Pregled bibliografske jedinice broj: 1194290
Ibrutinib as a salvage therapy after allogeneic HCT for chronic lymphocytic leukemia
Ibrutinib as a salvage therapy after allogeneic HCT for chronic lymphocytic leukemia // Bone marrow transplantation (Basingstoke), 55 (2020), 5; 884-890 doi:0.1038/s41409-019-0742-7 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1194290 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Ibrutinib as a salvage therapy after allogeneic
HCT for chronic
lymphocytic leukemia
Autori
Michallet, Mauricette ; Dreger, Peter ; Sobh, Mohamad ; Koster, Linda ; Hoek, Jennifer ; Boumendil, Ariane ; Scheid, Christof ; Fox, Christopher P ; Wulf, Gerald ; Krüger, William ; van Gelder, Michel ; Corradini, Paolo ; Russo, Domenico ; Passweg, Jakob ; Schoemans, Hélène ; Bethge, Wolfgang ; Schaap, Nicolaas ; Cornelissen, Jan ; Browne, Paul ; Duraković, Nadira ; Lutz, Muller ; Montoto, Silvia ; Kroger, Nicolaus ; Schetelig ; Johannes
Kolaboracija
French Cooperative Group for CLL ; SFGM-TC ; EBMT Chronic Malignancy and Lymphoma Working Parties
Izvornik
Bone marrow transplantation (Basingstoke) (0268-3369) 55
(2020), 5;
884-890
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
ibrutinib ; salvage ; bone marrow transplantation
Sažetak
The purpose of our study is to provide information on safety and efficacy of ibrutinib as salvage treatment after allo-HSCT for CLL. A total of 56 patients were included, 36 (64%) males ; median age at transplantation was 48 years (range: 35–64) and the median number of treatment lines prior to transplantation was 3 (1–10). The median time between allo-HSCT and Ibrutinib was 30 months (range: 1–140). Overall, 40 (71%) patients responded to Ibrutinib ; 23 (41%) PR, and 17 (30%) CR. At time of ibrutinib initiation, ten patients had active chronic GVHD that resolved under Ibrutinib, whilst a single patient developed limited de novo chronic GVHD on Ibrutinib. Fourteen patients discontinued ibrutinib, four because of toxicity and ten because of disease progression. Overall, 14 patients progressed (median PFS = 24 months) among them 10 died. Two- year OS and PFS probabilities were 72% (95% CI: 52–84) and 50% (95% CI: 32– 66), respectively. Patients with late relapse after allo-HSCT (≥24 months) had a better PFS after ibrutinib. Our study shows that ibrutinib can be safely administered for CLL relapse after allo-HSCT, with comparable efficacy to non-transplanted patients with high-risk disease.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
MZOS-108-1081872-1913 - LEUKEMIJE I TRANSPLANTACIJA KRVOTVORNIH MATIČNIH STANICA (Duraković, Nadira, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb,
Klinički bolnički centar Zagreb
Profili:
Nadira Duraković
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE