High-dose therapy (HDT) with autologous hematopoietic cell transplantation (autoHCT) has been considered the standard-of-care for relapsed chemosensitive classical Hodgkin lymphoma (cHL), since the end of the last century.1,2 While this simple and time-tested modality can eradicate disease in the majority of patients undergoing this procedure, recurrent cHL remains the most common cause of treatment failure and death following autoHCT. Several prognostic factors (primary refractory disease, early relapse after frontline treatment, poor patient performance status, extranodal involvement, positron emission tomography-avid residual disease prior to autoHCT, etc.) have been known to predict the risk of relapse after HDT and autoHCT.3 However, pharmacological interventions to mitigate the risk of lymphoma relapse after autoHCT had remained elusive, until the clinical availability of brentuximab vedotin.
Brentuximab vedotin is an anti-CD30 antibody conjugated by a protease-cleavable linker to a microtubule-disrupting agent, monomethyl auristatin E (MMAE). Brentuximab vedotin derives its antitumor activity by binding the antibody-drug conjugate (ADC) to CD30-expressing cells, leading to internalization of the ADC–CD30 complex followed by proteolytic cleavage and release of MMAE. MMAE disrupts the microtubule network by binding to tubulin within the cell, thereby causing cell cycle arrest and apoptotic death of the cell.4 The key phase II registration study of brentuximab vedotin (1.8 mg/kg every 3 weeks) in relapsed/refractory cHL (n=102; overall response rate = 75%)5 eventually paved the path to the prospective, multicenter, phase III randomized AETHERA trial, in which 327 patients with cHL at increased risk of progression after autoHCT, who had been treated with a minimum of two prior systemic therapies and had achieved a complete or partial remission or had stable disease at the time of autoHCT, were randomized to receive brentuximab vedotin consolidation or placebo (every 3 weeks for up to 16 cycles) after HDT.6 Patients were eligible for the study if they met one of the following criteria: primary refractory disease following first-line therapy, first remission duration of less than 12 months, or extranodal involvement at the start of salvage chemotherapy. After a median follow-up of 30 months, the estimated 2-year rate of progression-free survival by independent review was 63% (95% confidence interval [95% CI]: 55–70) in the brentuximab vedotin group and 51% (95% CI: 43–59) in the placebo group (hazard ratio = 0.57; 95% CI: 0·40–0·81). Overall survival was 88% at 2 years in both arms.
Table 1.Indications for brentuximab vedotin treatment of classical Hodgkin lymphoma approved by the United States Food and Drug Administration and the European Medicines Agency.
Of note, the AETHERA trial only enrolled cHL patients who had not previously received treatment with brentuximab vedotin. However, since publication of the results of AETHERA, brentuximab vedotin (at a dose of 1.2 mg/kg up to a maximum of 120 mg every 2 weeks in combination with doxorubicin, vinblastine, and dacarbazine) has become approved in the frontline setting based on the results of ECHELON17 (Table 1) and is being increasingly used in pre-autoHCT salvage regimens.8 Accordingly, in current clinical practice, the proportion of brentuximab vedotin-naïve high-risk cHL patients undergoing autoHCT is declining. While international consensus guidelines suggest the use of post-autoHCT brentuximab vedotin maintenance in high-risk cHL patients with limited prior exposure to brentuximab vedotin (defined as approximately ≤4-6 cycles),9 these recommendations lack supportive evidence.
In a Letter to the Editor published in this issue of Haematologica, Marouf et al.10 report a retrospective nationwide French cohort (AMAHRELIS) study, examining the real-life outcome of cHL patients who received post-transplant brentuximab vedotin maintenance (n=115) during 2012-2017. Since brentuximab vedotin received European Commission approval in 2016,11 it is not clear whether these patients were treated on local clinical trials or had access through compassionate use protocols. Compared to AETHERA, more patients in the AMAHRELIS cohort received escalated BEACOPP in first-line (16% vs. 37%), had a negative positron emission tomography scan prior to autoHCT (47% vs. 82%) and underwent more than one salvage therapies (43% vs. 51%). Ninety-five percent of patients in the AMAHRELIS cohort met the AETHERA definition of high-risk disease. More importantly, 70% (n=81) of patients in the AMAHRE-LIS cohort had been exposure to brentuximab vedotin prior to autoHCT. The mean number of brentuximab vedotin doses administered after autoHCT was 11 (range, 3-18), without difference between patients who had and had not been previously exposed to brentuximab vedotin. Treatment-related events led to maintenance discontinuation in 10% of patients, which is surprising, since nearly a third of brentuximab vedotin-naïve AETHERA patients discontinued treatment due to adverse events.8 The 2-year progression-free survival of patients in AMAHRELIS was 75% and was not affected by pre-transplant exposure to brentuximab vedotin. These rates seem to be numerically higher than rates reported in the AETHERA study; a potential explanation for these improved outcomes is a higher proportion of patients with complete metabolic remission in the retrospective cohort prior to transplantation. With limitations of a retrospective cohort in mind, these results are noteworthy and provide much needed evidence supporting the use of brentuximab vedotin maintenance after autoHCT in cHL patients with prior exposure to this agent. In the recent past, nonrandomized data on post-transplant maintenance with checkpoint inhibitors have shown a high degree of disease control.12 Whether checkpoint inhibitors are superior to brentuxi-mab vedotin in the post-transplant maintenance space merits examination, especially when considering the recent results of the KEYNOTE-204 trial showing a progression-free survival benefit of pembrolizumab compared with brentuximab vedotin, in patients with cHL who have relapsed after autoHCT or are ineligible for autoHCT.13
Footnotes
Correspondence
Disclosures
MH has received research support or funding from Takeda Pharmaceutical Company and Spectrum Pharmaceuticals; has provided consultancy services for Incyte Corporation, ADC Therapeutics, Omeros, MorphoSys, Kite, Genmab, SeaGen, and Gamida Cell; and has participated in speakers’ bureaus for Sanofi Genzyme, AstraZeneca, and BeiGene.
References
- Linch DC, Winfield D, Goldstone AH. Dose intensification with autologous bone-marrow transplantation in relapsed and resistant Hodgkin's disease: results of a BNLI randomised trial. Lancet. 1993; 341(8852):1051-1054. https://doi.org/10.1016/0140-6736(93)92411-LPubMedGoogle Scholar
- Schmitz N, Pfistner B, Sextro M. Aggressive conventional chemotherapy compared with high-dose chemotherapy with autologous haemopoietic stem-cell transplantation for relapsed chemosensitive Hodgkin's disease: a randomised trial. Lancet. 2002; 359(9323):2065-2071. https://doi.org/10.1016/S0140-6736(02)08938-9PubMedGoogle Scholar
- Satwani P, Ahn KW, Carreras J. A prognostic model predicting autologous transplantation outcomes in children, adolescents and young adults with Hodgkin lymphoma. Bone Marrow Transplant. 2015; 50(11):1416-1423. https://doi.org/10.1038/bmt.2015.177PubMedPubMed CentralGoogle Scholar
- Doronina SO, Toki BE, Torgov MY. Development of potent monoclonal antibody auristatin conjugates for cancer therapy. Nat Biotechnol. 2003; 21(7):778-784. https://doi.org/10.1038/nbt832PubMedGoogle Scholar
- Younes A, Gopal AK, Smith SE. Results of a pivotal phase II study of brentuximab vedotin for patients with relapsed or refractory Hodgkin's lymphoma. J Clin Oncol. 2012; 30(18):2183-2189. https://doi.org/10.1200/JCO.2011.38.0410PubMedPubMed CentralGoogle Scholar
- Moskowitz CH, Nademanee A, Masszi T. Brentuximab vedotin as consolidation therapy after autologous stem-cell transplantation in patients with Hodgkin’s lymphoma at risk of relapse or progression (AETHERA): a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet. 385(9980):1853-1862. https://doi.org/10.1016/S0140-6736(15)60165-9PubMedGoogle Scholar
- Connors JM, Jurczak W, Straus DJ. Brentuximab vedotin with chemotherapy for stage III or IV Hodgkin’s lymphoma. N Engl J Med. 2017; 378(4):331-344. https://doi.org/10.1056/NEJMoa1708984PubMedPubMed CentralGoogle Scholar
- Moskowitz AJ, Schöder H, Yahalom J. PET-adapted sequential salvage therapy with brentuximab vedotin followed by augmented ifosamide, carboplatin, and etoposide for patients with relapsed and refractory Hodgkin’s lymphoma: a non-randomised, open-label, single-centre, phase 2 study. Lancet Oncol. 2015; 16(3):284-292. https://doi.org/10.1016/S1470-2045(15)70013-6PubMedGoogle Scholar
- Kanate AS, Kumar A, Dreger P. Maintenance therapies for Hodgkin and non-Hodgkin lymphomas after autologous transplantation: a Consensus Project of ASBMT, CIBMTR, and the Lymphoma Working Party of EBMT. JAMA Oncol. 2019; 5(5):715-722. https://doi.org/10.1001/jamaoncol.2018.6278PubMedPubMed CentralGoogle Scholar
- Marouf A, Cottereau AS, Kanoun S. Outcomes of refractory or relapsed Hodgkin lymphoma patients with post autologous stem cell transplantation brentuximab vedotin maintenance : a French multicenter observational cohort study. Haematologica. 2022; 107(7):1685-1690. https://doi.org/10.3324/haematol.2021.279564PubMedPubMed CentralGoogle Scholar
- 2021. Publisher Full TextGoogle Scholar
- Armand P, Chen Y-B, Redd RA. PD-1 blockade with pembrolizumab for classical Hodgkin lymphoma after autologous stem cell transplantation. Blood. 2019; 134(1):22-29. https://doi.org/10.1182/blood.2019000215PubMedPubMed CentralGoogle Scholar
- Kuruvilla J, Ramchandren R, Santoro A. Pembrolizumab versus brentuximab vedotin in relapsed or refractory classical Hodgkin lymphoma (KEYNOTE-204): an interim analysis of a multicentre, randomised, open-label, phase 3 study. Lancet Oncol. 2021; 22(4):512-524. https://doi.org/10.1016/S1470-2045(21)00005-XPubMedGoogle Scholar
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