Risk-adapted treatment of acute promyelocytic leukemia with all-trans retinoic acid and anthracycline monochemotherapy: long-term outcome of the LPA 99 multicenter study by the PETHEMA Group

Author:

Sanz Miguel A.1,Montesinos Pau12,Vellenga Edo3,Rayón Consuelo4,de la Serna Javier5,Parody Ricardo6,Bergua Juan M.7,León Angel8,Negri Silvia9,González Marcos10,Rivas Concha11,Esteve Jordi12,Milone Gustavo13,González José D.14,Amutio Elena15,Brunet Salut16,García-Laraña J.17,Colomer Dolors12,Calasanz María J.18,Chillón Carmen10,Barragán Eva1,Bolufer Pascual1,Lowenberg Bob19

Affiliation:

1. Hospital Universitario La Fe, Valencia, Spain;

2. Department of Medicine of Universitat Autònoma de Barcelona, Barcelona, Spain;

3. University Hospital, Groningen, The Netherlands;

4. Hospital Central de Asturias, Oviedo, Spain;

5. Hospital 12 de Octubre, Madrid, Spain;

6. Hospital Universitario Virgen del Rocío, Sevilla, Spain;

7. Hospital San Pedro de Alcántara, Cáceres, Spain;

8. Hospital General, Jerez de la Frontera, Spain;

9. Hospital Carlos Haya, Málaga, Spain;

10. Hospital Universitario, Salamanca, Spain;

11. Hospital General, Alicante, Spain;

12. Hospital Clinic, Barcelona, Spain;

13. Fundaleu, Buenos Aires, Argentina;

14. Hospital Insular, Las Palmas, Spain;

15. Hospital de Cruces, Baracaldo, Spain;

16. Hospital Sant Pau, Barcelona, Spain;

17. Hospital Ramón y Cajal, Madrid, Spain;

18. Universidad de Navarra, Pamplona, Spain; and

19. Erasmus University Medical Center, Rotterdam, The Netherlands

Abstract

Abstract A previous report of the Programa de Estudio y Tratamiento de las Hemopatías Malignas (PETHEMA) Group showed that a risk-adapted strategy combining all-trans retinoic acid (ATRA) and anthracycline monochemotherapy for induction and consolidation in newly diagnosed acute promyelocytic leukemia results in an improved outcome. Here we analyze treatment outcome of an enlarged series of patients who have been followed up for a median of 65 months. From November 1999 through July 2005 (LPA99 trial), 560 patients received induction therapy with ATRA plus idarubicin. Patients achieving complete remission received 3 courses of consolidation followed by maintenance with ATRA and low-dose chemotherapy. The 5-year cumulative incidence of relapse and disease-free survival were 11% and 84%, respectively. These results compare favorably with those obtained in the previous LPA96 study (P = .019 and P = .04, respectively). This updated analysis confirms the high antileukemic efficacy, low toxicity, and high degree of compliance of a risk-adapted strategy combining ATRA and anthracycline monochemotherapy for consolidation therapy.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference13 articles.

1. Treatment of acute promyelocytic leukemia.;Sanz;Hematology Am Soc Hematol Educ Program,2006

2. Risk-adapted treatment of acute promyelocytic leukemia with all-trans retinoic acid and anthracycline monochemotherapy: a multicenter study by the PETHEMA Group.;Sanz;Blood,2004

3. Definition of relapse risk and role of non-anthracycline drugs for consolidation in patients with acute promyelocytic leukemia: a joint study of the PETHEMA and GIMEMA cooperative groups.;Sanz;Blood,2000

4. A modified AIDA protocol with anthracycline-based consolidation results in high antileukemic efficacy and reduced toxicity in newly diagnosed PML/RARa-positive acute promyelocytic leukemia.;Sanz;Blood,1999

5. Nonparametric estimations from incomplete observations.;Kaplan;J Am Stat Assoc,1958

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