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Patterns of care and treatment outcomes for primary thyroid lymphoma: a single institution study

机译:原发性甲状腺淋巴瘤的护理模式和治疗结局:单机构研究

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Purpose The aim of this study was to analyze the patterns of care and treatment outcomes in patients with primary thyroid lymphoma (PTL) in a single institution. Materials and Methods Medical records of 29 patients with PTL treated between April 1994 and February 2012 were retrospectively reviewed. Diagnosis was confirmed by biopsy (n = 17) or thyroidectomy (n = 12). Treatment modality and outcome were analyzed according to lymphoma grade. Results The median follow-up was 43.2 months (range, 3.8 to 220.8 months). The median age at diagnosis was 57 years (range, 21 to 83 years) and 24 (82.8%) patients were female. Twenty-five (86.2%) patients had PTL with stage IEA and IIEA. There were 8 (27.6%) patients with mucosa-associated lymphoid tissue (MALT) lymphoma and the remaining patients had high-grade lymphoma. Patients were treated with surgery (n = 2), chemotherapy (n = 7), radiotherapy (n = 3) alone, or a combination of these methods (n = 17). Treatment modalities evolved over time and a combination of modalities was preferred, especially for the treatment of high-grade lymphoma in recent years. There was no death or relapse among MALT lymphoma patients. Among high-grade lymphoma patients, 5-year overall survival (OS) and 5-year progression-free survival (PFS) were 75.6% and 73.9%, respectively. Complete remission after initial treatment was the only significant prognostic factor for OS (p = 0.037) and PFS (p = 0.003). Conclusion Patients with PTL showed a favorable outcome, especially with MALT lymphoma. Radiotherapy alone for MALT lymphoma and chemotherapy followed by radiotherapy for high-grade lymphoma can be effective treatment options for PTL.
机译:目的这项研究的目的是在单一机构中分析原发性甲状腺淋巴瘤(PTL)患者的护理模式和治疗结果。资料与方法回顾性分析了1994年4月至2012年2月间收治的29例PTL患者的病历。通过活检(n = 17)或甲状腺切除术(n = 12)确认诊断。根据淋巴瘤等级分析治疗方式和结果。结果中位随访时间为43.2个月(范围3.8至220.8个月)。诊断时的中位年龄为57岁(21至83岁),女性为24名(82.8%)。 25名(86.2%)患者患有IEA和IIEA分期的PTL。粘膜相关淋巴组织(MALT)淋巴瘤患者8例,占27.6%,其余患者为高度淋巴瘤。分别接受手术(n = 2),化学疗法(n = 7),放疗(n = 3)或这些方法的组合(n = 17)治疗。随着时间的流逝,治疗方式不断发展,并且首选多种方式,尤其是近年来治疗高度淋巴瘤的方式。 MALT淋巴瘤患者中没有死亡或复发。在高级别淋巴瘤患者中,5年总生存(OS)和5年无进展生存(PFS)分别为75.6%和73.9%。初始治疗后完全缓解是OS(p = 0.037)和PFS(p = 0.003)的唯一重要预后因素。结论PTL患者表现出良好的预后,尤其是MALT淋巴瘤。单独对MALT淋巴瘤进行放射治疗和化学疗法,然后对高级别淋巴瘤进行放射治疗可能是PTL的有效治疗选择。

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