TY - JOUR
T1 - Idelalisib treatment prior to allogeneic stem cell transplantation for patients with chronic lymphocytic leukemia
T2 - a report from the EBMT chronic malignancies working party
AU - Schetelig, Johannes
AU - Chevallier, Patrice
AU - van Gelder, Michel
AU - Hoek, Jennifer
AU - Hermine, Olivier
AU - Chakraverty, Ronjon
AU - Browne, Paul
AU - Milpied, Noel
AU - Malagola, Michele
AU - Socie, Gerard
AU - Delgado, Julio
AU - Deconinck, Eric
AU - Damaj, Ghandi
AU - Maury, Sebastian
AU - Beelen, Dietrich
AU - Quoc, Stephanie Nguyen
AU - Shankara, Paneesha
AU - Brecht, Arne
AU - Mayer, Jiri
AU - Hunault-Berger, Mathilde
AU - Bittenbring, Joerg
AU - Thieblemont, Catherine
AU - Lepretre, Stephane
AU - Baldauf, Henning
AU - de Wreede, Liesbeth C.
AU - Tournilhac, Olivier
AU - Yakoub-Agha, Ibrahim
AU - Kroeger, Nicolaus
AU - Dreger, Peter
N1 - Funding Information:
Conflict of interest JS—consultancy honoraria from AstraZeneca, Janssen, Roche, Gilead, Abbvie, Sanofi, Molmed; lecturer fees from AstraZeneca, Janssen, Roche, Gilead, Abbvie, Sanofi, Novartis; research support from Genzyme, Sanofi, GSK, Novartis, Abbvie. OH —consultancy honoraria from AB Science; research support from AB Science, Celgene, Alexion, and Inatherys. DG—consultancy honoraria from Roche, Takeda, Iqone; lecturer fees from Abbvie, Celgene, Sanofi-Genzyme; research support from Takeda. NK—lecturer fees from Neovii, Sanofi, Novartis, Kiadis, Celgene, Amgen, Riemser, Chugai, Janssen; research support from Novartis, Celgene, Riemser, Neovii. PD—consultancy for AbbVie, AstraZeneca, Gilead, Janssen, Novartis, Riemser, Roche; speakers bureau for AbbVie, Gilead, Novartis, Riemser, Roche; research support from Neovii and Riemser. The remaining authors declared no conflict of interest.
Publisher Copyright:
© 2020, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2021/3
Y1 - 2021/3
N2 - No studies have been reported so far on bridging treatment with idelalisib for patients with chronic lymphocytic leukemia (CLL) prior to allogeneic hematopoietic cell transplantation (alloHCT). To study potential carry-over effects of idelalisib and to assess the impact of pathway-inhibitor (PI) failure we performed a retrospective EBMT registry-based study. Patients with CLL who had a history of idelalisib treatment and received a first alloHCT between 2015 and 2017 were eligible. Data on 72 patients (median age 58 years) were analyzed. Forty percent of patients hadTP53(mut/del)CLL and 64% had failed on at least one PI. No primary graft failure occurred. Cumulative incidences of acute GVHD degrees II-IV and chronic GVHD were 51% and 39%, respectively. Estimates for 2-year overall survival (OS), progression-free survival (PFS), and cumulative incidences of relapse/progression (CIR) and non-relapse mortality NRM were 59%, 44%, 25%, and 31%. In univariate analysis, drug sensitivity was a strong risk factor. For patients who had failed neither PI treatment nor chemoimmunotherapy (CIT) the corresponding 2-year estimates were 73%, 65%, 15%, and 20%, respectively. In conclusion, idelalisib may be considered as an option for bridging therapy prior to alloHCT. Owing to the high risk for acute GVHD intensified clinical monitoring is warranted.
AB - No studies have been reported so far on bridging treatment with idelalisib for patients with chronic lymphocytic leukemia (CLL) prior to allogeneic hematopoietic cell transplantation (alloHCT). To study potential carry-over effects of idelalisib and to assess the impact of pathway-inhibitor (PI) failure we performed a retrospective EBMT registry-based study. Patients with CLL who had a history of idelalisib treatment and received a first alloHCT between 2015 and 2017 were eligible. Data on 72 patients (median age 58 years) were analyzed. Forty percent of patients hadTP53(mut/del)CLL and 64% had failed on at least one PI. No primary graft failure occurred. Cumulative incidences of acute GVHD degrees II-IV and chronic GVHD were 51% and 39%, respectively. Estimates for 2-year overall survival (OS), progression-free survival (PFS), and cumulative incidences of relapse/progression (CIR) and non-relapse mortality NRM were 59%, 44%, 25%, and 31%. In univariate analysis, drug sensitivity was a strong risk factor. For patients who had failed neither PI treatment nor chemoimmunotherapy (CIT) the corresponding 2-year estimates were 73%, 65%, 15%, and 20%, respectively. In conclusion, idelalisib may be considered as an option for bridging therapy prior to alloHCT. Owing to the high risk for acute GVHD intensified clinical monitoring is warranted.
KW - VENETOCLAX
KW - CLL
U2 - 10.1038/s41409-020-01069-w
DO - 10.1038/s41409-020-01069-w
M3 - Article
C2 - 33004942
SN - 0268-3369
VL - 56
SP - 605
EP - 613
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 3
ER -