Clinical trial · Interventional
Genexol-PM Versus Paclitaxel in Anthracycline-pretreated Metastatic Breast Cancer Patients
A Randomized Phase II Trial of Genexol-PM vs Paclitaxel in Anthracycline-pretreated Metastatic Breast Cancer Patients
NCT01169870CI-TRIAL-00006003withdrawnPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): withdrawn studies
Summary
Brief summary (as posted)
The purpose of this study is to evaluate the overall response rate of Genexol-PM compared with paclitaxel (cremophor-based paclitaxel) as palliative chemotherapy in anthracycline-pretreated patients with metastatic breast cancer.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Genexol-PM | Drug | Paclitaxel | ALIAS |
| Paclitaxel | Drug | Paclitaxel | ALIAS |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Genexol-PM
- description
- Genexol-PM 300mg/m2, diluted with 500ml of 5% dextrose or normal saline, intravenous infusion over 1 hour on day 1, every 3 week cycle.
- interventionNames
- Drug: Genexol-PM
- type
- ACTIVE_COMPARATOR
- label
- Paclitaxel
- description
- Paclitaxel 175mg/m2, diluted with 500ml of 5% dextrose or normal saline, intravenous infusion over 3 hour on day 1, every 3 week cycle.
- interventionNames
- Drug: Paclitaxel
Primary outcomes (1)
- measure
- overall response rate
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria:
1. Histologically or cytologically diagnosed stage IV or recurrent breast cancer patients according to American Joint Committee on Cancer (AJCC 6th ed.)
2. Prior chemotherapy at least one anthracycline-containing regimen, in either adjuvant or metastatic setting is requested.
3. Previous hormonal therapy in adjuvant setting is allowed.
4. Previous adjuvant taxane chemotherapy in an adjuvant setting is allowed, if taxane-free interval is more than 12 months
5. previous chemotherapy for metastatic disease is not allowed except for the regimen including anthracycline.
6. Previous chemotherapy including taxane for metastatic disease is not allowed.
7. Prior radiation therapy is allowed as long as the irradiated area is not the only source of measurable disease.
8. No other forms of cancer therapy, such as radiation, immunotherapy or chemotherapy for at least 4 weeks before the enrollment in therapy.
9. Major surgery other than biopsy within the past two weeks.
10. At least 18 years old
11. Performance status of 0, 1 and 2 on the ECOG criteria.
12. Disease status must be that of measurable disease defined as RECIST:
Lesions that can be accurately measured in at least one dimension \> 10 mm with chest x-ray, spiral CT scan, MRI, or physical examination
13. Estimated life expectancy of at least 12 weeks.
14. Patient compliance that allow adequate follow-up.
15. Adequate major organ function including the following:
①Hematologic function: WBC ³ 3,000/mm3 or absolute neutrophil count (ANC) ³ 1,500/mm3, platelet count ³ 100,000/mm3
②Hepatic function: bilirubin 1.5 x UNL , AST/ALT levels 2.5 x UNL
③Renal function: serum creatinine 1.5mg/dL
16. Grade of baseline neuropathy should not be more than grade 1 by NCI CTC v.3.0
17. Patients should sign an informed consent
18. women of childbearing age should use non-hormonal contraceptive method.
Exclusion Criteria:
1. Serious concurrent infection or nonmalignant illness that is uncontrolled or whose control may be jeopardized by complication of study therapy
2. Other malignancy with the past 5 years except adequately treated cutaneous basal cell carcinoma or uterine cervix in situ cancer
3. Psychiatric disorder that would preclude compliance.
4. uncontrolled CNS disease (eligible if the CNS disease is controlled with radiotherapy or corticosteroid)References
Publications (0)
Data not yet available
No reference posted for this study.