TY - JOUR
T1 - Secondary plasma cell leukemia
T2 - a multicenter retrospective study of 101 patients
AU - Jurczyszyn, Artur
AU - Castillo, Jorge J.
AU - Avivi, Irit
AU - Czepiel, Jacek
AU - Davila, Julio
AU - Vij, Ravi
AU - Fiala, Mark A.
AU - Gozzetti, Alessandro
AU - Grząśko, Norbert
AU - Milunovic, Vibor
AU - Hus, Iwona
AU - Mądry, Krzysztof
AU - Waszczuk-Gajda, Anna
AU - Usnarska-Zubkiewicz, Lidia
AU - Dębski, Jakub
AU - Atilla, Erden
AU - Beksac, Meral
AU - Mele, Giuseppe
AU - Sawicki, Waldemar
AU - Jayabalan, David
AU - Charliński, Grzegorz
AU - Gyula Szabo, Agoston
AU - Hajek, Roman
AU - Delforge, Michel
AU - Kopacz, Agnieszka
AU - Fantl, Dorotea
AU - Waage, Anders
AU - Crusoe, Edvan
AU - Hungria, Vania
AU - Richardson, Paul
AU - Laubach, Jacob
AU - Guerrero-Garcia, Thomas
AU - Liu, Jieqi
AU - Vesole, David H.
N1 - Publisher Copyright:
© 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2019/1/2
Y1 - 2019/1/2
N2 - This multicenter retrospective study included 101 patients (median age 62 years) with secondary plasma cell leukemia (sPCL). The median time from initial multiple myeloma diagnosis to sPCL was 31 months. Fifty-five out of 72 patients (75%) who received any therapy were treated with immunomodulators (IMiDs) and/or proteasome inhibitors (PIs), and 14/72 (19%) underwent salvage autologous stem cell transplantation (ASCT). The overall response rate in patients who received ASCT or PI (either alone or in combination) was higher than in those who did not (93% vs. 36% and 60% vs. 30%, respectively). The median overall survival (OS) in patients who received therapy was 4.2 months (95% CI: 1.3; 8.0) with a 1-year OS of 19%. Platelet count ≤100 × 10 9 /L at sPCL diagnosis was the only independent predictor of a poorer OS in treated patients (HR = 3.98, p =.0001). These findings suggest that patients with sPCL may benefit from salvage ASCT- and PI-based regimens.
AB - This multicenter retrospective study included 101 patients (median age 62 years) with secondary plasma cell leukemia (sPCL). The median time from initial multiple myeloma diagnosis to sPCL was 31 months. Fifty-five out of 72 patients (75%) who received any therapy were treated with immunomodulators (IMiDs) and/or proteasome inhibitors (PIs), and 14/72 (19%) underwent salvage autologous stem cell transplantation (ASCT). The overall response rate in patients who received ASCT or PI (either alone or in combination) was higher than in those who did not (93% vs. 36% and 60% vs. 30%, respectively). The median overall survival (OS) in patients who received therapy was 4.2 months (95% CI: 1.3; 8.0) with a 1-year OS of 19%. Platelet count ≤100 × 10 9 /L at sPCL diagnosis was the only independent predictor of a poorer OS in treated patients (HR = 3.98, p =.0001). These findings suggest that patients with sPCL may benefit from salvage ASCT- and PI-based regimens.
KW - Autologous stem cell transplantation
KW - proteasome inhibitors
KW - secondary plasma cell leukemia
UR - http://www.scopus.com/inward/record.url?scp=85049602239&partnerID=8YFLogxK
U2 - 10.1080/10428194.2018.1473574
DO - 10.1080/10428194.2018.1473574
M3 - Article
C2 - 29965787
AN - SCOPUS:85049602239
SN - 1042-8194
VL - 60
SP - 118
EP - 123
JO - Leukemia and Lymphoma
JF - Leukemia and Lymphoma
IS - 1
ER -