Clinical profile and outcome of children with anaplastic large cell lymphoma treated with short-course chemotherapy - ten years experience from a tertiary care center in a LMIC.

IF 1.2 4区 医学 Q4 HEMATOLOGY
Maharshi Trivedi, Priyakumari Thankamony, Manjusha Nair, Binitha Rajeswari, C S Guruprasad, V R Prasanth, Rekha A Nair, K M Jagathnath Krishna
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引用次数: 0

Abstract

Anaplastic large-cell lymphoma (ALCL) constitutes 10-15% of non-Hodgkin lymphoma in children. With short-course chemotherapy, outcome has improved up-to 90% in developed-countries. There is limited-data on outcome of pediatric ALCL treated with ALCL99 protocol from low-middle income countries. Children ≤14 years, diagnosed with ALCL between 1st January 2007 and 31st December 2016 were analyzed. Details regarding clinical-presentation and treatment were recorded and outcome was analyzed. Fourteen-children were diagnosed. Median-age was 114 months (range 24 - 162 months). Male:female ratio was 3.6:1. Stage-I, II and III disease was seen in three (21.4%), three (21.4%), and eight (57.1%) children, respectively. Low, standard and high-risk disease was seen in two (14.2%), six (42.9%) and six (42.9%), respectively. All children were treated using ALCL99 protocol. Three (21.4%) children had disease-progression/relapse and five (35.7%) died (three from treatment-related mortality, and two from disease). At median follow-up of 54-months, four-year EFS and OS were 64.3% and 64.3%, respectively. Log-rank test demonstrated female gender (p = 0.005), stage-III disease (p < 0.001), visceral-organ involvement (p = 0.035), high-risk disease (p = 0.016) and, serum albumin ≤3.5 g/dL (p = 0.031) associated with significantly worse 4-year EFS. Cox-regression analysis demonstrated female gender associated with poor EFS (p = 0.02) and female gender and visceral-organ involvement associated with poor OS (p = 0.02, p = 0.011, respectively). Good survival could be achieved for children with ALCL using uniform treatment protocol in a resource-limited setting, especially among low and standard-risk children. Female-sex, high-risk disease, stage-III disease, visceral organ involvement and low albumin levels were associated with poor outcome, however these findings need to be corroborated in larger studies.

短期化疗治疗儿童间变性大细胞淋巴瘤的临床概况和结果——LMIC三级护理中心的十年经验
间变性大细胞淋巴瘤(ALCL)占儿童非霍奇金淋巴瘤的10-15%。在发达国家,短期化疗的疗效提高了90%。中低收入国家使用ALCL99方案治疗小儿ALCL的结果数据有限。分析2007年1月1日至2016年12月31日诊断为ALCL的≤14岁儿童。记录临床表现和治疗的细节并分析结果。14名儿童被确诊。中位年龄为114个月(24 - 162个月)。男女比例为3.6:1。i、II和III期疾病分别出现在3例(21.4%)、3例(21.4%)和8例(57.1%)儿童中。低、标准和高危疾病分别为2例(14.2%)、6例(42.9%)和6例(42.9%)。所有患儿均采用ALCL99治疗方案。3名(21.4%)儿童出现疾病进展/复发,5名(35.7%)死亡(3名死于治疗相关死亡,2名死于疾病)。中位随访54个月时,4年EFS和OS分别为64.3%和64.3%。Log-rank检验显示,女性(p = 0.005)、iii期疾病(p = 0.035)、高危疾病(p = 0.016)和血清白蛋白≤3.5 g/dL (p = 0.031)与4年EFS显著恶化相关。cox回归分析显示,女性与较差的EFS相关(p = 0.02),女性和脏器受累与较差的OS相关(p = 0.02, p = 0.011)。在资源有限的情况下,使用统一的治疗方案,特别是在低风险和标准风险儿童中,ALCL儿童可以获得良好的生存率。女性、高危疾病、iii期疾病、脏器受累和低白蛋白水平与预后不良相关,但这些发现需要在更大规模的研究中得到证实。
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来源期刊
CiteScore
2.60
自引率
5.90%
发文量
71
审稿时长
6-12 weeks
期刊介绍: PHO: Pediatric Hematology and Oncology covers all aspects of research and patient management within the area of blood disorders and malignant diseases of childhood. Our goal is to make PHO: Pediatric Hematology and Oncology the premier journal for the international community of clinicians and scientists who together aim to define optimal therapeutic strategies for children and young adults with cancer and blood disorders. The journal supports articles that address research in diverse clinical settings, exceptional case studies/series that add novel insights into pathogenesis and/or clinical care, and reviews highlighting discoveries and challenges emerging from consortia and conferences. Clinical studies as well as basic and translational research reports regarding cancer pathogenesis, genetics, molecular diagnostics, pharmacology, stem cells, molecular targeting, cellular and immune therapies and transplantation are of interest. Papers with a focus on supportive care, late effects and on related ethical, legal, psychological, social, cultural, or historical aspects of these fields are also appreciated. Reviews on important developments in the field are welcome. Articles from scientists and clinicians across the international community of Pediatric Hematology and Oncology are considered for publication. The journal is not dependent on or connected with any organization or society. All submissions undergo rigorous peer review prior to publication. Our Editorial Board includes experts in Pediatric Hematology and Oncology representing a wide range of academic and geographic diversity.
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