Dührsen Ulrich, Bockisch Andreas, Hertenstein Bernd, Karsten Imke E, Kroschinsky Frank, Heuser Michael, Hochhaus Andreas, Höffkes Heinz-Gert, Behringer Dirk, Prange-Krex Gabriele, Tometten Mareike, Grieshammer Martin, Grigoleit Götz U, Schmalz Oliver, Jordan Karin, Bernhard Helga, Gaska Tobias, Giagounidis Aristoteles, Schroers Roland, Martens Uwe M, Held Gerhard, Klapper Wolfram, Jöckel Karl-Heinz, Nonnemacher Michael, Hüttmann Andreas
Klinik für Hämatologie und Stammzelltransplantation, Universitätsklinikum, Essen, Germany.
Klinik für Nuklearmedizin, Universitätsklinikum, Essen, Germany.
Blood Neoplasia. 2024 May 21;1(3):100018. doi: 10.1016/j.bneo.2024.100018. eCollection 2024 Sep.
The PETAL (Positron Emission Tomography-Guided Therapy of Aggressive Non-Hodgkin Lymphomas) trial investigated whether treatment intensification after 2 cycles of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP; plus rituximab [R] for CD20 lymphomas) improved survival in aggressive non-Hodgkin lymphoma. A total of 754 patients (87.5%) had a negative and 108 (12.5%) had a positive interim positron emission tomography (iPET) scan. iPET-positive patients were randomly assigned to receive another 6 (R-)CHOP cycles or 6 blocks of a more intensive protocol. Interim PET-negative patients received another 4 cycles of R-CHOP with or without 2 additional doses of R. After a median follow-up of 4 years, treatment intensification had not improved outcome. These results were confirmed after 10.3 years of follow-up. The present analysis also describes the management of relapse that was part of the study. Among 240 relapsing patients, 94 of 133 autologous transplantation-eligible patients (70.7%) and 16 of 107 ineligible patients (15.0%) received the salvage treatments recommended in the study protocol. Adherence to recommendations had no impact on outcome. Best results were seen after allogeneic transplantation, followed by autologous transplantation and treatment without transplantation (5-year overall survival rate, 64.3% vs 45.5% vs 22.6%), but patients undergoing allogeneic transplantation were significantly younger and their disease was well controlled at the time of transplantation. Early outcome prediction by iPET, alone or in combination with other methods, is a powerful tool to investigate the value of immunological treatment options for patients with a poor response to chemotherapy. This trial was registered at ClinicalTrials.gov as #NCT00554164.
PETAL(正电子发射断层扫描引导下的侵袭性非霍奇金淋巴瘤治疗)试验研究了在接受2个周期的环磷酰胺、多柔比星、长春新碱和泼尼松(CHOP;CD20淋巴瘤加用利妥昔单抗[R])治疗后强化治疗是否能提高侵袭性非霍奇金淋巴瘤的生存率。共有754例患者(87.5%)中期正电子发射断层扫描(iPET)结果为阴性,108例(12.5%)为阳性。iPET阳性患者被随机分配接受另外6个(R-)CHOP周期或6个疗程的更强化方案。iPET阴性患者接受另外4个周期的R-CHOP治疗,可加用或不加用2剂额外的R。中位随访4年后,强化治疗并未改善预后。随访10.3年后,这些结果得到了证实。本分析还描述了作为研究一部分的复发管理情况。在240例复发患者中,133例符合自体移植条件的患者中有94例(70.7%),107例不符合条件的患者中有16例(15.0%)接受了研究方案推荐的挽救治疗。遵循推荐对预后没有影响。异基因移植后的结果最佳,其次是自体移植和未进行移植的治疗(5年总生存率分别为64.3%、45.5%和22.6%),但接受异基因移植的患者明显更年轻,且移植时疾病得到了良好控制。单独或与其他方法联合使用iPET进行早期预后预测,是研究免疫治疗方案对化疗反应不佳患者价值的有力工具。该试验已在ClinicalTrials.gov注册,注册号为#NCT00554164。