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Hodgkin lymphoma

机译:霍奇金淋巴瘤

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Hodgkin lymphoma (HL) is a curable malignancy which shows a bimodal curve in incidence in economically developed countries; there is a putative association with Epstein-Barr virus. The WHO 2008 classification schema recognises two histological types of HL: the nodular lymphocyte predominant and the " classic" HL. The latter encompasses four entities: nodular sclerosis, mixed cellularity, lymphocyte depletion, and lymphocyte-rich. Most patients with HL present with asymptomatic superficial lymphadenopathy. The commonest sites of disease are the cervical, supraclavicular and mediastinal lymph nodes, while sub-diaphragmatic presentations and bone marrow and hepatic involvement are less common. Splenic involvement is usually concomitant with hepatic disease and systemic symptoms; extranodal presentations are quite rare. Systemic symptoms are present in ??35% of cases. The stage of disease is defined according to the Ann Arbor staging system or its Cotswolds variant, and staging work-up includes physical examination, chest X-rays, chest and abdominal CT scan, and bone marrow biopsy. 18FDG-PET (18fluordeoxyglucose positron emission tomography) plays a central role in staging, response assessment and prognosis definition.Classic HL usually spreads by contiguity within the lymphatic tissue network, with a late extension to adjacent and distant viscera. Mortality from HL has been progressively decreasing, as confirmed by the most recent 5-year survival figure of 81%. The list of putative prognostic factors in HL has been increasing, but most factors still require prospective validation. Some of these variables are used to stratify early-stage disease into " favourable" and " unfavourable" categories, with " unfavourable early-stage" being intermediate between " favourable early-stage" and " advanced-stage" .ABVD (adriamycin(doxorubicin), bleomycin, vinblastine, dacarbazine) combination chemotherapy followed by involved-field irradiation is the standard treatment for patients with early-stage HL, with a 5-year OS 95%. Several trials assessing less intensive approaches for patients with favourable early-stage HL are ongoing. More intensified combinations, such as the BEACOPP (bleomycin, etoposide, adriamycin, cyclophosphamide, vincristine (Oncovin), procarbazine, prednisone) regimen, are being investigated, usually in patients with unfavourable early-stage HL and interim PET+. ABVD is the standard chemotherapy treatment also for patients with advanced disease. Although some evidence suggests that more intensive combinations provide better disease control, the inevitable increased risk of relevant late toxicity worries investigators. Consequently, there has been a shift towards investigating the innovative strategy of a more aggressive schedule for patients with 18FDG-PET positive results after the first 2 courses of ABVD. High-dose chemotherapy supported by ASCT (autologous stem cell transplantation) is considered the standard of care in patients with HL which has relapsed after, or is refractory to conventional chemoradiotherapy, while allogeneic transplant is a suitable tool for patients with chemorefractory disease and patients failed after ASCT. ? 2012 Elsevier Ireland Ltd.
机译:霍奇金淋巴瘤(HL)是一种可治愈的恶性肿瘤,在经济发达国家显示出双峰曲线。推测与爱泼斯坦-巴尔病毒有关。 WHO 2008分类方案可识别HL的两种组织学类型:主要为结节性淋巴细胞和“经典” HL。后者包括四个实体:结节性硬化,混合细胞性,淋巴细胞耗竭和淋巴细胞丰富。大多数HL患者表现为无症状的浅表淋巴结肿大。疾病的最常见部位是颈,锁骨上和纵隔淋巴结,而-下表现和骨髓及肝受累则较少。脾脏受累通常伴有肝病和全身症状。结外的演示很少见。在35%的病例中出现全身症状。疾病的阶段根据Ann Arbor分期系统或其Cotswolds变种定义,分期检查包括体格检查,胸部X线检查,胸部和腹部CT扫描以及骨髓活检。 18FDG-PET(18氟脱氧葡萄糖正电子发射断层扫描)在分期,反应评估和预后定义中起着核心作用。经典HL通常通过邻近组织在淋巴组织网络内扩散,晚期延伸到邻近和远处的内脏。最近的5年生存率81%证实了HL的死亡率正在逐步下降。 HL的预后因素清单不断增加,但大多数因素仍需要前瞻性验证。这些变量中的一些变量用于将早期疾病分为“有利”和“不利”类别,其中“不利早期”介于“有利早期”和“晚期”之间。ABVD(阿霉素(阿霉素) ),博来霉素,长春碱,达卡巴嗪)联合化疗后再进行实地照射是早期HL患者(5年OS> 95%)的标准治疗方法。正在进行一些评估对早期HL有利的患者的低强度治疗方法的试验。通常在早期HL和中期PET +不良的患者中,正在研究更强化的组合,例如BEACOPP(博来霉素,依托泊苷,阿霉素,环磷酰胺,长春新碱(Oncovin),丙卡巴嗪,泼尼松)方案。 ABVD也是晚期患者的标准化疗方法。尽管一些证据表明,更密集的组合可以更好地控制疾病,但相关后期毒性的风险不可避免地增加,这使研究人员感到担忧。因此,已经开始研究创新的策略,即在ABVD的前2个疗程后针对18FDG-PET阳性结果的患者制定更积极的治疗方案。由ASCT(自体干细胞移植)支持的大剂量化学疗法被认为是HL患者的标准治疗方法,这种方法在常规放化疗后复发或难以治愈,而同种异体移植是化学性难治性疾病患者和失败者的合适工具。在ASCT之后。 ? 2012爱思唯尔爱尔兰有限公司

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