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Prospective multicenter study regarding the efficacy of Gemcitabine (gemzar) plus nab-Paclitaxel (Abraxane) regimen for locally advanced pancreatic cancer

Prospective multicenter study regarding the efficacy of Gemcitabine (gemzar) plus nab-Paclitaxel (Abraxane) regimen for locally advanced pancreatic cancer - GEAR study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000027775
Enrollment
37
Registered
2017-07-01
Start date
2017-07-20
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

pancreatic cancer

Interventions

Gemcitabine + nab-Paclitaxel regimen (Gemcitabine 1000mg/m2 nab-Panclitaxicel 125mg/2: day1,8,15 28day/course:2-4 course) and operation

Sponsors

Kyushu-Yamaguchi study group of therapy for pancreatobiliary cancer
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Histologically confirmed adenocarcinoma or adenosquamous carcinoma 2) BR-A pancreatic cancer 3) With measurable lesion(s) 4) Without distant metastasis 5) Without any further treatment for pancreatic cancer 6) Age more than 20 or less than 75 7)ECOG Performance Status 0-1 8) Without history of chemotherapy or radiotherapy 9)Adequate organ function 10) Sensory/motor neuropathy: None or Grade 1 11) Written informed consent

Exclusion criteria

Exclusion criteria: 1) Present or previous (within 5 years) double cancer except for carcinoma in situ 2) Pregnant females, possibly pregnant females, females feeding babies and males wishing partners' pregnancy 3) Active infection 4) Severe mental disorder 5) Interstitial pneumonia or pulmonary fibrosis 6) Severe heart disease, liver disease and uncontrolled diabetes 7) Patients positive for HBs antigen 8) Patients inadequate for enhanced CT scan 9) Severe allergy for drugs 10) Patients with inadequate condition

Design outcomes

Primary

MeasureTime frame
R0 resection rate

Secondary

MeasureTime frame
QOL assessment, Effectiveness of preoperative chemotherapy, pathological response rate, incidence rate of adverse events, relative dose intensity

Countries

Japan

Contacts

Public ContactYoshihiro Miyasaka

Kyushu University Department of Surgery and Oncology

yoshi-m@surg1.med.kyushu-u.ac.jp092-622-5441

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026