P-021: Experience with autologous stem-cell transplant (auto-SCT) in patients with systemic light-chain amyloidosis (LA) at our center

Auto-SCT is the standard first-line treatment in patients with LA and good personal status. This procedure achieves haematological responses >70% with an average survival rate of more than 8 years. Depending on patient characteristics and hospital guidelines, prior chemotherapy (CT) is administer...

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Bibliographic Details
Published in:Clinical lymphoma, myeloma and leukemia Vol. 21; p. S51
Main Authors: Carbonero, Javier Díaz, Guerrero, Elena Medina, Montaña, Albert Pérez, García, Antonio Gutierrez, Raga, Jose María Sánchez, del Carmen Ballester Ruíz, María, Moya, María Jiménez, León, Sandra Pérez, Rincón, Andrea Provencio, de Miguel, Leyre Bento, García, Andrés Novo, Maño, Lucía García, Mayol, Antonia Sampol
Format: Journal Article
Language:English
Published: Elsevier Inc 01-10-2021
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Summary:Auto-SCT is the standard first-line treatment in patients with LA and good personal status. This procedure achieves haematological responses >70% with an average survival rate of more than 8 years. Depending on patient characteristics and hospital guidelines, prior chemotherapy (CT) is administered, usually with Bortezomib-based regimens. The main determinant of survival in LA is cardiac involvement. The subgroup of patients with cardiac involvement and an indication for Auto-SCT is at the highest risk of complications and mortality and should therefore be strictly selected. Our objective is to review the experience in our center with Auto-SCT in patients with LA. A retrospective descriptive study was conducted at the Son Espases University Hospital between November 2012 and June 2021. Pre- and post-SCT clinical-biological data, complications during transplantation and progression-free survival (PFS) were analyzed. Eleven patients with a median age of 59 years at the time of Auto-SCT (range 41-69) were included, of whom 7 were male (64%). Ten patients (90.9%) had renal involvement at diagnosis and 6 (54.5%) had cardiac involvement. According to the Mayo Clinic 2013 prognostic staging score, 6 patients (54.5%) had stage I, 3 patients (27.3%) had stage II and 2 patients (18.2%) had stage IIIb (18.2%). All patients received pre Auto-SCT CT with bortezomib-based regimens. The median pre Auto-SCT left ventricular ejection fraction was 58% (41-79 range). Pre Auto-SCT organ-based chemotherapy response was: 8/10 patients (80%) with renal response; 1/6 patients (16.7%) with cardiac response. Pre Auto-SCT haematological response was: 7 patients (63.6%) complete remission, 1 patient (9%) very good partial response, 1 patient (9%) partial response, 1 patient (9%) stable disease and 1 patient (9%) not assessable. The median number of CD34+ cells infused into Auto-SCT was 3.66×106/kg. 10 patients (90.9%) received G-CSF from day +5. 10 patients (90.9%) developed complications during transplantation, 7 of them requiring admission to the Intensive Care Unit (ICU) with a median of 15 days of admission (range 1-24 days), mainly due to acute pulmonary edema - APE (85.7%). 3/7 patients requiring ICU admission passed away, leaving the Auto-SCT-related mortality rate at 27.3%. With a median follow-up of 36 months (range 5-90), a median PFS and an overall survival rate (OS) of 73% (95%CI 46-99) is observed. PFS and OS match because there are no progression events. Patients with cardiac involvement prior to Auto-SCT have a high risk of morbidity and mortality, with APE being the main complication in our study. Multidisciplinary management of these patients during Auto-SCT is essential to avoid complications.
ISSN:2152-2650
2152-2669
DOI:10.1016/S2152-2650(21)02155-8