Successful reversal of severe liver function impairment with Brentuximab vedotin in multiply relapsed/refractory classical Hodgkin lymphoma.
Adult
Aged
Antineoplastic Agents, Immunological
/ therapeutic use
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Brentuximab Vedotin
/ therapeutic use
Drug Resistance, Neoplasm
/ drug effects
Hodgkin Disease
/ drug therapy
Humans
Liver Diseases
/ etiology
Male
Neoplasm Recurrence, Local
/ drug therapy
Prognosis
Retrospective Studies
Journal
Journal of B.U.ON. : official journal of the Balkan Union of Oncology
ISSN: 2241-6293
Titre abrégé: J BUON
Pays: Cyprus
ID NLM: 100883428
Informations de publication
Date de publication:
Historique:
entrez:
27
1
2020
pubmed:
27
1
2020
medline:
20
6
2020
Statut:
ppublish
Résumé
To present our experience on the use of Brentuximab Vedotin (BV) in patients with relapsed/refractory classical Hodgkin Lymphoma (cHL) and severe liver function impairment with marked jaundice. Two patients with relapsed/refractory cHL were evaluated. BV was administered in the presence of liver dysfunction and severe jaundice due to liver infiltration by cHL, as confirmed by PET-CT. Complete blood counts, biochemical profile, physical and imaging findings were reviewed to assess BV efficacy and tolerance. Case 1 had stage IVB, mixed cellularity cHL. Following ABVD chemotherapy, the patient experienced a relapse and responded to IGEV (ifosfamide, gemcitabine, vinorelbine, steroids) chemotherapy followed by autologous stem cell transplantation (ASCT). Thereafter, he experienced a second relapse with constitutional symptoms, severe jaundice and pancytopenia. Liver involvement was confirmed by PET-CT. Case 2 was admitted with a very late relapse of cHL. After a single cycle of gemcitabine-vinorelbine chemotherapy, which was not tolerated, the patient developed fever, anemia and jaundice, with laboratory findings indicating bone marrow and liver infiltration. The latter was confirmed by PET-CT. Both patients received BV monotherapy according to its formal indication at the reduced dose of 1.2 mg/kg due to severe liver impairment and experienced a rapid clinical and laboratory improvement. BV was well tolerated and offered a clinical benefit for approximately 4 months. BV was safely administered to patients with relapsed/refractory cHL and severe liver function impairment with marked jaundice due to liver involvement, offering significant clinical improvement and reversal of liver abnormalities. BV may serve as a bridge to further salvage combination chemotherapy or a transplant procedure.
Substances chimiques
Antineoplastic Agents, Immunological
0
Brentuximab Vedotin
7XL5ISS668
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM