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Comparison between nanoliposomal irinotecan plus 5-FU/ folinic acid and S-1 monotherapy in metastatic pancreatic cancer: A propensity score-matched retrospective cohort study.

Comparison between nanoliposomal irinotecan plus 5-FU/ folinic acid and S-1 monotherapy in metastatic pancreatic cancer: A propensity score-matched retrospective cohort study. - Comparison between nanoliposomal irinotecan plus 5-FU/ folinic acid and S-1 monotherapy in metastatic pancreatic cancer: A propensity score-matched retrospective cohort study.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000048143
Enrollment
500
Registered
2022-06-23
Start date
2022-06-23
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

None listed

Sponsors

Japan Oncology Network in Hepatobiliary and Pancreas
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) NAPOLI-1 regimen or S-1 monotherapy is initiated as second-line therapy after failure of gemcitabine=based first-line therapy. 2) Therapy is introduced between September 1, 2019 and February 28, 2021 3) Diagnosis of adenocarcinoma by histological or cytological diagnosis of primary or metastatic lesions. 4) Pancreatic cancer with distant metastasis or recurrent pancreatic cancer by chest CT and abdominal/pelvic contrast-enhanced CT or abdominal/pelvic contrast-enhanced MRI. In the case of recurrent pancreatic cancer, the following items should be followed: a) The first treatment regimen after the diagnosis of recurrence is considered as the primary treatment. b) If postoperative adjuvant chemotherapy was administered, patients are eligible if at least 6 months have elapsed between the last administration of postoperative adjuvant chemotherapy and the recurrence (patients are eligible if the recurrence occurs on the same date 6 months after the last administration of postoperative adjuvant chemotherapy). c) The first treatment regimen after the diagnosis of recurrence is defined as first-line treatment. 5) Patients must not have used irinotecan (including nanoliposomal irinotecan) or fluoropyrimidines. 6) Patients must be at least 20 years of age at the time of enrollment.

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
Overall survival

Secondary

MeasureTime frame
Progression-free survival, Objective response rate, Disease control rate

Countries

Japan

Contacts

Public ContactHiroshi Imaoka

National Cancer Center Hospital East Hepatobiliary and Pancreatic Oncology

hiimaoka@east.ncc.go.jp+81-4-7133-1111

Outcome results

None listed

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