2017
DOI: 10.1016/s1470-2045(17)30696-4
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Incorporation of brentuximab vedotin into first-line treatment of advanced classical Hodgkin's lymphoma: final analysis of a phase 2 randomised trial by the German Hodgkin Study Group

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Cited by 104 publications
(79 citation statements)
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“…Phase 2 trials of checkpoint inhibitors, specifically nivolumab and pembrolizumab, have shown outstanding efficacy in adults with relapsed/refractory HL leading to their Food and Drug Administration (FDA) approval for these indications. The anti‐CD30 antibody–drug conjugate brentuximab vedotin (Bv) has shown efficacy in adults in both relapsed and up‐front settings . The combination of Bv with gemcitabine demonstrated high complete response rates in patients up to age 30 with relapsed/refractory HL …”
Section: Treatmentmentioning
confidence: 99%
See 1 more Smart Citation
“…Phase 2 trials of checkpoint inhibitors, specifically nivolumab and pembrolizumab, have shown outstanding efficacy in adults with relapsed/refractory HL leading to their Food and Drug Administration (FDA) approval for these indications. The anti‐CD30 antibody–drug conjugate brentuximab vedotin (Bv) has shown efficacy in adults in both relapsed and up‐front settings . The combination of Bv with gemcitabine demonstrated high complete response rates in patients up to age 30 with relapsed/refractory HL …”
Section: Treatmentmentioning
confidence: 99%
“…The anti-CD30 antibody-drug conjugate brentuximab vedotin (Bv) has shown efficacy in adults in both relapsed and upfront settings. 45,46 The combination of Bv with gemcitabine demonstrated high complete response rates in patients up to age 30 with relapsed/refractory HL. 47,48 Ongoing studies include a Phase 2 study investigating Bv in place of vincristine in the OEPA/COPDac regimen (NCT01920932) and Sequential randomized clinical trials in HL have led to steady improvements in disease-related survival and continued reductions in therapy-related toxicities.…”
Section: Treatmentmentioning
confidence: 99%
“…Meanwhile, German Hodgkin Study Group incorporated BV in BEACOPPesc resulting in hybrid regimens BrECAPP and BrECADD on 104 subjects. 5 Dosage of brentuximab vedotin was 1.8 mg/kg every 3 weeks. Concerning safety profile, grade IV hematologic toxicities were prominent occurring in 80% and 79% based on randomization, but BrECADD regimen had negligible organ-related toxicity.…”
Section: Introductionmentioning
confidence: 99%
“…To reduce short‐ and long‐term toxicity of BEACOPP escalated or improve efficacy of ABVD, variants of the regimens incorporating novel agents, such as the anti‐CD30 antibody‐drug conjugate brentuximab vedotin (BV) or the anti‐PD1 antibody nivolumab, are under investigation. Results of the randomized phase III ECHELON‐1 trial with BV‐AVD versus ABVD and a phase II trial investigating BV‐based BEACOPP variants were recently reported (Ansell et al , ; Connors et al , ; Eichenauer et al , ).…”
mentioning
confidence: 99%