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Single-cell Sequencing Analysis of Resectable/Borderline Resectable Pancreatic Cancer Patients

Single-cell Sequencing Analysis of Resectable/Borderline Resectable Pancreatic Cancer Patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06310902
Enrollment
40
Registered
2024-03-15
Start date
2024-03-01
Completion date
2026-09-01
Last updated
2024-03-15

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

Conditions

Pancreatic Neoplasms

Keywords

Pancreatic neoplasms, Single-cell sequencing, Immune microenvironment

Brief summary

Preoperative neoadjuvant chemotherapy is widely used in treating patients with borderline resectable pancreatic cancer (BRPC). However, there are limitations in this field. Treatment strategies and definitions for BRPC patients differ, and the efficacy and prognosis of neoadjuvant chemotherapy vary greatly.This study aims to utilize single-cell sequencing technology to investigate in-depth the composition and interactions of the tumor microenvironment in patients from the surgical-only group and the preoperative neoadjuvant chemotherapy group.

Interventions

DIAGNOSTIC_TESTSingle-cell Sequencing Analysis

Identification of rare cell populations, the characterization of cell types and subtypes, and the discovery of novel cell states.

Sponsors

Fujian Medical University Union Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* 18 years ≤ age ≤ 75 years. * Resectable/borderline resectable pancreatic cancer patients diagnosed based on pathological and preoperative imaging evaluation. * No prior history of any form of anti-tumor treatment. * At least one measurable lesion. * Eastern Cooperative Oncology Group (ECOG): 0-1. * Not participated in any other clinical studies before or during treatment. * Willingness to participate voluntarily in this study, signing an informed consent form.

Exclusion criteria

* History of any other malignant tumor, except for completely resected basal cell or squamous cell carcinoma of the skin or carcinoma in situ of the cervix, within the past 5 years. * Vaccination with live vaccines within 4 weeks prior to enrollment or during the study period. * Active autoimmune diseases or a history of autoimmune diseases within the past 4 weeks before enrollment. * Allogeneic bone marrow or organ transplantation. * Active gastric or duodenal ulcers, ulcerative colitis, or active bleeding from unresected tumors in the gastrointestinal tract, or other conditions determined by the investigator that may cause gastrointestinal bleeding or perforation. * Evidence or history of significant bleeding tendency within 3 months prior to enrollment (bleeding \>30 mL within 3 months, hematemesis, melena, or hematochezia), hemoptysis (\>5 mL of fresh blood within 4 weeks), or occurrence of thromboembolic events within 12 months (including stroke events and/or transient ischemic attacks).

Design outcomes

Primary

MeasureTime frameDescription
Bioinformatics analysis of single-cell sequencing resultsCollected during surgical treatmentUsing single-cell sequencing technology, in-depth analysis of surgical samples from resectable/borderline resectable pancreatic cancer patients is conducted to investigate the composition and interactions of the tumor microenvironment in pancreatic cancer.

Countries

China

Contacts

Primary ContactYu Pan, M.D.
yupan199002@163.com+86 18900316399

Outcome results

None listed

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