不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:EBV associated T- and NK-cell lymphoproliferative diseases: A comprehensive overview of clinical manifestations and novel therapeutic insights.
EBV associated T- and NK-cell lymphoproliferative diseases: A comprehensive overview of clinical manifestations and novel therapeutic insights.
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EBV是一种普遍存在的病毒,几乎感染了全世界所有人。大多数感染者无症状,不显示严重后遗症,而其他人可能发展为以EBV感染的T或NK细胞为特征的EBV阳性T和NK细胞淋巴增殖性疾病。这些疾病在亚洲和拉丁美洲人群中更为常见,提示遗传易感性是促成因素。修订后的WHO分类将这些淋巴增殖性疾病分类为:结外NK/T细胞淋巴瘤鼻型(ENKTL)、侵袭性NK细胞白血病(ANKL)、原发性EBV阳性淋巴结T或NK细胞淋巴瘤(NNKTL)、儿童系统性EBV阳性T细胞淋巴增殖性疾病(STCLC)、系统性慢性活动性EBV感染(sys CAEBV)、种痘样水疱病(HV)和严重蚊叮咬过敏(SMBA)。这些疾病分子发病机制的最新进展促进了新治疗策略的开发。由于这些疾病罕见且临床病理学重叠广泛,诊断和分类对临床医生和病理学家都具有挑战性。在本文中,我们旨在综述近期有助于设计新药的病理学发现、临床表现和鉴别诊断,以及建议的治疗干预措施,以更好地理解这些罕见疾病。
EBV is a ubiquitous virus that infects nearly all people around the world. Most infected people are asymptomatic and do not show serious sequelae, while others may develop Epstein-Barr virus (EBV)-positive T and NK-cell lymphoproliferations characterised by EBV-infected T or NK cells. These disorders are more common in Asian and Latin American people, suggesting genetic predisposition as a contributing factor. The revised WHO classification classifies the lymphoproliferative diseases as: extranodal NK/T-cell lymphoma nasal type (ENKTL), aggressive NK-cell leukemia (ANKL), primary EBV-positive nodal T or NK cell lymphoma (NNKTL), systemic EBV-positive T-cell lymphoproliferative disease of childhood (STCLC), systemic chronic active EBV infection (sys CAEBV), hydroa-vacciniforme (HV) and severe mosquito bite allergy (SMBA).
Recent advances in the molecular pathogenesis of these diseases have led to the development of new therapeutic strategies. Due to the infrequency of the diseases and broad clinicopathological overlap, the diagnosis and classification are challenging for both clinicians and pathologists. In this article, we aim to review the recent pathological findings which can be helpful for designing new drugs, clinical presentations and differential diagnoses, and suggested therapeutic interventions to provide a better understanding of these rare disorders.
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