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논문 기본 정보

자료유형
학술저널
저자정보
Yang Liang Boo (Hospital Sultanah Aminah) Helen Siew Yean Ting (Hospital Sultanah Aminah) Diana Fui Sing Yap (Hospital Enche’ Besar Hajjah Khalsom) See Guan Toh (Hospital Sultanah Aminah) Soo Min Lim (Hospital Sultanah Aminah)
저널정보
대한혈액학회 Blood Research Blood Research Vol.54 No.3
발행연도
2019.1
수록면
210 - 217 (8page)

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BackgroundClassical Hodgkin lymphoma (cHL) is a clinicopathologically unique, aggressive lympho-ma arising from germinal center B-cells and is one of the most curable hematological malignancies. This study aimed to determine the clinical course, treatment regimens, re-sponse rates, and survival data of patients diagnosed with cHL in a tertiary center.MethodsA retrospective review was conducted to include patients with a diagnosis of cHL from 2013 to 2017. Data of demographic and clinical characteristics, treatment regimens, and outcomes were collected and analyzed. ResultsWe recruited 94 patients with a median age of 27.0 [interquartile range (IQR), 12] years. Most of the patients were male (61.7%) and 73.4% were ethnic Malay. Nodular sclerosis was the most common histology (77.6%), followed by mixed cellularity (6.4%) and others (16%). The median follow-up time was 28.0 (IQR, 32) months. All patients received che-motherapy but only 13.8% received radiotherapy as consolidation. The doxor-ubicin-bleomycin-vinblastine-dacarbazine regimen was the most common (85.1%), fol-lowed by the escalated bleomycin-etoposide-doxorubicin-cyclophosphamide-vincristine- prednisolone-procarbazine regimen (14.9%). Following treatment, 76.1% of patients achieved complete response. The 2-year overall survival (OS) and progression-free sur-vival (PFS) of the entire cohort were 96.5% and 71.1%, respectively. The 2-year OS and PFS for advanced-stage disease were 93.9% and 62.8%, compared to 100% and 82.7% for early-stage disease, respectively (P=0.252 and P=0.052, respectively).ConclusionThis study provides insight into the clinical presentation and treatment outcomes among patients with cHL in Malaysia. A longer study duration is required to identify OS and PFS benefits and treatment-related complications for different chemotherapeutic regimens.

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