Long term follow-up of frontline Dasatinib in older patients with chronic myeloid leukemia in chronic phase treated outside clinical trials: a real-life cohort observational study.


Journal

Acta oncologica (Stockholm, Sweden)
ISSN: 1651-226X
Titre abrégé: Acta Oncol
Pays: England
ID NLM: 8709065

Informations de publication

Date de publication:
Nov 2021
Historique:
pubmed: 10 9 2021
medline: 15 10 2021
entrez: 9 9 2021
Statut: ppublish

Résumé

A limited amount of data has been published in chronic-phase chronic myeloid leukemia (CP-CML) patients aged >75 years treated frontline with second-generation tyrosine kinase inhibitors. To address this issue in a clinical 'real-life' setting, we retrospectively analyzed 45 CP-CML patients (pts) followed in 20 Italian Centers and treated frontline with dasatinib (DAS). Median age was 78.4 years (range 75-89.2 years). DAS starting dose was 100 mg QD in 35 pts (77.7%), 80 mg QD in 1 pts (2.2%) and 50 mg QD in 9 pts (20.1%), respectively. The median follow-up was 42.6 months (IQR 20.4 - 63.3). Grade 3 and 4 side effects, both hematological and non-hematological, were detected in 6 (13.3%) and 12 (26.6%) pts, respectively. Pleural effusions of all grades occurred in 13 pts (28.8%) after a median period of DAS exposure of 14.7 months (IQR 3.0 - 33.1). The rates of DAS dose reduction and permanent drug discontinuation were 53.3% and 20.0%, respectively. As the best response, 42/45 patients (93.3%) achieved a complete cytogenetic response (CCyR), 35/45 (77.7%) a major molecular response (MMR) and 24/45 (53.3%) a deep molecular response (both MR 4.0 and MR 4.5). Only 1 patient (2.2%) progressed to the blast phase after 13 months of therapy; 8 deaths were observed (1 CML-related and 7 CML-unrelated). Cumulative event-free survival and overall survival at 36 months were 64.7% (95%, CI 49.4 - 80.0) and 82.3% (95%, CI 70.3-94.3), respectively. These findings, although evaluated in a limited and selected cohort of patients, suggest that DAS might be effective in older patients (aged >75 years) affected by CP-CML with acceptable toxicity.

Sections du résumé

BACKGROUND BACKGROUND
A limited amount of data has been published in chronic-phase chronic myeloid leukemia (CP-CML) patients aged >75 years treated frontline with second-generation tyrosine kinase inhibitors.
AIMS OBJECTIVE
To address this issue in a clinical 'real-life' setting, we retrospectively analyzed 45 CP-CML patients (pts) followed in 20 Italian Centers and treated frontline with dasatinib (DAS).
PATIENTS AND METHODS METHODS
Median age was 78.4 years (range 75-89.2 years). DAS starting dose was 100 mg QD in 35 pts (77.7%), 80 mg QD in 1 pts (2.2%) and 50 mg QD in 9 pts (20.1%), respectively. The median follow-up was 42.6 months (IQR 20.4 - 63.3).
RESULTS RESULTS
Grade 3 and 4 side effects, both hematological and non-hematological, were detected in 6 (13.3%) and 12 (26.6%) pts, respectively. Pleural effusions of all grades occurred in 13 pts (28.8%) after a median period of DAS exposure of 14.7 months (IQR 3.0 - 33.1). The rates of DAS dose reduction and permanent drug discontinuation were 53.3% and 20.0%, respectively. As the best response, 42/45 patients (93.3%) achieved a complete cytogenetic response (CCyR), 35/45 (77.7%) a major molecular response (MMR) and 24/45 (53.3%) a deep molecular response (both MR 4.0 and MR 4.5). Only 1 patient (2.2%) progressed to the blast phase after 13 months of therapy; 8 deaths were observed (1 CML-related and 7 CML-unrelated). Cumulative event-free survival and overall survival at 36 months were 64.7% (95%, CI 49.4 - 80.0) and 82.3% (95%, CI 70.3-94.3), respectively.
CONCLUSION CONCLUSIONS
These findings, although evaluated in a limited and selected cohort of patients, suggest that DAS might be effective in older patients (aged >75 years) affected by CP-CML with acceptable toxicity.

Identifiants

pubmed: 34499575
doi: 10.1080/0284186X.2021.1971292
doi:

Substances chimiques

Protein Kinase Inhibitors 0
Imatinib Mesylate 8A1O1M485B
Dasatinib RBZ1571X5H

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1527-1533

Auteurs

Fabio Stagno (F)

Hematology Section and BMT Unit, Rodolico Hospital, AOU Policlinico Rodolico-San Marco, Catania, Italy.

Massimo Breccia (M)

Department of Precision and Translational Medicine, Sapienza University, Rome, Italy.

Mario Annunziata (M)

Hematology Section, Cardarelli Hospital, Naples, Italy.

Malgorzata Monika Trawinska (MM)

Hematology Section, S. Eugenio Hospital, Tor Vergata University, Rome, Italy.

Alessandra Iurlo (A)

Hematology Section, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Nicola Sgherza (N)

Hematology Unit, IRCCS "Casa Sollievo Sofferenza" Hospital, San Giovanni Rotondo, Italy.

Carmen Fava (C)

Hematology Section, Azienda Ospedaliera Mauriziano, Turin, Italy.

Antonella Gozzini (A)

Hematology Section, Careggi Hospital, Florence, Italy.

Luigiana Luciano (L)

Hematology Section, Federico II University, Naples, Italy.

Ida Carmosino (I)

Department of Precision and Translational Medicine, Sapienza University, Rome, Italy.

Massimiliano Bonifacio (M)

Hematology Section, Department of Medicine, University of Verona, Verona, Italy.

Federica Sorà (F)

Hematology Section, Policlinico A. Gemelli, IRCSS Catholic University, Rome, Italy.

Sabrina Leonetti Crescenzi (S)

Hematology Section, Azienda Ospedaliera San Giovanni-Addolorata, Rome, Italy.

Monica Crugnola (M)

Hematology Section and BMT Unit, AOU Parma, Parma, Italy.

Gabriele Gugliotta (G)

Hematology Section "Seragnoli", IRCCS AOU Bologna, University of Bologna, Bologna, Italy.

Sara Galimberti (S)

Hematology Section, University of Pisa, Pisa, Italy.

Cristina Bucelli (C)

Hematology Section, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Gioia Colafigli (G)

Department of Precision and Translational Medicine, Sapienza University, Rome, Italy.

Costanzo Feo (C)

Immunohematology and Transfusion Unit, AORN "Gaetano Rummo", Benevento, Italy.

Mario Tiribelli (M)

Hematology Section and BMT, University of Udine, Udine, Italy.

Endri Mauro (E)

Hematology Section, Dipartimento di Medicina Specialistica, Ca' Foncello Hospital, Treviso, Italy.

Antonella Russo Rossi (A)

Unit of Hematology and Stem Cell Transplantation, AOU Policlinico, Bari, Italy.

Attilio Guarini (A)

Unit of Hematology and Cell Therapy, IRCCS-Istituto Tumori "Giovanni Paolo II", Bari, Italy.

Elisabetta Abruzzese (E)

Hematology Section, S. Eugenio Hospital, Tor Vergata University, Rome, Italy.

Gianantonio Rosti (G)

Hematology Section, IRCCS "Dino Amadori", Meldola, Italy.

Francesco Di Raimondo (F)

Hematology Section and BMT Unit, Rodolico Hospital, AOU Policlinico Rodolico-San Marco, Catania, Italy.

Roberto Latagliata (R)

Hematology Section, Belcolle Hospital, Viterbo, Italy.

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