Verhoef Gregor, Robak Tadeusz, Huang Huiqiang, Pylypenko Halyna, Siritanaratkul Noppadol, Pereira Juliana, Drach Johannes, Mayer Jiri, Okamoto Rumiko, Pei Lixia, Rooney Brendan, Cakana Andrew, van de Velde Helgi, Cavalli Franco
University Hospital Leuven, Belgium
Medical University of Lodz, Copernicus Memorial Hospital, Poland.
Haematologica. 2017 May;102(5):895-902. doi: 10.3324/haematol.2016.152496. Epub 2017 Feb 9.
In the phase 3 LYM-3002 study comparing intravenous VR-CAP with R-CHOP in patients with newly-diagnosed, measurable stage II-IV mantle cell lymphoma, not considered or ineligible for transplant, the median progression-free survival was significantly improved with VR-CAP (24.7 14.4 months with R-CHOP; <0.001). This analysis evaluated the association between the improved outcomes and quality of responses achieved with VR-CAP R-CHOP in LYM-3002. Patients were randomized to six to eight 21-day cycles of VR-CAP or R-CHOP. Outcomes included progression-free survival, duration of response (both assessed by an independent review committee), and time to next anti-lymphoma treatment, evaluated by response (complete response/unconfirmed complete response and partial response), MIPI risk status, and maximum reduction of lymph-node measurements expressed as the sum of the product of the diameters. Within each response category, the median progression-free survival was longer for patients given VR-CAP than for those given R-CHOP (complete response/unconfirmed complete response: 40.9 19.8 months; partial response: 17.1 11.7 months, respectively); similarly, the median time to next anti-lymphoma treatment was longer among the patients given VR-CAP than among those treated with R-CHOP (complete response/unconfirmed complete response: not evaluable 26.6 months; partial response: 35.3 24.3 months). Within the complete/unconfirmed complete and partial response categories, improvements in progression-free survival, duration of response and time to next anti-lymphoma treatment were more pronounced in patients with low-and intermediate-risk MIPI treated with VR-CAP than with R-CHOP. In each response category, more VR-CAP than R-CHOP patients had a sum of the product of the diameters nadir of 0 during serial radiological assessments. Results of this analysis suggest a greater duration and quality of response in patients treated with VR-CAP in comparison with those treated with R-CHOP, with the improvements being more evident in patients with low- and intermediate-risk MIPI. .
在3期LYM - 3002研究中,对新诊断的、可测量的II - IV期套细胞淋巴瘤患者(不考虑或不符合移植条件)比较静脉注射VR - CAP与R - CHOP方案,VR - CAP组的中位无进展生存期显著改善(R - CHOP组为14.4个月,VR - CAP组为24.7个月;P<0.001)。该分析评估了LYM - 3002研究中VR - CAP与R - CHOP方案疗效改善与缓解质量之间的关联。患者被随机分配接受6至8个周期、每21天一次的VR - CAP或R - CHOP方案治疗。疗效指标包括无进展生存期、缓解持续时间(均由独立审查委员会评估)以及至下一次抗淋巴瘤治疗的时间,根据缓解情况(完全缓解/未确认的完全缓解和部分缓解)、MIPI风险状态以及淋巴结测量最大缩小值(以直径乘积之和表示)进行评估。在每个缓解类别中,接受VR - CAP治疗的患者中位无进展生存期长于接受R - CHOP治疗的患者(完全缓解/未确认的完全缓解:40.9个月对19.8个月;部分缓解:分别为17.1个月对11.7个月);同样,接受VR - CAP治疗的患者至下一次抗淋巴瘤治疗的中位时间长于接受R - CHOP治疗的患者(完全缓解/未确认的完全缓解:不可评估对26.6个月;部分缓解:35.3个月对24.3个月)。在完全/未确认的完全缓解和部分缓解类别中,接受VR - CAP治疗的低风险和中风险MIPI患者在无进展生存期、缓解持续时间和至下一次抗淋巴瘤治疗时间方面的改善比接受R - CHOP治疗的患者更显著。在每个缓解类别中,在系列影像学评估期间,VR - CAP组患者直径乘积之和最低点为0的人数多于R - CHOP组。该分析结果表明,与接受R - CHOP治疗的患者相比,接受VR - CAP治疗的患者缓解持续时间更长且质量更高,在低风险和中风险MIPI患者中改善更为明显。