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Blood advances · 2021

Role of radiotherapy to bulky sites of advanced Hodgkin lymphoma treated with ABVD: final results of FIL HD0801 trial.

СтатьяРандомизированное исследованиеНазвание и аннотация: Перевод пока не подготовлен
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Ricardi Umberto, Levis Mario, Evangelista Andrea, Gioia Daniela Maria, Sacchetti Gian Mauro, Gotti Manuel, Re Alessandro, Buglione Michela, Pavone Vincenzo, Nardella Antonio, Nassi Luca, Zanni Manuela, Franzone Paola, Frezza Giovanni Piero, Pulsoni Alessandro, Grapulin Lavinia, Santoro Armando, Rigacci Luigi, Simontacchi Gabriele, Tani Monica, Zaja Francesco, Abruzzese Elisabetta, Botto Barbara, Zilioli Vittorio Ruggero, Rota-Scalabrini Delia, Freilone Roberto, Ciccone Giovannino, Filippi Andrea Riccardo, Zinzani Pier Luigi

Аннотация

The role of consolidation radiotherapy (RT) for bulky lesions is controversial in patients with advanced-stage Hodgkin lymphoma who achieve complete metabolic response (CMR) after doxorubicin, bleomycin, vinblastine, dacarbazine (ABVD)-based chemotherapy. We present the final results of the Fondazione Italiana Linfomi HD0801 trial, which investigated the potential benefit of RT in that setting. In this phase 3 randomized study, patients with a bulky lesion at baseline (a mass with largest diameter ≥5 cm) who have CMR after 2 and 6 ABVD cycles were randomly assigned 1:1 to RT vs observation (OBS) with a primary endpoint of event-free survival (EFS) at 2 years. The sample size was calculated estimating an EFS improvement for RT of 20% (from 60% to 80%). The secondary end point was progression-free survival (PFS). One hundred sixteen patients met the inclusion criteria and were randomly assigned to RT or OBS. Intention-to-treat (ITT) analysis showed a 2-year EFS of 87.8% vs 85.8% for RT vs OBS (hazard ratio [HR], 1.5; 95% confidence interval [CI], 0.6-3.5; P = .34). At 2 years, ITT-PFS was 91.3% vs 85.8% (HR, 1.2; 95% CI, 0.5-3; P = .7). Patients in CMR randomly assigned to OBS had a good outcome, and the primary end point of a 20% benefit in EFS for RT was not met. However, the sample size was underpowered to detect a benefit of 10% or less, keeping open the question of a potential, more limited role of RT in this setting. This trial was registered at www.clinicaltrials.gov as #NCT00784537.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты