University of Cologne, Cologne, Germany.
J Clin Oncol. 2012 Mar 20;30(9):907-13. doi: 10.1200/JCO.2011.38.5807. Epub 2012 Jan 23.
In patients with early unfavorable Hodgkin's lymphoma (HL), combined modality treatment with four cycles of ABVD (adriamycin, bleomycin, vinblastine, and dacarbazine) and 30 Gy involved-field radiotherapy (IFRT) results in long-term tumor control of approximately 80%. We aimed to improve these results using more intensive chemotherapy.
Patients with newly diagnosed early unfavorable HL were randomly assigned to either four cycles of ABVD or an intensified treatment consisting of two cycles of escalated BEACOPP (bleomycin, etoposide, adriamycin, cyclophosphamide, vincristine, procarbazine, and prednisone) followed by two cycles of ABVD (2 + 2). Chemotherapy was followed by 30 Gy IFRT in both arms. The primary end point was freedom from treatment failure (FFTF); secondary end points included progression-free survival (PFS) and treatment-related toxicity.
With a total of 1,528 qualified patients included, the 2 + 2 regimen demonstrated superior FFTF compared with four cycles of ABVD (P < .001; hazard ratio, 0.44; 95% CI, 0.30 to 0.66), with a difference of 7.2% at 5 years (95% CI, 3.8 to 10.5). The difference in 5-year PFS was 6.2% (95% CI, 3.0% to 9.5%). There was more acute toxicity associated with 2 + 2 than with ABVD, but there were no overall differences in treatment-related mortality or secondary malignancies.
Intensified chemotherapy with two cycles of BEACOPP escalated followed by two cycles of ABVD followed by IFRT significantly improves tumor control in patients with early unfavorable HL.
在早期预后不良的霍奇金淋巴瘤(HL)患者中,采用 ABVD(阿霉素、博来霉素、长春碱和达卡巴嗪)联合四个周期和 30Gy 累及野放疗(IFRT)的联合治疗可使肿瘤长期控制率达到约 80%。我们旨在通过更强化的化疗来改善这些结果。
新诊断为早期预后不良 HL 的患者被随机分配到 ABVD 四个周期或强化治疗组,强化治疗组由两个周期递增 BEACOPP(博来霉素、依托泊苷、阿霉素、环磷酰胺、长春新碱、丙卡巴肼和泼尼松)加两个周期 ABVD(2+2)组成。两组均在化疗后接受 30Gy IFRT。主要终点是无治疗失败(FFTF);次要终点包括无进展生存(PFS)和治疗相关毒性。
共有 1528 名合格患者入组,2+2 方案与 ABVD 四个周期相比,FFTF 显著提高(P<0.001;风险比,0.44;95%CI,0.30 至 0.66),5 年差异为 7.2%(95%CI,3.8%至 10.5%)。5 年 PFS 的差异为 6.2%(95%CI,3.0%至 9.5%)。与 ABVD 相比,2+2 方案相关的急性毒性更大,但在治疗相关死亡率或继发性恶性肿瘤方面没有总体差异。
采用两个周期的递增 BEACOPP 加两个周期的 ABVD 加 IFRT 的强化化疗可显著改善早期预后不良 HL 患者的肿瘤控制。