HL-041 The Efficacy and Safety of BV-ICE Salvage Therapy for Relapsed/Refractory Hodgkin Lymphoma: A Single-Center
| dc.contributor.author | Amhaz, Ghid | |
| dc.contributor.department | Internal Medicine | |
| dc.contributor.faculty | Faculty of Medicine (FM) | |
| dc.contributor.institution | American University of Beirut | |
| dc.date.accessioned | 2025-01-24T11:43:39Z | |
| dc.date.available | 2025-01-24T11:43:39Z | |
| dc.date.issued | 2022 | |
| dc.description.abstract | Context: ASCT is the standard of care in R/R HL. Brentuximab-vedotin (BV) has been studied as maintenance post-ASCT, as single-agent after failure chemotherapy or in combination with different protocols. Objective: This study is to evaluate the CMR post salvage BV-ICE in patients with R/R HL prior to ASCT. The secondary endpoints: PFS, OS, RR, safety profile, and the delay to platelets and neutrophils engraftment post ASCT. Methods: Retrospective study of patients with R/R HL treated and followed at AUBMC between 2018 and 2021 Results: We identified 14 R/R HL patients, median age 30 yrs. 13 were nodular sclerosis (NS) subtype. 1 patient had mixed cellularity. All received ABVD initially. Median duration from diagnosis to relapse was 9.6 months. Patients were divided into 3 categories, 43% primary refractory, 21% relapsed within 3 to 12 months, 36% relapsed after 12 months from initial therapy. 57% were stage II on relapse and 36% stage IV. 14% received E-BEACOPP and 7% received DHAP as 1st salvage therapy. 21% received BV-ICE as 2nd salvage and 79% received BV-ICE as 1st salvage. Median duration from 1st relapse to BV-ICE was 1 month. BV was given on day 1 at 1.8mg/kg IV, etoposide 100 mg/m2 IV on days 1-3 and ifosfamide 5mg/m2 plus mesna 5g/m2 IV over 24 h on day 2, carboplatin IV AUC5 on day 2 for 2 cycles every 21-day cycle. All received GCSF 24hrs after treatment. Disease evaluation after 2nd cycle of BV-ICE using PET-FDG showed 93% CR and 7% PR. All did one attempt for SCC after cycle 2 without plerixafor. 93% were in CR and 7% in PR prior to transplant. The median PBSC collection was 14.7×106 CD34+cells/Kg, median of 10.96×106 CD34+ cells/Kg were infused. All received 3rd BV-ICE cycle and went into ASCT using BEAM conditioning. Median days to ANC engraftment was 9 and to platelet engraftment was 16.5. At day 100, 79% had CR, 14% PR, 7% had progression. After a median follow-up [E2] of 12.3 months the OS was 100% and PFS of 77%. Most common adverse event was hematological toxicity: 50% grade 3 anemia, 72% grade 3 thrombocytopenia, 72% FN. 7% developed grade 4 PN with reversible symptoms. Conclusions: BV-ICE as 1st salvage in R/R HL showed high ORR of 100% to be translated into improvement in DFS with acceptable toxicity profile. © 2022 Elsevier Inc. | |
| dc.identifier.doi | https://doi.org/10.1016/S2152-2650(22)01470-7 | |
| dc.identifier.eid | 2-s2.0-85138592597 | |
| dc.identifier.pmid | 36164021 | |
| dc.identifier.uri | http://hdl.handle.net/10938/30330 | |
| dc.language.iso | en | |
| dc.publisher | Elsevier Inc. | |
| dc.relation.ispartof | Clinical Lymphoma, Myeloma and Leukemia | |
| dc.source | Scopus | |
| dc.subject | Brentuximab vedotin | |
| dc.subject | Hl | |
| dc.subject | Hodgkin lymphoma | |
| dc.subject | Relapsed/refractory hl | |
| dc.subject | Salvage therapy | |
| dc.subject | Carboplatin | |
| dc.subject | Cd34 antigen | |
| dc.subject | Etoposide | |
| dc.subject | Fluorodeoxyglucose f 18 | |
| dc.subject | Granulocyte colony stimulating factor | |
| dc.subject | Ifosfamide | |
| dc.subject | Mesna | |
| dc.subject | Plerixafor | |
| dc.subject | Adult | |
| dc.subject | Allogeneic hematopoietic stem cell transplantation | |
| dc.subject | Anemia | |
| dc.subject | Article | |
| dc.subject | Cancer combination chemotherapy | |
| dc.subject | Cancer growth | |
| dc.subject | Cancer recurrence | |
| dc.subject | Cancer resistance | |
| dc.subject | Cancer staging | |
| dc.subject | Clinical evaluation | |
| dc.subject | Disease duration | |
| dc.subject | Drug efficacy | |
| dc.subject | Drug safety | |
| dc.subject | Engraftment | |
| dc.subject | Follow up | |
| dc.subject | Hodgkin disease | |
| dc.subject | Human | |
| dc.subject | Human cell | |
| dc.subject | Low drug dose | |
| dc.subject | Morning dosage | |
| dc.subject | Multiple cycle treatment | |
| dc.subject | Neutropenia | |
| dc.subject | Neutrophil | |
| dc.subject | Nodular sclerosis hodgkin lymphoma | |
| dc.subject | Overall survival | |
| dc.subject | Positron emission tomography | |
| dc.subject | Progression free survival | |
| dc.subject | Relapse | |
| dc.subject | Retrospective study | |
| dc.subject | Symptom | |
| dc.subject | Thrombocyte transfusion | |
| dc.subject | Thrombocytopenia | |
| dc.subject | Transplantation conditioning | |
| dc.title | HL-041 The Efficacy and Safety of BV-ICE Salvage Therapy for Relapsed/Refractory Hodgkin Lymphoma: A Single-Center | |
| dc.type | Article |
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