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Clinical networking results in continuous improvement of the outcome of patients with acute promyelocytic leukemia.
Koury, Luisa Corrêa de Araujo; Kim, Haesook T; Undurraga, Maria Soledad; Navarro-Cabrera, Juan Ramon; Salinas, Victor; Muxi, Pablo; Melo, Raul A M; Gloria, Ana Beatriz F; Pagnano, Katia B B; Nunes, Elenaide C; Bittencourt, Rosane Isabel; Rojas, Ninoska; Quintana Truyenque, Shirley Milenca; Ayala-Lugo, Ana Ilda; Oliver, Ana Carolina; de Figueiredo-Pontes, Lorena Lobo; Traina, Fabiola; Moreira, Frederico; Fagundes, Evandro M; Duarte, Bruno Kosa L; Mora-Alferez, Analí Pamela; Ortiz, Percy; Untama, Jose Luis; Tallman, Martin S; Ribeiro, Raul C; Ganser, Arnold; Dillon, Richard James; Valk, Peter J M; Sanz, Miguel A; Löwenberg, Bob; Berliner, Nancy; Rego, Eduardo M.
Affiliation
  • Koury LCA; University of São Paulo, Ribeirão Preto, Brazil.
  • Kim HT; Dana-Farber Cancer Inst., Boston, Massachusetts, United States.
  • Undurraga MS; Hospital del Salvador, Santiago, Chile.
  • Navarro-Cabrera JR; Edgardo Rebagliati Hospital, Lima, Peru.
  • Salinas V; Instituto de Previsión Social, Asunción, Paraguay.
  • Muxi P; Hospital Britanico, Montevideo, Uruguay.
  • Melo RAM; University of Pernambuco - UPE, Recife, Brazil.
  • Gloria ABF; Federal University of Minas Gerais, Belo Horizonte, Brazil.
  • Pagnano KBB; Universidade Estadual de Campinas (UNICAMP), Campinas, Brazil.
  • Nunes EC; Federal University of Parana, CURITIBA, Brazil.
  • Bittencourt RI; Hospital Clinicas de Porto Alegre, Porto Alegre, Brazil.
  • Rojas N; Edgardo Rebagliati Hospital, Lima, Peru.
  • Quintana Truyenque SM; Instituto Nacional de Enfermedades Neoplásicas, Lima, Peru.
  • Ayala-Lugo AI; Universidad Nacional de Asuncion. Instituto de Investigaciones en Ciencias de la Salud, San Lorenzo, Paraguay.
  • Oliver AC; Hospital Británico, Montevideo, Uruguay.
  • de Figueiredo-Pontes LL; Ribeirao Preto Medical School, Ribeirao Preto, Brazil.
  • Traina F; University of São Paulo at Ribeirão Preto Medical School, Ribeirão Preto, Brazil.
  • Moreira F; Hospital das Clinicas da Universidade de Sao Paulo, Sao Paulo, Brazil.
  • Fagundes EM; Hospital das Clínicas - Federal University of MInas Gerais, Belo Horizonte, Brazil.
  • Duarte BKL; University of Campinas, Campinas, Brazil.
  • Mora-Alferez AP; Instituto Nacional de Enfermedades Neoplásicas, Lima, Peru.
  • Ortiz P; Edgardo Rebagliati Martins National Hospital, Lima, Peru.
  • Untama JL; Edgardo Rebagliati Hospital, Lima, Peru.
  • Tallman MS; Memorial Sloan Kettering Cancer Center, Highland Park, Illinois, United States.
  • Ribeiro RC; St. Jude Children's Research Hospital, Memphis, Tennessee, United States.
  • Ganser A; Hannover Medical School, Hannover, Germany.
  • Dillon RJ; King's College, London, London, United Kingdom.
  • Valk PJM; Erasmus University Medical Center, Rotterdam, Netherlands.
  • Sanz MA; Valencia University Medical School, Spain.
  • Löwenberg B; Department of Hematology, Erasmus MC, Rotterdam, The Netherlands, Rotterdam, Netherlands.
  • Berliner N; Brigham and Women's Hospital, Boston, Massachusetts, United States.
  • Rego EM; University of São Paulo, Faculdade de Medicina, São Paulo, Brazil.
Blood ; 2024 May 28.
Article in En | MEDLINE | ID: mdl-38805638
ABSTRACT
The introduction of all-trans retinoic acid (ATRA) combined with anthracyclines has significantly improved the outcomes for patients with acute promyelocytic leukemia (APL), and this strategy remains the standard of care in countries where arsenic trioxide is not affordable. However, data from national registries and real-world databases indicate that low- and middle-income countries (LMIC) still face disappointing results, mainly due to high induction mortality and suboptimal management of complications. The American Society of Hematology established the International Consortium on Acute Leukemias (ICAL) to address this challenge through international clinical networking. Here, we present the findings from the ICAPL study involving 806 patients with APL recruited in Brazil, Chile, Paraguay, Peru, and Uruguay. The induction mortality rate has decreased to 14.6% compared to the pre-ICAL rate of 32%. Multivariable logistic regression analysis revealed as factors associated with induction death age ≥ 40 years, ECOG = 3, high-risk status based on the PETHEMA/GIMEMA classification, albumin level ≤ 3.5 g/dL, bcr3 PML/RARA isoform, the interval between presenting symptoms to diagnosis exceeding 48 hours, and the occurrence of central nervous system and pulmonary bleeding. With a median follow-up of 53 months, the estimated 4-year overall survival (OS) rate is 81%, the 4-year disease-free survival (DFS) rate is 80%, and the 4-year cumulative incidence of relapse (CIR) rate is 15%. These results parallel those observed in studies conducted in high-income countries, highlighting the long-term effectiveness of developing clinical networks to improve clinical care and infrastructure in LMIC.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Blood Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Blood Year: 2024 Document type: Article Affiliation country:
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