tulane Cancer Center Office of Clinical Research
 Clinical Trials Office - Tulane Cancer Center
Ph: 504-988-6121
  Baton Rouge
 Mary Bird Perkins Cancer Center - Baton Rouge
 Robert Veith
Ph: 225-767-0847
 Ochsner Health Center - Bluebonnet
 Jyotsna Fuloria
Ph: 225-761-5200
  Covington
 Ochsner Health Center - Covington
 Jyotsna Fuloria
Ph: 985-875-2828
866-624-7637
  New Orleans
 CCOP - Ochsner
 Jyotsna Fuloria
Ph: 504-842-3910
 MBCCOP - LSU Health Sciences Center
 Robert Veith
Ph: 504-568-5151
 Ochsner Cancer Institute at Ochsner Clinic Foundation
 Jyotsna Fuloria
Ph: 504-842-4360
888-624-7637
  Shreveport
 Christus Schumpert Cancer Treatment Center
 Clinical Trials Office - Christus Schumpert Cancer Treatment Center
Ph: 318-681-4763
 Feist-Weiller Cancer Center at Louisiana State University Health Sciences
 Clinical Trials Office - Feist-Weiller Cancer Center at Louisiana State University Health Sciences
Ph: 318-813-1412
Maine
  Augusta
 Harold Alfond Center for Cancer Care
 Donald Magioncalda, MD
Ph: 207-626-1000
  Scarborough
 Maine Center for Cancer Medicine and Blood Disorders - Scarborough
 Tracey Weisberg, MD
Ph: 207-885-7634
  York
 York Hospital's Oncology Treatment Center
 Jonathan Eneman
Ph: 207-351-3777
Maryland
  Cumberland
 Regional Cancer Center at Western Maryland Health System - Sacred Heart Campus
 Alida Podrumar
Ph: 301-723-5536
  Easton
 Shore Regional Cancer Center at Memorial Hospital - Easton
 Mary DeShields, MD
Ph: 410-819-3332
  Frederick
 Frederick Memorial Hospital Regional Cancer Therapy Center
 Brian O'Connor, MD
Ph: 301-662-8477
  Silver Spring
 Holy Cross Hospital
 Clinical Trials Office - Holy Cross Hospital
Ph: 310-754-7552
  Towson
 Cancer Institute at St. Joseph Medical Center
 Hector Silva
Ph: 410-337-1000
Massachusetts
  Attleboro
 Sturdy Memorial Hospital
 Michael Vasconcelles, MD
Ph: 617-632-5301
  Boston
 Tufts Medical Center Cancer Center
 John Nystrom
Ph: 617-636-6100
  Burlington
 Lahey Clinic Medical Center - Burlington
 Clinical Trials Office - Lahey Clinic Medical Center - Burlington
Ph: 781-744-8027
  Pittsfield
 Berkshire Hematology Oncology, PC
 Harvey Zimbler, MD
Ph: 413-496-8205
  Quincy
 Commonwealth Hematology-Oncology, PC - Quincy
 Susan Sajer, MD
Ph: 978-287-3436
  Worcester
 Saint Vincent Hospital at Worcester Medical Center
 Clinical Trials Office - Saint Vincent Hospital at Worcester Medical Center
Ph: 508-363-7018
 UMASS Memorial Cancer Center - University Campus
 Kathryn Edmiston, MD
Ph: 508-334-5141
Michigan
  Adrian
 Hickman Cancer Center at Bixby Medical Center
 Clinical Trials Office - Hickman Cancer Center at Bixby Medical Center
Ph: 517-265-0116
  Ann Arbor
 CCOP - Michigan Cancer Research Consortium
 Philip Stella, MD
Ph: 734-712-1000
 Saint Joseph Mercy Cancer Center
 Philip Stella, MD
Ph: 734-712-1000
  Dearborn
 Oakwood Cancer Center at Oakwood Hospital and Medical Center
 Clinical Trials Office - Oakwood Cancer Center at Oakwood Hospital and Medical Center
Ph: 313-593-8090
  Detroit
 Josephine Ford Cancer Center at Henry Ford Hospital
 Robert Chapman, MD
Ph: 313-916-1332
  Flint
 Genesys Hurley Cancer Institute
 Clinical Trials Office - Genesys Hurley Cancer Institute
Ph: 810-762-8057
  Grosse Pointe Woods
 Van Elslander Cancer Center at St. John Hospital and Medical Center
 Clincial Trials Office - Van Elslander Cancer Center at St. John Hospital and Medical Center
Ph: 313-343-3166
  Lansing
 Sparrow Regional Cancer Center
 Clinical Trials Office - Sparrow Regional Cancer Center
Ph: 517-364-2890
  Livonia
 St. Mary Mercy Hospital
 Philip Stella, MD
Ph: 734-712-1000
  Monroe
 Community Cancer Center of Monroe
 Paul Schaefer, MD
Ph: 419-479-5605
 Mercy Memorial Hospital - Monroe
 Paul Schaefer, MD
Ph: 419-479-5605
  Mount Clemens
 Clemens Regional Medical Center
 Clinical Trials Office - Ted B. Wahby Cancer Center at Mount Clemens General Hospital
Ph: 586-493-3426
  Pontiac
 St. Joseph Mercy Oakland
 Philip Stella, MD
Ph: 734-712-1000
  Port Huron
 Mercy Regional Cancer Center at Mercy Hospital
 Philip Stella, MD
Ph: 734-712-1000
  Royal Oak
 William Beaumont Hospital - Royal Oak Campus
 Clinical Trials Office - William Beaumont Hospital - Royal Oak Campus
Ph: 248-551-7695
  Saginaw
 Seton Cancer Institute at Saint Mary's - Saginaw
 Clinical Trials Office - Seton Cancer Institute - Saginaw
Ph: 989-776-8411
  Warren
 St. John Macomb Hospital
 Philip Stella, MD
Ph: 734-712-1000
Minnesota
  Duluth
 CCOP - Duluth
 Daniel Nikcevich, MD, PhD
Ph: 218-786-3625
 Duluth Clinic Cancer Center - Duluth
 Clinical Trials Office - Duluth Clinic Cancer Center - Duluth
Ph: 218-786-3308
 Miller - Dwan Medical Center
 Daniel Nikcevich, MD, PhD
Ph: 218-786-3625
Mississippi
  Jackson
 Jackson Oncology Associates, PLLC
 Jyotsna Fuloria
Ph: 601-355-2485
  Pascagoula
 Regional Cancer Center at Singing River Hospital
 James Clarkson, MD
Ph: 228-374-6296
Missouri
  Cape Girardeau
 Saint Francis Medical Center
 Bethany Sleckman, MD
Ph: 314-251-7057
  Columbia
 Ellis Fischel Cancer Center at University of Missouri - Columbia
 Clinical Trial Office - Ellis Fischel Cancer Center
Ph: 573-882-7440
  Saint Louis
 David C. Pratt Cancer Center at St. John's Mercy
 Clinical Trials Office - David C. Pratt Cancer Center at St. John's Mercy
Ph: 314-251-6770
 Siteman Cancer Center at Barnes-Jewish Hospital - Saint Louis
 Michael Naughton, MD
Ph: 314-996-8872
  Springfield
 CCOP - Cancer Research for the Ozarks
 Robert Carolla
Ph: 417-269-4520
 Hulston Cancer Center at Cox Medical Center South
 Robert Carolla
Ph: 417-269-5257
Montana
  Billings
 Billings Clinic - Downtown
 Clinical Trials Office - Billings Clinic - Downtown
Ph: 800-996-2663
  Email: research@billingsclinic.org
 CCOP - Montana Cancer Consortium
 Benjamin Marchello, MD
Ph: 406-238-6290
 Hematology-Oncology Centers of the Northern Rockies - Billings
 Benjamin Marchello, MD
Ph: 406-238-6290
 St. Vincent Healthcare Cancer Care Services
 Benjamin Marchello, MD
Ph: 406-238-6290
  Bozeman
 Bozeman Deaconess Cancer Center
 Benjamin Marchello, MD
Ph: 406-238-6290
  Butte
 St. James Healthcare Cancer Care
 Benjamin Marchello, MD
Ph: 406-238-6290
  Great Falls
 Great Falls Clinic - Main Facility
 Benjamin Marchello, MD
Ph: 406-238-6290
 Sletten Cancer Institute at Benefis Healthcare
 Benjamin Marchello, MD
Ph: 406-238-6290
  Havre
 Northern Montana Hospital
 Benjamin Marchello, MD
Ph: 406-238-6290
  Helena
 St. Peter's Hospital
 Benjamin Marchello, MD
Ph: 406-238-6290
  Kalispell
 Glacier Oncology, PLLC
 Benjamin Marchello, MD
Ph: 406-238-6290
 Kalispell Medical Oncology at KRMC
 Benjamin Marchello, MD
Ph: 406-238-6290
 Kalispell Regional Medical Center
 Benjamin Marchello, MD
Ph: 406-238-6290
  Missoula
 Montana Cancer Center at St. Patrick Hospital and Health Sciences Center
 Clinical Trials Office - Montana Cancer Center at St. Patrick Hospital and Health Sciences Center
Ph: 406-329-7029
 Montana Cancer Specialists at Montana Cancer Center
 Clinical Trials Office - Montana Cancer Specialists at Montana Cancer Center
Ph: 406-238-6962
Nebraska
  Grand Island
 Saint Francis Cancer Treatment Center at Saint Francis Memorial Health Center
 Elizabeth Reed, MD
Ph: 402-559-5388
Nevada
  Las Vegas
 CCOP - Nevada Cancer Research Foundation
 John Ellerton, MD, CM
Ph: 702-384-0013
  Reno
 Renown Institute for Cancer at Renown Regional Medical Center
 Steven Schiff, MD
Ph: 775-329-0873
New Hampshire
  Exeter
 Center for Cancer Care at Exeter Hospital
 Michael Buff
Ph: 603-580-6636
  Keene
 Kingsbury Center for Cancer Care at Cheshire Medical Center
 Steven Larmon
Ph: 603-354-5400
  Nashua
 Foundation Medical Partners
 Marcia Browne, MD
Ph: 781-237-0700
New Jersey
  Freehold
 CentraState Medical Center
 Jeffrey Silberberg, MD
Ph: 732-431-8400
  Ridgewood
 Valley Hospital - Ridgewood
 Thomas Rakowski, MD
Ph: 201-444-4526
  Sparta
 Frederick R. and Betty M. Smith Cancer Treatment Center
 Allison Zibelli, MD
Ph: 215-923-5676
  Summit
 Overlook Hospital
 Bonni Guerin
Ph: 908-522-2000
New Mexico
  Albuquerque
 Hematology Oncology Associates, PC
 Melanie Royce, MD, PhD
Ph: 505-272-6057
 Lovelace Medical Center - Downtown
 Melanie Royce, MD, PhD
Ph: 505-272-6057
 Presbyterian Cancer Treatment Center at Presbyterian Kaseman Hospital
 Melanie Royce, MD, PhD
Ph: 505-272-6057
 University of New Mexico Cancer Center
 Clinical Trials Office - University of New Mexico Cancer Center
Ph: 505-272-6972
  Santa Fe
 New Mexico Cancer Care Associates
 Clinical Trials Office - New Mexico Cancer Care Associates
Ph: 505-955-7910
New York
  Plattsburgh
 Fitzpatrick Cancer Center at Champlain Valley Physicians Hospital Medical Center
 Jan Duus, MD
Ph: 518-562-7110
  Rochester
 Highland Hospital of Rochester
 Richard Fisher, MD
Ph: 585-275-0842
 James P. Wilmot Cancer Center at University of Rochester Medical Center
 Richard Fisher, MD
Ph: 585-275-0842
 Lipson Cancer and Blood Center at Rochester General Hospital
 Peter Bushunow, MD
Ph: 585-922-4020
North Carolina
  Charlotte
 Blumenthal Cancer Center at Carolinas Medical Center
 Clinical Trials Office - Blumenthal Cancer Center at Carolinas Medical Center
Ph: 704-355-2884
  Durham
 Duke Cancer Institute
 Clinical Trials Office - Duke Cancer Institute
Ph: 888-275-3853
  Fayetteville
 Cape Fear Valley Medical Center Cancer Center
 Clinical Trial Office - Cape Fear Valley Medical Center Cancer Center
Ph: 910-609-4561
  Greenville
 Leo W. Jenkins Cancer Center at ECU Medical School
 Clinical Trials Office - Leo W. Jenkins Cancer Center at ECU Medical School
Ph: 252-744-2391
  Henderson
 Maria Parham Medical Center
 Jeffrey Crawford, MD
Ph: 919-681-9509
  Lumberton
 Southeastern Regional Medical Center
 Jeffrey Crawford, MD
Ph: 919-681-9509
  Oxford
 Granville Medical Center
 Jeffrey Crawford, MD
Ph: 919-681-9509
  Pinehurst
 FirstHealth Moore Regional Community Hospital Comprehensive Cancer Center
 Clinical Trials Office - FirstHealth Moore Regional Community Hospital Comprehensive Cancer Center
Ph: 910-715-2200
  Raleigh
 Duke Health Raleigh Hospital
 Jeffrey Crawford, MD
Ph: 919-681-9509
 Rex Cancer Center at Rex Hospital
 Clinical Trials Office - Rex Cancer Center
Ph: 919-784-7209
  Roxboro
 Person Memorial Hospital
 Jeffrey Crawford, MD
Ph: 919-681-9509
  Statesville
 Iredell Memorial Hospital
 Ruby Grimm, MD
Ph: 704-873-2219
  Winston-Salem
 Wake Forest University Comprehensive Cancer Center
 Clinical Trials Office - Wake Forest University Comprehensive Cancer Center
Ph: 336-713-6771
Ohio
  Bowling Green
 Wood County Oncology Center
 Paul Schaefer, MD
Ph: 419-479-5605
  Canton
 Aultman Cancer Center at Aultman Hospital
 Clinical Trials Office - Aultman Cancer Center at Aultman Hospital
Ph: 330-363-6891
  Chillicothe
 Adena Regional Medical Center
 Clinical Trials Office - Adena Regional Medical Center
Ph: 877-779-7585
  Cincinnati
 Charles M. Barrett Cancer Center at University Hospital
 Elizabeth Shaughnessy, MD
Ph: 513-584-8900
 Christ Hospital Cancer Center
 Robert Cody, MD
Ph: 513-321-4333
  Cleveland
 Case Comprehensive Cancer Center
 Clinical Trials Office - Case Comprehensive Cancer Center
Ph: 800-641-2422
  Clyde
 North Coast Cancer Care - Clyde
 Paul Schaefer, MD
Ph: 419-479-5605
  Columbus
 Doctors Hospital at Ohio Health
 Clinical Trials Office - Doctors Hospital at Ohio Health
Ph: 614-566-3275
 Grant Medical Center Cancer Care
 Clinical Trials Office - Grant Medical Center Cancer Care
Ph: 614-566-4475
 Mount Carmel Health - West Hospital
 J. Philip Kuebler, MD, PhD
Ph: 614-442-3130
 Riverside Methodist Hospital Cancer Care
 Clinical Trials Office - Riverside Methodist Hospital Cancer Care
Ph: 614-566-4475
  Delaware
 Grady Memorial Hospital
 J. Philip Kuebler, MD, PhD
Ph: 614-442-3130
  Lima
 Lima Memorial Hospital
 Paul Schaefer, MD
Ph: 419-479-5605
 St. Rita's Medical Center
 Clinical Trials Office - St. Rita's Medical Center
Ph: 419-226-9617
  Marietta
 Strecker Cancer Center at Marietta Memorial Hospital
 J. Philip Kuebler, MD, PhD
Ph: 614-442-3130
  Maumee
 Northwest Ohio Oncology Center
 Paul Schaefer, MD
Ph: 419-479-5605
 Paul Schaefer, MD
Ph: 419-479-5605
  Newark
 Licking Memorial Cancer Care Program at Licking Memorial Hospital
 J. Philip Kuebler, MD, PhD
Ph: 614-442-3130
  Norwalk
 Fisher-Titus Medical Center
 Paul Schaefer, MD
Ph: 419-479-5605
  Oregon
 St. Charles Mercy Hospital
 Paul Schaefer, MD
Ph: 419-479-5605
 Toledo Clinic - Oregon
 Paul Schaefer, MD
Ph: 419-479-5605
  Sandusky
 North Coast Cancer Care, Incorporated
 Paul Schaefer, MD
Ph: 419-479-5605
  Springfield
 Community Hospital of Springfield and Clark County
 J. Philip Kuebler, MD, PhD
Ph: 614-442-3130
  Sylvania
 Flower Hospital Cancer Center
 Clinical Trials Office - Flower Hospital Cancer Center
Ph: 419-824-1842
  Tiffin
 Mercy Hospital of Tiffin
 Paul Schaefer, MD
Ph: 419-479-5605
  Toledo
 CCOP - Toledo Community Hospital
 Paul Schaefer, MD
Ph: 419-479-5605
 Medical University of Ohio Cancer Center
 Clinical Trials Office - Medical University of Ohio Cancer Center
Ph: 419-383-6583
 St. Anne Mercy Hospital
 Paul Schaefer, MD
Ph: 419-479-5605
 St. Vincent Mercy Medical Center
 Paul Schaefer, MD
Ph: 419-479-5605
 Toledo Clinic, Incorporated - Main Clinic
 Paul Schaefer, MD
Ph: 419-479-5605
 Toledo Hospital
 Clinical Trials Office - Toledo Hospital
Ph: 419-824-1842
  Wauseon
 Fulton County Health Center
 Clinical Trials Office - Fulton County Health Center
Ph: 419-330-2708
  Westerville
 Mount Carmel St. Ann's Cancer Center
 J. Philip Kuebler, MD, PhD
Ph: 614-442-3130
  Wright-Patterson Afb
 United States Air Force Medical Center - Wright-Patterson
 Roger Wood
Ph: 937-257-9133
  Zanesville
 Genesis - Good Samaritan Hospital
 Clinical Trials Office - Genesis - Good Samaritan Hospital
Ph: 740-454-5232
Oklahoma
  Lawton
 Cancer Centers of Southwest Oklahoma, LLC - Lawton
 Nadim Nimeh, MD
Ph: 580-536-2121ext.113
  Norman
 Cancer Care Associates - Norman
 Vikki Canfield, MD
Ph: 405-751-4343
  Oklahoma City
 Cancer Care Associates - Mercy Campus
 Vikki Canfield, MD
Ph: 405-751-4343
 Cancer Care Associates at Troy and Dollie Smith Cancer Center
 Vikki Canfield, MD
Ph: 405-751-4343
  Tulsa
 Natalie Warren Bryant Cancer Center at St. Francis Hospital
 Joseph Lynch, MD
Ph: 918-494-8275
Oregon
  Milwaukie
 Providence Milwaukie Hospital
 Janet Ruzich
Ph: 503-513-8300
  Portland
 Adventist Medical Center
 Janet Ruzich
Ph: 503-257-2500
 CCOP - Columbia River Oncology Program
 Janet Ruzich
Ph: 503-216-6260
 Providence Cancer Center at Providence Portland Medical Center
 Clinical Trials Office - Providence Cancer Center at Providence Portland Medical Center
Ph: 503-215-6412
 Providence St. Vincent Medical Center
 Clinical Trials Office - Providence St. Vincent Medical Center
Ph: 503-215-6412
Pennsylvania
  Abington
 Rosenfeld Cancer Center at Abington Memorial Hospital
 Clinical Trials Office - Rosenfeld Cancer Center at Abington Memorial Hospital
Ph: 215-481-2402
  Doylestown
 Doylestown Hospital Cancer Center
 Mitchell Alden, DO
Ph: 215-345-8444
  East Stroudsburg
 Dale and Frances Hughes Cancer Center at Pocono Medical Center
 Allison Zibelli, MD
Ph: 215-923-5676
  Ephrata
 Ephrata Cancer Center at Ephrata Community Hospital
 Allison Zibelli, MD
Ph: 215-923-5676
  Erie
 Regional Cancer Center - Erie
 Carmen Pisc
Ph: 814-838-9000
  Hershey
 Penn State Hershey Cancer Institute at Milton S. Hershey Medical Center
 Clinical Trials Office - Penn State Hershey Cancer Institute at Milton S. Hershey Medical Center
Ph: 717-531-3779
  Email: CTO@hmc.psu.edu
  Langhorne
 St. Mary Regional Cancer Center
 Clinical Trials Office - St. Mary Regional Cancer Center
Ph: 215-710-4585
  Meadowbrook
 Charles A. & Betty Bott Cancer Center at Holy Redeemer Hospital
 Joseph Potz
Ph: 215-938-3555
  Media
 Riddle Memorial Hospital Cancer Center
 Allison Zibelli, MD
Ph: 215-923-5676
  Philadelphia
 Fox Chase Cancer Center - Philadelphia
 Clinical Trials Office - Fox Chase Cancer Center - Philadelphia
Ph: 215-728-4790
 Frankford Hospital Cancer Center - Torresdale Campus
 Allen Terzian, MD
Ph: 215-612-5250
  Pittsburgh
 Allegheny Cancer Center at Allegheny General Hospital
 Thomas Julian
Ph: 412-359-3336
866-680-0004
  Pottstown
 Pottstown Memorial Regional Cancer Center
 Wei Song, MD, PhD
Ph: 610-327-7555
  Reading
 McGlinn Family Regional Cancer Center at Reading Hospital and Medical Center
 Clinical Trials Office - McGlinn Family Regional Cancer Center
Ph: 610-988-9323
  Sayre
 Guthrie Cancer Center at Guthrie Clinic Sayre
 Clinical Trials Office - Guthrie Cancer Center at Guthrie Clinic Sayre
Ph: 800-836-0388
  Upland
 Associates in Hematology-Oncology, PC at Crozer Regional Cancer Center
 Allison Zibelli, MD
Ph: 215-923-5676
  West Grove
 Jennersville Regional Hospital
 Clinical Trials Office - Jennersville Regional Hospital
Ph: 610-869-1396
  Williamsport
 Susquehanna Cancer Center at Divine Providence Hospital
 Warren Robinson, Jr.
Ph: 570-326-8000
  York
 York Cancer Center at Apple Hill Medical Center
 Amir Tabatabai, MD
Ph: 717-741-9229
Rhode Island
  Pawtucket
 Memorial Hospital of Rhode Island
 Anthony Thomas, DO
Ph: 401-729-2700
South Carolina
  Anderson
 AnMed Cancer Center
 Clinical Trials Office - AnMed Cancer Center
Ph: 864-512-1000
  Charleston
 Hollings Cancer Center at Medical University of South Carolina
 Clinical Trials Office - Hollings Cancer Center at Medical University of South Carolina
Ph: 843-792-9321
 Roper St. Francis Cancer Center at Roper Hospital
 James Orcutt, MD
Ph: 843-577-2276
  Columbia
 South Carolina Oncology Associates, PA
 William Babcock
Ph: 803-461-3000
  Spartanburg
 CCOP - Upstate Carolina
 Clinical Trials Office - CCOP - Upstate Carolina
Ph: 800-486-5941
 Gibbs Regional Cancer Center at Spartanburg Regional Medical Center
 Clinical Trials Office - Gibbs Regional Cancer Center
Ph: 800-486-5941
South Dakota
  Sioux Falls
 Sanford Cancer Center at Sanford USD Medical Center
 Clinical Trials Office - Sanford Cancer Center
Ph: 605-328-1367
Tennessee
  Franklin
 Vanderbilt-Ingram Cancer Center - Cool Springs
 Ingrid Mayer, MD
Ph: 615-322-4967
  Jackson
 West Tennessee Cancer Center at Jackson-Madison County General Hospital
 Clinical Trials Office - West Tennessee Cancer Center
Ph: 731-425-6865
  Memphis
 University of Tennessee Cancer Institute - Memphis
 Clinical Trials Office - University of Tennessee Cancer Institute
Ph: 901-448-3303
  Nashville
 Vanderbilt Breast Center at One Hundred Oaks
 Ingrid Mayer, MD
Ph: 615-322-4967
 Vanderbilt-Ingram Cancer Center
 Clinical Trials Office - Vanderbilt-Ingram Cancer Center
Ph: 800-811-8480
Texas
  Fort Sam Houston
 Brooke Army Medical Center
 Clinical Trials Office - Brooke Army Medical Center
Ph: 210-916-4837
  Lackland AFB
 Wilford Hall Medical Center
 John Renshaw
Ph: 210-292-7100
  Laredo
 Doctor's Hospital of Laredo
 Gary Unzeitig, MD
Ph: 956-726-3691
  San Antonio
 University of Texas Health Science Center at San Antonio
 Anand Karnad, MD
Ph: 210-567-4777
Virginia
  Charlottesville
 Martha Jefferson Hospital Cancer Care Center
 Robert Pritchard, MD
Ph: 434-982-8390
  Fredericksburg
 Fredericksburg Oncology, Incorporated
 Paul Schaefer, MD
Ph: 419-479-5605
  Lynchburg
 Lynchburg Hematology-Oncology Clinic
 John Leach MacNeill, MD
Ph: 434-947-5925
  Newport News
 Peninsula Cancer Institute - Newport News Office
 Guy Tillinghast
Ph: 757-534-5555
Washington
  Spokane
 Rockwood Clinic Cancer Treatment Center
 Clinical Trials Office - Rockwood Clinic Cancer Treatment Center
Ph: 509-838-2531 ext. 6880
  Tacoma
 Madigan Army Medical Center - Tacoma
 Richard Reed
Ph: 206-968-1110
  Vancouver
 Northwest Cancer Specialists at Vancouver Cancer Center
 Janet Ruzich
Ph: 360-944-9889
West Virginia
  Charleston
 West Virginia University Health Sciences Center - Charleston
 Steven Jubelirer, MD
Ph: 304-388-8380
  Morgantown
 Mary Babb Randolph Cancer Center at West Virginia University Hospitals
 Jame Abraham, MD
Ph: 304-293-4229
Wisconsin
  Elkhorn
 Vince Lombardi Cancer Center at Aurora Lakeland Medical Center - Elkhorn
 Dhimant Patel, MD
Ph: 920-288-4180
  Fond du Lac
 Central Wisconsin Cancer Program at Agnesian HealthCare
 Clinical Trials Office - Central Wisconsin Cancer Program at Agnesian HealthCare
Ph: 800-494-2927
  Franklin
 Oncology Alliance - Franklin
 Rubina Qamar
Ph: 414-529-3210
  Glendale
 Oncology Alliance, SC - Milwaukee - East
 Clinical Trials Office - Oncology Alliance, SC - Milwaukee - East
Ph: 414-906-4480
  Green Bay
 St. Vincent Hospital Regional Cancer Center
 Clinical Trials Office - St. Vincent Hospital Regional Cancer Center
Ph: 920-433-8889
 Vince Lombardi Cancer Clinic - Green Bay at Aurora BayCare Medical Center
 Clinical Trials Office - Vince Lombardi Cancer Clinic - Green Bay at Aurora BayCare Medical Center
Ph: 414-649-5717
  Kenosha
 Oncology Alliance - Kenosha South
 Rubina Qamar
Ph: 262-942-9644
  La Crosse
 Franciscan Skemp Healthcare - La Crosse Campus
 Paula Gill
Ph: 608-785-0940
 Gundersen Lutheran Center for Cancer and Blood
 Clinical Trials Office - Gundersen Lutheran Cancer Center
Ph: 608-775-2385
  Email: cancerctr@gundluth.org
  Manitowoc
 Holy Family Memorial Medical Center Cancer Care Center
 Clinical Trials Office - Holy Family Memorial Medical Center Cancer Care Center
Ph: 920-320-2749
  Marinette
 Vince Lombardi Cancer Clinic - Marinette
 Dhimant Patel, MD
Ph: 920-288-4180
  Mequon
 Columbia Saint Mary's Hospital - Ozaukee
 Carl Olson, MD
Ph: 414-291-1556
  Milwaukee
 Aurora Sinai Medical Center
 Clinical Trials Office - Aurora Sinai Medical Center
Ph: 414-649-5717
 Columbia-Saint Mary's Cancer Care Center
 Clinical Trials Office - Columbia-St. Mary's Cancer Care Center
Ph: 414-326-1739
 Medical Consultants, Limited
 Jonathan Treisman, MD
Ph: 414-385-3086
 Oncology Alliance, SC - Milwaukee - South
 Rubina Qamar
Ph: 414- 384-5111
 Wheaton Franciscan Cancer Care - St. Joseph
 Norwood Anderson, MD
Ph: 414-874-1100
  Oconomowoc
 Regional Cancer Center at Oconomowoc Memorial Hospital
 Clinical Trials Office - Regional Cancer Center at Oconomowoc Memorial Hospital
Ph: 262-928-7878
  Oshkosh
 Vince Lombardi Cancer Clinic - Oshkosh
 Magdalena Flejsierowicz
Ph: 920-303-8700
  Summit
 Aurora Medical Center
 Dhimant Patel, MD
Ph: 920-288-4180
  Two Rivers
 Vince Lombardi Cancer Clinic - Two Rivers
 Dhimant Patel, MD
Ph: 920-288-4180
  Waukesha
 Waukesha Memorial Hospital Regional Cancer Center
 Clinical Trials Office - Waukesha Memorial Hospital Regional Cancer Center
Ph: 262-928-7632
  Wauwatosa
 Oncology Alliance, SC - Milwaukee - West
 Rubina Qamar
Ph: 414-476-8450
  West Allis
 Aurora Women's Pavilion of West Allis Memorial Hospital
 Magdalena Flejsierowicz
Ph: 414-978-3000
Wyoming
  Casper
 Rocky Mountain Oncology
 Benjamin Marchello, MD
Ph: 406-238-6290
  Sheridan
 Welch Cancer Center at Sheridan Memorial Hospital
 Benjamin Marchello, MD
Ph: 406-238-6290
Australia
New South Wales
  Coffs Harbour
 Coffs Harbour Health Campus
 John Forbes
Ph: 61-2-6656-7820
  Waratah
 Newcastle Mater Misericordiae Hospital
 John Forbes
Ph: 61-2-4921-1211
Canada
British Columbia
  Kelowna
 British Columbia Cancer Agency - Centre for the Southern Interior
 Barbara Czerkawski
Ph: 250-712-3900
  Penticton
 Penticton Regional Hospital
 Deepu Mirchandani, MD, MS
Ph: 306-655-2690
  Surrey
 BCCA - Fraser Valley Cancer Centre
 Lee Ann Martin
Ph: 604-930-2098
800-587-2885
  Vancouver
 British Columbia Cancer Agency - Vancouver Cancer Centre
 Stephen Chia
Ph: 604-877-6000
800-663-3333
  Victoria
 British Columbia Cancer Agency - Vancouver Island Centre
 Andrew Attwell
Ph: 250-519-5500
Manitoba
  Winnipeg
 CancerCare Manitoba
 Debjani Grenier, MD
Ph: 204-235-3394
New Brunswick
  Saint John
 Saint John Regional Hospital
 Margot Burnell, MD
Ph: 506-648-6884
Ontario
  Sudbury
 Northeastern Ontario Regional Cancer Centre
 Pedro Lopez, MD
Ph: 705-522-6237ext.2320
Quebec
  Montreal
 CHUM - Hotel Dieu Hospital
 Andre Robidoux, MD
Ph: 514-890-8000ext.15535
 Hopital Notre-Dame du CHUM
 Andre Robidoux, MD
Ph: 514-890-8000ext.15535
Saskatchewan
  Regina
 Allan Blair Cancer Centre at Pasqua Hospital
 Muhammad Salim, MD
Ph: 306-766-2203
Peru
  Lima
 Instituto Nacional de Enfermedades Neoplasicas
 Carlos Vallejos-Sologuren, MD, FACP
Ph: 511-620-4995

Related Information

Featured trial article

Registry Information
Official Title Program for the Assessment of Clinical Cancer Tests (PACCT-1): Trial Assigning Individualized Options for Treatment: The TAILORx Trial
Trial Start Date 2006-04-07
Trial Completion Date 2014-04-07 (estimated)
Registered in ClinicalTrials.gov NCT00310180
Date Submitted to PDQ 2006-02-27
Information Last Verified 2011-07-22
NCI Grant/Contract Number CA21115

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.

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