HL-007: Brentuximab Vedotin Consolidation Therapy after Autologous Stem-Cell Transplantation in Patients with High-Risk Hodgkin Lymphoma: Multi-Center Retrospective Study

Autor: Güray Saydam, Mehmet Hilmi Dogu, Elif Birtas Atesoglu, Murat Ozbalak, Meltem Ayli, Sevgi Kalayoglu Besisik, Zübeyde Nur Özkurt, Leylagül Kaynar, Gülsüm Özet, Meltem Kurt Yuksel, Murat Albayrak, Mustafa Pehlivan, Birol Yildiz, Ant Uzay, Irfan Yavasoglu, Tuğçe Nur Yiğenoğlu, Mehmet Sönmez, Ozan Salim, Rahsan Yildirim, Tayfur Toptas, Tugrul Elverdi, Selami Kocak Toprak, Özgür Mehtap, Ahmet Kursad Gunes, Orhan Ayyildiz, Meliha Nalcaci, Olga Meltem Akay, Hasan Sami Goksoy, Sinem Civriz Bozdag, Burhan Ferhanoglu, Sebnem Izmir Guner, Fevzi Altuntaş, İpek Yönal Hindilerden
Rok vydání: 2021
Předmět:
Zdroj: Clinical Lymphoma Myeloma and Leukemia. 21:S368-S369
ISSN: 2152-2650
Popis: Context The AETHERA trial reported an increased progression-free survival (PFS) when brentuximab vedotin (BV) was used as maintenance therapy in high-risk Hodgkin lymphoma (HL) after autologous stem cell transplantation (ASCT). Objective To determine the impact and safety of BV as maintenance after ASCT in real-world patients. Design Patients with relapsed/refractory HL started on BV consolidation therapy after ASCT due to high risk of relapse, between January 2016 and July 2019, from 25 institutions, were retrospectively analyzed. Setting All patients were followed by the bone marrow transplantation team of their hospital. Patients or Other Participants Seventy-five patients were included in the study. The median follow-up time was 26 months. The most common high-risk features were primary refractory or relapsed disease Interventions BV consolidation was initiated within 6 months of ASCT and administered at a dose of 1.8 mg/kg intravenous infusion over 30 min every 3 weeks for up to 16 cycles in an outpatient setting. Main Outcome Features The primary endpoint of the study was PFS; secondary endpoints were safety and overall survival (OS). Results At the time of analysis, 42 patients completed consolidation courses, and BV was discontinued in 33 patients. Fifty patients had an ongoing response (CR in 41, PR in six, and SD in three patients), 25 had progressed. Ten died in the follow-up, eight with progressive disease and two due to infection while in CR. The 2-years PFS and OS rates were 67.75% (95% CI:0.55–0.77) and 87.61% (95% CI:0.76–0.94), respectively. Seventeen patients (23%) received BV in the pre-ASCT treatment lines, and there was no survival difference between the BV naive and BV exposed groups. The most common adverse events were neutropenia (27%) and peripheral neuropathy (21%). Sixteen patients (21.3%) experienced grade 3 or 4 toxicity. BV was discontinued due to AE in 12 patients. Conclusions Consolidation with BV after ASCT can achieve a 2-year PFS of 67.75% (95% CI: 0.55–0.75) with an acceptable toxicity profile.
Databáze: OpenAIRE
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