| | db_trialID | db_groupID | db_PrimarySiteCode1 | db_PrimarySiteCode2 | Endorsed By | Protocol Description | Eligibility |
| 5 |
1
| RTOG 0625/ACRIN 6677 | Recurrent GBM |
BRAIN
RTOG 0625/ACRIN 6677
Recurrent GBM
| db_researchSpecialtyID | db_trialID | db_SpecialtyID | |
| 2 | 5 | 2 |
Medical Oncology
|
| A Randomized Phase II Trial of Bevacizumab with Irinotecan or Bevacizumab with Temozolomide in recurrent GBM |
| db_EligibilityTrialID | db_trialID | |
| 7 | 5 |
- Pt must have rec’d prior temozolomide
|
| 8 | 5 |
- Prior tx with SRS, Gliadel wafer or brachytherapy okay
|
| 10 | 5 |
- Unequivocal radiographic evidence for progression by MRI within 14 days
|
| 289 | 5 |
- Contact (561) 955-4800
|
|
| 6 |
1
| RTOG 0627 | Recurrent GBM |
BRAIN
RTOG 0627
Recurrent GBM
| db_researchSpecialtyID | db_trialID | db_SpecialtyID | |
| 4 | 6 | 1 |
Radiation Oncology
|
| 5 | 6 | 2 |
Medical Oncology
|
| Phase II Trial of Dasatinib in patients with recurrent GBM treated with RT + temozolomide |
| db_EligibilityTrialID | db_trialID | |
| 11 | 6 |
- MRI or CT brain done within 10 days prior to registration
|
| 12 | 6 |
- Gliadel wafer use excluded
|
| 13 | 6 |
- Scan showing recurrent/progressive GBM
|
| 290 | 6 |
- Contact (561) 955-4800
|
|
| 8 |
1
| NCCTG 0574 | Cerebral Mets |
BRAIN
NCCTG 0574
Cerebral Mets
| db_researchSpecialtyID | db_trialID | db_SpecialtyID | |
| 8 | 8 | 1 |
Radiation Oncology
|
| Phase III Randomized Trial of the Role of Whole Brain RT in Addition to Radiosurgery in Patients with 1 to 3 Cerebral Metastases |
| db_EligibilityTrialID | db_trialID | |
| 16 | 8 |
- 1-3 presumed brain mets from a histologically confirmed extra-cerebral tumor site (lung, breast, prostate)
|
| 17 | 8 |
- Will receive tx with a gamma knife or a linear accelerator-based SRS system
|
| 291 | 8 |
- Contact (561) 955-4800
|
|
| 9 |
2
| BRCH | PET/PEM/MRI |
BREAST
BRCH
PET/PEM/MRI
| db_researchSpecialtyID | db_trialID | db_SpecialtyID | |
| 68 | 9 | 3 |
Radiology/Women’s Center
|
| Prospective Study of the Role of Positron Emission Mammography & PET in Pre-Surgical Staging of Breast Cancer |
| db_EligibilityTrialID | db_trialID | |
| 18 | 9 |
- Bx-proven breast ca
|
| 19 | 9 |
- No type I or uncontrolled type II diabetes
|
| 20 | 9 |
- May have had MRI at BRCH or outside
|
| 292 | 9 |
- Contact (561) 955-4800
|
|
| 10 |
2
| Naviscan | PEM/MRI |
BREAST
Naviscan
PEM/MRI
| db_researchSpecialtyID | db_trialID | db_SpecialtyID | |
| 12 | 10 | 3 |
Radiology/Women’s Center
|
| Prospective Multicenter Study of the Role of Positron Emission Mammography in Pre-Surgical Planning for Breast Cancer |
| db_EligibilityTrialID | db_trialID | |
| 21 | 10 |
- Bx-proven breast ca
|
| 22 | 10 |
- No type I or uncontrolled type II diabetes
|
| 23 | 10 |
- No previous MRI within 1 year
|
| 293 | 10 |
- Contact (561) 955-4800
|
|
| 11 |
2
| NSABP B39 | WBI vs PBI |
BREAST
NSABP B39
WBI vs PBI
| db_researchSpecialtyID | db_trialID | db_SpecialtyID | |
| 13 | 11 | 1 |
Radiation Oncology
|
| A Randomized Phase III Study of Conventional Whole Breast Irradiation vs. Partial Breast Irradiation for Women with Stage 0, I or II Breast Cancer |
| db_EligibilityTrialID | db_trialID | |
| 24 | 11 |
- DCIS or invasive ca, stage 0, I or II
|
| 25 | 11 |
- Tumor less than or equal to 3 cm
|
| 26 | 11 |
- DCIS – must be < 50 y/o, any ER/PR
|
| 27 | 11 |
- Invasive ca EXCLUDED if > or = 50 y/o AND node neg AND receptor positive
|
| 294 | 11 |
- Contact (561) 955-4800
|
|
| 12 |
2
| ECOG PACCT-1 | Oncotype score to determine tx assignment |
BREAST
ECOG PACCT-1
Oncotype score to determine tx assignment
| db_researchSpecialtyID | db_trialID | db_SpecialtyID | |
| 14 | 12 | 2 |
Medical Oncology
|
| Trial Assigning Individualized Options for Treatment using Oncotype DX Assay Recurrence Score (RS 11-25 are randomized to chemo + hormonal tx OR hormonal tx only ; <11 receive only hormonal tx and > 25 receive chemo and hormonal tx)
Register before or after
|
| db_EligibilityTrialID | db_trialID | |
| 28 | 12 |
- ER + and/or PR +
|
| 29 | 12 |
- Her2/neu not over-expressed
|
| 30 | 12 |
- Axillary node negative & age < 75
|
| 31 | 12 |
- Tumor 1.1 to 5 cm or 5 mm to 1 cm and unfavorable histological features
|
| 32 | 12 |
- Candidate for chemo + hormonal therapy
|
| 262 | 12 |
- Placement of MammoSite excludes pt
|
| 295 | 12 |
- Contact (561) 955-4800
|
|
| 18 |
2
| SWOG 0307 | Bisphosphonate |
BREAST
SWOG 0307
Bisphosphonate
| db_researchSpecialtyID | db_trialID | db_SpecialtyID | |
| 22 | 18 | 2 |
Medical Oncology
|
| Phase III Trial of Bisphosphonates as Adjuvant Therapy for Primary Breast Cancer
Zolodrenic acid vs. Clodronate vs. Ibandronate
|
| db_EligibilityTrialID | db_trialID | |
| 53 | 18 |
- Invasive ca, stage I-III
|
| 54 | 18 |
- Prior tx with bisphosphonate ok, must d/c
|
| 55 | 18 |
- Must enroll within 84 days of surgery
|
| 296 | 18 |
- Contact (561) 955-4800
|
|
| 19 |
2
| NCIC MA17R | Hormonal Therapy |
BREAST
NCIC MA17R
Hormonal Therapy
| db_researchSpecialtyID | db_trialID | db_SpecialtyID | |
| 19 | 19 | 2 |
Medical Oncology
|
| Phase III Randomized Double-Blind Randomization to Letrozole or Placebo for women previously diagnosed with breast cancer completing five years of AI either as initial therapy or after tamoxifen |
| db_EligibilityTrialID | db_trialID | |
| 56 | 19 |
- Invasive breast cancer (DCIS excluded)
|
| 57 | 19 |
- Must have completed 4.5-6 years of an AI
|
| 58 | 19 |
- May have rec’d tamoxifen prior to AI
|
| 59 | 19 |
- Last dose of AI and randomization must be < 2 years
|
| 297 | 19 |
- Contact (561) 955-4800
|
|
| 20 |
2
| NSABP B42 | Hormonal Therapy |
BREAST
NSABP B42
Hormonal Therapy
| db_researchSpecialtyID | db_trialID | db_SpecialtyID | |
| 21 | 20 | 2 |
Medical Oncology
|
| A Clinical Trial to Determine the Efficacy of Five Years of Letrozole Compared to Placebo in Patients Completing Five Years of Hormonal Therapy Consisting of and AI or Tamoxifen Followed by an AI in Prolonging Disease-Free Survival in Post-Menopausal Women with Hormone Receptor Positive Invasive Br |
| db_EligibilityTrialID | db_trialID | |
| 60 | 20 |
- Duration of initial hormonal therapy may be 57-63 months, pt must be randomized within 6 months following completion;
|
| 61 | 20 |
- Therapy must have been an AI or up to 3 years of tamoxifen followed by an AI, no tamoxifen during years 4 and 5
|
| 62 | 20 |
- Can pre-register pt to receive letrozole at no cost to complete the 5 years of tx if:
|
| 63 | 20 |
- A) 2-4.5 years of AI; or B) 2-3 years tamoxifen; or C) 2-4.5 years combination of tamoxifen (≤ 3 years) followed by an AI
|
| 303 | 20 |
- Contact (561) 955-4800
|
|
| 22 |
2
| NSABP B37 | Recurrence |
BREAST
NSABP B37
Recurrence
| db_researchSpecialtyID | db_trialID | db_SpecialtyID | |
| 35 | 22 | 2 |
Medical Oncology
|
| A Randomized Clinical Trial of Adjuvant Chemotherapy for Radically Resected Loco-Regional Relapse of Breast Cancer
Randomized to observation or chemo, +/- RT, hormonal therapy +/-trastuzumab
|
| db_EligibilityTrialID | db_trialID | |
| 69 | 22 |
- 1st local and/or regional recurrence
|
| 70 | 22 |
- Medically suitable for chemo
|
| 71 | 22 |
- No bilateral malignancy
|
| 72 | 22 |
- No prior recurrence, prior breast RT=okay
|
| 73 | 22 |
- HER2 neu expression is permitted
|
| 298 | 22 |
- Contact (561) 955-4800
|
|
| 23 |
2
| CALGB 40302 | Endocrine therapy-stage III or IV, HER2 expression |
BREAST
CALGB 40302
Endocrine therapy-stage III or IV, HER2 expression
| db_researchSpecialtyID | db_trialID | db_SpecialtyID | |
| 94 | 23 | 2 |
Medical Oncology
|
| Endocrine Therapy With or Without Inhibition of EGF and HER2 Growth Factor Receptors: A Randomized, Double-Blind, Placebo-Controlled Phase III Trial for Postmenopausal Women with Estrogen-Receptor Positive Advanced Breast Cancer
|
|