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Aplastic anemia in the elderly: a nationwide survey on behalf of the French Reference Center for Aplastic Anemia

Authors :
Lucile Bussot
Anne Banos
Matthieu Resche-Rigon
Delphine Lebon
Fiorenza Barraco
Didier Bouscary
Jerome Tamburini
Natacha Maillard
Fabrice Jardin
Laurence Simon
Flore Sicre de Fontbrune
Ambroise Marçais
Adrien Contejean
Jean-Yves Cahn
Pierre Hirsch
Lionel Adès
Louis Terriou
Régis Peffault de Latour
Gérard Socié
Marion Alcantara
Etienne Lengliné
Luc Mathieu Fornecker
Cécile Moluçon-Chabrot
Service d'hématologie clinique
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Henri Mondor-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)
Centre de Recherche Épidémiologie et Statistique Sorbonne Paris Cité (CRESS (U1153 / UMR_A_1125 / UMR_S_1153))
Université Paris Diderot - Paris 7 (UPD7)-Université Sorbonne Paris Cité (USPC)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de la Recherche Agronomique (INRA)
Service de biostatistique et information médicale de l’hôpital Saint Louis (Equipe ECSTRA) (SBIM)
Hopital Saint-Louis [AP-HP] (AP-HP)
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut national du cancer [Boulogne] (INCA)-Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM)
Hôpital Cochin [AP-HP]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
Groupe d'étude des proliférations lymphoïdes (GPL)
Université de Rouen Normandie (UNIROUEN)
Normandie Université (NU)-Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM)
Génomique et Médecine Personnalisée du Cancer et des Maladies Neuropsychiatriques (GPMCND)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Rouen Normandie (UNIROUEN)
Normandie Université (NU)-Normandie Université (NU)
CIC - Biotherapie - GHU Ouest APHP (CIC-BT 502)
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Necker - Enfants Malades [AP-HP]
Université de Paris (UP)
Institut Cochin (IC UM3 (UMR 8104 / U1016))
Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Service d'immuno-hématologie pédiatrique [CHU Necker]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Necker - Enfants Malades [AP-HP]
University Paris Descartes Sorbonne Paris Cité, Imagine Institute, Paris
CHU Amiens-Picardie
CHU Estaing [Clermont-Ferrand]
CHU Clermont-Ferrand
Hôpital Claude Huriez [Lille]
CHU Lille
Centre Hospitalier Lyon Sud [CHU - HCL] (CHLS)
Hospices Civils de Lyon (HCL)
Hôpital de Bayonne
CH de la Côte Basque
Centre Hospitalier Universitaire [Grenoble] (CHU)
Centre de Recherche Saint-Antoine (CRSA)
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)
Hôpital de la Milétrie
Centre hospitalier universitaire de Poitiers (CHU Poitiers)
CHU Strasbourg
service hématologie Strasbourg
Service d’Hématologie Biologique [CHU Clermont-Ferrand]
CHU Gabriel Montpied [Clermont-Ferrand]
CHU Clermont-Ferrand-CHU Clermont-Ferrand-CHU Estaing [Clermont-Ferrand]
Département d'Oncologie et Hématologie [Strasbourg]
Les Hôpitaux Universitaires de Strasbourg (HUS)
Service d'Hémato-oncologie [CHU Saint-Louis]
Groupe Hospitalier Saint Louis - Lariboisière - Fernand Widal [Paris]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
DESSAIVRE, Louise
Université Paris Descartes - Paris 5 (UPD5)
Université Sorbonne Paris Cité (USPC)
CHU Necker - Enfants Malades [AP-HP]
Centre de Lutte Contre le Cancer Henri Becquerel Normandie Rouen (CLCC Henri Becquerel)
Université Paris Diderot - Paris 7 (UPD7)
Le CHCB, Centre Hospitalier de la Côte Basque
CHU Saint-Antoine [AP-HP]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)
CHU Pitié-Salpêtrière [AP-HP]
Ecotaxie, microenvironnement et développement lymphocytaire (EMily (UMR_S_1160 / U1160))
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité)
CHU Grenoble
Source :
Haematologica, HAEMATOLOGICA, HAEMATOLOGICA, 2019, 104 (2), pp.256-262. ⟨10.3324/haematol.2018.198440⟩, BLOOD, BLOOD, 2018, 132 (1), ⟨10.1182/blood-2018-99-113359⟩, Haematologica, Ferrata Storti Foundation, 2019, 104 (2), pp.256-262. ⟨10.3324/haematol.2018.198440⟩, Blood, Blood, American Society of Hematology, 2018, 132 (1), ⟨10.3324/haematol.2018.198440⟩
Publication Year :
2019
Publisher :
Ferrata Storti Foundation, 2019.

Abstract

Introduction Aplastic anemia (AA) is a rare but potentially life-threatening disease that frequently occurs in older patients. Various therapeutic options can be proposed and data regarding the ideal first line treatment of AA in this ageing population remains scarce. Methods We conducted a retrospective nationwide multicenter study in France to examine current treatments for AA patients over 60 years old within a 10-year period (1/1/2007 to 12/31/2016). Our aims were to evaluate efficacy and tolerance of AA treatment, and to analyze predictive factors for response and survival. Patients who were diagnosed with AA by a bone marrow biopsy at the age of 60 or over were included in the study. Results Over the course of a decade, 88 patients (median age 68.5) were identified in 19 centers, with a median follow-up of 32.1 months; 49% were women, the median Charlson comorbidity index was 2 (range 0-6), the median performance status was 1 (range 0-3), 21% had very severe (vSAA) and 36% severe AA. We analyzed 184 treatment lines which comprised ATG-CsA (33%, including 72% with horse ATG), CsA alone (14%), androgen alone (14%), eltrombopag alone (10%), CsA associated with androgen or eltrombopag (9%), and other treatments (20%). First-line treatment was ATG-CsA for half of patients. Comparisons of patients treated in first line with ATG-CsA, CsA or other treatments revealed that patients receiving ATG-CsA were significantly younger (66 years, vs. 71.5 vs. 71.5, respectively, p=0.007), more frequently female (61%, vs. 50% vs. 27%, p=0.02) and had a lower platelet count (8x109/L, vs. 12x109/L vs. 15x109/L, p=0.025). We found no difference with respect to weight, Charlson comorbidity index score, performance status or disease severity between first line treatment regimens. After first-line therapy, 32% of patients achieved a complete response (CR), and 15% a partial response (PR). After the 181 assessable treatment lines, 19% achieved CR and 19% a PR. Median time until best response was 151 days. The overall response rate (ORR) was 62% with ATG-CsA (70% as a first-line treatment), 35% with CsA alone (39% as first-line), 22% with eltrombopag, and 21% with androgen. The ORR in patients over 70 years receiving ATG-CsA (n=16) was 81% (50% achieving a CR). Responses were significantly better in first line and in patients with good performance status, as well as in those that had received ATG-CsA (ORR of 70% after first-line treatment). In a multivariable analysis using ATG-CsA as a baseline, we found that CsA alone (OR 0.35 (0.13;0.96), p=0.042), eltrombopag (OR 0.12 (0.03;0.54), p=0.0057) and androgens (OR 0.17 (0.05;0.58), p=0.0047) were all individually associated with lower response rates. The main complications were infections (grade III/IV, 35% of treatment lines including 9 deaths (5%)), and renal issues (grade-III/IV, 29%). ATG-CsA was associated with significantly more infectious complications (72% vs. 24%, p Conclusion Our study showed a significantly better ORR with ATG-CsA than other regimens for treatment of AA in elderly, with more complications but no more death. Age per se is not a limiting factor for treatment with ATG-CsA: this regimen should be used as first-line treatment in elderly patients if they have a good performance status and low comorbidity index score. Among patients with adverse performance status or comorbidities contra-indicating the use of ATG, CsA alone or in combination may be safely used. Other strategies might be reserved for later courses of treatments. Supportive care may have a great impact on survival in this population. Disclosures Ades: JAZZ: Honoraria; Takeda: Membership on an entity's Board of Directors or advisory committees; silent pharma: Consultancy; Celgene: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding. Peffault De Latour:Pfizer Inc.: Consultancy, Honoraria, Research Funding; Amgen Inc.: Research Funding; Novartis: Consultancy, Honoraria, Research Funding; Alexion Pharmaceuticals, Inc.: Consultancy, Honoraria, Research Funding.

Details

Language :
English
ISSN :
15928721, 03906078, 00064971, and 15280020
Volume :
104
Issue :
2
Database :
OpenAIRE
Journal :
Haematologica
Accession number :
edsair.doi.dedup.....89602c8b98cb275d058720196704ba27
Full Text :
https://doi.org/10.3324/haematol.2018.198440⟩