CD30 in PTCLS: correlation between RNA and protein levels in a large european series from the LYSA

Détails

ID Serval
serval:BIB_354606609734
Type
Actes de conférence (partie): contribution originale à la littérature scientifique, publiée à l'occasion de conférences scientifiques, dans un ouvrage de compte-rendu (proceedings), ou dans l'édition spéciale d'un journal reconnu (conference proceedings).
Sous-type
Abstract (résumé de présentation): article court qui reprend les éléments essentiels présentés à l'occasion d'une conférence scientifique dans un poster ou lors d'une intervention orale.
Collection
Publications
Institution
Titre
CD30 in PTCLS: correlation between RNA and protein levels in a large european series from the LYSA
Titre de la conférence
12th International Conference on Malignant Lymphoma
Auteur(s)
Bossard C., Dobay M.P., Lamant L., Missiglia E., Parrens M., Martin A., Tournillac C., Haioun C., Bonnet C., Berger F., Bouchind'homme B., Delarue R., Rousset T., Thiebault S., Picquenot J., Fabiani B., Delorenzi M., Gaulard P., de Leval L.
Adresse
Lugano, Switzerland, June 19-22, 2013
ISBN
0278-0232
ISSN-L
146-147
Statut éditorial
Publié
Date de publication
06/2013
Volume
31
Série
Hematological Oncology
Pages
146-147
Langue
anglais
Notes
Oral presentation
Résumé
Introduction: CD22 is expressed on most B-non-Hodgkin lymphomas (NHL);
inotuzumab ozogamicin (INO) is an anti-CD22 antibody conjugated to calicheamicin.
This study evaluated the safety and tolerability of INO plus R-CVP in patients (pts) with
relapsed/refractory CD22+ B-NHL. Efficacy data were also collected.
Methods: Part 1 of this open-label study identified a maximum tolerated dose (MTD)
of INO 0.8mg/m,2 on day 2 plus R-CVP (rituximab 375mg/m,2 cyclophosphamide
750mg/m,2 and vincristine 1.4mg/m,2 on day 1; prednisone 40mg/m,2 on days 1-5)
every 21 days. Subsequently, pts were enrolled in the MTD confirmation cohort (part
2, n = 10), which required a dose-limiting toxicity rate of <33% in cycle 1 and <4
pts discontinuing prior to cycle 3 due to an adverse event (AE) in the MTD expansion
cohort (part 3, n = 22), which explored preliminary activity.
Results: Parts 2 and 3 enrolled 32 pts: 16 pts with diffuse large B-cell lymphoma, 15
with follicular lymphoma and one with mantle cell lymphoma. Median age was
64.5 years (range 44-81 years); 34% of pts had 1 prior regimen, 34% had 2, 28% had
≥3 and 3% had none (median 2; range 0-6).Median treatment duration was five cycles
(range 1-6). Part 2 confirmed the MTD as standard dose R-CVP plus INO 0.8mg/m,2;
2/10 pts had a dose-limiting toxicity (grade 3 increased ALT/AST, grade 4 neutropenia
requiring G-CSF). One pt discontinued because of an AE prior to cycle 3.
Common treatment-related AEs were thrombocytopenia (78%), neutropenia (66%), fatigue
(50%), leukopenia (50%), nausea (41%) and lymphopenia (38%); common grade
3/4 AEs were neutropenia (63%), thrombocytopenia (53%), leukopenia (38%) and
lymphopenia (31%). There was one case of treatment-related fatal pneumonia with
grade 4 neutropenia. Ten pts discontinued treatment due to AEs; thrombocytopenia/delayed
platelet recovery was the leading cause (grade 1/2, n = 6; grade 3/4, n = 3). Objective
response rate (ORR) was 77% (n = 24/31 evaluable pts), including 26% (n=8/31)
with complete response (CR); three pts had stable disease. Of the pts with follicular
lymphoma, ORR was 100% (n = 15/15), including seven pts with CR. Of the pts with
diffuse large B-cell lymphoma, ORR was 60% (n = 9/16), including one pt with CR.
Conclusions: Results suggest that INOplus R-CVP has acceptable toxicity and promising
activity in relapsed/refractory CD22+ B-NHL. The most common grade 3/4 AEs were
hematologic. Follow-up for progression-free and overall survival is ongoing.
Création de la notice
05/07/2013 11:09
Dernière modification de la notice
20/08/2019 14:22
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