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Journal of Clinical Oncology, Vol 19, Issue 20 (October), 2001: 4023-4028
© 2001 American Society for Clinical Oncology

Extramedullary Involvement at Relapse in Acute Promyelocytic Leukemia Patients Treated or Not With All-Trans Retinoic Acid: A Report by the Gruppo Italiano Malattie Ematologiche dell’Adulto

By Giorgina Specchia, Francesco Lo Coco, Marco Vignetti, Giuseppe Avvisati, Paola Fazi, Francesco Albano, Francesco Di Raimondo, Bruno Martino, Felicetto Ferrara, Carmine Selleri, Vincenzo Liso, Franco Mandelli

From the Department of Hematology, University of Bari, Bari; Dipartimento di Biotecnologie Cellulari ed Ematologia, Università "La Sapienza," and Ematologia, Università "Campus Bio-Medico," Rome; Divisione di Ematologia, Ospedale Ferrarotto, Catania; Divisione di Ematologia-Oncologia, Azienda Ospedale "Bianchi-Melacrino-Morelli," Reggio Calabria; and Divisione di Ematologia, Ospedale "A. Cardarelli," and Ematologia, "Università Federico II," Naples, Italy.

Address reprint requests to G. Specchia, MD, Department of Hematology, University of Bari, Policlinico, Piazza G. Cesare 11, 70124 Bari, Italy; email: emadhba{at}cimedoc.uniba.it

PURPOSE: Recent reports of extramedullary disease (EMD) at recurrence in acute promyelocytic leukemia (APL) have raised increasing concern about a possible role of retinoic acid (RA) therapy.

PATIENTS AND METHODS: We analyzed the risk of developing EMD localization at relapse in APL patients enrolled onto two consecutive studies of the Gruppo Italiano Malattie Ematologiche dell’Adulto. The studies investigated chemotherapy alone (LAP0389) versus RA plus chemotherapy (AIDA).

RESULTS: When all relapse types were taken into account, 94 (51%) of 184 patients and 131 (18%) of 740 patients who attained hematologic remission underwent relapse in the LAP0389 and AIDA studies, respectively (P < .0001). EMD localization was documented in five (5%) of 94 and 16 (12%) of 131 patients (P = .08). Hematologic and/or molecular relapse was diagnosed concomitantly in all but two patients with EMD in the AIDA study. For patients in the LAP0389 and AIDA series, the probability of EMD localization of any type at relapse was 3% and 4.5%, respectively (P = .79), while the probability of CNS involvement was 0.6% and 2% (P = .28). No significant differences were found with regard to mean WBC count and promyelocytic leukemia/retinoic acid receptor-alpha junction type in comparisons of patients with EMD and hematologic relapse.

CONCLUSION: APL patients receiving all-trans retinoic acid in addition to chemotherapy have no increased risk of developing EMD at relapse as compared with those treated with chemotherapy alone.


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