Tratamento do mieloma múltiplo com VMCP: revisão de 52 casos

Detalhes bibliográficos
Autor(a) principal: Pinto, Carlos Frederico Distéfano
Data de Publicação: 2023
Outros Autores: 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.
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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spelling 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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status_str publishedVersion
dc.identifier.uri.fl_str_mv https://rbc.inca.gov.br/index.php/revista/article/view/3005
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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
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dc.relation.none.fl_str_mv https://rbc.inca.gov.br/index.php/revista/article/view/3005/1870
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dc.publisher.none.fl_str_mv INCA
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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
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institution INCA
reponame_str Revista Brasileira de Cancerologia (Online)
collection Revista Brasileira de Cancerologia (Online)
repository.name.fl_str_mv Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
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