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Clinical Features and Treatment Outcomes of Children with Anaplastic Large Cell Lymphoma
Asma Mehreen1, Rabia Wali1, Saima Riaz2
1Department of Paediatric Oncology, Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, Pakistan.
Insights
Pediatric Anaplastic Large Cell Lymphoma (ALCL) shows poor outcomes, with hematological toxicity and febrile neutropenia being leading causes of mortality. Improved supportive care is crucial for better survival rates in children with ALCL.
Area of Science:
- Pediatric Oncology
- Hematology
- Cancer Research
Background:
- Anaplastic Large Cell Lymphoma (ALCL) is a distinct type of non-Hodgkin lymphoma.
- Pediatric ALCL presents unique clinical and prognostic features compared to adult forms.
- Understanding clinical characteristics and treatment outcomes is vital for improving pediatric cancer care.
Purpose of the Study:
- To delineate the clinical features and treatment strategies for pediatric patients diagnosed with ALCL.
- To evaluate the treatment outcomes and survival rates in this specific pediatric cohort over a decade.
- To identify factors influencing prognosis and mortality in pediatric ALCL.
Main Methods:
- A retrospective-observational study was conducted.
- Medical records of pediatric patients (age < 20 years) with histopathologically confirmed ALCL were reviewed.
- Data spanning January 2005 to December 2015 from Shaukat Khanum Memorial Cancer Hospital and Research Centre were analyzed using descriptive statistics.
Main Results:
- Forty pediatric patients (67.5% males) with ALCL (CD30+) were analyzed.
- Common clinical features included B symptoms (80%), nodal (97.5%), mediastinal (20%), visceral (40%), and cutaneous involvement (15%).
- ALK positivity was observed in 48% of patients, with Stage III disease in 72.5%. Five-year event-free survival (EFS) was 30% and overall survival (OS) was 60%.
Conclusions:
- Pediatric ALCL is associated with unfavorable outcomes.
- Hematological toxicity and associated febrile neutropenia were the primary causes of mortality.
- Enhancing supportive care measures is essential to improve survival in pediatric ALCL patients.
Objective:
To describe clinical features and treatment options in pediatric patients with ALCL (Anaplastic large cell lymphoma) and their outcome over a span of 10 years.
Study Design:
A retrospective-observational study.
Place And Duration Of Study:
Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, from January 2005 to December 2015.
Methodology:
Medical records of pediatric patients with anaplastic large cell lymphoma was retrospectively collected after IRB approval. Data was reviewed for patients confirmed on histopathology and age less than 20 years at the time of diagnosis to see clinical features and treatment outcomes. Descriptive statistics were applied.
Results:
A total of 40 children, 27 males (67.5%) and 13 females (32.5%) with ALCL (CD30 +), were reviewed. B symptoms were present in 32 (80%) patients, nodal involvement in 39 (97.5%), and mediastinum involvement was present in 8 (20%) patients. Visceral (lung, liver, spleen) and cutaneous involvement was seen in 16 (40%) and 6 (15%) patients, respectively. ALK was positive in 19 patients (48%) and Bone marrow was involved in 3 patients (7.5%). Stage III was seen in 29 (72.5%). All patients were treated on ALCL 99 protocol. Five-year EFS (event-free survival) and OS (overall survival) was 30 and 60%, respectively. There were 7 relapses, 2 progressive disease, 16 death and 3 refusal for treatment.
Conclusion:
This analysis shows poor outcomes in pediatric ALCL. The most common cause of mortality was hematological toxicity and febrile neutropenia associated with it. Supportive care needs to be improved. Key Words: Clinical features, Outcomes, Anaplastic large cell lymphoma (ALCL), Children.
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