Incidence and outcome after first molecular versus overt recurrence in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia included in the ALL Ph08 trial from the Spanish PETHEMA Group.


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
15 08 2019
Historique:
received: 09 01 2019
revised: 08 03 2019
accepted: 18 03 2019
pubmed: 24 4 2019
medline: 19 5 2020
entrez: 24 4 2019
Statut: ppublish

Résumé

Disease recurrence occurs in 20% to 40% of adults with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) who are treated with chemotherapy and tyrosine kinase inhibitors (TKIs). In the current study, the authors report the incidence, treatment, and outcome after first disease recurrence in young and older adults treated in the ALL Ph08 trial (ClinicalTrials.gov identifier NCT01491763). Patients aged 18 to 55 years with de novo Ph+ ALL were treated with imatinib concurrently with standard-dose induction and consolidation therapy followed by allogeneic hematopoietic stem cell transplantation (allo-HSCT) when possible. In patients with first disease recurrence, the authors analyzed the type of recurrence, timing, location, presence of kinase domain mutations, type of treatment, and outcomes. Of the 125 patients, 28 patients (22%) developed disease recurrence before (4 patients) or after (24 patients) HSCT, with the recurrences being molecular in 11 patients (39%) and overt in 17 patients (61%). T315I was the most common mutation noted at the time of disease recurrence. Change in TKI was the most frequent treatment for patients with molecular disease recurrence whereas rescue chemotherapy and TKI change followed by second allo-HSCT when possible were performed for the most part in patients with overt disease recurrence. A total of 20 patients (71%) achieved response. The median disease-free survival (DFS) and overall survival (OS) were 8.5 months and 15.3 months, respectively. A trend for better DFS and OS was observed in patients with molecular recurrence compared with those with overt recurrence (median of 16.9 months vs 6.3 months [P = .05] and 28.7 months vs 11.5 months [P = .05] for DFS and OS, respectively). Disease recurrence was frequent in young and older adults with Ph+ ALL who were treated with imatinib and chemotherapy with HSCT. Although the majority of patients responded to rescue therapy, their outcomes were poor, especially with regard to overt disease recurrence.

Sections du résumé

BACKGROUND
Disease recurrence occurs in 20% to 40% of adults with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) who are treated with chemotherapy and tyrosine kinase inhibitors (TKIs). In the current study, the authors report the incidence, treatment, and outcome after first disease recurrence in young and older adults treated in the ALL Ph08 trial (ClinicalTrials.gov identifier NCT01491763).
METHODS
Patients aged 18 to 55 years with de novo Ph+ ALL were treated with imatinib concurrently with standard-dose induction and consolidation therapy followed by allogeneic hematopoietic stem cell transplantation (allo-HSCT) when possible. In patients with first disease recurrence, the authors analyzed the type of recurrence, timing, location, presence of kinase domain mutations, type of treatment, and outcomes.
RESULTS
Of the 125 patients, 28 patients (22%) developed disease recurrence before (4 patients) or after (24 patients) HSCT, with the recurrences being molecular in 11 patients (39%) and overt in 17 patients (61%). T315I was the most common mutation noted at the time of disease recurrence. Change in TKI was the most frequent treatment for patients with molecular disease recurrence whereas rescue chemotherapy and TKI change followed by second allo-HSCT when possible were performed for the most part in patients with overt disease recurrence. A total of 20 patients (71%) achieved response. The median disease-free survival (DFS) and overall survival (OS) were 8.5 months and 15.3 months, respectively. A trend for better DFS and OS was observed in patients with molecular recurrence compared with those with overt recurrence (median of 16.9 months vs 6.3 months [P = .05] and 28.7 months vs 11.5 months [P = .05] for DFS and OS, respectively).
CONCLUSIONS
Disease recurrence was frequent in young and older adults with Ph+ ALL who were treated with imatinib and chemotherapy with HSCT. Although the majority of patients responded to rescue therapy, their outcomes were poor, especially with regard to overt disease recurrence.

Identifiants

pubmed: 31012967
doi: 10.1002/cncr.32156
doi:

Substances chimiques

Protein Kinase Inhibitors 0
Imatinib Mesylate 8A1O1M485B

Banques de données

ClinicalTrials.gov
['NCT01491763']

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2810-2817

Informations de copyright

© 2019 American Cancer Society.

Auteurs

Josep-Maria Ribera (JM)

Department of Clinical Hematology, ICO Badalona-Hospital Germans Trias i Pujol, Josep Carreras Leukemia Research Institute, Autonomous University of Barcelona, Badalona, Spain.

Olga García (O)

Department of Clinical Hematology, ICO Badalona-Hospital Germans Trias i Pujol, Josep Carreras Leukemia Research Institute, Autonomous University of Barcelona, Badalona, Spain.

María-José Moreno (MJ)

Department of Hematology, Hospital of the Virgen de la Victoria, Malaga, Spain.

Pere Barba (P)

Department of Hematology, Vall d'Hebron University Hospital, Autonomous University of Barcelona, Barcelona, Spain.

Irene García-Cadenas (I)

Department of Hematology, Hospital of Sant Pau, Barcelona, Spain.

Santiago Mercadal (S)

Department of Hematology, ICO-Hospital Duran i Reynals, L'Hospitalet de Llobregat, Catalonia, Spain.

Pau Montesinos (P)

Department of Hematology, Le Fe University and Polytechnic Hospital, Valencia, Spain.

Manuel Barrios (M)

Department of Hematology, Carlos Haya Hospital, Malaga, Spain.

José González-Campos (J)

Department of Hematology, Virgen del Rocio University Hospital, Seville, Spain.

Daniel Martínez-Carballeira (D)

Department of Hematology, Central Hospital of Asturias, Oviedo, Spain.

Cristina Gil (C)

Department of Hematology, General University Hospital of Alicante, Alicante, Spain.

Jordi Ribera (J)

Department of Clinical Hematology, ICO Badalona-Hospital Germans Trias i Pujol, Josep Carreras Leukemia Research Institute, Autonomous University of Barcelona, Badalona, Spain.

Susana Vives (S)

Department of Clinical Hematology, ICO Badalona-Hospital Germans Trias i Pujol, Josep Carreras Leukemia Research Institute, Autonomous University of Barcelona, Badalona, Spain.

Andrés Novo (A)

Department of Hematology, Son Espases Hospital, Palma de Mallorca, Spain.

Marta Cervera (M)

Department of Hematology, ICO-Hospital Joan XXIII, Tarragona, Spain.

Josefina Serrano (J)

Department of Hematology, Reina Sofia Hospital, Cordoba, Spain.

Esperanza Lavilla (E)

Department of Hematology, Lucus Augusti Hospital, Lugo, Spain.

Eugenia Abella (E)

Department of Hematology, del Mar Hospital, Barcelona, Spain.

Mar Tormo (M)

Department of Hematology, Clinical Hospital, Valencia, Spain.

María-Luz Amigo (ML)

Department of Hematology, Morales Meseguer University General Hospital, Murcia, Spain.

María-Teresa Artola (MT)

Department of Hematology, Donostia University Hospital, San Sebastian, Spain.

Eulalia Genescà (E)

Department of Clinical Hematology, ICO Badalona-Hospital Germans Trias i Pujol, Josep Carreras Leukemia Research Institute, Autonomous University of Barcelona, Badalona, Spain.

Pilar Bravo (P)

Department of Hematology, Fuenlabrada University Hospital, Madrid, Spain.

Daniel García-Belmonte (D)

Department of Hematology, La Zarzuela Hospital, Madrid, Spain.

Antoni García-Guiñón (A)

Department of Hematology, Arnau de Vilanova Hospital, Lleida, Spain.

Jesús-María Hernández-Rivas (JM)

Department of Hematology, University Hospital of Salamanca, Salamanca, Spain.

Evarist Feliu (E)

Department of Clinical Hematology, ICO Badalona-Hospital Germans Trias i Pujol, Josep Carreras Leukemia Research Institute, Autonomous University of Barcelona, Badalona, Spain.

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