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A real world study of gemcitabine combined with nab-paclitaxel in the treatment of locally advanced or metastatic pancreatic cancer

A real world study of gemcitabine combined with nab-paclitaxel in the treatment of locally advanced or metastatic pancreatic cancer

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027729
Enrollment
Unknown
Registered
2019-11-24
Start date
2019-11-25
Completion date
Unknown
Last updated
2020-07-13

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

Conditions

pancreatic cancer

Interventions

experimental group:gemcitabine combined with nab-paclitaxel

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) patients with locally advanced or metastatic pancreatic cancer confirmed by pathology; 2) adenocarcinoma of pancreatic duct confirmed by cytology or histology; 3) have not received any systematic anti-tumor treatment before; 4) aged 18 to 80 years; 5) estimated survival time >=3 months; 6) ECoG PS score 0-1; 7) there is at least one measurable tumor focus: on spiral CT, the long diameter >=10 mm, the short diameter >=15 mm; on general CT or physical examination, the maximum diameter must be >=20 mm; 8) patients participate voluntarily and sign informed consent.

Exclusion criteria

Exclusion criteria: 1) those who are known to be seriously allergic to gemcitabine and albumin Paclitaxel; 2) patients with obvious coagulation mechanism disorder, active bleeding and bleeding tendency; 3) have other malignant tumor history within 5 years (except for skin basal cell carcinoma and cervical carcinoma in situ which are fully treated); 4) interstitial pneumonia or pulmonary fibrosis; 5) uncontrollable pleural effusion or ascites; 6) patients with serious uncontrolled internal diseases, acute infection and recent history of myocardial infarction (within 3 months); 7) pregnancy or lactation, as well as childbearing age patients who refuse to take appropriate contraceptive measures in the process of this trial; 8) patients not suitable for the study were judged by the researchers.

Design outcomes

Primary

MeasureTime frame
OS;

Secondary

MeasureTime frame
PFS;ORR;AE;QOL;

Countries

China

Contacts

Public ContactDan Cao

West China Hospital, Sichuan University

caodan316@163.com+86 18980605963

Outcome results

None listed

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