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Predicting Response to Chemotherapy in Colorectal Cancer Via Multi-dimensional Analyses of the Tumor Associated Neutrophils

Zhongshan Hospital,Fudan University

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06495827
Enrollment
653
Registered
2024-07-11
Start date
2010-07-31
Completion date
2023-08-31
Last updated
2024-07-11

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

Conditions

Tumor Associated Neutrophils

Brief summary

A single biomarker is not adequate to identify patients with colorectal cancer (CRC) who have the potential to benefit from adjuvant therapy, presumably owing to the complexity of tumor-infiltrating immune cells (TIICs). The density and spatial organization of TIICs has not been definitely established to explore their predictive value. This study aimed to investigate the prognostic significance of TIICs and its biological predictive value in CRC.

Interventions

OTHERNo different intenvention

No different intenvention

Sponsors

Fudan University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. Voluntarily sign a written ICF. 2. The Eastern Cancer Collaborative Organization (ECOG) has a physical fitness score of 0 or 1. 3. The expected survival period is ≥ 3 months. 5\. Subjects diagnosed with metastatic colorectal adenocarcinoma by histology or cytology. 6\. Colorectal cancer patients who have not received systematic anti-tumor therapy in the past.

Exclusion criteria

1. Subjects suffered from other malignant tumors within 3 years before enrollment, except for cured local tumors (such as basal cell skin cancer, squamous cell skin cancer, superficial bladder cancer, cervical carcinoma in situ, etc.). 2. Simultaneously enroll in another clinical study, unless it is an observational, non-interference clinical study or a follow-up period of an intervention study. 3. Received systematic anti-tumor therapy (chemotherapy) within 3 weeks prior to the first administration

Design outcomes

Primary

MeasureTime frameDescription
PFSFrom date of operation until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 120 monthsFrom date of operation until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 120 months

Outcome results

None listed

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