Pilot Study to Evaluate the Impact of Denosumab on Disseminated Tumor Cells (DTC) in Patients With Early Stage Breast Cancer
This trial is active, not recruiting.
|Condition||early stage breast cancer|
|Sponsor||Hope Rugo, MD|
|Collaborator||University of California, San Francisco|
|Start date||November 2012|
|End date||June 2015|
|Trial size||45 participants|
|Trial identifier||NCT01545648, UCSF Protocol No. 117527|
The purpose of this study is to see whether taking denosumab for 12 months in women with a significant number of disseminated tumor cells in the bone marrow can reduce the number of these cells below a significant level.
|Endpoint classification||efficacy study|
|Intervention model||single group assignment|
Reduction of bone marrow DTC
time frame: Bone marrow assessments at baseline and 6 and 12 months.
Disseminated tumor cell counts
time frame: Bone marrow assessments at baseline and 6 and 12 months.
Male or female participants at least 18 years old.
Inclusion Criteria: 1. Patients ≥18 years of age with histologically or cytologically confirmed stage I, II, or III breast cancer. 2. ECOG Performance Status of 0 or 1 3. Prior therapy: 1. Prior adjuvant therapy is not required for participation in this study. 2. If adjuvant or neoadjuvant treatment with chemotherapy is recommended, it must be completed before study start, and not more than 18 months prior to study start. 3. If adjuvant or neoadjuvant treatment with trastuzumab (Herceptin®) is recommended, patients should have received at least 3 months of therapy before eligibility bone marrow is performed. 4. Patients who have had surgery following neoadjuvant chemotherapy or hormonal therapy are eligible 5. Patients must have completed definitive surgery and have completely resected disease. 6. Concomitant hormonal therapy is allowed. 7. Concomitant adjuvant trastuzumab is permitted 8. If adjuvant hormonal treatment is recommended, patients should have received at least 3 months of therapy before screening bone marrow is performed. 4. Bone marrow aspirate positive by IE/FC assay within 12 weeks of study entry 1. Definition of positive: >10 DTC/ml 2. Timing of bone marrow aspiration to determine study eligibility i.If patient is to receive either no adjuvant therapy or hormonal therapy alone, the aspiration may be performed at diagnosis as part of the large micrometastasis study at UCSF, or following diagnosis if the patient received initial surgery elsewhere. This is also true for patients who have surgery following neoadjuvant therapy for breast cancer. ii.If the patient is to receive adjuvant chemotherapy, the aspiration will be performed at least three weeks after chemotherapy has been completed. iii.For trastuzumab and hormone therapy, see above. 5. Laboratory studies 1. Liver function tests within normal limits, including total bilirubin, alkaline phosphatase, and AST (elevation of total bilirubin due to Gilbert's disease is allowed). - Gilbert's disease: a common hereditary cause of increased indirect bilirubin, but with normal direct bilirubin. 2. Calculated creatinine clearance (calculated GFR) > 30 ml/min 6. Ability to understand and sign informed consent 7. Patients who have had surgery following neoadjuvant chemotherapy or hormonal therapy are eligible to participate in this trial. Exclusion Criteria: 1. Karnofsky performance status < 90% 2. Patients participating in this study are not allowed to receive bisphosphonate therapy during the study period, either oral or intravenous. 3. Patients who completed adjuvant or neoadjuvant therapy more than 18 months prior to study screening. 4. A history of malignancy within the last 5 years except basal cell carcinoma of skin. 5. A history of human immunodeficiency virus (HIV) infection. 6. Severe, concurrent illness that would likely prevent the patient from being able to comply with the study protocol. 7. Pregnant or lactating women and women of child-bearing potential who are not using an effective method of birth control. 8. Significant dental disease that requires major intervention during the study period, such as tooth extraction 9. Significant coagulopathy that would prevent safe bone marrow aspiration
|Official title||Pilot Study to Evaluate the Impact of Denosumab on Disseminated Tumor Cells (DTC) in Patients With Early Stage Breast Cancer|
|Principal investigator||Hope Rugo, MD|
|Description||The presence of disseminated tumor cells (DTC) in the bone marrow in women with early stage breast cancer is an important prognostic factor associated with an increase in both recurrence and disease-associated death. In a pooled analysis of 4703 invasive breast cancer patients, detection of DTC in the bone marrow was associated with an increase in disease recurrence, distant metastases, and death from breast cancer over a median follow-up period of 5.2 years. Subsequent studies have demonstrated that the presence of DTC in the bone marrow of women with early breast cancer following completion of adjuvant therapy have an even greater impact on the risk of recurrence and death from breast cancer. Multivariate analysis demonstrated that the presence of marrow cells was an independent prognostic factor for reduced breast cancer specific survival with a relative risk of 6.3 (2.3-17.6, p<0.0001). Clearly, the detection of DTC in women with early stage breast cancer is a marker for increased risk of relapse and death, and this could serve as a unique indicator to select higher risk patients for intervention with targeted therapeutics. It has long been recognized that there is close relationship between bone and immune system, recent studies also suggests that in addition to monocytes/macrophage, T cells (especially Th17, a subset of T helper cells that produces IL-17), B cells and dendritic cells all play an important role in osteoclast formation. RANKL, in addition to its effect on osteoclasts, also induces local inflammation. Several recent studies have demonstrated that the presence of tumor associate macrophages (TAM) is associated with more aggressive disease, and a worse outcome. Preclinical data suggests that TAM plays an important role in promoting metastases and resistance to therapy. In addition to RANKL, there are other genes secreted by breast cancer cells, including TGF-β, TNF associated factor 6 (TRAF6), Hypoxia Induced Factor -1 (HIF-1) and Bone morphogenetic protein 2 (BMP2), also involve in bone-cancer "vicious cycle" and induce RANKL expression. Cytokines, such as IL-4, IL-6, IL-17, TNF-α and CSF-1, also play an important role in osteolysis and immune response in bone microenvironment by regulating TAM function (CSF-1, IL-4 and IL-17) and RANKL expression. Recently, CD47 and Signal Regulatory Protein α (SIRPA) were also shown to impair macrophage function, and associated with increased risk for recurrence in patients with breast cancer. The investigators hypothesize that patients with higher DTC may have higher expression of RANKL and chronic inflammatory cytokines. The investigators plan to evaluate the expression of RANK, RANKL, TRAF6, BMP2, CSF-1, CD47, IL-17 and SIRPA on isolated DTC and bone marrow hematopoietic cells, and correlate these results to the outcome of patients enrolled in the trial. The investigators hypothesize that treatment with denosumab will decrease the number of DTC in women with early stage breast cancer who have completed adjuvant or neoadjuvant cytotoxic therapy possibly by preventing cancer cell migration, and by promoting cancer cell death by changing the bone into a "hostile" environment . The investigators propose to conduct a non-randomized phase II trial testing this hypothesis in women with early stage breast cancer and persistent DTC following adjuvant systemic therapy. Patients with DTC will receive denosumab monthly for 6 months, then every 3 months for a total of one-year treatment, to mirror the schedule utilized in the ongoing randomized phase III denosumab versus placebo D-CARE trial. DTC will be monitored following 6 months and 12 months of therapy. The investigators anticipate that this treatment will reverse the "vicious cycle" between bone and cancer cells.|
Call for more information