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Solid Pseudopapillary Neoplasm of the PancreasSPNNCT07183280

Multicentric Database for Solid Pseudopapillary Neoplasm of the Pancreas

An observational study of Solid Pseudopapillary Neoplasm of the Pancreas, run by Fudan University at 1 site in China.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

To establish and maintain a reliable multicenter real-world database for pancreatic SPN, providing high-quality data and evidence-based support for clinical/translational research. Read more about this study

Who is it for?
Any age
What is being tested?
operation
How many people
2,000 participants
Where
1 siteChina
Study dates
1 Sep 2025to 30 Dec 2041
How long will I take part?
10 Years
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: To establish and maintain a reliable multicenter real-world database for pancreatic SPN, providing high-quality data and evidence-based support for clinical/translational research.

Who may be able to join

  • No restrictions on age, gender, or performance status;
  • Pathologically/cytologically confirmed SPN;
  • Compliance with follow-up requirements;

Who cannot join

  • Non-neoplastic pancreatic lesions;
  • Non-pancreatic primary tumors;
  • Non-compliance with follow-up;

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

China1 site, 1 recruiting
  • Shanghai Cancer Center

    Shanghai, Special Administrative Region, 200032

    Guopei Luo, +86868621641755, luoguopei@hotmail.com

    Recruiting

Other trials in China

About this study

Official title: The Construction and Maintenance of A Real World Study Multicentric Database for Solid Pseudopapillary Neoplasm of the Pancreas

To establish and maintain a reliable multicenter real-world database for pancreatic SPN, providing high-quality data and evidence-based support for clinical/translational research.

Read the detailed description

Pancreatic solid pseudopapillary neoplasm (SPN) is a low-grade malignant tumor, accounting for 0.2%-2.7% of pancreatic tumors, with unique histological and biological characteristics. Its pathological features include solid-cystic and pseudopapillary structures. SPN occurs predominantly in younger individuals, with a median age of 27-31 years. Male patients tend to be older than female patients, but the incidence is significantly higher in females. This gender disparity may be related to hormonal factors or genetic susceptibility. Although most patients have excellent prognosis (10-year survival rate >95%), approximately 10% may develop metastasis or recurrence, particularly in cases with high-risk pathological features. Reported incidence rates are higher in Asia than in Western countries, with Chinese multicenter studies indicating SPN constitutes 2.8% of pancreatic tumors. SPN exhibits significant differences from other pancreatic tumors in epidemiology, morphology, immunophenotype, and genetics, warranting classification as a distinct pathological entity for clinical management and prognostic evaluation.

Real-world study (RWS) refers to the systematic collection of patient health data in real-world clinical settings [real-world data (RWD)] to address predefined medical questions, employing multidisciplinary methods for comprehensive analysis to generate real-world evidence (RWE). RWS can inform clinical decision-making, support drug development and regulatory decisions, and guide public health policies through pharmacoeconomic evaluations. As an important complement and extension to randomized controlled trials (RCTs), RWS has gained increasing attention globally in recent years. In May 2019, the U.S. FDA issued draft guidance on "Submitting Documents Using Real-World Data and Real-World Evidence to FDA for Drugs and Biologics", detailing the use of RWD/RWE for regulatory approvals. China's NMPA released the "Guideline for Real-World Evidence to Support Drug Development and Evaluation (Trial)" in January 2020, formally incorporating RWE into drug development and regulatory frameworks. Similar initiatives exist in Japan, South Korea, and the EU. As of June 2020, over 2,000 RWS studies were registered globally, including 300+ in China (70+ related to oncology).

SPN is insensitive to chemotherapy and radiotherapy, with complete surgical resection being the cornerstone of cure. R0 resection (negative margins) reduces recurrence and improves survival. For resectable SPN, surgery is strongly recommended. Despite being classified as malignant, SPN exhibits indolent growth with excellent outcomes. Most patients undergoing R0 resection achieve cure. Organ-preserving techniques (e.g., enucleation, spleen-preserving distal pancreatectomy) and minimally invasive approaches (laparoscopic/robotic) are prioritized to reduce complications and enhance quality of life. However, large-scale evidence comparing surgical approaches (minimally invasive vs. open; standard vs. limited resection) remains limited.

Given SPN's rarity and slow research progress, the investigators propose establishing a multicenter RWS database to:

  1. Design a tailored database system for SPN, retrospectively collecting clinical data from Shanghai Pancreatic Tumor Institute and other centers;
  2. Prospectively collect and maintain SPN patient data to support clinical and translational research.
Being tested
operation
Keywords
Solid Pseudopapillary Neoplasm of the Pancreas, Multicenter real-world database

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • operationOther

    Enucleation, spleen-preserving distal pancreatectomy, or duodenum-preserving pancreatic head resection, etc

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Overall survival

    OS: OS of subjects from recruiting to the time of death from any cause

    Measured: 12 month

Secondary outcomes (1)
  1. Disease free survival (DFS)

    Disease free survival (DFS) is calculated from completion of surgery and ends when the first event (recurrence/progression/death) occurs.

    Measured: up to 10 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Sep 2025
  2. Study start1 Sep 2025
  3. Primary completion30 Dec 2040 (estimated)
  4. Study completion30 Dec 2041 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
2,000 participants (estimated)
Target duration
10 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT07183280
Sponsor's protocol ID
PTCA199-15
Acronym
SPN
Status last verified
Sep 2025
First submitted
8 Sep 2025
Last updated
19 Sep 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Hua Y, Hong X, Dai M, Li J, Yang S, Guo J, Wang W, Xu Q, Han X, Wang M, Huang N, Zheng H, Kleeff J, Liu Q, Wu W, Zhang T, Liao Q, Zhao Y. Local resection for solid pseudopapillary neoplasms of the pancreas shows improved postoperative gastrointestinal function and reduced mental stress: a multiquestionnaire survey from a large cohort. Int J Surg. 2023 Dec 1;109(12):3815-3826. doi: 10.1097/JS9.0000000000000702.

    PubMed 37830944
  • Xiao Z, Fan Z, Yang F, Qadan M, Ray S, An Y, Wang P, Xiao W, Wu X, Zhou B, Sheng J, Long J, Zhu D, Zhou Y, Wen Y, Chen X, Zhou L, Cheng W, Song Y, Xu J, Ni Q, Warshaw A, Zhan H, Fu D, Yu X, Luo G. Organ-preserving surgery for solid pseudopapillary neoplasm of the pancreas: A multicentric study. Eur J Cancer. 2026 Sep 12;247:117053. doi: 10.1016/j.ejca.2026.117053. Online ahead of print.

    PubMed 42759262

Questions about this trial

What is this clinical trial studying?

An observational study of Solid Pseudopapillary Neoplasm of the Pancreas, run by Fudan University at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 19 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Huanyu Xia, MD (+86 2164175590 ext. 1307, xiahuanyu@fudanpci.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Overall survival (time frame: 12 month). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07183280, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Sep 2025.

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