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Clinical Trials (PDQ®)

  • First Published: 11/28/2007
  • Last Modified: 5/25/2012

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Phase III Randomized Study of Adjuvant Chemotherapy Comprising Carboplatin and Paclitaxel With Versus Without Bevacizumab and/or Secondary Cytoreduction Surgery in Patients With Platinum-Sensitive Recurrent Ovarian Epithelial Cancer, Primary Peritoneal Cavity Cancer, or Fallopian Tube Cancer

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

Alternate Title

Carboplatin and Paclitaxel With or Without Bevacizumab After Surgery in Treating Patients with Recurrent Ovarian Epithelial Cancer, Primary Peritoneal Cavity Cancer, or Fallopian Tube Cancer

Basic Trial Information

PhaseTypeStatusAgeSponsorProtocol IDs
Phase IIITreatmentActive18 and overNCIGOG-0213
GOG-0213, NCT00565851

Special Category: NCI Web site featured trial

Objectives

Primary

  1. To determine if surgical secondary cytoreduction in addition to adjuvant chemotherapy comprising carboplatin and paclitaxel with or without bevacizumab increases the duration of overall survival of patients with recurrent platinum-sensitive ovarian epithelial cancer, primary peritoneal cavity cancer, or fallopian tube cancer.
  2. To determine if the addition of bevacizumab to the second-line and maintenance phases of treatment increases the duration of overall survival relative to second-line paclitaxel and carboplatin alone in these patients.

Secondary

  1. To determine if the addition of bevacizumab to the second-line and maintenance phase of treatment increases the duration of progression-free survival relative to second-line paclitaxel and carboplatin alone in these patients.
  2. To prospectively determine the incidence of carboplatin and paclitaxel hypersensitivity in these patients undergoing retreatment with both agents as first recurrence therapy.
  3. To determine if surgical secondary cytoreduction in addition to adjuvant chemotherapy increases quality of life (QOL) of patients with recurrent platinum-sensitive ovarian epithelial cancer or primary peritoneal cavity cancer, as measured by the FACT-O trial outcome index and Rand SF-36 physical functioning scale.
  4. To determine if the addition of bevacizumab to the second-line and maintenance phases of treatment increases QOL relative to second-line paclitaxel and carboplatin alone in patients with recurrent platinum-sensitive ovarian epithelial cancer or primary peritoneal cavity cancer.

Entry Criteria

Disease Characteristics:

  • Patients must have histologic diagnosis of ovarian epithelial carcinoma, primary peritoneal cavity carcinoma, or fallopian tube carcinoma
    • Recurrent disease*
      • Patients whom have already undergone secondary cytoreduction for recurrent disease are excluded

     [Note: *Patients with biochemical recurrence, by definition, are not eligible for surgical randomization and should be considered for the chemotherapy randomization alone. (This eligibility criterion does not apply to patients enrolled after August 7, 2011)]

  • The following histologic epithelial cell types** are allowed:
    • Serous adenocarcinoma
    • Endometrioid adenocarcinoma
    • Mucinous adenocarcinoma
    • Undifferentiated carcinoma
    • Clear cell adenocarcinoma
    • Mixed epithelial carcinoma
    • Transitional cell carcinoma
    • Malignant Brenner Tumor
    • Adenocarcinoma not otherwise specified

     [Note: **Prior histologic diagnosis of borderline, low malignant potential (grade 0) epithelial carcinoma that was surgically resected and subsequently developed an unrelated, new invasive ovarian epithelial or primary peritoneal cavity cancer allowed provided the histological criteria for epithelial cell type is met]

  • Patients with synchronous primary endometrial cancer or a past history of primary endometrial cancer are excluded, unless all of the following conditions are met:
    • Stage not greater than I-B
    • No more than superficial myometrial invasion
    • No vascular or lymphatic invasion
    • No poorly differentiated subtypes, including papillary serous, clear cell or other FIGO grade 3 lesions

  • Patients must have had a complete response to front-line platinum-taxane therapy (at least 3 cycles) and a treatment-free interval without clinical evidence of progressive disease lasting at least 6 months
    • Front-line therapy may have included a biologic agent (e.g., bevacizumab) but an interval of at least 6 months must have elapsed after completion of therapy
    • A complete response to front-line chemotherapy must include the following:
      • Negative physical exam
      • Negative pelvic exam
      • Normalization of CA125, if elevated at baseline
      • Negative radiographic assessment of disease
    • Front-line treatment may include maintenance therapy following complete clinical or pathological response provided recurrent disease is not identified earlier than 6 months following completion of all anticancer treatment
      • Patients receiving maintenance biological therapy or hormonal therapy are eligible provided their recurrence is documented more than 6 months from primary cytotoxic chemotherapy completion (includes maintenance chemotherapy) AND a minimum of 4 weeks has elapsed since their last infusion of biological therapy
      • Patients enrolled on GOG-0198 or patients receiving hormonal therapy for biochemical or non-measurable recurrence disease are eligible provided their recurrence is documented more than 6 months following the completion of primary cytotoxic chemotherapy AND a minimum of 4 weeks must have elapsed since their last exposure to hormonal therapy (This eligibility criterion does not apply to patients enrolled after August 7, 2011)

  • Clinically evident measurable or nonmeasurable disease*** defined as at least one lesion that can be accurately measured in at least one dimension (longest dimension to be recorded)
    • Each lesion must be ≥ 20 mm when measured by conventional techniques, MRI or CT scan, or ≥ 10 mm when measured by spiral CT scan
    • Nonmeasurable disease defined by symptomatic ascites or pleural effusion***
    • Patients with clinically evident measurable or nonmeasurable disease*** must also have any 1 of the following:
      • CA-125 > 2 times upper limit of normal
      • Histologic confirmation of recurrence in the absence of an elevated CA-125 and measurable disease

     [Note: ***Patients with nonmeasurable, clinically evident disease, by definition, are not eligible for surgical randomization and should be considered for the chemotherapy randomization alone. Only measurable disease is permitted as of 8-7-2011.]

  • Patients enrolled after August 7, 2011 must be candidates for cytoreductive surgery and consent to have their surgical treatment determined by randomization

Prior/Concurrent Therapy:

  • See Disease Characteristics
  • No more than 1 prior regimen of chemotherapy (maintenance therapy is not considered a second regimen)
  • No prior radiotherapy to any portion of the abdominal cavity or pelvis
  • No prior chemotherapy for any other abdominal or pelvic tumor other than ovarian, fallopian tube, or primary peritoneal cancer
  • No major surgical procedure, open biopsy, or dental extractions or other dental surgery/procedure that results in an open wound within the past 28 days
  • No placement of vascular access device or core biopsy within the past 7 days
  • No concurrent immunotherapy or radiotherapy
  • No anticipation of need for major surgical procedure during the course of the study

Patient Characteristics:

Inclusion criteria:

  • GOG performance status of 0, 1, or 2
  • Platelet count ≥ 100,000/mm3
  • Absolute neutrophil count ≥ 1,500/mm3
  • Creatinine (non-IDMS) ≤ 1.5 times upper limit of normal (ULN)
  • Total bilirubin ≤ 1.5 times ULN
  • SGOT/AST and alkaline phosphatase ≤ 2.5 times ULN (< 5.0 times ULN in the presence of liver metastasis)
  • Urine protein-to-creatinine ratio < 1.0 mg/dL
  • Signed an approved informed consent and authorization permitting release of personal health information
  • Patients with allergic (i.e., hypersensitivity) reactions to these chemotherapeutic agents are eligible if they were successfully retreated following a desensitization program or protocol

Exclusion criteria:

  • Patients who require parenteral hydration or nutrition and have evidence of partial bowel obstruction or perforation
  • Patients with uncontrolled infection
  • Patients with concurrent severe medical problems unrelated to the malignancy that would significantly limit full compliance with the study or expose the patient to extreme risk or decreased life expectancy
  • Patients with peripheral neuropathy ≥ grade 2
  • Patients with a history of allergic reactions to carboplatin and/or paclitaxel or chemically similar compounds
  • Patients with known hypersensitivity to Chinese hamster ovary cell products or other recombinant human or humanized antibodies
  • Patients of childbearing potential not practicing adequate contraception or patients who are pregnant or nursing
  • Patients with other invasive malignancies, with the exception of nonmelanoma skin cancer, or patients who had (or have) any evidence of the other cancer present within the past 5 years or whose previous cancer treatment contraindicates this protocol therapy
  • Patients with active bleeding or pathologic conditions that carry high risk of bleeding such as a known bleeding disorder, coagulopathy, or tumor involving major vessels
  • Patients with a history or evidence upon physical examination of CNS disease, including primary brain tumor, seizures not controlled with standard medical therapy, any brain metastases, or a history of stroke within the past 5 years
  • Patients with clinically significant cardiovascular disease including any of the following:
    • Significant cardiac conduction abnormalities (e.g., PR interval > 0.24 sec or 2nd or 3rd degree atrioventricular block)
    • Uncontrolled hypertension, defined as systolic blood pressure (BP) > 150 mm Hg or diastolic BP > 90 mm Hg
    • Myocardial infarction, cardiac arrhythmia, or unstable angina within the past 6 months
    • New York Heart Association grade II or greater congestive heart failure
    • Serious cardiac arrhythmia requiring medication
    • Grade II or greater peripheral vascular disease except episodes of ischemia < 24 hrs in duration that are managed non-surgically and without permanent deficit
    • History of cerebrovascular accident within the past 6 months
    • No significant traumatic injury within the past 28 days

Expected Enrollment

360

Outcomes

Primary Outcome(s)

Overall survival

Secondary Outcome(s)

Progression-free survival
Frequency and severity of adverse events

Outline

This is a multicenter study. Patients are assigned to 1 of 2 treatment groups. Patients who are not candidates for surgical cytoreduction (i.e., those for whom complete cytoreduction in the estimation of the investigator is impossible or a medical infirmity precludes exploration and debulking) are eligible to receive chemotherapy after randomization (does not apply to patients enrolled onto the study after August 7, 2011). Patients who are eligible for surgery undergo abdominal exploration with cytoreduction and undergo tumor tissue collection and complete a quality-of-life questionnaire before and after surgery. All patients are then randomized to 1 of 2 treatment arms.

  • Arm I: Patients receive paclitaxel IV over 3 hours or docetaxel IV over 1 hour and carboplatin over 30 minutes on day 1.

  • Arm II: Patients receive chemotherapy as in arm I and bevacizumab IV over 30-90 minutes on day 1.

Treatment in both arms repeats every 21 days in the absence of disease progression or unacceptable toxicity. Patients with measurable disease achieving a clinical response (CR) receive 6-8 courses of therapy. Patients with stable disease or partial regression receive a maximum of 6 courses. Patients without measurable lesions as determined by a CT scan prior to initiating study treatment continue therapy for 6 courses or, if CA-125 normalizes, for 2 cycles beyond CA-125 normalization, whichever is greater. Patients in arm II then receive a maintenance regimen comprising bevacizumab IV over 30-90 minutes. Treatment with bevacizumab alone repeats every 3 weeks in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed periodically for 10 years.

Trial Contact Information

Trial Lead Organizations

Gynecologic Oncology Group

Robert Coleman, MD, Protocol chair
Ph: 713-745-3357; 800-392-1611
Email: rcoleman@mdanderson.org
Scott Eisenkop, MD, FACOG, Protocol co-chair
Ph: 408-378-6131
Deborah Armstrong, MD, Protocol co-chair
Ph: 410-614-2743
Email: darmstro@jhmi.edu
Thomas Herzog, MD, Protocol co-chair
Ph: 212-305-3410
Email: th2135@columbia.edu
Paul Sabbatini, MD, Protocol co-chair
Ph: 212-639-6423; 800-525-2225

Trial Sites

U.S.A.
Alaska
  Anchorage
 Providence Cancer Center
 Clinical Trials Office - Providence Cancer Center
Ph: 907-261-3109
California
  Long Beach
 Todd Cancer Institute at Long Beach Memorial Medical Center
 Robert Bristow
Ph: 562-933-0900
  Los Angeles
 Jonsson Comprehensive Cancer Center at UCLA
 Clinical Trials Office - Jonsson Comprehensive Cancer Center at UCLA
Ph: 888-798-0719
 Kaiser Permanente Medical Center - Los Angeles
 Scott Lentz, MD
Ph: 323-783-4018
  Mountain View
 Palo Alto Medical Foundation
 Albert Pisani
Ph: 650-934-7000
  San Francisco
 UCSF Helen Diller Family Comprehensive Cancer Center
 Clinical Trials Office - UCSF Helen Diller Family Comprehensive Cancer Center
Ph: 877-827-3222
  Stanford
 Stanford Cancer Center
 Clinical Trials Office - Stanford Cancer Center
Ph: 650-498-7061
  Email: cctoffice@stanford.edu
Colorado
  Aurora
 Aurora Presbyterian Hospital
 Eduardo Pajon, MD
Ph: 303-399-8020ext2261
 University of Colorado Cancer Center at UC Health Sciences Center
 Clinical Trials Office - University of Colorado Cancer Center
Ph: 720-848-0650
  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
 Presbyterian - St. Luke's Medical Center
 Clinical Trials Office - Presbyterian - St. Luke's Medical Center
Ph: 303-839-6000
 Rose Medical Center
 Eduardo Pajon, MD
Ph: 303-399-8020ext2261
 St. Anthony Central Hospital
 Eduardo Pajon, MD
Ph: 303-399-8020ext2261
 St. Joseph Hospital
 Eduardo Pajon, MD
Ph: 303-399-8020ext2261
  Englewood
 Rocky Mountain Gynecologic Oncology
 Kevin Davis, MD
Ph: 303-781-9090
 Swedish Medical Center
 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
  Littleton
 Littleton Adventist Hospital
 Eduardo Pajon, MD
Ph: 303-399-8020ext2261
  Lone Tree
 Sky Ridge 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
  Loveland
 McKee Medical Center
 Eduardo Pajon, MD
Ph: 303-399-8020ext2261
  Parker
 Parker Adventist Hospital
 Eduardo Pajon, MD
Ph: 303-399-8020ext2261
  Pueblo
 St. Mary - Corwin Regional Medical Center
 Eduardo Pajon, MD
Ph: 303-399-8020ext2261
  Thornton
 North Suburban Medical Center
 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
  Hartford
 Helen and Harry Gray Cancer Center at Hartford Hospital
 Clinical Trials Office - Helen and Harry Gray Cancer Center
Ph: 860-545-5363
 Saint Francis/Mount Sinai Regional Cancer Center at Saint Francis Hospital and Medical Center
 Philip Stella, MD
Ph: 734-712-1000
  New Britain
 George Bray Cancer Center at the Hospital of Central Connecticut - New Britain Campus
 Clinical Trials Office - George Bray Cancer Center
Ph: 860-224-5660
Delaware
  Lewes
 Tunnell Cancer Center at Beebe Medical Center
 Clinical Trials Office - Tunnell Cancer Center
Ph: 302-645-3171
  Newark
 CCOP - Christiana Care Health Services
 Clinical Trial Office - CCOP - Christiana Care Health Services
Ph: 302-623-4450
Florida
  Fort Myers
 Florida Gynecologic Oncology - Fort Myers
 Edward Grendys, MD
Ph: 239-992-0077
  Saint Petersburg
 Women's Cancer Associates
 James LaPolla, MD
Ph: 727-821-9688
Georgia
  Augusta
 MBCCOP - Medical College of Georgia Cancer Center
 Sharad Ghamande, MD
Ph: 706-721-3992
  Columbus
 John B. Amos Cancer Center
 Clinical Trials Office - John B. Amos Cancer Center
Ph: 706-660-6404
  Gainesville
 Northeast Georgia Medical Center
 Andrew Green
Ph: 770-535-3553
  Savannah
 Curtis and Elizabeth Anderson Cancer Institute at Memorial Health University Medical Center
 Clinical Trials Office - Curtis and Elizabeth Anderson Cancer Institute
Ph: 912-350-8568
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
 Robert H. Lurie Comprehensive Cancer Center at Northwestern University
 Clinical Trials Office - Robert H. Lurie Comprehensive Cancer Center at Northwestern University
Ph: 312-695-1301
  Email: cancer@northwestern.edu
 Rush University Medical Center
 Clinical Trials Office - Rush University Medical Center
Ph: 312-942-5498
  Email: clinical_trials@rush.edu
 University of Chicago Cancer Research Center
 Clinical Trials Office - University of Chicago Cancer Research Center
Ph: 773-834-7424
  Hinsdale
 Gynecologic Oncology
 Sudarshan Sharma, MD
Ph: 630-856-6757
  Springfield
 Regional Cancer Center at Memorial Medical Center
 Clinical Trials Office - Regional Cancer Center at Memorial Medical Center
Ph: 217-788-4233
  Urbana
 CCOP - Carle Cancer Center
 Clinical Trials Office - CCOP - Carle Cancer Center
Ph: 800-446-5532
Indiana
  Elkhart
 Elkhart Clinic, LLC
 Michael Rodriguez
Ph: 574-296-3200
 Elkhart General Hospital
 Michael Rodriguez
Ph: 574-294-2621
 Michiana Hematology-Oncology, PC - Elkhart
 Michael Rodriguez
Ph: 574-389-0414
  Indianapolis
 Indiana University Melvin and Bren Simon Cancer Center
 Clinical Trials Office - Indiana University Cancer Center
Ph: 317-274-2552
 St. Vincent Oncology Center
 Gregory Sutton, MD
Ph: 317-415-6740
  Kokomo
 Howard Community Hospital
 Michael Rodriguez
Ph: 765-453-8571
  La Porte
 Center for Cancer Therapy at LaPorte Hospital and Health Services
 Michael Rodriguez
Ph: 219-326-2683
  Mishawaka
 Michiana Hematology-Oncology, PC - South Bend
 Michael Rodriguez
Ph: 574-234-5123
 Saint Joseph Regional Medical Center
 Michael Rodriguez
Ph: 574-237-7111
  Munster
 Community Hospital
 Mohamad Kassar
Ph: 219-836-4503
  Plymouth
 Michiana Hematology Oncology PC - Plymouth
 Michael Rodriguez
Ph: 574-936-2585
  South Bend
 CCOP - Northern Indiana CR Consortium
 Michael Rodriguez
Ph: 574-647-7370
800-284-7370
 Memorial Hospital of South Bend
 Clinical Trials Office - Memorial Hospital of South Bend
Ph: 800-284-7370
 Michiana Hematology-Oncology, PC - South Bend
 Michael Rodriguez
Ph: 574-234-5123
  Westville
 Michiana Hematology Oncology PC - La Porte
 Michael Rodriguez
Ph: 219-324-1790
Iowa
  Des Moines
 CCOP - Iowa Oncology Research Association
 Robert Behrens
Ph: 515-244-7586
888-244-6061
 John Stoddard Cancer Center at Iowa Lutheran Hospital
 Clinical Trials Office - John Stoddard Cancer Center at Iowa Lutheran Hospital
Ph: 515-241-8704
 John Stoddard Cancer Center at Iowa Methodist Medical Center
 Clinical Trials Office - John Stoddard Cancer Center at Iowa Methodist Medical Center
Ph: 515-241-6727
 Medical Oncology and Hematology Associates at John Stoddard Cancer Center
 Robert Behrens
Ph: 515-282-2921
 Medical Oncology and Hematology Associates at Mercy Cancer Center
 Robert Behrens
Ph: 515-643-8740
 Mercy Cancer Center at Mercy Medical Center - Des Moines
 Robert Behrens
Ph: 515-643-8206
888-221-4849
  Iowa City
 Holden Comprehensive Cancer Center at University of Iowa
 Cancer Information Service
Ph: 800-237-1225
Kansas
  Chanute
 Cancer Center of Kansas, PA - Chanute
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
  Dodge City
 Cancer Center of Kansas, PA - Dodge City
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
  El Dorado
 Cancer Center of Kansas, PA - El Dorado
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
  Fort Scott
 Cancer Center of Kansas - Fort Scott
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
  Independence
 Cancer Center of Kansas-Independence
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
  Kingman
 Cancer Center of Kansas, PA - Kingman
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
  Liberal
 Cancer Center of Kansas, PA - Liberal
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
  Newton
 Cancer Center of Kansas, PA - Newton
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
  Overland Park
 Saint Luke's Hospital - South
 Rakesh Gaur, MD
Ph: 913-948-5588
  Parsons
 Cancer Center of Kansas, PA - Parsons
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
  Prairie Village
 CCOP - Kansas City
 Rakesh Gaur, MD
Ph: 913-948-5588
  Pratt
 Cancer Center of Kansas, PA - Pratt
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
  Salina
 Cancer Center of Kansas, PA - Salina
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
  Wellington
 Cancer Center of Kansas, PA - Wellington
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
  Wichita
 Associates in Womens Health, PA - North Review
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
 Cancer Center of Kansas, PA - Wichita
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
 Cancer Center of Kansas, PA - Medical Arts Tower
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
 CCOP - Wichita
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
 Via Christi Cancer Center at Via Christi Regional Medical Center
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
  Winfield
 Cancer Center of Kansas, PA - Winfield
 Shaker Dakhil, MD, FACP
Ph: 316-262-4467
Louisiana
  Baton Rouge
 Woman's Hospital
 Giles Fort, MD
Ph: 225-358-1071
Maryland
  Baltimore
 Greater Baltimore Medical Center Cancer Center
 Clinical Trials Office - Greater Baltimore Medical Center Cancer Center
Ph: 443-849-3706
  Elkton MD
 Union Hospital of Cecil County
 Mark Borowsky
Ph: 410-398-4000
Massachusetts
  Worcester
 UMASS Memorial Cancer Center - University Campus
 Susan Zweizig, MD
Ph: 508-334-1160
Michigan
  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
 University of Michigan Comprehensive Cancer Center
 Clinical Trials Office - University of Michigan Comprehensive Cancer Center
Ph: 800-865-1125
  Battle Creek
 Battle Creek Health System Cancer Care Center
 Gilbert Padula
Ph: 616-966-8000
  Big Rapids
 Mecosta County Medical Center
 Gilbert Padula
Ph: 231-796-8691
  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
 Barbara Ann Karmanos Cancer Institute
 Clinical Trials Office - Barbara Ann Karmanos Cancer Institute
Ph: 313-576-9363
 Josephine Ford Cancer Center at Henry Ford Hospital
 Thomas Buekers
Ph: 313-916-1850
888-734-5322
  Flint
 Hurley Medical Center
 Clinical Trials Office - Hurley Medical Center
Ph: 810-762-8057
  Grand Rapids
 Butterworth Hospital at Spectrum Health
 Gilbert Padula
Ph: 616-391-2799
 CCOP - Grand Rapids
 Gilbert Padula
Ph: 616-391-1230
 Gynecologic Oncology of West Michigan
 Gordon Downey, MD
Ph: 616-957-3398
 Lacks Cancer Center at Saint Mary's Health Care
 Gilbert Padula
Ph: 616-752-5222
  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
  Jackson
 Foote Memorial Hospital
 Philip Stella, MD
Ph: 734-712-1000
  Kalamazoo
 Borgess Medical Center
 Raymond Lord, MD
Ph: 269-373-7458
 Bronson Methodist Hospital
 Raymond Lord, MD
Ph: 269-373-7458
 West Michigan Cancer Center
 Clinical Trials Office - West Michigan Cancer Center
Ph: 269-373-7458
  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
  Muskegon
 Mercy General Health Partners
 Gilbert Padula
Ph: 231-672-2000
  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
  Reed City
 Spectrum Health Reed City Hospital
 Gilbert Padula
Ph: 231-832-3271
  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
  Saint Joseph
 Lakeside Cancer Specialists, PLLC
 Michael Rodriguez
Ph: 269-428-4411
  St. Joseph
 Lakeland Regional Cancer Care Center - St. Joseph
 Michael Rodriguez
Ph: 269-983-8698
800-303-8399
  Traverse City
 Munson Medical Center
 Gilbert Padula
Ph: 231-935-6202
  Warren
 St. John Macomb Hospital
 Philip Stella, MD
Ph: 734-712-1000
Minnesota
  Burnsville
 Fairview Ridges Hospital
 Patrick Flynn, MD
Ph: 612-863-8585
  Coon Rapids
 Mercy and Unity Cancer Center at Mercy Hospital
 Patrick Flynn, MD
Ph: 612-863-8585
  Duluth
 St. Luke's Hospital Cancer Care Center
 Tanya Repka, MD, FACP
Ph: 218-726-3081
  Edina
 Fairview Southdale Hospital
 Clinical Trials Office - Fairview Southdale Hospital
Ph: 612-625-3650
  Fridley
 Mercy and Unity Cancer Center at Unity Hospital
 Patrick Flynn, MD
Ph: 612-863-8585
  Hutchinson
 Hutchinson Area Health Care
 Patrick Flynn, MD
Ph: 612-863-8585
  Maplewood
 HealthEast Cancer Care at St. John's Hospital
 Patrick Flynn, MD
Ph: 612-863-8585
 Minnesota Oncology - Maplewood
 Patrick Flynn, MD
Ph: 612-863-8585
  Minneapolis
 Hennepin County Medical Center - Minneapolis
 Clinical Trials Office - Hennepin County Medical Center - Minneapolis
Ph: 612-873-5911
 Virginia Piper Cancer Institute at Abbott - Northwestern Hospital
 Clinical Trials Office - Virginia Piper Cancer Institute
Ph: 612-863-5654
  New Ulm
 New Ulm Medical Center
 Patrick Flynn, MD
Ph: 612-863-8585
  Robbinsdale
 Humphrey Cancer Center at North Memorial Outpatient Center
 Clinical Trials Office - Humphrey Cancer Center at North Memorial Outpatient Center
Ph: 763-520-1893
  Saint Louis Park
 CCOP - Metro-Minnesota
 Patrick Flynn, MD
Ph: 612-863-8585
 Park Nicollet Cancer Center
 Patrick Flynn, MD
Ph: 612-863-8585
  Saint Paul
 United Hospital
 Patrick Flynn, MD
Ph: 612-863-8585
  Shakopee
 St. Francis Cancer Center at St. Francis Medical Center
 Patrick Flynn, MD
Ph: 612-863-8585
  St. Paul
 Regions Hospital Cancer Care Center
 Clinical Trials Office - Regions Hospital Cancer Care Center
Ph: 651-254-1517
  Stillwater
 Lakeview Hospital
 Patrick Flynn, MD
Ph: 612-863-8585
  Waconia
 Ridgeview Medical Center
 Patrick Flynn, MD
Ph: 612-863-8585
  Willmar
 Willmar Cancer Center at Rice Memorial Hospital
 Patrick Flynn, MD
Ph: 612-863-8585
  Woodbury
 Minnesota Oncology - Woodbury
 Patrick Flynn, MD
Ph: 612-863-8585
Mississippi
  Jackson
 St. Dominic Cancer Center
 Donald Seago
Ph: 601-200-3070
 University of Mississippi Cancer Clinic
 James Thigpen, MD
Ph: 601-984-5590
Missouri
  Columbia
 Ellis Fischel Cancer Center at University of Missouri - Columbia
 Clinical Trial Office - Ellis Fischel Cancer Center
Ph: 573-882-7440
  Kansas City
 Research Medical Center
 Rakesh Gaur, MD
Ph: 913-948-5588
 Saint Luke's Cancer Institute at Saint Luke's Hospital
 Rakesh Gaur, MD
Ph: 913-948-5588
  Lee's Summit
 Saint Luke's East - Lee's Summit
 Rakesh Gaur, MD
Ph: 913-948-5588
  Saint Louis
 Siteman Cancer Center at Barnes-Jewish Hospital - Saint Louis
 David Mutch, MD
Ph: 314-362-3181
  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
 St. John's Regional Health Center
 Robert Carolla
Ph: 417-820-2000
Nebraska
  Omaha
 Methodist Estabrook Cancer Center
 Peter Morris, MD
Ph: 402-354-5250
Nevada
  Las Vegas
 Women's Cancer Center - La Canada
 Nick Spirtos, MD
Ph: 408-866-3843
  Reno
 Renown Institute for Cancer at Renown Regional Medical Center
 Peter Lim
Ph: 775-982-5050
866-559-0558
New Jersey
  Marlton
 Fox Chase Virtua Health Cancer Program at Virtua Memorial Hospital Marlton
 Clinical Trials Office - Fox Chase Virtua Health Cancer Program at Virtua Memorial Hospital Marlton
Ph: 888-847-8823
  Morristown
 Carol G. Simon Cancer Center at Morristown Memorial Hospital
 Daniel Tobias
Ph: 973-971-6100
800-247-9580
  Neptune
 Jersey Shore Cancer Center at Jersey Shore University Medical Center
 Henry Sprance, MD, PhD
Ph: 732-776-4128
  New Brunswick
 Cancer Institute of New Jersey at UMDNJ - Robert Wood Johnson Medical School
 Clinical Trials Office - Cancer Institute of New Jersey
Ph: 732-235-8675
  Phillipsburg
 Women’s Institute for Gynecologic Cancer and Special Pelvic Surgery
 David Silver, MD
Ph: 702-427-4999
  Voorhees
 Cancer Institute of New Jersey at Cooper - Voorhees
 Clinical Trials Office - Cancer Institute of New Jersey at Cooper University Hospital - Voorhees
Ph: 856-325-6757
New Mexico
  Albuquerque
 Southwest Gynecologic Oncology Associates, Incorporated
 Carolyn Muller, MD
Ph: 505-272-0185
 University of New Mexico Cancer Center
 Clinical Trials Office - University of New Mexico Cancer Center
Ph: 505-272-6972
  Las Cruces
 University of New Mexico Cancer Center - South
 Carolyn Muller, MD
Ph: 505-272-0185
New York
  Albany
 Women's Cancer Care Associates
 Thomas Morrissey
Ph: 518-458-1390
  Brooklyn
 SUNY Downstate Medical Center
 Ovadia Abulafia, MD
Ph: 718-270-2152
  Lake Success
 Monter Cancer Center of the North Shore-LIJ Health System
 Veena John
Ph: 516-734-8959
  Manhasset
 Don Monti Comprehensive Cancer Center at North Shore University Hospital
 Clinical Trials Office - Don Monti Comprehensive Cancer Center at North Shore University Hospital
Ph: 516-734-8900
  New Hyde Park
 Long Island Jewish Medical Center
 Veena John
Ph: 718-470-7000
800-371-7111
  New York
 Herbert Irving Comprehensive Cancer Center at Columbia University Medical Center
 Clinical Trials Office - Herbert Irving Comprehensive Cancer Center at Columbia University Medical Center
Ph: 212-305-8615
 Memorial Sloan-Kettering Cancer Center
 Mario Leitao, Jr.
Ph: 212-639-8895
800-525-2225
 Mount Sinai Medical Center
 Jamal Rahaman
Ph: 212-241-6500
 NYU Cancer Institute at New York University Medical Center
 Stephanie Blank, MD
Ph: 212-263-2668
  Stony Brook
 Stony Brook University Cancer Center
 Clinical Trials Office - Stony Brook University Cancer Center
Ph: 800-862-2215
North Carolina
  Burlington
 Alamance Cancer Center at Alamance Regional Medical Center
 Janak Choksi, MD
Ph: 336-538-7737
  Chapel Hill
 Lineberger Comprehensive Cancer Center at University of North Carolina - Chapel Hill
 Clinical Trials Office - Lineberger Comprehensive Cancer Center
Ph: 877-668-0683; 919-966-4432
  Charlotte
 Blumenthal Cancer Center at Carolinas Medical Center
 Clinical Trials Office - Blumenthal Cancer Center at Carolinas Medical Center
Ph: 704-355-2884
 Presbyterian Cancer Center at Presbyterian Hospital
 Clinical Trials Office - Presbyterian Cancer Center at Presbyterian Hospital
Ph: 704-384-5369
  Durham
 Duke Cancer Institute
 Clinical Trials Office - Duke Cancer Institute
Ph: 888-275-3853
  Greensboro
 Moses Cone Regional Cancer Center at Wesley Long Community Hospital
 Clinical Trials Office - Moses Cone Regional Cancer Center at Wesley Long Community Hospital
Ph: 336-621-8374
  Raleigh
 Duke Health Raleigh Hospital
 Angeles Secord, MD
Ph: 919-684-3765
  Winston-Salem
 Wake Forest University Comprehensive Cancer Center
 Clinical Trials Office - Wake Forest University Comprehensive Cancer Center
Ph: 336-713-6771
Ohio
  Akron
 McDowell Cancer Center at Akron General Medical Center
 Eric Jenison, MD
Ph: 330-344-6041
 Summa Center for Cancer Care at Akron City Hospital
 Clinical Trials Office - Akron City Hospital
Ph: 330-375-6101
  Canton
 Aultman Cancer Center at Aultman Hospital
 Clinical Trials Office - Aultman Cancer Center at Aultman Hospital
Ph: 330-363-6891
  Cincinnati
 Charles M. Barrett Cancer Center at University Hospital
 William Richards
Ph: 806-796-1317
  Cleveland
 Case Comprehensive Cancer Center
 Clinical Trials Office - Case Comprehensive Cancer Center
Ph: 800-641-2422
 Cleveland Clinic Cancer Center at Fairview Hospital
 Clinical Trials Office - Cleveland Clinic Cancer Center at Fairview Hospital
Ph: 216-476-9362
 Cleveland Clinic Taussig Cancer Center
 Clinical Trials Office - Cleveland Clinic Taussig Cancer Center
Ph: 866-223-8100
 MetroHealth Cancer Care Center at MetroHealth Medical Center
 Peter Rose, MD
Ph: 216-444-1712
  Columbus
 Arthur G. James Cancer Hospital and Richard J. Solove Research Institute at Ohio State University Comprehensive Cancer Center
 Ohio State University Cancer Clinical Trial Matching Service
Ph: 866-627-7616
  Email: osu@emergingmed.com
 Riverside Methodist Hospital Cancer Care
 Clinical Trials Office - Riverside Methodist Hospital Cancer Care
Ph: 614-566-4475
  Dayton
 David L. Rike Cancer Center at Miami Valley Hospital
 Clinical Trials Office - David L. Rike Cancer Center at Miami Valley Hospital
Ph: 937-208-2079
  Kettering
 Charles F. Kettering Memorial Hospital
 Clinical Trials Office - Charles F. Kettering Memorial Hospital
Ph: 937-298-3399 ext. 57556
  Mayfield Heights
 Hillcrest Cancer Center at Hillcrest Hospital
 Peter Rose, MD
Ph: 216-444-1712
  Mentor
 Lake/University Ireland Cancer Center
 Steven Waggoner, MD
Ph: 216-844-5011
Oklahoma
  Oklahoma City
 Oklahoma University Cancer Institute
 Robert Mannel, MD
Ph: 405-271-8787
  Tulsa
 Cancer Care Associates - Saint Francis Campus
 Robert Mannel, MD
Ph: 405-271-8787
Oregon
  Portland
 Knight Cancer Institute at Oregon Health and Science University
 Clinical Trials Office - Knight Cancer Institute at Oregon Health and Science University
Ph: 503-494-1080
  Email: trials@ohsu.edu
 Northwest Cancer Specialists at Rose Quarter Cancer Center
 William Winter, III
Ph: 503-228-6509
Pennsylvania
  Abington
 Rosenfeld Cancer Center at Abington Memorial Hospital
 Clinical Trials Office - Rosenfeld Cancer Center at Abington Memorial Hospital
Ph: 215-481-2402
  Allentown
 Morgan Cancer Center at Lehigh Valley Hospital - Cedar Crest
 Richard Boulay, MD
Ph: 610-402-3650
  Bethlehem
 St. Luke's Cancer Network at St. Luke's Hospital
 Nicholas Taylor
Ph: 610-954-3580
  Danville
 Geisinger Cancer Institute at Geisinger Health
 Clinical Trials Office - Geisinger Cancer Institute
Ph: 570-271-5251
  Hazleton
 Geisinger Hazleton Cancer Center
 James Bosscher
Ph: 570-459-2901
  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
  Philadelphia
 Abramson Cancer Center of the University of Pennsylvania
 Clinical Trials Office - Abramson Cancer Center of the University of Pennsylvania
Ph: 800-474-9892
 Fox Chase Cancer Center - Philadelphia
 Clinical Trials Office - Fox Chase Cancer Center - Philadelphia
Ph: 215-728-4790
 Fox Chase Cancer Center CCOP Research Base
 Clinical Trials Office - Fox Chase Cancer Center CCOP Research Base
Ph: 215-728-2983
 Joan Karnell Cancer Center at Pennsylvania Hospital
 Patricia Ford, MD
Ph: 215-829-6088
  Reading
 McGlinn Family Regional Cancer Center at Reading Hospital and Medical Center
 Clinical Trials Office - McGlinn Family Regional Cancer Center
Ph: 610-988-9323
  State College
 Geisinger Medical Group - Scenery Park
 James Bosscher
Ph: 814-231-4560
  Wilkes-Barre
 Frank M. and Dorothea Henry Cancer Center at Geisinger Wyoming Valley Medical Center
 Clinical Trials Office - Frank M. and Dorothea Henry Cancer Center at Geisinger Wyoming Valley Medical Center
Ph: 570-271-5251
Rhode Island
  Providence
 Women and Infants Hospital of Rhode Island
 Clinical Trials Office - Women and Infants Hospital of Rhode Island
Ph: 401-274-1122
South Dakota
  Rapid City
 Black Hills Obstetrics & Gynecology LLP
 Helen Frederickson, MD
Ph: 605-343-9224
  Sioux Falls
 Avera Cancer Institute
 Luis Rojas-Espaillat
Ph: 605-322-3000
 Sanford Cancer Center at Sanford USD Medical Center
 Clinical Trials Office - Sanford Cancer Center
Ph: 605-328-1367
Texas
  Dallas
 Simmons Comprehensive Cancer Center at University of Texas Southwestern Medical Center - Dallas
 Clinical Trials Office - Simmons Comprehensive Cancer Center at University of Texas Southwestern Medical Center - Dallas
Ph: 866-460-4673; 214-648-7097
  Fort Sam Houston
 Brooke Army Medical Center
 Clinical Trials Office - Brooke Army Medical Center
Ph: 210-916-4837
  Galveston
 University of Texas Medical Branch
 Clinical Trials Office - University of Texas Medical Branch
Ph: 409-772-1950
  Houston
 M. D. Anderson Cancer Center at University of Texas
 Clinical Trials Office - M. D. Anderson Cancer Center at the University of Texas
Ph: 713-792-3245
 Methodist Hospital
 Aparna Kamat
Ph: 713-441-1010
Utah
  Salt Lake City
 Huntsman Cancer Institute at University of Utah
 Clinical Trials Office - Huntsman Cancer Institute at University of Utah
Ph: 801-581-4477
  Email: clinical.trials@hci.utah.edu
Vermont
  Burlington
 Fletcher Allen Health Care - University Health Center Campus
 Clinical Trials Office - Fletcher Allen Health Care
Ph: 802-656-8990
Virginia
  Charlottesville
 University of Virginia Cancer Center
 Susan Modesitt
Ph: 434-924-9333
800-223-9173
  Richmond
 Virginia Commonwealth University Massey Cancer Center
 Clinical Trials Office -Virginia Commonwealth University Massey Cancer Center
Ph: 804-628-1939
Washington
  Bellingham
 PeaceHealth Medical Group, PC at St. Joseph Hospital
 Benjamin Greer, MD
Ph: 206-685-2463
  Bremerton
 Harrison Medical Center
 Benjamin Greer, MD
Ph: 206-685-2463
 Olympic Hematology and Oncology
 Benjamin Greer, MD
Ph: 206-685-2463
  Everett
 Providence Regional Cancer Partnership
 Benjamin Greer, MD
Ph: 206-685-2463
  Mount Vernon
 Skagit Valley Hospital Cancer Care Center
 Benjamin Greer, MD
Ph: 206-685-2463
  Poulsbo
 Harrison Poulsbo Hematology and Onocology
 Benjamin Greer, MD
Ph: 206-685-2463
  Seattle
 Fred Hutchinson Cancer Research Center
 Benjamin Greer, MD
Ph: 206-685-2463
 Group Health Central Hospital
 Clinical Trials Office - Group Health Central Hospital
Ph: 206-287-2900
 Northwest Hospital and Medical Center
 Benjamin Greer, MD
Ph: 206-685-2463
 Pacific Gynecology Specialists
 Benjamin Greer, MD
Ph: 206-685-2463
 Seattle Cancer Care Alliance
 Clinical Trials Office - Seattle Cancer Care Alliance
Ph: 800-804-8824
 Swedish Cancer Institute at Swedish Medical Center - First Hill Campus
 Benjamin Greer, MD
Ph: 206-685-2463
 University Cancer Center at University of Washington Medical Center
 Benjamin Greer, MD
Ph: 206-685-2463
  Sequim
 Olympic Medical Cancer Center
 Benjamin Greer, MD
Ph: 206-685-2463
  Spokane
 Cancer Care Northwest - Spokane South
 Clinical Trials Office - Cancer Care Northwest - Spokane South
Ph: 509-228-1083
 Rockwood Clinic Cancer Treatment Center
 Clinical Trials Office - Rockwood Clinic Cancer Treatment Center
Ph: 509-838-2531 ext. 6880
  Tacoma
 Franciscan Cancer Center at St. Joseph Medical Center
 Clinical Trials Office - Franciscan Cancer Center
Ph: 253-426-6914
 MultiCare Regional Cancer Center at Tacoma General Hospital
 Clinical Trials Office - MultiCare Regional Cancer Center
Ph: 253-403-3229
  Walla Walla
 St. Mary Regional Cancer Center at St. Mary Medical Center
 Benjamin Greer, MD
Ph: 206-685-2463
  Wenatchee
 Wenatchee Valley Medical Center
 Clinical Trials Office - Wenatchee Valley Medical Center
Ph: 509-665-5800
Wisconsin
  Green Bay
 Green Bay Oncology, Limited at St. Mary's Hospital
 Jonathan Tammela
Ph: 920-884-3135
 Green Bay Oncology, Limited at St. Vincent Hospital Regional Cancer Center
 Jonathan Tammela
Ph: 920-432-6049
 St. Vincent Hospital Regional Cancer Center
 Clinical Trials Office - St. Vincent Hospital Regional Cancer Center
Ph: 920-433-8889
  Madison
 University of Wisconsin Paul P. Carbone Comprehensive Cancer Center
 Clinical Trials Office - University of Wisconsin Paul P. Carbone Comprehensive Cancer Center
Ph: 608-262-5223
  Marinette
 Bay Area Cancer Care Center at Bay Area Medical Center
 Jonathan Tammela
Ph: 715-735-6523
888-788-2070
  Milwaukee
 Aurora Sinai Medical Center
 Clinical Trials Office - Aurora Sinai Medical Center
Ph: 414-649-5717
 Medical College of Wisconsin Cancer Center
 Clinical Trials Office - Medical College of Wisconsin Cancer Center
Ph: 414-805-4380
 Vince Lombardi Cancer Clinic at Aurora St. Luke's Medical Center
 Clinical Trials Office - Vince Lombardi Cancer Clinic
Ph: 414-649-5717
  Sheboygan
 Vince Lombardi Cancer Clinic - Sheboygan
 Clinical Trials Office - Vince Lombardi Cancer Clinic - Sheboygan
Ph: 414-649-7200
  Two Rivers
 Vince Lombardi Cancer Clinic - Two Rivers
 Andrew Yetter
Ph: 920-793-6000
  Wausau
 University of Wisconcin Cancer Center at Aspirus Wausau Hospital
 Clinical Trials Office - University of Wisconsin Cancer Center
Ph: 608-262-5223
  West Allis
 Aurora Women's Pavilion of West Allis Memorial Hospital
 Peter Johnson, MD (Contact information may not be current)
Ph: 262-549-6662
Japan
  Hiroshima City
 Hiroshima University Hospital
 Hisaya Fujiwara
Ph: 81-82-261-3131
  Kagoshima City, Kagoshima
 Kagoshima City Hospital
 Masayuki Hatae, MD
Ph: 81-99-224-2101
  Kure
 National Hospital Organization - Medical Center of Kure
 Kazuhiro Takehara
Ph: 81-82-322-3111
  Minato-ku, Tokyo
 Jikei University School of Medicine Hospital
 Kyosuke Yamada
Ph: 81-3-3603-2111
  Niigata City
 Niigata University Medical and Dental Hospital
 Tetsuro Yahata
  Saitama
 Saitama Medical University International Medical Center
 Keiichi Fujiwara, MD, PhD
Ph: 81-42-984-4637
  Sapporo
 Hokkaido University Hospital
 Noriaki Sakuragi
Ph: 81-11-716-1161 ext. 6000
  Sendai
 Tohoku University Graduate School of Medicine
 Nobuo Yaegashi
Ph: 81-22-274-1111
  Tokyo
 National Cancer Center Hospital
 Mayu Yunokawa
Ph: 81-3-3542-2511
  Tottori
 Tottori University Hospital
 Junzo Kigawa, MD, PhD
Ph: 81-859-33-1111
Iwate
  Morioka
 Iwate Medical University Hospital
 Toru Sugiyama
Ph: 81-19-651-5111
Republic of Korea
  Goyang-si
 National Cancer Center - Korea
 Sang Park
Ph: 82-031-920-0001
  Jung-Ku
 Dongsan Medical Center of Keimyung University
 Chi-Heum Cho
Ph: 82-53-250-7114
  Seoul
 Asan Medical Center - University of Ulsan College of Medicine
 Young-Tak Kim
Ph: 82-2-224-3210
 Catholic University of Korea College of Medicine
 Jong-Sup Park
Ph: 82-2-593-5141
 Ewha Womans University Hospital
 Seung Kim
Ph: 82-2-760-5114
 Korea Cancer Center Hospital
 Moon-Hong Kim
Ph: 82-2-9702-114
 Samsung Medical Center
 Duk-Soo Bae
Ph: 82-2-3410-0200, 0220
 Seoul National University Hospital
 Soon-Beom Kang
Ph: 82-2-763-5110
  Suwon
 Ajou University Hospital
 Hee-Sug Ryu

Related Information

Featured trial article

Registry Information
Official Title A Phase III Randomized Controlled Clinical Trial of Carboplatin and Paclitaxel alone or in Combination with Bevacizumab (NSC #704865, IND #7921) followed by Bevacizumab and Secondary Cytoreduction Surgery in Platinum-Sensitive, Recurrent Ovarian, Peritoneal Primary and Fallopian Tube Cancer
Trial Start Date 2007-12-07
Trial Completion Date 2009-12-17 (estimated)
Registered in ClinicalTrials.gov NCT00565851
Date Submitted to PDQ 2007-10-29
Information Last Verified 2012-05-26
NCI Grant/Contract Number CA27469

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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