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Efficacy and safety of albumin-bound paclitaxel combined with platinum as first-line chemotherapy for patients with residual tumor after initial reduction in advanced ovarian cancer: a prospective one-arm study and mechanism based on PDX model

Efficacy and safety of albumin-bound paclitaxel combined with platinum as first-line chemotherapy for patients with residual tumor after initial reduction in advanced ovarian cancer: a prospective one-arm study and mechanism based on PDX model

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200057542
Enrollment
Unknown
Registered
2022-03-14
Start date
2022-03-14
Completion date
Unknown
Last updated
2023-10-22

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

Conditions

Ovarian Cancer

Interventions

Experimental group:nab-paclitaxel in combination with carboplatin

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Women aged 18-80 years. 2. Patients with epithelial ovarian cancer/tubal cancer/primary peritoneal cancer confirmed by pathology in our hospital. 3. FIGO stage was stage III-IV. 4. Initial tumor cell reduction was performed, which was evaluated as incomplete tumor reduction after surgery, and albumin-bound paclitaxel + carboplatin adjuvant chemotherapy was performed. 5. ECOG score: 0-2; Life expectancy >3 months; No obvious abnormalities in organ function: (1) Liver function: total bilirubin = 60ml/min; (3) Blood function: neutrophils >= 3x10^9/L; Platelet count >= 80x10^9/L, hemoglobin >= 7g/dL. 6. Patients give informed consent to the basic contents of the study, and can complete the treatment as planned and continue to follow up. 7. There is no history of other malignancies that may interfere with the comparison of treatment or study effectiveness.

Exclusion criteria

Exclusion criteria: 1. Pregnant or breastfeeding patients. 2. Inability to give informed consent to research content and interventions. 3. Preoperative neoadjuvant chemotherapy.

Design outcomes

Primary

MeasureTime frame
2-year progression-free survival rate;

Secondary

MeasureTime frame
chemotherapy related adverse events;incidence of post-operative complications;quality of life;

Countries

China

Contacts

Public ContactLinghu Hua

The First Affiliated Hospital of Chongqing Medical University

linghu_hua@126.com+86 15023075926

Outcome results

None listed

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