Improving acute promyelocytic leukemia (APL) outcome in developing countries through networking, results of the International Consortium on APL

Eduardo Magalhães Rego(Universidade de São Paulo), Haesook T. Kim(Dana-Farber Cancer Institute), Guillermo J. Ruíz‐Argüelles(Clínica Ruiz), María Soledad Undurraga(Hospital del Salvador), Marı́a del Rosario Uriarte, Rafael Henriques Jácomo(Universidade de São Paulo), Cesar Homero Gutiérrez‐Aguirre(Hospital Universitario Dr José Eleuterio Gonzalez), Raul Antônio Morais Melo(Fundação Hemopa), Rosane Bittencourt(Universidade Federal do Rio Grande do Sul), Ricardo Pasqüini(Universidade Federal do Paraná), Kátia Bórgia Barbosa Pagnano(Universidade Estadual de Campinas (UNICAMP)), Evandro M. Fagundes(Universidade Federal de Minas Gerais), Maria de Lourdes Chauffaille(Universidade Federal de São Paulo), Carlos Chiattone(Santa Casa Hospital), Lem Martínez, Luis Meillón(Centro Medico Nacional Siglo XXI), David Gómez‐Almaguer(Hospital Universitario Dr José Eleuterio Gonzalez), Hau C. Kwaan(Northwestern University), Javier Garcés‐Eisele(Clínica Ruiz), Robert E. Gallagher(Albert Einstein College of Medicine), Charlotte M. Niemeyer(University Medical Center Freiburg), Stanley L. Schrier(Stanford University), Martin S. Tallman(Memorial Sloan Kettering Cancer Center), David Grimwade(King's College London), Arnold Ganser(Medizinische Hochschule Hannover), Nancy Berliner(Brigham and Women's Hospital), Raul C. Ribeiro(St. Jude Children's Research Hospital), Francesco Lo‐Coco(University of Rome Tor Vergata), Bob Löwenberg(Erasmus MC), Miguel Á. Sanz(Hospital Universitari i Politècnic La Fe)
Blood
January 14, 2013
Cited by 152Open Access
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Abstract

Thanks to modern treatment with all-trans retinoic acid and chemotherapy, acute promyelocytic leukemia (APL) is now the most curable type of leukemia. However, this progress has not yielded equivalent benefit in developing countries. The International Consortium on Acute Promyelocytic Leukemia (IC-APL) was established to create a network of institutions in developing countries that would exchange experience and data and receive support from well-established US and European cooperative groups. The IC-APL formulated expeditious diagnostic, treatment, and supportive guidelines that were adapted to local circumstances. APL was chosen as a model disease because of the potential impact on improved diagnosis and treatment. The project included 4 national coordinators and reference laboratories, common clinical record forms, 5 subcommittees, and laboratory and data management training programs. In addition, participating institutions held regular virtual and face-to-face meetings. Complete hematological remission was achieved in 153/180 (85%) patients and 27 (15%) died during induction. After a median follow-up of 28 months, the 2-year cumulative incidence of relapse, overall survival (OS), and disease-free survival (DFS) were 4.5%, 80%, and 91%, respectively. The establishment of the IC-APL network resulted in a decrease of almost 50% in early mortality and an improvement in OS of almost 30% compared with historical controls, resulting in OS and DFS similar to those reported in developed countries.


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