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Will BEACOPP be the standard for high risk Hodgkin lymphoma patients in advanced stages?

机译:BEACOPP将成为晚期高危霍奇金淋巴瘤患者的标准吗?

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Hodgkin Lymphoma (HL) has become one of the most curable cancers, even in adulthood, through continuous improvement of therapeutic options and their verification by large multicenter trials. Today more than 95% of patients with HL in early stages and in advanced stages 85-90% can be cured. Nevertheless, these good results are threatened by treatment associated toxicities such as infertility, cardiopulmonary toxicity and secondary malignancies. It is therefore the aim of future trial generations both to maintain the excellent treatment results and to minimize late effects. In 1964 for the first time deVita et al. described the MOPP polychempotherapy for patients with advanced HL which led to cure rates in more than 50%. Around ten years later Bonadonna et al. established the non cross resistant alternative regime to MOPP, ABVD which nowadays is accepted as "gold standard" for the treatment of advanced HL. MOPP and/or ABVD and furthermore the alternating MOPP/ABVD or the MOPP/ABV hybrid with and without the help of consolidative radiation resulted in around 70% long term survival rates, 30-40% of patients experienced tumor progression or relapses within 5 years. This led the German Hodgkin Study Group (GHSG) [Diehl V, Franklin J, Pfreundschuh M, Lathan B, Paulus U, Hasenclever D, et al. Standard and increased-dose BEACOPP chemotherapy compared with COPP-ABVD for advanced Hodgkin's disease. N Engl J Med 2003; 348: 2386-95] to improve the efficacy of COPP/ABVD by time- and dose-intensification, omission of Velban and Dacarbazin and adding Etoposide resulting in the BEACOPP principle. From the initial pilot studies in 1992 three trial generations, HD9, HD12, HD15, have now established this principle as one of the most effective chemotherapy regimen in advanced HL. We certainly hope that it will not last another 20 years to establish the BEACOPP regimen as an attractive curative treatment option for at least the high risk cohorts of HL.
机译:霍奇金淋巴瘤(HL)已通过不断改进治疗方案并通过大型多中心试验进行验证,甚至在成年期也已成为最可治愈的癌症之一。如今,超过95%的HL患者在早期和晚期可以治愈85-90%。然而,这些良好的结果受到与治疗有关的毒性的威胁,例如不育,心肺毒性和继发性恶性肿瘤。因此,下一代试验的目的是保持出色的治疗效果并最大程度地减少后期影响。 1964年,deVita等首次提出。描述了MOPP多化学疗法用于晚期HL患者,治愈率超过50%。大约十年后,Bonadonna等人。建立了MOPP,ABVD的无交叉耐药替代方案,如今已被公认是治疗晚期HL的“金标准”。 MOPP和/或ABVD以及进一步的交替MOPP / ABVD或MOPP / ABV混合体在有无辅助照射的情况下均可达到约70%的长期存活率,其中30-40%的患者在5年内经历了肿瘤进展或复发。这导致了德国霍奇金研究小组(GHSG)[Diehl V,Franklin J,Pfreundschuh M,Lathan B,Paulus U,Hasenclever D等。标准和加大剂量的BEACOPP化疗与COPP-ABVD相比可治疗晚期霍奇金病。 N Engl J Med 2003; 348:2386-95]通过时间和剂量增强,省略Velban和Dacarbazin并添加依托泊苷来产生BEACOPP原理来提高COPP / ABVD的疗效。从1992年的初步试验研究开始,三个试验代,即HD9,HD12,HD15,现已确立了该原则,是晚期HL中最有效的化疗方案之一。我们当然希望,将BEACOPP方案确立为至少对HL高危人群的一种有吸引力的治疗选择不会再持续20年。

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