# Comprehensive study of anaplastic large cell lymphoma: clinicopathological features from Indonesia

**Authors:** Agnes Stephanie Harahap, Ivana Santoso, Stefanny Charles, Nadia Ayu Mulansari, Maria Francisca Ham

PMC · DOI: 10.1186/s13104-025-07354-5 · 2025-07-09

## TL;DR

This study examines the clinicopathological features of anaplastic large cell lymphoma in Indonesia, highlighting differences between ALK-positive and ALK-negative cases.

## Contribution

The study provides insights into ALCL epidemiology and outcomes in an Indonesian population.

## Key findings

- ALK-positive ALCL cases had better survival and earlier-stage disease compared to ALK-negative cases.
- ALK-negative patients had a shorter median survival of 23 months.
- B symptoms and high ECOG-PS scores were linked to poor outcomes.

## Abstract

Anaplastic large cell lymphoma (ALCL) is a rare and aggressive CD30-positive non-Hodgkin lymphoma with histopathological features overlapping Hodgkin and T-cell lymphomas. ALK-positive ALCL shows a better prognosis than ALK-negative cases, which are often associated with advanced disease. This study evaluates the epidemiological profile of ALCL in Indonesian population and its distinct histopathological characteristics and immunohistochemical expression patterns.

Among 93 ALCL cases (2013–2023) enrolled at Dr. Cipto Mangunkusumo Hospital, 13.9% were primary cutaneous ALCL, while 86.1% were systemic ALCL (consisted of 53.7% ALK-positive and 46.3% ALK-negative). ALK-positive patients were older (p = 0.009), with earlier-stage disease (p = 0.032) and nodal predilection (p = 0.032). ALK-negative cases demonstrated a shorter median survival of 23 months compared to ALK-positive cases of 28 months. Poor outcomes were associated with B symptoms and high Eastern Cooperative Oncology Group Performance Status (ECOG-PS) scores. Given that this study was conducted at a single, government-operated tertiary care teaching hospital in Indonesia’s capital, validation through multicenter prospective studies is warranted to further refine diagnostic and therapeutic strategies.

The online version contains supplementary material available at 10.1186/s13104-025-07354-5.

## Linked entities

- **Proteins:** ALK (ALK receptor tyrosine kinase), TNFRSF8 (TNF receptor superfamily member 8)
- **Diseases:** anaplastic large cell lymphoma (MONDO:0020325), non-Hodgkin lymphoma (MONDO:0018908), Hodgkin lymphoma (MONDO:0004952), T-cell lymphoma (MONDO:0015760)

## Full-text entities

- **Genes:** TNFRSF8 (TNF receptor superfamily member 8) [NCBI Gene 943] {aka CD30, D1S166E, Ki-1}, ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}
- **Diseases:** ALCL (MESH:D017728), non-Hodgkin lymphoma (MESH:D008228), B (MESH:D006509), Hodgkin and T-cell lymphomas (MESH:D016399)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12243422/full.md

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Source: https://tomesphere.com/paper/PMC12243422