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Construction of a risk prediction model for severe neutropenia in cancer patients after chemotherapy based on immune-inflammatory indicators

Building a Risk Prediction Model for Severe Neutropenia in Cancer Patients After Chemotherapy Based on Immune-Inflammatory Indicators

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600128410
Enrollment
Unknown
Registered
2026-07-20
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Severe neutropenia in cancer patients after chemotherapy

Interventions

Observation group:None

Sponsors

Xi'an Daxing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 - 80 years old, gender not restricted; 2. Diagnosed with malignant tumor and receiving chemotherapy treatment in our hospital; 3. Has complete basic clinical data and relevant laboratory test results before chemotherapy; 4. Has blood routine test results within 7 - 14 days after chemotherapy, which can determine whether grade 3 or above neutropenia occurs; 5. Medical records are complete and can meet the needs of research analysis; 6. The same patient is only included in the first chemotherapy cycle to avoid repeated inclusion.

Exclusion criteria

Exclusion criteria: 1. Those who had ANC < 1.0×10^9/L before chemotherapy; 2. Those with concurrent hematological diseases or clear abnormalities in bone marrow hematopoietic function; 3. Those with acute infections, severe inflammatory reactions or febrile diseases; 4. Those who have received other treatments in the recent period that may significantly affect bone marrow function and whose effects cannot be distinguished, such as those who have used white blood cell stimulants/hormones within the last 4 weeks and whose bone marrow function has been affected; 5. Those whose blood routine results are missing 7-14 days after chemotherapy and cannot determine the main outcome; 6. Those with severe lack of key clinical data or laboratory examination data, which cannot meet the needs of research analysis; 7. Pregnant or lactating patients; 8. Those whose test time window does not match, whose chemotherapy and pre-chemotherapy conditions are inconsistent, or whose extreme values cannot be verified.

Design outcomes

Primary

MeasureTime frame
Occurrence of severe neutropenia within 7–14 days after chemotherapy;

Secondary

MeasureTime frame
C-reactive protein level;proportion of CD28-positive T cells ; CD4/CD8 ratio;Interferon-gamma, IFN-?;Systemic immune-inflammation index, SII;White blood cell count,WBC;Tumor necrosis factor-alpha, TNF-a;Hemoglobin,Hb; interleukin-10 level ;Platelet count, PLT;Platelet-to-lymphocyte ratio, PLR;Lymphocyte count,LYM;proportion of PD-1-positive T cells ;Absolute neutrophil count,ANC;Monocyte-to-lymphocyte ratio, MLR;Neutrophil-to-lymphocyte ratio, NLR;Monocyte count, MONO; interleukin-6 level;

Countries

China

Contacts

Public ContactJINGJING TIE

Xi'an Daxing Hospital

18291765773@163.com+86 26 2616166

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026