|
BREAST |
|
|
SOFT(IBCSG24-02/BIG 2-02) |
Suppression of Ovarian Function Trial. A Phase III Trial Evaluating the Role of Ovarian Function Suppression and the Role of Exemestane Adjuvant Therapies for Premenopausal Women with Endocrine Responsive Breast Cancer Tamoxifen versus Ovarian Function Suppression + Tamoxifen versus Ovarian Function Suppression + Exemestane |
|
NSABP |
A Clinical Trial of Adjuvant Therapy Comparing Six Cycles of 5-Fluorouracil (5-FU), Epirubicin and Cyclophosphamide (FEC) to Four Cycles of Adriamycin and Cyclophosphamide (AC) in Patients with Node-Negative Breast Cancer |
|
B-36 |
|
|
B-38 |
A Phase III adjuvant trial comparing three chemotherapy regimens in women with node-positive breast cancer: Docetaxel/Doxorubicin/Cyclophosphamide (TAC); dose-dense (DD) Doxorubicin/Cyclophosphamide followed by DD Paclitaxel (DD AC→P); DD AC followed by DD Paclitaxel plus Gemcitabine (DD AC→PG) |
|
B-39 |
A randomized phase III study of conventional whole breast irradiation (WBI) versus partial breast irradiation (PBI) for women with stage 0, I, or II breast cancer |
|
SWOG S0307 |
Phase III Trial of Bisphosphonates as Adjuvant Therapy for Primary Breast Cancer |
|
BRE 63 |
A Phase II Trial of Combination Gemcitabine Carboplatin with or without Trastuzumab in Patients with Metastatic Breast Cancer |
|
NCIC CTG |
A Randomized Phase III Trial of Exemestane versus Anastrozole in Postmenopausal Women with Receptor-Positive Primary Breast Cancer |
|
MA 27 | |
|
Perifosine 208 |
A Phase II Trial of Two Schedules of Perifosine in Combination with Endocrine Therapy for Patients with Estrogen Receptor or Progesterone Receptor Positive Metastatic Breast Cancer |
|
BRE 73 |
Phase II Trial of Dose Dense Neoadjuvant Gemcitabine, Epirubicin, ABI-007 (GEA) in Locally Advanced and/or Inflammatory Breast Cancer |
|
BRE 89 |
Phase II Trial of Vinflunine with or without Trastuzumab in Patients with Metastatic Breast Cancer |
|
GE JUNCTION AND STOMACH |
|
|
GIST |
Gastrointestinal Stromal Tumors (GIST) Registry Protocol |
|
SWOG S0414 |
Cetuximab Plus Cisplatin, Irinotecan and Thoracic Radiotherapy (TRT) for Locally Advanced (Non-Metastatic), Clinically Unresectable Esophageal Cancer: A Phase II Trial with Molecular Correlates |
|
SWOG S0356 |
Oxaliplatin plus Protracted Infusion 5-Fluorouracil and Radiation for Potentially Curable Esophageal Cancer: A Phase II Trial with Molecular Correlates |
|
CALGB |
A Phase III Trial of Adjuvant Chemoradiation after Resection of Gastric and Gastroesophageal Adenocarcinoma |
|
80101 | |
COLORECTAL |
|
|
NSABP R-04 |
A Clinical Trial Comparing Preoperative Radiation Therapy and Capecitabine with or without Oxaliplatin with Preoperative Radiation Therapy and Continuous Intravenous Infusion of 5-Fluorouracil with or without Oxaliplatin in the Treatment of Patients with Operable Carcinoma of the Rectum |
|
MACCO-A |
Microarray analysis of colon cancer outcome-A |
|
C-08 |
A Phase III Clinical Trial Comparing Infusional 5-Fluorouracil (5-FU), Leucovorin, and Oxaliplatin (mFOLFOX6) Every Two Weeks with Bevacizumab to the Same Regimen without Bevacizumab for the Treatment of Patients with Resected Stages II and III Carcinoma of the Colon |
|
GI 65 |
Phase II Study of 5-Fluorouracil, Bevacizumab, and Radiation Followed by Modified FOLFOX6 and Bevacizumab in the Adjuvant Treatment of Patients with Stage II/III Rectal Cancer |
|
XELOX Colorectal |
“XELOX – A-DVS” (Dense vs. Standard): A Randomized Study of Intermittent Capecitabine in Combination with Oxaliplatin (XELOX Q3W) and Bevacizumab versus Intermittent Capecitabine in Combination with Oxaliplatin (XELOX Q2W) and Bevacizumab as First-Line Treatment for Patients with Metastatic Colorectal Cancer |
|
GENITOURINARY |
|
|
CALGB |
A Randomized, double-blind, placebo-controlled phase III study of early versus standard Zoledronic acid to prevent skeletal related events in men with prostate cancer metastatic to bone |
|
90202 |
|
|
Perifosine 215 |
A Placebo-Controlled, Double-Blind Trial of Perifosine in Combination with Docetaxel and Prednisone for Patients with Metastatic Androgen Independent Prostate Cancer |
|
HEMATOLOGICAL |
|
|
ECO-1 |
A Phase II study using Alemtuzumab combined with Fludarabine for the treatment of B-cell chronic lymphocytic leukemia (B-CLL) |
|
LymphoCare |
An Observational Study of Treatment, Outcomes and Prognosis in Patients with Follicular Non-Hodgkin’s Lymphoma |
|
LYM 28 |
Phase II Trial of Brief Duration Combination Chemotherapy (CNOP or CVP) and Rituximab with Prophylactic Pegfilgrastim (Neulasta), Followed by Maintenance Rituximab in Elderly/Poor Performance Status Patients with Large B-Cell Non-Hodgkin’s Lymphoma |
|
PIX 301 |
Pixantrone (BBR 2778) versus other chemotherapeutic agents for third-line single agent treatment of patients with relapsed aggressive NHL: A randomized, controlled, phase III comparative trial |
|
SWOG S0106 |
A Phase III Study of the Addition of Gemtuzumab Ozogamicin (Mylotarg) Induction Therapy versus Standard Induction with Daunomycin and Cytosine Arabinoside followed by Consolidation and Subsequent Randomization to Post-Consolidation Therapy with Gemtuzumab Ozogamicin (Mylotarg) or No Additional Therapy for Patients under Age 56 with Previously Untreated deNovo Acute Myeloid Leukemia (AML) |
|
SWOG S0016 |
A Phase III Trial of CHOP + Rituximab vs. CHOP + Iodine-131-Labeled Monoclonal Anti-B1 Antibody (Tositumomab) for Treatment of Newly Diagnosed Follicular Non-Hodgkin’s Lymphomas |
|
SWOG S0313 |
Evaluation of CHOP Plus Involved Field Radiotherapy Followed by Yttrium-90 Ibritumomab Tiuxetan for Stages I, IE, and Non-Bulky Stages II and IIE CD20 Positive, High-Risk Localized, Aggressive Histologies of Non-Hodgkin’s Lymphoma, Phase II |
|
DACO-016 |
Randomized Phase 3 Trial of Decitabine versus Patient’s Choice with Physician’s Advice of Either Supportive Care or Low-Dose Cytarabine for the Treatment of Older Patients with Newly Diagnosed Acute Myeloid Leukemia |
|
MELANOMA |
|
|
Luitpold |
Phase III study of Taxoprexin injection versus Dacarbazine in patients with metastatic malignant melanoma |
|
LUNG |
|
|
RTOG
0412/ |
Phase III Randomized Trial of Preoperative Chemotherapy versus Preoperative Concurrent Chemotherapy and Thoracic Radiotherapy Followed by Surgical Resection and Consolidation Chemotherapy in Favorable Prognosis Patients with Stage IIIA (N2) Non-Small Cell Lung Cancer |
|
OSI3364g Tarceva |
A Phase III, Multicenter, Placebo-Controlled, Double-Blind, Randomized Clinical Trial to Evaluate the Efficacy of Bevacizumab in Combination with TarcevaÔ (Erlotinib) Compared with Tarceva Alone for Treatment of Advanced Non-Small Cell Lung Cancer (NSCLC) after Failure of Standard First-Line Chemotherapy |
|
Perifosine 201 |
A Phase I/II Trial of Perifosine in the Treatment of Non-Small Cell Lung Cancer |
|
Bayer 11961 (Sorafenib) |
A Randomized Controlled Trial Comparing Safety and Efficacy of Carboplatin and Paclitaxel plus or minus Sorafenib (BAY 43-9006) in Chemonäive Patients with Stage IIIB-IV Non-Small Cell Lung Cancer (NSCLC) |
|
LUN 90 |
A Phase II Trial of Irinotecan, Carboplatin, and Bevacizumab in the Treatment of Patients with Extensive Stage Small Cell Lung Cancer |
|
LUN 120 |
Phase II Study of Higher Dose Weekly Topotecan in the 2nd Line Treatment of Patients with Relapsed Extensive Stage Small Cell Lung Cancer |
|
PANCREATIC |
We have no pancreatic studies at this time. |
|
HEAD AND NECK |
We have no head and neck studies at this time. |
|
MISCELLANEOUS |
|
|
CRASH |
Chemotherapy Risk Assessment Score for High Age Patients; Design and Validation |
|
Moffitt | |
|
UNK PRI 12 |
A Randomized, Phase III Comparison of Gemcitabine/ Irinotecan Followed by ZD1839 (Iressaâ) versus Paclitaxel/Carboplatin/Etoposide Followed by ZD1839 (Iressaâ) in the First-Line Treatment of Patients with Carcinoma of Unknown Primary Site |
|
Perifosine 207 |
A Phase IIA Trial of Two Schedules of Perifosine in Patients for Whom No Standard Therapy Exists |
|
GI
Outcomes |
Total Cancer Care Quality Improvement Protocol for Colorectal Cancer |
|
TCC—Total Cancer Care (MCC 14690) |
Total Cancer Care: A Partnership with High Risk and/or Diagnosed Cancer Patients for Life |
|
PBI |
Partial Breast Irradiation Registry |
For More
Information:
If you would like
additional information about the Center for Research, please send your name,
company or practice name, address and telephone number to the following
address:
The Watson Clinic Center for
Research
1600 Lakeland Hills Blvd
Lakeland, FL 33805
Attn: Noreen
McGowan, BSN CCRC Administrative Coordinator
Phone (863) 688-6826 · FAX (863)
688-5842
Please indicate which of the following type(s) of information you would like:·