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Author Spotlight: Advancing Cancer Associated Thrombosis Research in Rodent Models
Published on: January 5, 2024
Pediatric cancer-associated thrombosis: Analysis from a tertiary care cancer center in India
Nidhi Dhariwal1,2, Venkata Rama Mohan Gollamudi1,2, K P Sangeetha3
1Division of Pediatric Oncology, Department of Medical Oncology, Tata Memorial Hospital, Mumbai, Maharashtra, India.
Insights
Pediatric cancer-associated thrombosis (PCAT) affects 2.4% of children, predominantly older children with hematolymphoid malignancies. While most cases resolve with treatment, PCAT negatively impacts event-free survival, underscoring the need for preventative strategies.
Area of Science:
- Oncology
- Pediatrics
- Hematology
Background:
- Thrombotic events (TEs) are well-documented in adult cancer patients, but data on pediatric cancer-associated thrombosis (PCAT) remain limited.
- This study prospectively investigated the incidence, characteristics, and outcomes of PCAT in children with malignancies.
Purpose of the Study:
- To determine the incidence and risk factors of pediatric cancer-associated thrombosis.
- To analyze the clinical presentation, management, and outcomes of TEs in children undergoing cancer treatment.
Main Methods:
- A prospective analysis of children under 15 years with confirmed malignancies treated at a tertiary cancer center in India.
- Data collection included demographic information, malignancy type, TE occurrence, site, management with low molecular weight heparin (LMWH), and survival outcomes.
- Statistical analysis identified factors associated with PCAT, including age, malignancy type, and treatment risk group.
Main Results:
- The incidence of PCAT was 2.44% (150/6132 children), with TEs occurring most frequently during chemotherapy (74.0%) and in the central nervous system (39.3%).
- Hematolymphoid malignancies (3.23%) were more prone to PCAT than solid tumors (1.58%). Acute myeloid leukemia (AML) and non-Hodgkin lymphoma showed higher incidences.
- Older age (>10 years), AML, and non-Hodgkin lymphoma were significant risk factors for TEs. PCAT was associated with reduced 2-year event-free survival in hematolymphoid malignancies.
Conclusions:
- PCAT occurs in 2.4% of pediatric cancer patients, primarily affecting older children with hematolymphoid malignancies early in their treatment course.
- Most TEs resolved with LMWH treatment, and mortality directly attributable to TEs was low (4.66%).
- PCAT significantly impacts event-free survival in hematolymphoid malignancies, highlighting the critical need for effective prevention strategies in this vulnerable population.
Background And Aims:
Thrombotic events (TEs) have been extensively studied in adult cancer patients, but data in children are limited. We prospectively analyzed pediatric cancer-associated thrombosis (PCAT) in children with malignancies.
Methods:
Children below 15 years of age with confirmed malignancies, treated at a large tertiary cancer center in India from July 2015 to March 2020 developing any TE were eligible. A standardized approach for detection and management was followed. Data were collected after informed consent.
Results:
Of 6132 eligible children, 150 (2.44%) had 152 TEs, with median age 8.5 years and male:female of 1.83:1. Most TEs occurred on chemotherapy: 111 (74.0%). The most common site was central nervous system (CNS) 59 (39.3%), followed by upper-limb venous system 37 (24.7%). Hemato-lymphoid (HL) malignancies were more prone to PCAT than solid tumors (ST) (incidence 3.23% vs. 1.58%; odds ratio [OR] = 2.06, 95% confidence interval [CI] [1.36-2.88]; p < .001). Malignancies associated with PCAT were acute lymphoblastic leukemia (ALL) 2.94%, acute myeloid leukemia (AML) 6.66%, and non-Hodgkin lymphomas 5.35%. Response imaging done in 106 (70.7%) children showed complete to partial resolution in almost 90% children. Death was attributable to TE in seven (4.66%) children. Age above 10 years (OR 2.33, 95% CI [1.59-3.41]; p < .001), AML (OR 4.62, 95% CI [1.98-10.74]; p = .0062), and non-Hodgkin lymphoma (OR 4.01, 95% CI [1.15-14.04]; p = .029) were significantly associated with TEs. In ALL, age more than 10 years (OR 1.86, 95% CI [1.06-3.24]; p < .03), T-ALL (OR 3.32, 95% CI [1.69-6.54]; p = .001), and intermediate-risk group (OR 4.97, 95% CI [1.12-22.02]; p = .035) were significantly associated with thrombosis. The 2-year event-free survival (EFS) for HL malignancies with PCAT was 55.3% versus 72.1% in those without PCAT (p = .05), overall survival (OS) being 84.6% versus 80.0% (p = .32).
Conclusion:
Incidence of PCAT was 2.4%, and occurred predominantly in older children with hematolymphoid malignancies early in treatment. Most resolved completely with low molecular weight heparin (LMWH) and mortality was low. In hematolymphoid malignancies, PCAT reduce EFS, highlighting the need for prevention.
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