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Research of gemcitabine and capecitabine in treatment of advanced breast cancer

Research of gemcitabine and capecitabine in treatment of advanced breast cancer

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-PRNC-13003611
Enrollment
Unknown
Registered
2013-09-16
Start date
2013-09-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced breast cancer

Interventions

Case series:Pharmacological interventions

Sponsors

First Affiliated Hospital of Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 75 Years

Inclusion criteria

Inclusion criteria: Aged 20 to 75 years; ECOG performance status of 0 to 2; Pathological examination confirmed the presence of breast cancer recurrence/metastasis; With at least one measurable lesion (bone metastases, ascites and pleural effusion is not considered measurable lesions);Bone marrow, kidney and liver functions are normal; Expected survival time of at least 6 months; Had received prior anthracycline and taxane chemotherapy but without vinblastine, platinum-based drugs.Submitted a written informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Fluoropyrimidine drug allergies; 3. History of organ transplants; 4. Long-term use of systemic corticosteroids treatment history; 5. Current or previous history of brain tumor metastasis; 6. Serious concurrent diseases such as severe liver disease (such as cirrhosis), kidney disease, lung disease, or uncontrolled diabetes; 7. Observe significant ECG abnormalities or clinical manifestations of an apparent heart disease.

Design outcomes

Primary

MeasureTime frame
Gene mutations;TTP;PFS;OS;CR+PR;

Secondary

MeasureTime frame
toxicity;

Countries

China

Contacts

Public ContactShen Peng

Medical oncology, First Affiliated Hospital of Zhejiang University

shenp@zju.edu.cn+86 0571-87236557

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026