Treatment Protocols
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Current Treatment Protocols

 Updated 9/5/08

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Contact Information

Montana Cancer Consortium 90 Poly Dr  Suite 2      Billings, MT  59101      Phone 406-259-2245      800-528-3340                 Fax  259-2682                Email mccinfo@mtcancer.org
 


 

Index

List by Protocol Number

Brain Gynecologic Lymphoma
Breast Head and Neck Melanoma
Gastrointestinal Leukemia Myeloma
Genitourinary Lung Sarcoma and other

BRAIN

NCCTG N0779    Consent    HIPAA    Protocol  

Phase II Study of Vorinostat (SAHA) in combination with Bortezomib (PS-341) in Patients with Recurrent Glioblatoma Multiforme

NCCTG N0272A(phase 1) Consent  HIPAA Protocol (temporary closure Arm C-EIAC's patients)     NCCTG N0272B(phase 2) Consent       

A Phase I/II Trial of Imatinib Mesylate (Gleevec) in Treatment of Recurrent Oligodendroglioma and Mixed Oligoastrocytoma

RTOG R0625  Consent     HIPAA     Protocol   Application    Information  (Temporary closure)

A Randomized Phase II Trial of Bevacizumab with Irinotecan or Bevacizumab with Temozolomide in Recurrent Glioblastoma

Central Lymphoma Repository Tissue Procurement Protocol for Relapse or Recurrent Disease, Ancillary

Brain Mets

NCCTG N0574  Consent   HIPAA    Protocol

Phase III Randomized Trial of the Role of Whole Brain Radiation Therapy in Addition to Radiosurgery in Patients with One to Three Cerebral Metastases

BREAST

      Breast DCIS

      Breast - Node Positive

    Breast - Node Negative

CTSU PACCT-1   TAILORx   Consent   HIPAA   Fast Facts    Protocol     Patient Information

Program for the Assessment of Clinical Cancer Tests (PACCT-1):  Trial Assigning Individualized Options for Treatment:  The TAILORx Trial

NSABP B-36   Consent   HIPAA    Fast Facts     Protocol 

A Clinical Trial of Adjuvant Therapy Comparing Six Cycles of 5-Fluorouracil, Epirubicin and Cyclophosphamide to Four Cycles of Adriamycin and Cyclophosphamide, With or Without Celecoxib, in patients with Node-Negative Breast Cancer

   Breast -  Node Positive or Negative

CTSU N063D ALTTO     Consent    HIPAA   Fast Facts    Protocol    

A Randomized, Multi-center, Open-label, Phase III Study of Adjuvant Lapatinib, Trastuzumab, Their Sequence and Their Combination in Patients with HER2/ErbB2 Positive Primary Breast Cancer

SWOG S0221    Consent   HIPAA    Protocol     Fast Facts   Antioxidant Use   

Phase III Trial of Continuous Schedule AC + G vs. Q-2 Week Schedule AC, Followed by Paclitaxel Given Either Every 2 Weeks or Weekly for 12 Weeks as Postoperative Adjuvant Therapy in Node-Positive or High-Risk Node Negative Breast Cancer

SWOG S0307    Consent    HIPAA   Fast Facts    Protocol

Phase III Trial of Bisphosphonates as Adjuvant Therapy for Primary Breast Cancer

CTSU CALGB 40101    Consent     HIPAA   Fast Facts    Protocol    

Cyclophosphamide and Doxorubicin vs. Paclitaxel as Adjuvant Therapy for Breast Cancer in Women with 0-3 Positive Axillary Lymph Nodes

CTSU CALGB 70301   Consent     HIPAA   Schema      Protocol

Quality of Life, Employment, and Informal Care Cost Analysis in Women Receiving Adjuvant Chemotherapy (Adjunct study for C40101)

CTSU E5103  Consent    HIPAA   Fast Facts    Protocol

A Double-blind Phase III Trial of Doxorubicin and Cyclophosphamide followed by Paclitaxel and Bevacizumab or Placebo in Patients with Lymph Node Positive and High-risk Lymph Node Negative Breast Cancer

CTSU N0434 (MA.27D)    Consent    HIPAA    Fast Facts    Protocol

Association of Breast Density Changes, Plasma Hormone Changes and Breast Cancer Recurrence (Companion MA.27D)

NSABP B-39        Consent    HIPAA    Fast Facts     Protocol    (Closed to specific patients)

A Randomized Phase III Study of Conventional Whole Breast Irradiation versus Partial Breast Irradiation for Women with Stage 0, I or II Breast Cancer

NSABP B-40   Consent   HIPAA   Fast Facts    Protocol    

A Randomized Phase III Trial of Neoadjuvant Therapy in Patients with Palpable and Operable Breast Cancer Evaluating the Effect on Pathologic Complete Response (pCR) of Adding Capecitabine or Gemcitabine to Docetaxel when Administered Before AC with or without Bevacizumab and Correlative Science Studies Attempting to Identify Predictors of High Likelihood for pCR with Each of the Regimens

NSABP B-41    Consent   HIPAA   Fast Facts    Protocol    (Hold for regulatory) (Temporary closure 6/11/08)

A Randomized Phase III Trial of Neoadjuvant Therapy for Patients with Palpable and Operable HER2-Positive Breast Cancer Comparing the Combination of Trastuzumab Plus Lapatinib to Trastuzumab and to Lapatinib Administered with Weekly Paclitaxel Following AC Accompanied by Correlative Science Studies to Identify Predictors of Pathologic Complete Response

NSABP B-42   Consent  Consent #2-Reg.  HIPPA HIPPA-Reg. Protocol   

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 an Aromatase Inhibitor (AI) or Tamoxifen Followed by an AI in Prolonging Disease-Free Survival in Postmenopausal Women with Hormone Receptor Positive Breast Cancer

        Ovarian Function Failure

SWOG S0230    Consent     HIPAA   Fast Facts    Protocol

Phase III Trial of LHRH Analog Administration During Chemotherapy to Reduce Ovarian Failure Following Standard Adjuvant Chemotherapy in Early Stage, Hormone-Receptor Negative Breast Cancer

    Breast - Inflammatory

    Breast - Relapse

NSABP B-37     Consent   HIPAA    Fast Facts    Protocol 

A Randomized Clinical Trial of Adjuvant Chemotherapy for Radically Resected Loco-regional Relapse of Breast Cancer

    Breast - Metastatic

SWOG S0226    Consent     HIPAA  Fast Facts    Protocol

Phase III Randomized Trial of Anastrozole vs. Anastrozole and Fulvestrant as First-Line Therapy for Post Menopausal Women with Metastatic Breast Cancer

SWOG S0500    Consent    HIPAA   Fast Facts     Protocol

A Randomized Phase II Trial to Test the Strategy of Changing Therapy vs Maintaining Therapy for Metastatic Breast Cancer Patients Who Have Elevated Circulating Tumor Cell Levels at First Follow-up Assessment

SWOG S0622      Consent     HIPAA    Fast Facts     Protocol

Phase II Studies of Two Different Schedules of Dasatinib (NSC-732517) in Bone-Metastasis Predominant Metastatic Breast Cancer

CTSU CALGB 40302   Consent    HIPAA   Fast Facts  Protocol     Investigator letter

Endocrine Therapy with or without Inhibition of EGF and HER2 Growth Factor Receptors:   A Randomized, Double-Blinded, Placebo-controlled Phase III Trial of Fulvestrant with or without Lapatinib for Postmenopausal Women with Hormone Receptor Positive Advanced Breast Cancer

CTSU E1105  Consent    HIPAA    Fast Facts Protocol   

A Randomized Phase III Double-Blind Placebo-Controlled Trial of First-line Chemotherapy and Trastuzumab with or without Bevacizumab for Patients with HER-2/NEU Over-expressing Metastatic Breast Cancer

NCCTG N0539    Consent     HIPAA     Protocol   (Study requires N0392 adjunct study)

Phase II Trial of Fulvestrant and Bevacizumab in Patients with Metastatic Breast Cancer Previously Treated with an Aromatase Inhibitor

    Breast-Other

SWOG JMA.17R    Consent    HIPAA    Protocol  

A Double Blind Randomization To Letrozole or Placebo For Women Previously Diagnosed with Primary Breast Cancer Completing Five Years of Adjuvant Aromatase Inhibitor Either as Initial Therapy or After Tamoxifen (including those in the MA.17 study)

NSABP BP-59      Consent     HIPAA     Fast Facts     Protocol  

Bone Marrow Analysis in Early-Stage Breast Cancer

IBCSG 24-02    Consent    HIPAA   Fast Facts    Protocol

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

NCCTG N063I  Consent     HIPAA     Protocol 

Changes in Breast Density and Plasma Hormone Levels After One Year of Aromatase Inhibitor Therapy

GASTROINTESTINAL

  Colon - Rectal

NSABP LTS-01    Consent    HIPAA    Protocol 

Patient Reported Outcomes in Long-term Survivors with Colon and Rectal Cancer

SWOG S0600   Consent    HIPAA   Fast Facts    Protocol     (temporary closure 6/9/08)

Phase III Trial of Irinotecan-Based Chemotherapy Plus Cetuximab with or without Bevacizumab as Second-Line Therapy for Patients with Metastatic Colorectal Cancer who have Progressed on Bevacizumab with Either FOLFOX, OPTIMOX, or XELOX

CTSU E5202    Consent    HIPAA     Protocol

A Randomized Phase II Study Comparing 5-FU, Leucovorin and Oxaliplatin vs 5-FU, Leucovorin, Oxaliplatin and Bevacizumab in Patients with Stage II Colon Cancer at High Risk for Recurrence to Determine Prospectively the Prognostic Value of Molecular Markers

CTSU N0147     Consent    HIPAA   Fast Facts     Protocol    (temporary closure 6/9/08)

A Randomized Phase III Trial of Irinotecan and/or Oxaliplatin Plus 5-Fluorouracil/Leucovorin with or without Cetuximab (C225) after Curative Resection for Patients with Stage III Colon Cancer

NSABP C-10    Consent    HIPAA    Fast Facts     Protocol

A Phase II Trial of 5-Fluorouracil, Leucovorin, and Oxaliplatin (mFOLFOX6) Chemotherapy plus Bevacizumab for Patients with Unresectable Stage IV Colon Cancer and a Synchronous Asymptomatic Primary Tumor

CTSU CALGB 80405     Consent   HIPAA    Fast Facts     Protocol   (Closure QOL) (temporary closure 6/9/08)

A Phase III Trial of Irinotecan/5-FU/Leucovorin or Oxaliplatin/5-FU/Leucovorin with Bevacizumab, or Cetuximab or with the Combination of Bevacizumab and Cetuximab for Patients with Untreated Metastatic Adenocarcinoma of the Colon or Rectum

NCCTG N0543  Consent    HIPAA     Protocol

A Phase II Trial of Pharmacogenetic-Based Dosing of Irinotecan, Oxaliplatin, and Capecitabine as First-Line Therapy for Advanced Small Bowel Adencarcinoma

      Rectal

NSABP R-04    Consent     Consent tissue   HIPAA     Fast Facts     Protocol

A Clinical Trial Comparing Preoperative Radiation Therapy and Capecitabine with Preoperative Radiation Therapy and Continuous Intravenous Infusion of 5-Fluorouracil in the Treatment of Patients with Operable Carcinoma of the Rectum

CTSU E5204    Consent    HIPAA    Fast Facts    Protocol

Intergroup Randomized Phase III Study of Postoperative Oxaliplatin, 5-Fluorouracil, and Leucovorin versus Oxaliplatin, 5-Fluorouracil, Leucovorin and Bevacizumab for Patients with Stage II or III Rectal Cancer Receiving Preoperative Chemoradiation

    Stomach

CTSU C80101  Consent   HIPAA     Fast Facts     Protocol

A Phase III Intergroup Trial of Adjuvant Chemoradiation after Resection of Gastric or Gastroesophageal Adenocarcinoma

    Esophageal

RTOG R0436    Consent   HIPAA   Protocol  

A Phase III Trial Evaluating the Addition of Cetuximab to Paclitaxel, Cisplatin, and Radiation for Patients With Esophageal Cancer Who Are Treated Without Surgery

    Pancreas

None

     Gallbladder

None

     Other

SWOG S0502    Consent    HIPAA   Protocol    

A Phase III Randomized Trial of Imatinib, with or without Bevacizumab  in Patients with Metastatic or Unresectable Gastrointestinal Stromal Tumors

GENITOURINARY

    Prostate

SWOG 9346      Consent     HIPAA    Protocol     (closure 9/1/2008)

Intermittent Androgen Deprivation in Patients with Stage D2 Prostate Cancer

SWOG S0421      Consent    HIPAA     Protocol

Phase III Study of Docetaxel and Atrasentan Versus Docetaxel and Placebo for Patients with Advanced Hormone Refractory Prostate Cancer

CTSU E3805   Consent  HIPPA  Protocol  

CHAARTED:  Chemohormonal Therapy versus Androgen Ablation Randomized Trial for Extensive Disease in Prostate Cancer

CTSU CALGB 90202    Consent    HIPAA   Fast Facts     Protocol

A Randomized, Double-blind, Placebo-controlled Phase III Study of Early vs. Standard Zoledronic Acid to Prevent Skeletal-related Events in Men with Prostate Cancer Metastatic to Bone

CTSU CALGB 90203    Consent    HIPAA    Protocol

Randomized Phase III Study of Neoadjuvant Docetaxel and Androgen Deprivation Prior to Radical Prostatectomy vs Immediate Radical Prostatectomy in Patients with High-Risk, Clinically Localized Prostate Cancer

CTSU MDA-3410    Consent    HIPAA    Fast Facts     Protocol  

A Prospective Randomized Phase II Trial Comparing Consolidation Therapy With or Without Strontium-89 Following Induction Chemotherapy in Androgen-Independent Prostate Cancer

CTSU RTOG 0521    Consent   Consent for Tissue      HIPAA    Protocol

A Phase III Protocol of Androgen Suppression (AS) and Radiotherapy (RT) vs AS and RT Followed by Chemotherapy with Doxetaxel and Prednisone for Localized High-Risk Prostate Cancer

CTSU RTOG 0415    Consent   HIPAA    Fast Facts    Protocol                                                                                                    Pre-registration requirements (see section 5.0 of the protocol)

A Phase III Randomized Study of Hypofractinated 3D-CRT/IMRT Versus Conventionally Fractionated 3D-CRT/IMRT in Patients with Favorable-Risk Prostate Cancer

RTOG R0534  Consent     HIPAA     Protocol  

A Phase III Trial Of Short Term Androgen Deprivation With Pelvic Lymph Node Or Prostate Bed Only Radiotherapy (SPORT) In Prostate Cancer Patients With A Rising PSA After Radical Prostatectomy

    Bladder/Urothelium

SWOG S0337     Consent    HIPAA      Protocol 

A Phase III Blinded Study of Immediate Post-TURBT Instillation of Gemcitabine Versus Saline in Patients with Newly Diagnosed or Occasionally Recurring Grade I/II Superficial Bladder Cancer

SWOG S0353     Consent     HIPAA     Fast Facts     Protocol

Phase II Study of Intravesical Gemcitabine in Patients with Superficial Bladder Cancer Who Have Progressed Despite Intravesical BCG

    Germ Cell Malignancies

none

   Renal

CTSU E2805    Consent   HIPAA      Fast Facts    Protocol   

A Randomized, Double-Blind Phase III Trial of Adjuvant Sunitinib versus Sorafenib versus Placebo in Patients with Resected Renal Cell Carcinoma

CTSU E2804   Consent    HIPAA     Protocol    

The BeST Trial: A Randomized Phase II Study of VEGF, RAF kinase, and mTOR Combination Targeted Therapy (CTT) with Bevacizumab, Sorafenib and Temsirolimus in Advanced Renal Cell Carcinoma

GYNECOLOGIC

      Ovarian

CTSU GOG 0218    Consent      HIPAA    Fast Facts    Protocol

A Phase III Trial of Carboplatin and Paclitaxil plus Placebo versus Carboplatin and Paclitaxil plus Concurrent Bevacizumab followed by Placebo versus Carboplatin and Paclitaxil plus Concurrent and Extended Bevacizumab in Women with Newly Diagnosed, Previously Untreated Suboptimal Advanced Stage Epithelial Ovarian and Primary Peritoneal Cancer

    Cervical

CTSU GOG 0219    Consent   HIPAA    Fast Facts    Protocol

A Phase III Randomized Trial of Weekly Cisplatin and Radiotherapy versus Cisplatin and Tirapazamine and Radiotherapy in Stage IB2, IIA, IIIB, and IVA Cervical Cancer Limited to the Pelvis

    Endometrial

CTSU GOG 0209    Consent   HIPAA    Fast Facts     Protocol  (Temporarily closed to patients who have received any prior external RT)

Randomized Phase III Trial of Doxorubicin/Cisplatin/Paclitaxel and G-CSF vs. Carboplatin/Paclitaxel in Patients with Stage III & IV or Recurrent Endometrial Cancer

HEAD & NECK

CTSU E1302    Consent    HIPAA    Fast Facts    Protocol   (Arm C partial closure)

Phase III Randomized, Placebo-Controlled Trial of Docetaxel Versus Docetaxel Plus ZD1839(Iressa, Gefitinib) in Performance Status 2 or Previously Treated Patients with Recurrent or Metastatic Head and Neck Cancer

RTOG R0435   Consent     HIPAA     Protocol    Training                                                                                                         Pre-registration requirements (see section 5.0 of the protocol)

Randomized, Phase III, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Palifermin (NSC#740548m IND 6370) for the Reduction of Oral Mucositis in Patients with Locally-Advanced Head and Neck Cancer Receiving Radiation Therapy with concurrent Chemotherapy (Followed by surgery for Selected Patients)

CTSU RTOG 0522    Consent    HIPAA    Fast Facts    Protocol        PET Requirements and Credentialing

A Phase III Trial of Concurrent Accelerated Radiation and Chemotherapy vs Concurrent Accelerated Radiation, Chemotherapy and Cetuximab (C225) for Stage III and IV Head and Neck Carcinoma

LEUKEMIA

    Acute Leukemia

SWOG 9007       Consent     HIPAA    Protocol

Cytogenetics Studies in Leukemia Patients, Ancillary

SWOG 9910       Consent    HIPAA   Protocol

Leukemia Centralized Reference Laboratories and Tissue Repositories Consent to Perform Cellular and Molecular Studies in Leukemia Patients

SWOG S0106    Consent   HIPAA    Protocol

A Phase III Study of the Addition of Gemtuzumab Ozogamicin During Induction Therapy vs. Standard Induction with Daunomycin and Cytosine Arabinoside Followed by Consolidation and Subsequent Randomization to Post-Consolidation Therapy with Gemruzumab Ozogamicin or No Additional Therapy for Patients Under Age 56 with Previously Untreated De Novo Acute Myeloid Leukemia

SWOG S0535    Consent   HIPAA  Protocol

Phase II Study of ATRA, Arsenic Trioxide and Gemtuzumab Ozogamicin in Patients with Previously-untreated High-risk Acute Promyelocytic Leukemia

SWOG S0605    Consent    HIPAA    Protocol

A Phase II Study of Lenalidomide (Revlimid) (NSC-703813) for Previously Untreated Non-M3 Deletion 5Q Acute Myeloid Leukemia (AML) in Patients Age 60 or Older Who Decline Remission Induction Chemotherapy

SWOG S0521   Consent    HIPAA    Protocol

A Randomized Trial of Maintenance vs Observation for Patients with Previouslly Untreated Low and Intermediate risk Acute Promyelocytic Leukemia (APL), Phase III

CTSU E2902    Consent   HIPAA    Fast Facts     Protocol  

A Phase III Randomized Study of Farnesyl Transferase Inhibitor R115777 in Acute Myeloid Leukemia (AML) Patients in Second or Subsequent Remission or in Remission after Primary Induction Failure

CTSU E1900    Consent    HIPAA     Protocol   (Arm D Suspended) (temporary closure 2/16/08)

A Phase III Trial in Adult Acute Myeloid Leukemia:  Daunorubicin Dose-Intensification and Gentuzumab-Ozogamicin Consolidation Therapy Prior to Autologous Stem Cell Transplantation Study

SWOG E1905   Consent    HIPAA   Protocol    (Temporary Closure)

A Randomized Phase II Trial of Azacitidine with or without the Histone Deacetylase Inhibitor MS-275 for the Treatment of Myelodysplastic Syndrome, Chronic Myelomonocytic Leukemia (dysplastic type), and Acute Myeloid Leukemia with Multilineage Dysplasia

    Chronic Leukemia

SWOG S0325    Consent      HIPAA     Protocol      (Arm II only closed to accrual)

A Phase IIb Study of Molecular Responses to Imatinib at Standard or Increased Doses for Previously Untreated Patients with Chronic Myelogenous Leukemia (CML) in Chronic Phase

NCCTG N0683   Consent     HIPAA     Protocol  

A Phase II Study of Sunitinib Malate for Treatment of Patients with Relapsed/Refractory Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Lymphoma (SLL)

SWOG E1905   Consent   HIPAA   Protocol   (Temporary closure)

A Randomized Phase II Trial of Azacitidine with or without the Histone Deacetylase Inhibitor MS-275 for the Treatment of Myeolodysplastic Syndrome, Chronic Myelomonocytic Leukemia (dysplastic type), and Acute Myeloid Leukemia with Multilineage Dysplasia

    Lymphoblastic Leukemia

SWOG S0333    Consent    HIPAA      Protocol   

A Phase II Study of Double Induction Chemotherapy for Newly Diagnosed Non-L3 Adult Acute Lymphoblastic Leukemia with Investigation of Minimal Residual Disease and Risk of Relapse Following Maintenance Chemotherapy

SWOG C10403   Consent     HIPAA      Protocol     (MCC treats adults only -- must be > 18 yrs)

An Intergroup Phase II Clinical Trial for Adolescents and Young Adults with Untreated Acute Lymphoblastic Leukemia

CTSU C10501   Consent    HIPAA    Fast Facts    Protocol    

A Phase III Intergroup CLL Study of Asymptomatic Patients with Untreated CLL Randomized to Early Intervention vs Observation with Later Treatment in Hi-Risk Genetic Subset with IgVh Unmutated Disease 

LUNG 

SWOG 9925    Protocol    (NO CONSENT)

Lung Cancer Specimen Repository Protocol, Ancillary    

Non-Small Cell

SWOG 0229    Consent    HIPAA    Protocol

A Randomized Trial Assessing the Effects of Exercise on Patients with Locally-Advanced Non-Small Cell Lung Cancer Undergoing Curative-Intent Combined Modality Therapy (Ancillary to S0023)

SWOG S0424   Consent    HIPAA    Fast Facts    Protocol     (study open only to non-smokers - fewer than 100 cigarettes in lifetime)

Molecular Epidemiology Case-Series Study of Non-Small Cell Lung Cancer in Smoking and Non-Smoking Women and Men

SWOG S0429    Consent    HIPAA    Fast Facts    Protocol

A Pilot (Phase I) Study of Weekly Docetaxel and Cetuximab Chemoradiation for Poor Risk    Stage III Non-Small Cell Lung Cancer

SWOG S0526    Consent    HIPAA   Fast Facts   Protocol    (permanent closure 10/1/08)

Phase II Trial of Pemetrexed in Patients with Selected Stage IIIB and IV Bronchioalveolar Carcinoma (BAC)

SWOG S0636     Consent     HIPAA   Fast Facts   Protocol     

A Phase II Trial of the Combination of OSI-774 (Erlotinib; NSC-718781) and Bevacizumab (Rhumab VEGF; NSC-704865) in Never-Smokers with Stage IIIB and IV Primary NSCLC Adenocarcinomas

SWOG E5597    Consent     HIPAA    Protocol

Phase III Chemoprevention Trial of Selenium Supplementation in Persons with Resected Stage I Non-Small Cell Lung Cancer

NCCTG N0528   Consent   HIPAA    Protocol    

A Randomized Phase II Study of Gemcitabine and Carboplatin With or Without AZD2171 as First-Line Therapy in Advanced Non-Small Cell Lung Cancer

NCCTG N0626    Consent    HIPAA     Protocol 

A Phase II Randomized Study of Pemetrexed With Sorafenib Versus Pemetrexed Alone as Second-line Therapy in Patients With Advanced Non-Small Cell Lung Cancer

RTOG R0617     Consent     HIPAA     Protocol   

A Randomized Phase III Comparison of Standard-Dose (60 Gy) Versus High-Dose (74 Gy) Conformal Radiotherapy with Concurrent and Consolidation Carboplatin/Paclitaxel in Patients With Stage IIIA/IIIB Non-Small Cell Lung Cancer

CTSU E1505     Consent   HIPAA    Fast Facts     Protocol  

A Phase III Randomized Trial of Adjuvant Chemotherapy with or without Bevacizumab for Patients with Completely Resected Stage IB (> 4 cm) - IIIA Non-Small Cell Lung Cancer

    Small Cell

CTSU C30610   Consent    HIPAA       Protocol   

Phase III Comparison of Thoracic Radiotherapy Regimens in Patients with Limited Small Cell Lung Cancer also Receiving Cisplatin and Etoposide

RTOG R0623   Consent    HIPAA   Protocol  

A Phase II Trial of Combined Modality Therapy with Growth Factor Support for Patients with Limited Stage Small Cell Lung Cancer

   Lung-Other

NCCTG N0623     Consent    HIPAA   Protocol    

Phase II Study of GW786034 in Patients with Malignant Pleural Mesothelioma

SWOG S0635    Consent    HIPAA    Fast Facts    Protocol  

Phase II Trial of the Combination of OSI-774(Erlotinib) and Bevacizumab in Stage IIIB and IV Bronchoalveolar Carcinoma (BAC) and Adencarcinoma with BAC Features (AdenoBAC)

LYMPHOMA

SWOG 8819        (NO CONSENT)    Protocol

Central Lymphoma Repository Tissue Procurement                                                             

SWOG 8947   Consent   HIPAA   Protocol

Central Lymphoma Serum Repository                                                                                   

SWOG 9245  Consent     HIPAA    Protocol

Central Lymphoma Repository Tissue Procurement Protocol for Relapse or Recurrent Disease

    Hodgkin's

   Non-Hodgkin's

SWOG S0016      Consent    HIPAA   Fast Facts    Protocol  (Closing 9/15/2008)

A Phase III Trial of CHOP vs. CHOP + Rituximab vs. CHOP + Iodine 131 Labeled Monoclonal Anti-B1 Antibody (Tositumomab) for Treatment of Newly Diagnosed Follicular Non-Hodgkin’s Lymphoma  (Closure Arm 1)    

SWOG S0350    Consent    HIPAA    Fast Facts    Protocol    

Phase II Trial of Cisplatin Plus Etoposide Plus Gemcitabine Plus Solumedrol in Peripheral T-cell Non-Hodgkin's Lymphoma

SWOG S0433      Consent    HIPAA    Fast Facts    Protocol 

Iodine-131-Labeled Monoclonal Anti-B1 Antibody in Combination with Cyclophosphamide, Doxorubicin, Vincristine, Prednisone, and Rituximab Therapy for Patients Greater Than or Equal to Age 60 with Advanced Stage Diffuse Large B-Cell NHL

SWOG S0515     Consent    HIPAA    Fast Facts    Protocol   (closing 9/15/2008)

Phase II Trial of Standard Dose Cyclophosphamide, Doxorubicin, Vincristine, Prednisone (CHOP) and Rituximab Plus Bevacizumab for Advanced Stage Diffuse Large B-Cell NHL

SWOG S0520    Consent    HIPAA    Fast Facts    Protocol

Phase II Study of PXD101 in Relapsed and Refractory Aggressive B-Cell Lymphomas

CTSU E 4402     Consent    HIPAA    Fast Facts     Protocol   (closing 9/12/2008)

A Randomized Phase III Trial Comparing Two Different Rituximab Dosing Regimens for Patients with Low Tumor Burden Indolent Non-Hodgkin's Lymphoma

CTSU CALGB 50303    Consent    HIPAA    Fast Facts    Protocol

Randomized Study of R-CHOP versus Dose-Adjusted EPOCH-R With Molecular Profiling in Untreated DeNovo Diffuse Large B-Cell Lymphomas

NCCTG N0682    Consent    HIPAA    Protocol

A Phase II Clinical Trial of Denileukin Diftitox in Combination with Rituximab in Previously Untreated Follicular B-Cell Non-Hodgkin's Lymphoma

NCCTG N0683   Consent     HIPAA     Protocol  

A Phase II Study of Sunitinib Malate for Treatment of Patients with Relapsed/Refractory Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Lymphoma (SLL)

    Mantle Cell

NCCTG N038H    Consent    HIPAA    Protocol    (temporary closure 9/4/08))

A Phase II Study of CCI-779 in Combination with Rituximab in Patients with Relapsed or Refractory Mantle Cell Lymphoma

Melanoma    

SWOG S0438  Consent   HIPAA      Protocol   (temporary closure 9/4/08) 

A Randomized Phase II Trial of BAY 43-9006 (Sorafenib) with Either CCI-779 (Temsirolimus) or R115777 (Tipifarnib) in Metastatic Melanoma                     

SWOG S0512    Consent    HIPAA    Protocol     (temporary closure effective 3/1/08)

Phase II Trial of BAY 43-9006(Sorafenib) in Combination with Carboplatin and Paclitaxel in Patients with Metastatic Uveal Melanoma

NCCTG N0675   Consent    HIPAA   Protocol  

A Phase II Study of Temozolomide and Everolimus (RAD-001) Therapy for Metastatic Melanoma

Myeloma

CTSU C100104    Consent     HIPAA    Protocol

A Phase III Randomized, Double-blind Study of Maintenance Therapy with CC-5013 or Placebo Following Autologous Stem Cell Transplantation for Multiple Myeloma

CTSU E1A05   Consent     HIPAA     Protocol   Schema    Fast Facts

Randomized Phase III Trial of Consolidation Therapy with Bortezomib (VelcadeŽ) - Lenalidomide (RevlimidŽ) - Dexamethasone (VRD) versus Bortezomib (VelcadeŽ) - Dexamethasone (VD) for Patients with Multiple Myeloma Who Have Completed a Dexamethasone-Based Induction Regimen

CTSU E1A06     Consent      HIPAA    Protocol 

An Intergroup Phase III Randomized Controlled Trial Comparing Melphalan, Prednisone and Thalidomide Versus Melphalan, Prednisone and Lenalidomide in Newly Diagnosed Myeloma Patients Who Are Not Candidates for High-Dose Therapy

SWOG S0115      Consent     HIPAA   Fast Facts    Protocol

Phase II Trial Evaluating Modified High Dose Melphalan and Autologous Peripheral Blood Stem Cell Supported Transplantation for High Risk Patients with Multiple Myeloma and/or Light Chain Amyloidosis

SWOG S0120       Consent     HIPAA      Fast Facts    Protocol 

A Prospective Observational Biologic Study of Asymptomatic Patients With Monoclonal Gammopathy and Plasma Proliferative Disorders

 SWOG S0309    (No Consent)   HIPAA    Protocol

Myeloma Specimen Repository Protocol, Ancillary

SWOG S0434    Consent    HIPAA    Protocol     (Temporary closure 7/1/08)

A Phase II Trial of BAY 43-9006 (Sorafenib) in Patients with Relapsing or Resistant Multiple Myeloma Previously Treated with Bortezomib

SWOG S0777   Consent