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Cohort study of patients with initially unresectable pancreatic cancer in whom conversion surgery is planned after FOLFIRINOX or gemcitabine plus nab-paclitaxel therapy

Cohort study of patients with initially unresectable pancreatic cancer in whom conversion surgery is planned after FOLFIRINOX or gemcitabine plus nab-paclitaxel therapy - PC-CURE-1

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000035668
Enrollment
360
Registered
2019-01-26
Start date
2019-03-04
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

Unresectable pancreatic cancer

Interventions

None listed

Sponsors

Federation of Asian Clinical Oncology (FACO)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with initially pathological confirmed adenocarcinoma and consitent with pancreatic ductal adenocarcinoma including papillary adenocarcinoma, tubular adenocarcinoma, poor differentiated adenocarcinoma, or adenosquamous carcinoma by diagnostic imaging 2. Locally advanced or distant metastatic disease before starting of chemotherapy 3. FOLFIRINOX (including modified regimen) or gemcitabine plus nab-paclitaxel initially performed 4. Diagnosed as resectable disease after chemotherapy by imaging, then laparotomy or continuation of chemotherapy performed

Exclusion criteria

Exclusion criteria: 1. Borderline resectable disease by NCCN Guidelines Ver 2.2018 is excluded in this study. Solid tumor contact with the CA >180 degrees is classified to unrsectable. 2. Recurrent disease 3. Response to chemotherapy according to RECIST ver 1.1 was PD 4. Heavy ion radiotherapy or proton beam therapy performed before laparotomy 5. Diagnosed as unresectable disease by examination laparoscopic when was intented to conversion surgery 6. Resection of metastatic lesions at conversion surgery. However, patients can be registered unless they are pathologically demonstrated to have cancer after dissection of the 16th lymph node or hepatectomy. 7. Peritoneal lavage cytology positive

Design outcomes

Primary

MeasureTime frame
Overall survival from the day when resection was considered to be possible (day of examination)

Secondary

MeasureTime frame
Relapse-free survival, post-resection survival, mode of relapse, presence or absence of hospital death, and surgery-related complications

Countries

Japan,Asia(except Japan)

Contacts

Public ContactMami Sakurai

Federation of Asian Clinical Oncology (FACO) Tokyo Office

faco-office@jsco.or.jp03-5542-0546

Outcome results

None listed

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