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Development and validation of a Nomogram integrating the prognostic nutritional index for predicting Chemotherapy-Induced myelosuppression in patients with Gynecological cancers

Development and validation of a Nomogram integrating the prognostic nutritional index for predicting Chemotherapy-Induced myelosuppression in patients with Gynecological cancers

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121329
Enrollment
Unknown
Registered
2026-03-30
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Gynecologic cancers (GCs)

Interventions

External Group:None
Internal Group:None

Sponsors

Affiliated Qingyuan Hospital, Guangzhou Medical University (Qingyuan People's Hospital)
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Diagnosed with primary gynecological malignancy (including cervical cancer, ovarian cancer, endometrial cancer, etc.) confirmed by histopathology; 2. Age >= 18 years; 3. Scheduled to receive first-time chemotherapy regimens containing platinum-based agents and/or taxanes, such as neoadjuvant or adjuvant chemotherapy; 4. Completed at least 3 cycles of chemotherapy with complete blood routine monitoring data; 5. Complete blood routine and biochemical test results available within one week prior to chemotherapy.

Exclusion criteria

Exclusion criteria: 1. Presence of grade II or higher myelosuppression prior to chemotherapy (according to CTCAE v5.0 criteria); 2. Concurrent other primary malignancies or previous history of chemotherapy or radiotherapy; 3. Coexisting severe hematologic diseases (e.g., aplastic anemia, myelodysplastic syndrome, etc.); 4. Coexisting severe hepatic or renal dysfunction (Child – Pugh class C, or eGFR < 30 mL/min/1.73 m²); 5. Active infection or uncontrolled autoimmune disease; 6. Anticipated inability to collect complete clinical data;

Design outcomes

Primary

MeasureTime frame
Prognostic Nutritional Index(PNI);

Secondary

MeasureTime frame
Laboratory parameters: serum albumin, hemoglobin, neutrophil count, peripheral blood lymphocyte count, platelet count.;Disease and treatment data: tumor type, FIGO stage, tumor diameter (longest), distant metastasis (yes/no), chemotherapy regimen (drug, dose, cycle), surgery before chemotherapy (yes/no).;The model evaluation metrics include discrimination, calibration, and clinical utility.;

Countries

China

Contacts

Public ContactCaifang Wang

Affiliated Qingyuan Hospital, Guangzhou Medical University (Qingyuan People's Hospital)

2386966483@qq.com+86 763 3113803

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026