Tratamento do mieloma múltiplo com VMCP: revisão de 52 casos
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Revista Brasileira de Cancerologia (Online) |
Texto Completo: | https://rbc.inca.gov.br/index.php/revista/article/view/3005 |
Resumo: | Fifty-two patients were treated for multiple myeloma between November 1987andAugust 1992 at the Santa Casa de Misericórdia de Belo Horizonte General Hospital with VMCP (vincristine, melphalan, cyclophosphamide and prednisone) every28 days. Twenty-six patients with bone lesions received palliative radiotherapy. Fifteen (28.8%) were stage IIIA; 32 (61.5%) stage IIIB; five (7.6%) stage I and II by the Salmon and Durie staging system, as used by the SWOG. The response criteria used, when available, was also the proposed by SWOG. Seven patients reached the complete remission, 12 partial remission, 20had stable disease and 13 had progressiva disease. The overall survival was 41 months. Toxicity was well tolerated in the majority of the group. Grade 3-4 toxicity was reached at least once in 30.8%. Three patients died of neutropenic sepsis and 1 of gastrointestinal toxicity. Eight patients are lost of follow-up. The authors considered the actual regimen safe and with satisfactory results. |
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Tratamento do mieloma múltiplo com VMCP: revisão de 52 casosMieloma MúltiploPoliquimioterapiaFatores PrognósticosMultiple MyelomaChemotherapyPrognostic FactorsFifty-two patients were treated for multiple myeloma between November 1987andAugust 1992 at the Santa Casa de Misericórdia de Belo Horizonte General Hospital with VMCP (vincristine, melphalan, cyclophosphamide and prednisone) every28 days. Twenty-six patients with bone lesions received palliative radiotherapy. Fifteen (28.8%) were stage IIIA; 32 (61.5%) stage IIIB; five (7.6%) stage I and II by the Salmon and Durie staging system, as used by the SWOG. The response criteria used, when available, was also the proposed by SWOG. Seven patients reached the complete remission, 12 partial remission, 20had stable disease and 13 had progressiva disease. The overall survival was 41 months. Toxicity was well tolerated in the majority of the group. Grade 3-4 toxicity was reached at least once in 30.8%. Three patients died of neutropenic sepsis and 1 of gastrointestinal toxicity. Eight patients are lost of follow-up. The authors considered the actual regimen safe and with satisfactory results.Cinqüenta e dois pacientes estudados entre novembro de 1987 e agosto de 1992 tendo sido submetidos a um ou mais ciclos de quimioterapia com VMCP (vincristina 2 mg IV dl; melphalan 4 mg/m2 VO d2-5; ciclofosfamida 100 mg/rrf VO d2-5 e prednisona 100 mg VO d2-5 - repetidos a cada 28 dias, ou conforme a toxicidade hematológica). Vinte e seis pacientes foram submetidos a radioterapia concomitante. Foi utilizado o estadiamento proposto pelo SWOG (Durie e Salmon, 1975), onde 15 (28,8%) pacientes foram estadiados como IIIA e 32 (61,5%) como IIIB, quatro (7,4%>) como II e um (2,2%) como I. Os critérios de resposta foram os mesmos adotados pelo SWOG; porém, consideramos também como Resposta Parcial (RP) a melhora do PS em um ponto ou mais. Sete pacientes entraram em Remissão Completa, 12 em Remissão Parcial e 20 foram considerados com Doença Está vele 13 não responderam ao tratamento. A Sobrevida Mediana para todos os pacientes, calculada pelo método de Kaplan-Meier, foi de 41 meses. A toxicidade foi tolerável na maioria dos pacientes, sendo grau 3-4 em 16 (30,8%) pacientes em pelo menos um episódio. A principal toxicidade dose limitante foi hematológica. Três pacientes morreram por leucopenia e infecção e um por toxicidade gastrointestinal (7,6%>). Oito pacientes estão perdidos do follow-up. Os autores consideram o esquema eficaz e com resultados compatíveis com os da literatura, com toxicidade dentro das expectativas.INCA2023-06-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionRelato de Casoapplication/pdfhttps://rbc.inca.gov.br/index.php/revista/article/view/300510.32635/2176-9745.RBC.1994v40n4.3005Revista Brasileira de Cancerologia; Vol. 40 No. 4 (1994): Oct./Nov./Dec.; 207-213Revista Brasileira de Cancerologia; Vol. 40 Núm. 4 (1994): oct./nov./dic.; 207-213Revista Brasileira de Cancerologia; v. 40 n. 4 (1994): out./nov./dez.; 207-2132176-9745reponame:Revista Brasileira de Cancerologia (Online)instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)instacron:INCAporhttps://rbc.inca.gov.br/index.php/revista/article/view/3005/1870https://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessPinto, Carlos Frederico Distéfano Silva, Alexandre J. Fenelon Moreira, Wagner Brant Cabral Filho, SebastiãoNascimento, EduardoLopes, Eugênio B. Brandão, Eduardo C.Teixeira, João Augusto M.Vieira, Maria do CarmoAlvares, Maria N.Novaes, Nedda Maria V.2023-06-19T13:30:23Zoai:rbc.inca.gov.br:article/3005Revistahttps://rbc.inca.gov.br/index.php/revistaPUBhttps://rbc.inca.gov.br/index.php/revista/oairbc@inca.gov.br0034-71162176-9745opendoar:2023-06-19T13:30:23Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)false |
dc.title.none.fl_str_mv |
Tratamento do mieloma múltiplo com VMCP: revisão de 52 casos |
title |
Tratamento do mieloma múltiplo com VMCP: revisão de 52 casos |
spellingShingle |
Tratamento do mieloma múltiplo com VMCP: revisão de 52 casos Pinto, Carlos Frederico Distéfano Mieloma Múltiplo Poliquimioterapia Fatores Prognósticos Multiple Myeloma Chemotherapy Prognostic Factors |
title_short |
Tratamento do mieloma múltiplo com VMCP: revisão de 52 casos |
title_full |
Tratamento do mieloma múltiplo com VMCP: revisão de 52 casos |
title_fullStr |
Tratamento do mieloma múltiplo com VMCP: revisão de 52 casos |
title_full_unstemmed |
Tratamento do mieloma múltiplo com VMCP: revisão de 52 casos |
title_sort |
Tratamento do mieloma múltiplo com VMCP: revisão de 52 casos |
author |
Pinto, Carlos Frederico Distéfano |
author_facet |
Pinto, Carlos Frederico Distéfano Silva, Alexandre J. Fenelon Moreira, Wagner Brant Cabral Filho, Sebastião Nascimento, Eduardo Lopes, Eugênio B. Brandão, Eduardo C. Teixeira, João Augusto M. Vieira, Maria do Carmo Alvares, Maria N. Novaes, Nedda Maria V. |
author_role |
author |
author2 |
Silva, Alexandre J. Fenelon Moreira, Wagner Brant Cabral Filho, Sebastião Nascimento, Eduardo Lopes, Eugênio B. Brandão, Eduardo C. Teixeira, João Augusto M. Vieira, Maria do Carmo Alvares, Maria N. Novaes, Nedda Maria V. |
author2_role |
author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Pinto, Carlos Frederico Distéfano Silva, Alexandre J. Fenelon Moreira, Wagner Brant Cabral Filho, Sebastião Nascimento, Eduardo Lopes, Eugênio B. Brandão, Eduardo C. Teixeira, João Augusto M. Vieira, Maria do Carmo Alvares, Maria N. Novaes, Nedda Maria V. |
dc.subject.por.fl_str_mv |
Mieloma Múltiplo Poliquimioterapia Fatores Prognósticos Multiple Myeloma Chemotherapy Prognostic Factors |
topic |
Mieloma Múltiplo Poliquimioterapia Fatores Prognósticos Multiple Myeloma Chemotherapy Prognostic Factors |
description |
Fifty-two patients were treated for multiple myeloma between November 1987andAugust 1992 at the Santa Casa de Misericórdia de Belo Horizonte General Hospital with VMCP (vincristine, melphalan, cyclophosphamide and prednisone) every28 days. Twenty-six patients with bone lesions received palliative radiotherapy. Fifteen (28.8%) were stage IIIA; 32 (61.5%) stage IIIB; five (7.6%) stage I and II by the Salmon and Durie staging system, as used by the SWOG. The response criteria used, when available, was also the proposed by SWOG. Seven patients reached the complete remission, 12 partial remission, 20had stable disease and 13 had progressiva disease. The overall survival was 41 months. Toxicity was well tolerated in the majority of the group. Grade 3-4 toxicity was reached at least once in 30.8%. Three patients died of neutropenic sepsis and 1 of gastrointestinal toxicity. Eight patients are lost of follow-up. The authors considered the actual regimen safe and with satisfactory results. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-06-05 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Relato de Caso |
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article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://rbc.inca.gov.br/index.php/revista/article/view/3005 10.32635/2176-9745.RBC.1994v40n4.3005 |
url |
https://rbc.inca.gov.br/index.php/revista/article/view/3005 |
identifier_str_mv |
10.32635/2176-9745.RBC.1994v40n4.3005 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://rbc.inca.gov.br/index.php/revista/article/view/3005/1870 |
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https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
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https://creativecommons.org/licenses/by/4.0 |
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openAccess |
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INCA |
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INCA |
dc.source.none.fl_str_mv |
Revista Brasileira de Cancerologia; Vol. 40 No. 4 (1994): Oct./Nov./Dec.; 207-213 Revista Brasileira de Cancerologia; Vol. 40 Núm. 4 (1994): oct./nov./dic.; 207-213 Revista Brasileira de Cancerologia; v. 40 n. 4 (1994): out./nov./dez.; 207-213 2176-9745 reponame:Revista Brasileira de Cancerologia (Online) instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) instacron:INCA |
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Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) |
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INCA |
institution |
INCA |
reponame_str |
Revista Brasileira de Cancerologia (Online) |
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Revista Brasileira de Cancerologia (Online) |
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Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) |
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rbc@inca.gov.br |
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