早期滤泡性淋巴瘤患者的局部放疗和可测量残留疾病驱动的免疫疗法(FIL MIRO):一项前瞻性多中心 2 期试验的最终结果。

IF 15.4 1区 医学 Q1 HEMATOLOGY Lancet Haematology Pub Date : 2024-07-01 DOI:10.1016/S2352-3026(24)00143-1
Alessandro Pulsoni, Simone Ferrero, Maria Elena Tosti, Stefano Luminari, Alessandra Dondi, Federica Cavallo, Francesco Merli, Anna Marina Liberati, Natalia Cenfra, Daniela Renzi, Manuela Zanni, Carola Boccomini, Andrés J M Ferreri, Sara Rattotti, Vittorio Ruggero Zilioli, Silvia Anna Bolis, Patrizia Bernuzzi, Gerardo Musuraca, Gianluca Gaidano, Tommasina Perrone, Caterina Stelitano, Alessandra Tucci, Paolo Corradini, Sara Bigliardi, Francesca Re, Emanuele Cencini, Clara Mannarella, Donato Mannina, Melania Celli, Monica Tani, Giorgia Annechini, Giovanni Manfredi Assanto, Lavinia Grapulin, Anna Guarini, Marzia Cavalli, Lucia Anna De Novi, Riccardo Bomben, Elena Ciabatti, Elisa Genuardi, Daniela Drandi, Irene Della Starza, Luca Arcaini, Umberto Ricardi, Valter Gattei, Sara Galimberti, Marco Ladetto, Robin Foà, Ilaria Del Giudice
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引用次数: 0

摘要

背景:早期滤泡性淋巴瘤的主要治疗方法是局部放疗,抗CD20单克隆抗体(mAb)也可能发挥作用。我们的目的是采用可测量残留疾病(MRD)驱动的方法评估这些疗法的效果:这项前瞻性、多中心、2 期试验在意大利林福米基金会(FIL)的 27 个中心进行。符合条件的参与者为新确诊、组织学确诊为滤泡性淋巴瘤(I期或II期;I-IIIa级)的成人(≥18岁)。患者最初接受为期12天、24Gy的涉野放疗;放疗后或随访期间MRD阳性的患者接受8次静脉注射(每次1000毫克;每周1次)抗CD20 mAb ofatumumab。主要终点是接受累及野放疗后MRD呈阳性、接受ofatumumab治疗后MRD呈阴性的患者比例。如果患者在入组时外周血或骨髓样本中BCL2::IGH重排阳性,则纳入主要终点分析人群。MRD阳性是指外周血或骨髓中BCL2::IGH重排持续存在,由FIL MRD网络实验室集中评估。该试验已在EudraCT注册,编号为2012-001676-11.研究结果:2015年5月2日至2018年6月1日期间,我们共招募了110名参与者,其中106人(96%)符合条件并接受了参与场放疗。其中,105人(99%)为白人,1人(1%)为黑人,50人(47%)为男性,56人(53%)为女性。在可评估BCL2::IGH状态的105名参与者中,32人(30%)在基线时检测到BCL2::IGH重排。放疗后,30 名患者中有 12 人(40%)达到 MRD 阴性状态,其中 3 人(25%)的阴性状态持续时间较长(至少 36 或 42 个月)。对于放疗后MRD呈阳性的患者,在25例可评估的患者中,有23例(92%;95% CI 74-99)患者的MRD呈阴性。在中位随访46-1个月(IQR 42-8-50-8)后,这23名患者中有14人(61%)仍处于完全应答状态,MRD阴性。最常见的3-4级不良反应是输液相关反应,有4名患者出现这种情况:解读:局部放疗通常无法根除滤泡性淋巴瘤。MRD驱动的抗CD20单克隆抗体巩固治疗可使几乎所有患者达到分子缓解,并降低长期复发率。因此,MRD驱动的巩固治疗具有临床优势:意大利AIRC癌症研究基金会、诺华国际公司和葛兰素史克公司。
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Local radiotherapy and measurable residual disease-driven immunotherapy in patients with early-stage follicular lymphoma (FIL MIRO): final results of a prospective, multicentre, phase 2 trial.

Background: The mainstay of treatment for early-stage follicular lymphoma is local radiotherapy, with a possible role for anti-CD20 monoclonal antibody (mAb). We aimed to evaluate the effect of these treatments using a measurable residual disease (MRD)-driven approach.

Methods: This prospective, multicentre, phase 2 trial was conducted at 27 centres of the Fondazione Italiana Linfomi (FIL) in Italy. Eligible participants were adults (≥18 years) with newly diagnosed, histologically confirmed follicular lymphoma (stage I or II; grade I-IIIa). Patients were initially treated with 24 Gy involved-field radiotherapy over 12 days; those who were MRD-positive after radiotherapy or during follow-up received eight intravenous doses (1000 mg per dose; one dose per week) of the anti-CD20 mAb ofatumumab. The primary endpoint was the proportion of patients who were MRD-positive after involved-field radiotherapy and became MRD-negative after ofatumumab treatment. Patients were included in the primary endpoint analysis population if they were positive for BCL2::IGH rearrangement at enrolment in peripheral blood or bone marrow samples. MRD positivity was defined as the persistence of BCL2::IGH rearrangement in peripheral blood or bone marrow, assessed centrally by laboratories of the FIL MRD Network. The trial was registered with EudraCT, 2012-001676-11.

Findings: Between May 2, 2015, and June 1, 2018, we enrolled 110 participants, of whom 106 (96%) were eligible and received involved-field radiotherapy. Of these, 105 (99%) were White, one (1%) was Black, 50 (47%) were male, and 56 (53%) were female. Of 105 participants in whom BCL2::IGH status was evaluable, 32 (30%) had a detectable BCL2::IGH rearrangement at baseline. After radiotherapy, 12 (40%) of 30 patients reached MRD-negative status, which was long-lasting (at least 36 or 42 months) in three (25%). In those who were MRD-positive after radiotherapy, ofatumumab induced MRD-negativity in 23 (92%; 95% CI 74-99) of 25 evaluable patients. After a median follow-up of 46·1 months (IQR 42·8-50·8), 14 (61%) of these 23 patients remain in complete response and are MRD-negative. The most common grade 3-4 adverse events were infusion-related reactions, observed in four patients.

Interpretation: Local radiotherapy is frequently not associated with the eradication of follicular lymphoma. An MRD-driven, anti-CD20 monoclonal antibody consolidation enables molecular remission to be reached in almost all patients and is associated with a reduced incidence of relapse over time. A clinical advantage of an MRD-driven consolidation is therefore suggested.

Funding: AIRC Foundation for Cancer Research in Italy, Novartis International, and GlaxoSmithKline.

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来源期刊
Lancet Haematology
Lancet Haematology HEMATOLOGY-
CiteScore
26.00
自引率
0.80%
发文量
323
期刊介绍: Launched in autumn 2014, The Lancet Haematology is part of the Lancet specialty journals, exclusively available online. This monthly journal is committed to publishing original research that not only sheds light on haematological clinical practice but also advocates for change within the field. Aligned with the Lancet journals' tradition of high-impact research, The Lancet Haematology aspires to achieve a similar standing and reputation within its discipline. It upholds the rigorous reporting standards characteristic of all Lancet titles, ensuring a consistent commitment to quality in its contributions to the field of haematology.
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