Faizan Mahwish, Taj Mary M, Anwar Saadia, Asghar Nyla, Ahmad Alia, Lancaster Donna, Atra Ayad, Ali Agha Shabbir
Department of Paediatric Haematology/Oncology and Bone Marrow Transplant, Birmingham Children Hospital, Steel House Lane, B4 6NH Birmingham, UK.
Department of Paediatric Oncology, Royal Marsden Hospital, Downs Road, Sutton, London, UK SM2 5PT.
J Coll Physicians Surg Pak. 2016 Nov;26(11):904-907.
To compare differences in demographics and outcomes in childhood Hodgkin lymphoma (HL) presenting at the Children's Hospital Lahore (CHL), and Royal Marsden Hospital (RMH), UK.
An observational comparative study.
From January 2011 to February 2012 at CH, Lahore and from October 2008 to February 2012 at RMH, UK.
Consecutive HL patients (50 from each hospital) were inducted. Data regarding age, gender, staging, histopathology and outcome were analysed. Clinical and pathological staging done according to Ann-Arbor and World Health Organization classification. Treatment duration was 6-8 months. They were followed for 6 months post-treatment. Frequencies of variables were noted and compared. Chi-square test was used for determining significance.
Patients from Children's Hospital, Lahore were younger (mean 7.9 years) with male predominance (n=42, 84%). Histopathology showed Mixed Cellularity (MC) in 32 (64%), Nodular Sclerosis (NS) in 5 (10%), Lymphocyte Rich in 4 (8%) and lymphocyte depleted in 1 (2%), nodular lymphocyte predominant (NLP) in 1 (2%) each. Majority presented in stage IV (n=25,50%), or stage III (n=20,40%). Constitutional B symptoms were present in 37 (74%). Bone marrow involvement observed in 23 (46%). Remission was achieved in 42 (84%) patients; 2 (4%) relapsed, 4 (8%) expired and 2 (4%) left against medical advice. In contrast, RMH patients were older (mean 11.8 years.) and 30 (60%) were males. NS (n=40,80%) and NLP (n=6,12%) types were predominant. Two (4%) patients were in stage I, 27 (54%) in stage II, 12 (24%) in stage III and 9 (18%) presented in stage IV. Fourteen (28%) had B-symptoms. None had bone marrow disease. Event free survival was 46 (92%). Four (8%) patients relapsed. Three responded to second line therapy and one relapsed postautologous transplant.
Significant differences were observed in age at presentation, stage, histopathology and extent of bone marrow involvement between the groups. Of interest is the bone marrow involvement in stage IV patients in Pakistan. Delayed diagnosis account for advanced stage but difference in pathological subtype needs further study.
比较拉合尔儿童医院(CHL)和英国皇家马斯登医院(RMH)收治的儿童霍奇金淋巴瘤(HL)患者在人口统计学和治疗结果方面的差异。
一项观察性比较研究。
2011年1月至2012年2月在拉合尔儿童医院,2008年10月至2012年2月在英国皇家马斯登医院。
纳入连续的HL患者(每家医院50例)。分析有关年龄、性别、分期、组织病理学和治疗结果的数据。根据Ann-Arbor和世界卫生组织分类进行临床和病理分期。治疗疗程为6 - 8个月。治疗后随访6个月。记录并比较变量的频率。采用卡方检验确定显著性。
拉合尔儿童医院的患者年龄较小(平均7.9岁),以男性为主(n = 42,84%)。组织病理学显示,混合细胞型(MC)32例(64%),结节硬化型(NS)5例(10%),富于淋巴细胞型4例(8%),淋巴细胞消减型1例(2%),结节性淋巴细胞为主型(NLP)各1例(2%)。大多数患者为IV期(n = 25,50%)或III期(n = 20,40%)。37例(74%)有全身B症状。23例(46%)观察到骨髓受累。42例(84%)患者实现缓解;2例(4%)复发,4例(8%)死亡,2例(4%)自行出院。相比之下,皇家马斯登医院的患者年龄较大(平均11.8岁),30例(60%)为男性。NS型(n = 40,80%)和NLP型(n = 6,12%)为主。2例(4%)患者为I期,27例(54%)为II期,12例(24%)为III期,9例(18%)为IV期。14例(28%)有B症状。无骨髓疾病患者。无事件生存期为46例(92%)。4例(8%)患者复发。3例对二线治疗有反应,1例自体移植后复发。
两组在就诊年龄、分期、组织病理学和骨髓受累程度方面存在显著差异。值得关注的是巴基斯坦IV期患者的骨髓受累情况。诊断延迟导致分期较晚,但病理亚型的差异需要进一步研究。