Roberto José Pessoa de Magalhães Filho1, Edvan Crusoe2, Eloisa Riva3, Willen Bujan4, Guilhermo Conte5, Juan Ramon Navarro Cabrera6, Diana Katerine Garcia7, Guilhermo Quintero Vega8, Jose Macias9, Jose Willian Oliveros Alvear10, Mercedes Royg11, Lidiane Andino Neves12, Jose Luis Lopez Dopico13, German Espino14, Douglas Rosales Ortiz15, Zurelis Socarra16, Dorotea Fantl17, Guillermo J Ruiz-Arguelles18, Angelo Maiolino19, Vania Tietsche de Moraes Hungria20, Jean-Luc Harousseau21, Brian Durie22. 1. Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil. Electronic address: robmag@hucff.ufrj.br. 2. Universidade Federal da Bahia, Salvador, Brazil. 3. Hospital de clinicas de Uruguay, Montevideo, Uruguay. 4. Universidad Costa Rica, San Jose, Costa Rica. 5. Hospital Clinico de la Universidad del Chile, Santiago, Chile. 6. Hospital Edgardo Rebagliati, Lima, Peru. 7. Instituto de Oncologia Dr Heriberto Pieter (IOHP), Santo Domingo, Dominican Republic. 8. Fundacion de Santa Fe de Bogota, Bogota, Colombia. 9. Universidad Mayor de San Simon, Cochabamba, Bolivia. 10. Universidad de Guayaquil, Guayaquil, Ecuador. 11. Hospital de Clinicas de Paraguay, Asuncion, Paraguay. 12. Hospital Central del Instituto de Prevision Social Paraguay, Asuncion, Paraguay. 13. Banco Municipal de Sangre DC, Caracas, Venezuela. 14. Complejo Hospitalario de la Caja de Seguro Social, Panama city, Panama. 15. Hospital Manolo Morales, Managua, Nicaragua. 16. Instituto de Hematologia y Oncologia Cuba, Habana, Cuba. 17. Hospital Italiano de Buenos Aires, Caba, Buenos Aires, Argentina. 18. Centro de Hematologia y Medicina Interna Mexico, Puebla, Mexico. 19. Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil. 20. Irmandade Santa Casa de Misericordia de Sao Paulo, Sao Paulo, Brazil. 21. Groupe Confluent, Nantes, France. 22. Cedar-Sinai Medical Center, Los Angeles, CA.
Abstract
INTRODUCTION: Latin American countries (LATAMC) represent a large fraction of patients treated for multiple myeloma (MM) worldwide. In order to understand the difficulty of access to anti-myeloma therapy in LATAMC, we designed this study that explores areas involved in the availability of drugs, such as health care systems, approval times, coverage of new agents, old drugs, use of generics, and the first-line treatments. MATERIAL AND METHODS: We collected data from 16 countries in 2015. RESULTS: The majority of LATAMC (88%; n = 14) had mixed public and private coverage, with patients with MM cared for in public institutions. Although bortezomib and lenalidomide were approved in 100% and 73% in LATAMC, these figures did not translate to real-world practice as one-half of the nations reported unequal access to the new agents (thalidomide, bortezomib, and lenalidomide) in both public and private systems. Conversely, cheaper old drugs, represented by melphalan, were not available commercially in 44% (n = 7) of nations. Thus, first-line MM treatments for old and young patients in public practice were triplets with thalidomide-alkylating agent-steroid, whereas in private practice, treatments involved bortezomib-alkylating agent-steroid. An alarming rate of 30% of the nations reported suboptimal regimens (eg, VAD [vincristine, adriamycin, and dexamethasone]) or the impossibility of transplantation. CONCLUSION: Our data indicates that bortezomib and transplant are still an unmet medical necessity in public systems. In the complex puzzle of myeloma drug access in LATAMC, important issues, such as the adjustment of disparities between health systems, the incorporation of new drugs with an economic cost-effectiveness view, and the re-establishment of essential old drugs, can be a platform to the future.
INTRODUCTION: Latin American countries (LATAMC) represent a large fraction of patients treated for multiple myeloma (MM) worldwide. In order to understand the difficulty of access to anti-myeloma therapy in LATAMC, we designed this study that explores areas involved in the availability of drugs, such as health care systems, approval times, coverage of new agents, old drugs, use of generics, and the first-line treatments. MATERIAL AND METHODS: We collected data from 16 countries in 2015. RESULTS: The majority of LATAMC (88%; n = 14) had mixed public and private coverage, with patients with MM cared for in public institutions. Although bortezomib and lenalidomide were approved in 100% and 73% in LATAMC, these figures did not translate to real-world practice as one-half of the nations reported unequal access to the new agents (thalidomide, bortezomib, and lenalidomide) in both public and private systems. Conversely, cheaper old drugs, represented by melphalan, were not available commercially in 44% (n = 7) of nations. Thus, first-line MM treatments for old and young patients in public practice were triplets with thalidomide-alkylating agent-steroid, whereas in private practice, treatments involved bortezomib-alkylating agent-steroid. An alarming rate of 30% of the nations reported suboptimal regimens (eg, VAD [vincristine, adriamycin, and dexamethasone]) or the impossibility of transplantation. CONCLUSION: Our data indicates that bortezomib and transplant are still an unmet medical necessity in public systems. In the complex puzzle of myeloma drug access in LATAMC, important issues, such as the adjustment of disparities between health systems, the incorporation of new drugs with an economic cost-effectiveness view, and the re-establishment of essential old drugs, can be a platform to the future.
Authors: Maira A Castañeda-Avila; Karen J Ortiz-Ortiz; Carlos R Torres-Cintrón; Brenda M Birmann; Mara M Epstein Journal: Int J Cancer Date: 2019-03-30 Impact factor: 7.396
Authors: Heinz Ludwig; Wolfram Poenisch; Stefan Knop; Alexander Egle; Martin Schreder; Daniel Lechner; Roman Hajek; Eberhard Gunsilius; Karl Jochen Krenosz; Andreas Petzer; Katja Weisel; Dietger Niederwieser; Hermann Einsele; Wolfgang Willenbacher; Thomas Melchardt; Richard Greil; Niklas Zojer Journal: Br J Cancer Date: 2019-09-27 Impact factor: 7.640
Authors: Vania Tietsche de Moraes Hungria; Deborah M Martínez-Baños; Christian R Peñafiel; Carlos E Miguel; Jorge Vela-Ojeda; Guillermina Remaggi; Fernando B Duarte; Carmen Cao; Maria S Cugliari; Telma Santos; Gerardo Machnicki; Mariana Fernandez; Mariana Grings; Eric M Ammann; Jennifer H Lin; Yen-Wen Chen; Yu-Ning Wong; Paula Barreyro Journal: Br J Haematol Date: 2019-08-07 Impact factor: 6.998