St. Joseph Cancer Center - Clinical Trials: Breast
 

Early Stage:

  • None currently

Stage 0, I, or II:

  • RTOG 0413: A Randomized Phase III Study of Conventional Whole Breast Irradiation vs Partial Breast Irradiation for Women with Stage 0, I, or II Breast Cancer

T1-3, Node Negative:

  • CTSU 40101: Randomized Study, Cyclosphosphamide and Doxorubicin (4 vs. 6 Cycles) vs. Paclitaxel (12 Weeks vs. 18 Weeks) as Adjuvant Therapy for Women with Node-Negative Breast Cancer: A 2x2 Factorial, Phase III

  • CTSU PACCT-1: Program for the Assessment of Clinical Trial Tests (PACCT-1):
    Trial Assigning Individualized Options for Treatment: The TAYLORx Trial

Stage I, II, III:

  • SWOG 0221: 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 Post-Operative Adjuvant Therapy in Node-Positive or High-Risk Node Negative Breast Cancer.

  • SWOG 0230: 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.

  • SWOG 0307: Phase III Trial of Bisphosphonates as Adjuvant Therapy for Primary Breast Cancer.

  • CTSU 24-02: Phase III Trial Evaluating the Role of Ovarian Function Suppression and the Role of Exemestane as Adjuvant Therapies for Premenopausal Women with Endocrine Responsive Breast Cancer. (SOFT Trial)

  • NSABP B-42: 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

  • NASBP B-40: 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

  • JMA17R:  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)

  • CTSU N063D:  Adjuvant Lapatinib and/or Trastuzumab Treatment Optimisation (ALTTO) study: A Randomised, Multi-Centre, Open-Label, Phase III Study of Adjuvant Lapatinib, Trastuzumab, Their Sequence and Their Combination in Patients with HER2/ErbB2 Positive Primary Breast Cancer

Stage II, III:

  • None Currently

Stage IV:

  • SWOG 0226: Phase III Randomized Trail of Anastrozole vs Anastrozole and Fulvestrant as First Line Therapy for Post Menopausal Women with Metastatic Breast Cancer.

  • NSABP B-37: A Randomized Clinical Trial of Adjuvant Chemotherapy for Radically Resected Loco-regional Relapse of Breast Cancer

  • SWOG 0500: A Randomized Phase III Trial to test the Strategy of Changing therapy Versus Maintaining Therapy for Metastatic Breast cancer Patients who have Elevated Circulating Tumor Cells at First Follow-Up Assessment

  • CTSU E1105: 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

  • CTSU C40302:  Endocrine Therapy with or without Inhibition of EGF and HER2 Growth Factor Receptors: A Randomized, Double-Blind, Placebo-Controlled Phase III Trial of Fulvestrant with or without Lapatinib (GW572016) for Postmenopausal Women with Estrogen-Receptor Positive Advanced Breast Cancer

For more information on the above clinical trials: Cheryl Patz, RN, OCN, CCRC, 360.715.4133

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