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NCT Number: NCT06310902

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

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.

Recruiting

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Fujian Medical University Union Hospital

Fuzhou, Fujian, 350001, China

Location status: Recruiting

Location contact

Yu Pan, M.D

CONTACT

[email protected]

+86 18900316399

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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).

Treatment and study plan

Single-cell Sequencing Analysis

Diagnostic Test

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

Primary outcomes

  1. Bioinformatics analysis of single-cell sequencing results

    Time frame: Collected during surgical treatment

    Using 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.

Study contacts

Contact information is provided by the study sponsor or research team.

Yu Pan, M.D.

CONTACT

[email protected]

+86 18900316399

Sponsors and collaborators

Lead sponsor

Fujian Medical University Union Hospital

Other

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Mar 15, 2024
Registry last updated
Mar 15, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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