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Monocytosis as a prognostic factor for survival in stage IB and IIA cervical cancer
Wan Kyu Eo1, Byung Su Kwon2, Ki Hyung Kim2
1Department of Internal Medicine, College of Medicine, Kyung Hee University, Seoul, Korea.
Insights
Monocytosis, indicated by a high absolute monocyte count, and larger tumor size are key indicators of poorer survival in early-stage cervical cancer patients. These hematologic parameters offer prognostic value for progression-free and overall survival.
Area of Science:
- Oncology
- Hematology
- Gynecologic Oncology
Background:
- Cervical cancer prognosis relies on clinical factors.
- Hematologic parameters from white blood cell counts may offer additional prognostic insights.
Purpose of the Study:
- To evaluate white blood cell count and differential count-derived parameters as prognostic factors for survival in stage IB and IIA cervical cancer.
- To determine the independent prognostic value of absolute monocyte count (AMC) and other hematologic markers.
Main Methods:
- Retrospective analysis of 233 patients with stage IB/IIA cervical cancer.
- Assessment of demographic, clinicopathologic, and laboratory data.
- Multivariate analysis to identify prognostic factors for progression-free survival (PFS) and overall survival (OS).
Main Results:
- Absolute monocyte count (AMC) and tumor size were significant independent prognostic factors for both PFS and OS.
- Monocytosis (elevated AMC) showed a strong association with reduced survival (HR for OS: 23.29).
- Lymph node involvement also impacted OS, but AMC and tumor size were stronger predictors.
Conclusions:
- Monocytosis and increased tumor size are independent prognostic factors for PFS and OS in early-stage cervical cancer.
- AMC is a valuable hematologic marker for predicting outcomes in these patients.
- Further research may explore therapeutic strategies targeting monocyte pathways.
Abstract:
Objective: To measure hematologic parameters derived from the white blood cell (WBC) count and differential count (DC) as prognostic factors for survival in patients with stage IB and IIA cervical cancer. Methods: We retrospectively examined demographic, clinicopathologic, and laboratory parameters in a cohort of 233 patients with International Federation of Gynecology and Obstetrics stage IB and IIA cervical cancer who underwent surgical resection. We further assessed the effects of the WBC count and DC-derived hematologic parameters on progression-free survival (PFS) and overall survival (OS) after controlling for other parameters. Results: Patients were followed up for a median of 46.6 months (range, 9-142 months). The Kaplan-Meier estimates of PFS and OS at 5 years were 88.5% and 92.3%, respectively. In a multivariate analysis, we identified the absolute monocyte count (AMC) (hazard ratio [HR], 11.78; P <0.001) and tumor size (HR, 5.41; P = 0.003) as the strongest prognostic factors affecting PFS. We also identified AMC (HR, 23.29; P <0.001), tumor size, (HR, 5.27; P = 0.033), and lymph node involvement (HR, 3.90; P = 0.027) as the strongest prognostic factors affecting OS. AMC remained prognostic with respect to PFS or OS in a Cox model that controlled for the neutrophil-lymphocyte ratio or lymphocyte-monocyte ratio, although neither ratio was a significant prognostic factor for survival. Conclusions: Monocytosis and an increased tumor size were found to be independent prognostic factors affecting both PFS and OS in patients with stage IB and IIA cervical cancer.
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