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Surgery for Pancreatic Cancer With Oligo-Metastasis

Surgery/Destruction for Stage IV Pancreatic Cancer With Oligo-Metastatic Disease

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04196816
Acronym
SPaM
Enrollment
200
Registered
2019-12-12
Start date
2020-01-01
Completion date
2020-12-01
Last updated
2020-12-29

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

Conditions

Pancreatic Cancer, Pancreatic Surgery

Keywords

Surgery, Metastasis surgery, Survival, Multimodal treatment, Stage IV

Brief summary

Pancreatic cancer is increasing in incidence and will be the second leading cause of cancer-related deaths in 2030 in the West. Only 10 to 15% of patients are eligible for curative resection with long-term survival rarely exceeding 20% at 5 years. The management of metastatic or recurrent diseases can not, unfortunately, be recommended to date because of limited data available (INCA 2019). However, recent, low-strength publications have reported encouraging results on the long-term survival of stage IV or recurrent patients. The aim of the present retrospective cohort study is to analyze results of surgery/destruction of metastatic synchronous or metachronous disease or local recurrence in patients with stage IV pancreatic cancer

Interventions

None listed

Sponsors

Université Montpellier
CollaboratorOTHER
Association de Chirurgie hepato-bilio-pancreatique et transplantation (ACHBT)
CollaboratorUNKNOWN
Federation de recherche en chirurgie digestive (FRENCH)
CollaboratorUNKNOWN
Club Français du Pancreas (CFP)
CollaboratorUNKNOWN
University Hospital, Montpellier
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 95 Years
Healthy volunteers
No

Inclusion criteria

\- Patients who had resection or destruction of one or more synchronous or metachronous metastases or local recurrence of pancreatic adenocarcinoma Details: * synchronous lesions, metachrones can be included * all distant lesions (hepatic, pulmonary) can be included * documented lymph node involvement after analysis of the specimen (hepatic hilum, mesenteric root, retroperitoneal or inter-aortic-cellar) can be included * patients with local recurrence who underwent surgical treatment

Exclusion criteria

\- Patient who reject the study protocol

Design outcomes

Primary

MeasureTime frameDescription
Overall survival3 yearsOverall survival at 3 years (percentage of patients alive). Overall survival (OS) (time from diagnosis until death, regardless of cause)

Secondary

MeasureTime frameDescription
Progression-free survival3 yearsProgression-free survival (percentage of patients without recurrence) at 3 years. Progression-free survival (PFS) (time from diagnosis to time of first radiological evidence of local, regional, or distant relapse, or death due to any cause)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026