Neoadjuvant Doxorubicin, Polyglutamate Paclitaxel, Capecitabine and Metronomic Chemotherapy in Breast Cancer
Overview[ - collapse ][ - ]
| Purpose | The investigators propose to conduct a clinical trial of neoadjuvant treatment utilizing chemotherapy formulations with favorable toxicity profiles: weekly doxorubicin, PPX and capecitabine. It is expected this combination will at least maintain the efficacy of a traditional chemotherapy regimen but will be associated with less toxicity, particularly nausea, vomiting and alopecia. In order to accomplish this the investigators have designed a chemotherapy regimen whose components (or administration schedule) are associated with minimal or no alopecia and are also considered to have low emetogenic potential. In an attempt to improve the efficacy of the regimen the investigators plan to study an alternate schedule of cyclophosphamide and methotrexate administration (metronomic chemotherapy) which appears to inhibit angiogenesis and therefore enhance the activity of conventional cytotoxic chemotherapy administered concurrently. In this trial the investigators aim to determine the clinical and pathologic response rate of 12 weeks of doxorubicin followed by 4 cycles of PPX and capecitabine. Metronomic chemotherapy with cyclophosphamide and methotrexate will be administered during the 24 weeks of chemotherapy. |
|---|---|
| Condition | Breast Cancer |
| Intervention | Drug: doxorubicin, paclitaxel poliglumex, capecitabine, cyclophosphamide, methotrexate |
| Phase | Phase 2 |
| Sponsor | University of Southern California |
| Responsible Party | University of Southern California |
| ClinicalTrials.gov Identifier | NCT01227408 |
| First Received | January 8, 2009 |
| Last Updated | October 22, 2010 |
| Last verified | October 2010 |
Tracking Information[ + expand ][ + ]
| First Received Date | January 8, 2009 |
|---|---|
| Last Updated Date | October 22, 2010 |
| Start Date | February 2009 |
| Estimated Primary Completion Date | Not Provided |
| Current Primary Outcome Measures | Response [Time Frame: At surgical resection on about week 30] [Designated as safety issue: No] |
| Current Secondary Outcome Measures | Toxicity [Time Frame: Every 4 weeks] [Designated as safety issue: Yes] |
Descriptive Information[ + expand ][ + ]
| Brief Title | Neoadjuvant Doxorubicin, Polyglutamate Paclitaxel, Capecitabine and Metronomic Chemotherapy in Breast Cancer |
|---|---|
| Official Title | Phase II Clinical Trial of Neoadjuvant Weekly Doxorubicin, Polyglutamate Paclitaxel, Capecitabine and Metronomic Chemotherapy in Breast Cancer |
| Brief Summary | The investigators propose to conduct a clinical trial of neoadjuvant treatment utilizing chemotherapy formulations with favorable toxicity profiles: weekly doxorubicin, PPX and capecitabine. It is expected this combination will at least maintain the efficacy of a traditional chemotherapy regimen but will be associated with less toxicity, particularly nausea, vomiting and alopecia. In order to accomplish this the investigators have designed a chemotherapy regimen whose components (or administration schedule) are associated with minimal or no alopecia and are also considered to have low emetogenic potential. In an attempt to improve the efficacy of the regimen the investigators plan to study an alternate schedule of cyclophosphamide and methotrexate administration (metronomic chemotherapy) which appears to inhibit angiogenesis and therefore enhance the activity of conventional cytotoxic chemotherapy administered concurrently. In this trial the investigators aim to determine the clinical and pathologic response rate of 12 weeks of doxorubicin followed by 4 cycles of PPX and capecitabine. Metronomic chemotherapy with cyclophosphamide and methotrexate will be administered during the 24 weeks of chemotherapy. |
| Detailed Description | Not Provided |
| Study Type | Interventional |
| Study Phase | Phase 2 |
| Study Design | Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment |
| Condition | Breast Cancer |
| Intervention | Drug: doxorubicin, paclitaxel poliglumex, capecitabine, cyclophosphamide, methotrexate doxorubicin 20mg/m2 weekly x 12 wks, cyclophosphamide 50 mg PO qd x 12 wks, methotrexate 2.5 mg PO bid d1,2 wkly x 12. One week later paclitaxel poliglumex 135mg/m2 IV every 3 wks plus capecitabine 825 mg/m2 PO bid x 14days x 4 cycles |
| Study Arm (s) | Not Provided |
Recruitment Information[ + expand ][ + ]
| Recruitment Status | Withdrawn |
|---|---|
| Estimated Enrollment | 42 |
| Estimated Completion Date | Not Provided |
| Estimated Primary Completion Date | February 2009 |
| Eligibility Criteria | Inclusion Criteria: - SWOG performance status of 0-2 - Projected life expectancy of at least 3 months - Female age 18 years and over - Provision of informed consent prior to any study-related procedures. - Hormone receptor positive or negative tumor - Her 2 neu negative tumor - Negative pregnancy test for women of childbearing potential - Patients must agree to use some form of contraception while on this study at initiation and for the duration of participation in the study. Sexually active males must also use a reliable and appropriate method of contraception. Post-menopausal women must be amenorrheic for at least 12 months to be considered of non-childbearing potential. - ANC > 1500, Platelet count > 100,000, Hemoglobin > 9.0 - Serum creatinine < 1.5 mg/dl - Hepatic function: Patients must have adequate liver functions: AST or ALT < 2.5 X upper limit of normal (ULN), alkaline phosphatase < 2.5 X upper limit of normal. Serum Bilirubin < 1.5 mg - Peripheral neuropathy grade 0-1 - No other concomitant therapy directed at the cancer is allowed. Exclusion Criteria: - Serum bilirubin > 1.5 the upper limit of reference range (ULRR) - Serum creatinine >1.5 - Prior therapy for this tumor. - Clinical Congestive Heart Failure - Women who are currently pregnant or breast feeding. - Receipt of any investigational agents within 30 days prior to commencing study treatment - Prior radiation must not have included ≥ 30% of major bone marrow containing areas (pelvis, lumbar spine) - No other prior malignancy is allowed except for the following: adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, lobular carcinoma in-situ of the breast (LCIS), or any other cancer from which the patient has been disease-free for 5 years. Patients with prior invasive breast cancer or ductal carcinoma in-situ (DCIS) are eligible if they have been disease free for 5 years and did not receive prior treatment with doxorubicin and/or a taxane. |
| Gender | Female |
| Ages | 18 Years |
| Accepts Healthy Volunteers | No |
| Contacts | Not Provided |
| Location Countries | United States |
Administrative Information[ + expand ][ + ]
| NCT Number | NCT01227408 |
|---|---|
| Other Study ID Numbers | 1B-08-7 |
| Has Data Monitoring Committee | Yes |
| Information Provided By | University of Southern California |
| Study Sponsor | University of Southern California |
| Collaborators | Cell Therapeutics |
| Investigators | Not Provided |
| Verification Date | October 2010 |
Locations[ + expand ][ + ]
| USC/Norris Comprehensive Cancer Center | Los Angeles, California, United States, 90033 |
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