AIDA 0493 protocol for newly diagnosed acute promyelocytic leukemia: very long-term results and role of maintenance

Author:

Avvisati Giuseppe1,Lo-Coco Francesco23,Paoloni Francesca Paola4,Petti Maria Concetta5,Diverio Daniela6,Vignetti Marco6,Latagliata Roberto6,Specchia Giorgina7,Baccarani Michele8,Di Bona Eros9,Fioritoni Giuseppe10,Marmont Filippo11,Rambaldi Alessandro12,Di Raimondo Francesco13,Kropp Maria Grazia14,Pizzolo Giovanni15,Pogliani Enrico M.16,Rossi Giuseppe17,Cantore Nicola18,Nobile Francesco19,Gabbas Attilio20,Ferrara Felicetto21,Fazi Paola4,Amadori Sergio2,Mandelli Franco4,

Affiliation:

1. Unità Operativa Complessa di Ematologia e Terapia Cellulare, Università Campus Bio-Medico, Roma, Italy;

2. Dipartimento di Bipatologia, Università Tor Vergata, Roma, Italy;

3. Laboratorio di Neuro-Oncoematologia, Fondazione Santa Lucia, Roma, Italy;

4. Fondazione GIMEMA-ONLUS, Roma, Italy;

5. Divisione di Ematologia, Istituto Nazionale per i Tumori Regina Elena, Roma, Italy;

6. Dipartimento di Biotecnologie Cellulari ed Ematologia, Università Sapienza, Roma, Italy;

7. Unità Operativa Ematologia 1, Università degli Studi, Bari, Italy;

8. Istituto di Ematologia ed Oncologia Medica L.e A. Seràgnoli, Università degli Studi, Bologna, Italy;

9. Divisione di Ematologia, Ospedale S. Bortolo, Vicenza, Italy;

10. Unità Operativa Ematologia Clinica, Azienda USL, Pescara, Italy;

11. Divisione di Ematologia Molinette, Ospedale Maggiore S.G. Battista, Torino, Italy;

12. Divisione di Ematologia, Ospedali Riuniti, Bergamo, Italy;

13. Divisione di Ematologia, Ospedale Ferrarotto, Università degli Studi, Catania, Italy;

14. Unità Operativa Ematologia, Azienda Ospedaliera Pugliese Ciaccio, Catanzaro, Italy;

15. Divisione di Ematologia, Policlinico G.B. Rossi, Università degli Studi, Verona, Italy;

16. Clinica Ematologica, Università Milano Bicocca, Nuovo Ospedale S. Gerardo dei Tintori, Monza, Italy;

17. Divisione di Ematologia, Spedali Civili, Brescia, Italy;

18. Divisione di Ematologia, Azienda Ospedaliera S. G. Moscati, Avellino, Italy;

19. Dipartimento Ematologia-Oncologia, Azienda Ospedaliera Bianchi-Melacrino-Morelli, Reggio Calabria, Italy;

20. Divisione di Ematologia, Ospedale S. Francesco, Nuoro, Italy; and

21. Divisione di Ematologia, Azienda Ospedaliera di Rilievo Nazionale, A. Cardarelli, Napoli, Italy

Abstract

Abstract All-trans-retinoic acid (ATRA) has greatly modified the prognosis of acute promyelocytic leukemia; however, the role of maintenance in patients in molecular complete remission after consolidation treatment is still debated. From July 1993 to May 2000, 807 genetically proven newly diagnosed acute promyelocytic leukemia patients received ATRA plus idarubicin as induction, followed by 3 intensive consolidation courses. Thereafter, patients reverse-transcribed polymerase chain reaction–negative for the PML-RARA fusion gene were randomized into 4 arms: oral 6-mercaptopurine and intramuscular methotrexate (arm 1); ATRA alone (arm 2); 3 months of arm1 alternating to 15 days of arm 2 (arm 3); and no further therapy (arm 4). Starting from February 1997, randomization was limited to ATRA-containing arms only (arms 2 and 3). Complete remission was achieved in 761 of 807 (94.3%) patients, and 681 completed the consolidation program. Of these, 664 (97.5%) were evaluated for the PML-RARA fusion gene, and 586 of 646 (90.7%) who tested reverse-transcribed polymerase chain reaction–negative were randomized to maintenance. The event-free survival estimate at 12 years was 68.9% (95% confidence interval, 66.4%-71.4%), and no differences in disease-free survival at 12 years were observed among the maintenance arms.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference38 articles.

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

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