Acute promyelocytic leukemia (APL) in very old patients: real-life behind protocols.


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: 1 9 2021
medline: 15 10 2021
entrez: 31 8 2021
Statut: ppublish

Résumé

Acute promyelocytic leukemia (APL) is uncommon among subjects aged ≥ 70 years and the better therapeutic strategy represents an unmet clinical need. This prompted us to explore our real-life data on a retrospective cohort of 45 older APL patients (≥ 70 years) consecutively diagnosed at eight different hematologic institutions in Latium, Italy, from July 1991 to May 2019. Two patients (4.4%) died from early hemorrhagic complications before treatment could begin. Twenty-two patients (51.1%) (Group A) were enrolled or treated according to standard clinical protocols, while 21 (48.8%) (Group B) received an ATRA-based personalized approach due to poor performance status. Morphologic complete remission (CR) after induction therapy was achieved in 33 patients (76.7%) with 100% of patients in Group A and 52.3% in Group B ( The present analysis highlights that almost half of the patients received sub-optimal induction treatments and registered dismal outcomes demonstrating the importance of adopting standard therapies instead of modified or reduced personalized approaches also in the setting of frail older patients.

Sections du résumé

BACKGROUND BACKGROUND
Acute promyelocytic leukemia (APL) is uncommon among subjects aged ≥ 70 years and the better therapeutic strategy represents an unmet clinical need.
MATERIALS AND METHODS METHODS
This prompted us to explore our real-life data on a retrospective cohort of 45 older APL patients (≥ 70 years) consecutively diagnosed at eight different hematologic institutions in Latium, Italy, from July 1991 to May 2019.
RESULTS RESULTS
Two patients (4.4%) died from early hemorrhagic complications before treatment could begin. Twenty-two patients (51.1%) (Group A) were enrolled or treated according to standard clinical protocols, while 21 (48.8%) (Group B) received an ATRA-based personalized approach due to poor performance status. Morphologic complete remission (CR) after induction therapy was achieved in 33 patients (76.7%) with 100% of patients in Group A and 52.3% in Group B (
CONCLUSIONS CONCLUSIONS
The present analysis highlights that almost half of the patients received sub-optimal induction treatments and registered dismal outcomes demonstrating the importance of adopting standard therapies instead of modified or reduced personalized approaches also in the setting of frail older patients.

Identifiants

pubmed: 34461798
doi: 10.1080/0284186X.2021.1971291
doi:

Substances chimiques

Tretinoin 5688UTC01R
Arsenic Trioxide S7V92P67HO

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1520-1526

Auteurs

Serena Rosati (S)

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

Carmelo Gurnari (C)

Department of Biomedicine and Prevention, PhD in Immunology, Molecular Medicine and Applied Biotechnology, University of Rome Tor Vergata, Rome, Italy.
Translational Hematology and Oncology Research Department, Taussig Cancer Center, Cleveland Clinic, Cleveland, USA.

Massimo Breccia (M)

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

Ida Carmosino (I)

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

Emilia Scalzulli (E)

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

Enrico Montefusco (E)

Hematology, Ospedale Sant'Andrea, Rome, Italy.

Salvatore Perrone (S)

Hematology, Polo Universitario Pontino, "Sapienza", Via A. Canova S.M. Goretti Hospital, Latina, Italy.

Ombretta Annibali (O)

Unit of Hematology and Stem Cell Transplantation, Campus Bio-Medico University, Rome, Italy.

Vincenza Martini (V)

UOC Ematologia, Ospedale "Fabrizio Spaziani", Frosinone, Italy.

Giulio Trapè (G)

Hematology, Belcolle Hospital, Viterbo, Italy.

Gioia Colafigli (G)

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

Malgorzata Trawinska (M)

Hematology, Ospedale S. Eugenio, Roma, Italy.

Clara Minotti (C)

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

Giuseppe Cimino (G)

Hematology, Polo Universitario Pontino, "Sapienza", Via A. Canova S.M. Goretti Hospital, Latina, Italy.

Agostino Tafuri (A)

Hematology Institute, La Sapienza University of Rome, S. Andrea Hospital, Rome, Italy.

Giuseppe Avvisati (G)

Unit of Hematology and Stem Cell Transplantation, Campus Bio-Medico University, Rome, Italy.

Maurizio Martelli (M)

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

Maria Teresa Voso (MT)

Laboratorio di Neuro-Oncoematologia, Fondazione Santa Lucia, Rome, Italy.
Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.

Roberto Latagliata (R)

Department of Translational and Precision Medicine, Sapienza University, Rome, Italy.
Hematology, Belcolle Hospital, Viterbo, Italy.

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Classifications MeSH