Skip navigation
Universidade Federal da Bahia |
Repositório Institucional da UFBA
Use este identificador para citar ou linkar para este item: https://repositorio.ufba.br/handle/ri/40887
Registro completo de metadados
Campo DCValorIdioma
dc.creatorOliveira, Lucas Villasboas de-
dc.date.accessioned2025-01-13T16:06:44Z-
dc.date.available2025-01-13T16:06:44Z-
dc.date.issued2024-12-18-
dc.identifier.citationOLIVEIRA, Lucas Villasboas de. Dose de prednisona usada no tratamento de linfoma difuso de grandes células B, uma revisão sistemática e metanálise. Orientadora: Juliana de Andrade Santos; Coorientador: Alessandro de Moura Almeida. 2024. 25 f. Trabalho de Conclusão de Curso (Especialização em Hematologia e Hemoterapia) - Programa Residência Medica, Hospital Universitário Professor Edgard Santos, Faculdade de Medicina da Bahia, Universidade Federal da Bahia, Salvador, 2024.pt_BR
dc.identifier.urihttps://repositorio.ufba.br/handle/ri/40887-
dc.description.abstractBackground: Chemoimmunotherapy using rituximab, cyclophosphamide, doxorubicin hydrochloride (hydroxydaunomycin), vincristine sulfate (Oncovin), and prednisone (R-CHOP) has been the standard of care treatment of DLBCL for over 20 years. Despite its widespread usage, there is no accepted standard for the dose of prednisone in this setting which varies from fixed dose (100mg daily for 5 days) to different levels of BSA-adjusted dosage (ranging from 40-100 mg/m2 daily for 5 days). BSA-adjusted dosage results in high doses of prednisone administered to patients with increased body surface area which may lead to significant adverse events. We performed a systematic review and meta-analysis to determine if fixeddose prednisone during R CHOP therapy results in equivalent outcomes compared to BSA adjusted dosing. Methods: A comprehensive search of several databases from each database's inception to April 29th, 2024, English language, was conducted. The databases included Ovid MEDLINE and Epub Ahead of Print, In-Process & Other Non-Indexed Citations, and Daily, Ovid EMBASE, Ovid Cochrane Central Register of Controlled Trials, Ovid Cochrane Database of Systematic Reviews, and Scopus. The search strategy was designed and conducted by an experienced librarian with input from the study's principal investigator. Controlled vocabulary supplemented with keywords was used to search for prospective clinical studies of R-CHOP for adult patients with untreated DLBCL. Search results were reviewed independently by 2 members of the study team for final inclusion. Discrepancies were adjudicated by a third member and reviewed by the senior author. Prednisone dosage and clinical outcomes were abstracted from the available public data. Meta-analysis was performed using the metafor package in R version 4.2.2 by applying a mixed effects model to combine results from the multiple studies. The analysis was first conducted overall to determine the general effect, and then stratified by prednisone dose (fixed- vs. BSAadjusted) to explore dose-dependent variations in outcomes. Results: Our search resulted in 2287 entries which were individually reviewed by the study team. A total of 30 studies with a combined sample size of 3573 treated patients fulfilled the inclusion criteria and were included in the final analysis set. Nineteen (63%) studies with a combined sample size of 1930 patients (median 155, range 12-399) used fixed-dose prednisone. Eleven (37%) studies with a combined sample size of 1643 patients (median 70, range 9-439) used BSA-adjusted dosing. Overall survival at 2 years for all studies was 84% (SD 78%-91%) and did not differ between fixed-dose (88%, SD 79%-97%) and BSA-adjusted dose (82%, 73%-91%). Progression-free survival at 2 years for all studies was 77% (SD 68%-85%) and did not differ between fixed-dose (80%, SD 68%-93%) and BSA-adjusted dose (74%, SD 62%-86%). Complete response rate for all studies was 70% (SD 61%-80%) and did not differ between fixed-dose (67%, SD 54%-81%) and BSA-adjusted dose (77%, SD 64%-89%). Conclusion: The result of our systematic review and meta-analysis combining 30 prospective studies and a total of 3573 patients with newly diagnosed DLBCL treated with frontline R-CHOP found no difference in clinical outcomes between patients treated with fixed-dose and BSA-adjusted dose prednisone. Our findings provide scientific evidence for the widespread practice of capping prednisone at the maximum dose of 100 mg daily for 5 days, potentially avoiding unnecessary adverse effects from BSA-adjusted dosing.pt_BR
dc.languageporpt_BR
dc.publisherUniversidade Federal da Bahiapt_BR
dc.rightsAcesso Abertopt_BR
dc.subjectLinfoma Difuso de Grandes Células Bpt_BR
dc.subjectPrednisonapt_BR
dc.subjectDosagempt_BR
dc.subjectEnsaio clínico randomizadopt_BR
dc.subjectEnsaios Clínicos Controlados Aleatórios como Assuntopt_BR
dc.subject.otherLymphoma, Large B-Cell, Diffusept_BR
dc.subject.otherPrednisonept_BR
dc.subject.otherDosagept_BR
dc.subject.otherRandomized controlled trialspt_BR
dc.subject.otherRandomized Controlled Trials as Topicpt_BR
dc.titleDose de prednisona usada no tratamento de linfoma difuso de grandes células B, uma revisão sistemática e metanálisept_BR
dc.title.alternativePrednisone dosing in diffuse large B-Cell lymphoma treatment: a systematic review and meta-analysispt_BR
dc.typeTrabalho de Conclusão de Cursopt_BR
dc.publisher.initialsUFBApt_BR
dc.publisher.countryBrasilpt_BR
dc.subject.cnpqCNPQ::CIENCIAS BIOLOGICASpt_BR
dc.subject.cnpqCNPQ::CIENCIAS DA SAUDE::MEDICINA::CLINICA MEDICA::HEMATOLOGIApt_BR
dc.contributor.advisor1Santos, Juliana de Andrade-
dc.contributor.advisor1Latteshttp://lattes.cnpq.br/2229346307055389pt_BR
dc.contributor.advisor-co1Almeida, Alessandro de Moura-
dc.contributor.advisor-co1Latteshttp://lattes.cnpq.br/2229346307055389pt_BR
dc.contributor.referee1Almeida, Alessandro de Moura-
dc.contributor.referee1Latteshttp://lattes.cnpq.br/2229346307055389pt_BR
dc.creator.Latteshttp://lattes.cnpq.br/9507260983830891pt_BR
dc.description.resumoIntrodução: A imunoquimioterapia utilizando rituximabe, ciclofosfamida, cloridrato de doxorrubicina (hidroxidaunomicina), sulfato de vincristina (Oncovin) e prednisona (R-CHOP) tem sido o tratamento padrão para o linfoma difuso de grandes células B (LDGCB) há mais de 20 anos. Apesar de seu uso disseminado, não há um padrão aceito na dose de prednisona nesse cenário. Há duas estratégias, a primeira com dose fixa (100mg diários por cinco dias) e a segunda com a dose ajustada pela área de superfície corpórea (ASC), que varia de 40-100mg/m² diários por cinco dias. Essa segunda estratégia resulta em altas doses de prednisona administradas a pacientes com área de superfície corporal aumentada, o que pode levar a eventos adversos significativos. Foi feita uma revisão sistemática e metanálise para determinar se a prednisona em dose fixa durante o tratamento com R-CHOP resultaria em desfechos equivalentes em comparação com a dose ajustada pela ASC. Métodos: Uma busca abrangente em várias bases de dados, na língua inglesa foi feita em junho de 2022 e atualizada em abril de 2024. As bases de dados incluiram: Ovid MEDLINE, Epub Ahead of Print, In-Process & Other Non-Indexed Citations and Daily, Ovid EMBASE, Ovid Cochrane Central Register of Controlled Trials, Ovid Cochrane Database of Systematic Reviews e Scopus. A estratégia de busca foi elaborada pelo investigador principal do estudo e conduzida por um bibliotecário experiente. Palavras-chaves foram usadas para buscar estudos clínicos prospectivos de pacientes adultos com diagnóstico de Linfoma Difuso de Grandes Células B e que nunca foram tratados com R-CHOP. Os resultados da busca foram revisados por dois membros da equipe, de forma independente para seleção e inclusão final. Discrepâncias foram resolvidas por um terceiro membro e revisadas pelo autor sênior. A dose de prednisona e os desfechos clínicos foram extraídos dos dados públicos disponíveis. A metanálise foi realizada usando o pacote metafor versão R 4.2.2, aplicando um modelo de efeitos mistos para combinar os resultados dos múltiplos estudos. A análise foi conduzida primeira de forma ampla para determinar o efeito geral e, em seguida, estratificada por dose de prednisona (fixa versus ajustada pela ASC) para explorar variações dependentes da dose nos desfechos. Resultados: Um total de 2287 artigos foi revisado individualmente pelos pesquisadores, e selecionados 30 estudos, com um tamanho amostral combinado de 3573 pacientes tratados, que atenderam aos critérios de inclusão para análise final. Dezenove (63%) estudos, com um tamanho amostral combinado de 1930 pacientes (mediana de 155, intervalo de 12-399), usaram prednisona em dose fixa. Onze (37%) estudos, com um tamanho amostral combinado de 1643 pacientes (mediana de 70, intervalo de 9-439), usaram a dose ajustada pela ASC. A sobrevida global (SG) em 2 anos para todos os estudos foi de 84% (DP 78%-91%) e não houve diferença entre a dose fixa (88%, DP 79%-97%) e a dose ajustada pela ASC (82%, 73%-91%). A progressão livre de doença (PLD) em dois anos para todos os estudos foi de 77% (DP 68%-85%) e não houve diferença entre a dose fixa (80%, DP 68%-93%) e a dose ajustada pela ASC (74%, DP 62%-86%). A taxa de resposta completa (TRC) para todos os estudos foi de 70% (DP 61%-80%) e não houve diferença entre a dose fixa (67%, DP 54%-81%) e a dose ajustada pela ASC (77%, DP 64%-89%). Conclusão: O resultado desta sistemática e metanálise, combinando 30 estudos prospectivos e um total de 3573 pacientes diagnosticados com LDGCB tratados com R-CHOP em primeira linha, não encontrou diferença nos desfechos clínicos entre pacientes tratados com prednisona em dose fixa e dose ajustada pela ASC. Essa revisão sistemática e metanálise fornecem evidências científicas para a prática disseminada de limitar a prednisona à dose máxima de 100mg diários por cinco dias, potencialmente evitando efeitos adversos desnecessários da dose ajustada pela ASC.pt_BR
dc.publisher.departmentFaculdade de Medicina da Bahiapt_BR
dc.relation.references1. Greer JP, Arber DA, Glader B, List AF, Means RT Jr, Rodgers GM, et al. Wintrobe's clinical hematology. 15th ed. Philadelphia: Wolters Kluwer; 2024. p. 6968. 2. Soffer B, Chihara D, Rosenwald A. Epidemiology, clinical manifestations, pathologic features, and diagnosis of diffuse large B-cell lymphoma. UpToDate [Internet]. 2022 Jul 29 [cited 2024 Dec 3]. Available from: https://www.uptodate.com/contents/epidemiology-clinical-manifestationspathologic-features-and-diagnosis-of-diffuse-large-b-celllymphoma?search=Epidemiology%2C%20clinical%20manifestations%2C%20 pathologic%20features%2C%20and%20diagnosis%20of%20diffuse%20large %20Bcell%20lymphoma&source=search_result&selectedTitle=1%7E122&usage_ty pe=default&display_rank=1 3. Galaznik A, Bell JA, Hamilton L, Ogbonnaya A, Hennenfent K, Eaddy MT, et al. Economic impact and healthcare utilization in patients with diffuse large Bcell lymphoma (DLBCL) in routine clinical care in the United States (US) - a claims database study. Blood. 2023;130(Suppl 1):2185. doi: 10.1182/blood2023-171479. 4. Coiffier B, Lepage E, Brière J, Herbrecht R, Tilly H, Bouabdallah R, et al. CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients 1 with diffuse large-B-cell lymphoma. N Engl J Med. 2002;346(4):23542. 5. Perini GF, Soares A. Outros tumores. In: Neto MC, et al. Guia de protocolos e medicamentos para tratamento em oncologia e hematologia. São Paulo: Hospital Israelita Albert Einstein; 2013. p. 139-54. 6. National Comprehensive Cancer Network. NCCN clinical practice guidelines in oncology: B-cell lymphomas [Internet]. Version 3.2024. 2024 [cited 2024 Dec 16]. Available from: https://www.nccn.org/guidelines/guidelinesdetail?category=1&id=1456 7. Collins G. R-CHOP-21/CHOP-21. NHS Thames Valley Strategic Clinical Network. 2023;1(7):1-8. 8. Armitage JO. How I treat patients with diffuse large B-cell lymphoma. Blood. 2007;110(1):29-36. 9. Melchardt T, Egle A, Greil R. How I treat diffuse large B-cell lymphoma. ESMO Open. 2023;8(1). 10. Saag K, Curtis JR, Saag MG. Major adverse effects of systemic glucocorticoids. UpToDate [Internet]. 2024 Jan 8 [cited 2024 Dec 3]. Available from: https://www.uptodate.com/contents/major-adverse-effects-of-systemicglucocorticoids?search=prednisone%20side%20effects&source=search_ result&selectedTitle=1%7E150&usage_type=default&display_r ank=1#H4 11. Waljee AK, Rogers MA, Lin P, Singal AG, Stein JD, Marks RM, et al. Short term use of oral corticosteroids and related harms among adults in the United States: population based cohort study. BMJ. 2017;357:j1415. 22 12. de Oliveira LV, Al-Jarrad A, Mwangi R, Moe C, Nedved AN, Hampel PJ, et al. Can I cap the prednisone? a systematic review and meta-analysis comparing fixed-dose with body surface area (BSA)-adjusted prednisone in untreated diffuse large B-cell lymphoma (DLBCL). Blood. 2024;144(Suppl 1):7588-9. doi: 10.1182/blood-2024-210544. 13. Tilly H, Morschhauser F, Sehn LH, Friedberg JW, Trněný M, Sharman JP, et al. Polatuzumab Vedotin in Previously Untreated Diffuse Large B-Cell Lymphoma. N Engl J Med. 2022;386(4):351-63. 14. Song Y, Zhou H, Zhang H, Liu W, Shuang Y, Zhou K, et al. Efficacy and Safety of the Biosimilar IBI301 Plus Standard CHOP (I-CHOP) in Comparison With Rituximab Plus CHOP (R-CHOP) in Patients with Previously Untreated Diffuse Large B-Cell Lymphoma (DLBCL): A Randomized, Double-Blind, Parallel-Group, Phase 3 Trial. Adv Ther. 2021;38(4):1889-1903. 15. Sancho JM, Fernández-Alvarez R, Gual-Capllonch F, et al. R-COMP versus R-CHOP as first-line therapy for diffuse large B-cell lymphoma in patients ≥60 years: Results of a randomized phase 2 study from the Spanish GELTAMO group. Cancer Med. 2021;10:1314-1326. https://doi.org/10.1002/cam4.3730 16. Hegazy SK, El-Haggar SM, Alhassanin SA, El-berri EI. Comparative randomized trial evaluating the effect of proton pump inhibitor versus histamine 2 receptor antagonist as 1 an adjuvant therapy in diffuse large B-cell lymphoma. 2 Med Oncol. 2021;38(4):4. https://doi.org/10.1007/s12032-02001452-z 17. Yhim HY, Yoon DH, Kim SJ, Yang D-H, Eom H-S, Kim KH, et al. First-Line Treatment for Primary Breast Diffuse Large B-Cell Lymphoma Using Immunochemotherapy and Central Nervous System Prophylaxis: A Multicenter Phase 2 Trial. Cancers (Basel). 2020;12(8):2192. Published 2020 Aug 6. doi:10.3390/cancers12082192 18. Swinnen LJ, Li H, Quon A, Gascoyne R, Hong F, Ranheim EA, et al. Response-adapted therapy for aggressive non-Hodgkin's lymphomas based on early [18F] FDG-PET scanning: ECOG-ACRIN Cancer Research Group study (E3404). British Journal of Haematology. 2015;170(1):56-65. doi:10.1111/bjh.13389 19. Takemura S, Tomita N, Koharazawa H, Fujimaki K, Harano H, Hyo R, et al. Phase II study of CHOP-GR therapy in diffuse large B-cell lymphoma. Int J Hematol. 2012;96(3):241-6. 20. Spina M, Balzarotti M, Uziel L, Ferreri AJM, Fratino L, Magagnoli M, et al. Modulated Chemotherapy According to Modified Comprehensive Geriatric Assessment in 100 Consecutive Elderly Patients with Diffuse Large B-Cell Lymphoma. The Oncologist. 2012;17(7):838-46. 21. Mounier N, Heutte N, Thieblemont C, Briere J, Gaulard P, Van Den Neste E, et al. Ten-Year Relative Survival and Causes of Death in Elderly Patients Treated With R-CHOP or CHOP in the GELA LNH-985 Trial. Clin Lymphoma Myeloma Leuk. 2012;12(3):151-4. 22. Manolopoulos L, Gomatos IP, Leandros E, Alevizos L, Georgiou N, Giotakis J, et al. Use of Rituximab in Combination with Conventional Chemotherapy for the Treatment of Non-Hodgkin’s Lymphoma of the Head and Neck. In Vivo. 2009;23(4):475-8. 23 23. Voulgarelis M, Giannouli S, Tzioufas AG, Moutsopoulos HM. Long term remission of Sjögren's syndrome associated aggressive B cell non-Hodgkin's lymphomas following combined B cell depletion therapy and CHOP (cyclophosphamide, doxorubicin, vincristine, prednisone). Ann Rheum Dis. 2006;65(8):1033-1037. doi:10.1136/ard.2005.046193 24. Pfreundschuh M, Trümper L, Österborg A, Pettengell R, Trneny M, Imrie K, et al. CHOP-like chemotherapy plus rituximab versus CHOP-like chemotherapy alone in young patients with good-prognosis diffuse large-B-cell lymphoma: a randomised controlled trial by the MabThera International Trial (MInT) Group. Lancet Oncol. 2006;7(5):379-91. doi:10.1016/S1470-2045(06)70664-7 25. Boué F, Gabarre J, Gisselbrecht C, Reynes J, Cheret A, Bonnet F, et al. Phase II Trial of CHOP Plus Rituximab in Patients With HIV-Associated NonHodgkin's Lymphoma. J Clin Oncol. 2006;24(25):4123-4128. doi:10.1200/JCO.2005.05.4684 26. Feugier P, Van Hoof A, Sebban C, Solal-Celigny P, Bouabdallah R, Fermé C, et al. Long-Term Results of the R-CHOP Study in the Treatment of Elderly Patients With Diffuse Large B-Cell Lymphoma: A Study by the Groupe d'Etude des Lymphomes de l'Adulte. J Clin Oncol. 2005;23(18):4117-4126. doi:10.1200/JCO.2005.09.131 27. Mounier N, Briere J, Gisselbrecht C, Emile J-F, Lederlin P, Sebban C, et al. Rituximab plus CHOP (R-CHOP) overcomes bcl-2-associated resistance to chemotherapy in elderly patients with diffuse large B-cell lymphoma (DLBCL). Blood. 2003;101(11):4279-84. 28. Coiffier B, Lepage E, Herbrecht R, et al. Rituximab plus CHOP (R-CHOP) is superior to CHOP alone in elderly patients with diffuse large B-cell lymphoma (DLCL): interim results of a randomized GELA trial. Blood. 2001;96(1):223a. 29. Kim DW, Byun JM, Lee J-O, Kim JK, Koh Y. Chemotherapy delivery time affects treatment outcomes of female patients with diffuse large B cell lymphoma. JCI Insight. 2023;8(2):e164767. doi:10.1172/jci.insight.164767 30. Held G, Thurner L, Poeschel V, Ott G, Schmidt C, Christofyllakis K, et al. Radiation and Dose-densification of R-CHOP in Primary Mediastinal B-cell Lymphoma: Subgroup Analysis of the UNFOLDER Trial. HemaSphere. 2023;7(7):917. 31. Tilly H, Morschhauser F, Sehn LH, Friedberg JW, Trněný M, Sharman JP, et al. Polatuzumab Vedotin in Previously Untreated Diffuse Large B-Cell Lymphoma. N Engl J Med. 2022;386(4):351-63. 32. Saito T, Nagai H, Izutsu K, Ando K, Igarashi T, Izumi T, et al. A phase II Japanese trial of 90-minute rituximab infusion for untreated B-cell lymphoma. Jpn J Clin Oncol. 2024;54(4):444-51. 33. Qin Y, Song Y, Wang D, Bai O, Feng J, Sun X, et al. Long-term outcomes with HLX01 (HanliKang®), a rituximab biosimilar, in previously untreated patients with diffuse large B-cell lymphoma: 5-year follow-up results of the phase 3 HLX01-NHL03 study. BMC Cancer. 2024;24(1):124. Published 2024 Jan 24. doi:10.1186/s12885-024-11876-9 34. Ou W, Jiang T, Zhang N, et al. Role of HDL cholesterol in anthracyclineinduced subclinical cardiotoxicity: a prospective observational study in patients with diffuse large B-cell lymphoma treated with R-CHOP. BMJ Open 2024;14:e074541. doi:10.1136/bmjopen-2023-074541 24 35. Shi Q, He Y, Yi H-M, Mu R-J, Jiang X-F, Fu D, et al. Positron emission tomography-adapted therapy in low-risk diffuse large B-cell lymphoma: results of a randomized, phase III, non-inferiority trial. Cancer Commun. 2023;43:896908. https://doi.org/10.1002/cac2.12462 36. Jin J, Ji D, Xia Z, Xue K, Zhang Q, Liu Y, et al. Four cycles of R-CHOP followed by two applications of rituximab based on negative interim PET/CT: an analysis of a prospective trial. BMC Cancer. 2022;22(1):403. https://doi.org/10.1186/s12885-022-09486-4 37. Luminari S, Montanini A, Caballero D, Bologna S, Notter M, Dyer MJS, et al. Nonpegylated liposomal doxorubicin (Myocet™) combination (R-COMP) chemotherapy in elderly patients with diffuse large B-cell lymphoma (DLBCL): results from the phase II EUR018 trial. Ann Oncol. 2010;21(7):1492-9. doi:10.1093/annonc/mdp544 38. Coiffier B, Thieblemont C, Van Den Neste E, et al. Long-term outcome of patients in the LNH-98.5 trial, the first randomized study comparing rituximabCHOP to standard CHOP chemotherapy in DLBCL patients: a study by the Groupe d'Etudes des Lymphomes de l'Adulte. Blood. 2010;116(12):20402045. 39. Cho H-J, Eom H-S, Kim H-J, Kim I-S, Lee GW, Kong S-Y. Glutathione-Stransferase genotypes influence the risk of chemotherapy-related toxicities and prognosis in Korean patients with diffuse large B-cell lymphoma. Cancer Genet Cytogenet. 2010;198(1):40-46. doi:10.1016/j.cancergencyto.2009.12.004pt_BR
dc.type.degreeEspecializaçãopt_BR
dc.publisher.courseMEDICINApt_BR
Aparece nas coleções:Trabalho de Conclusão de Curso (Especialização) - Programa de Residência Médica (Faculdade de Medicina)

Arquivos associados a este item:
Arquivo Descrição TamanhoFormato 
Lucas Villasboas TCC Especialização.pdfTCC Residência Hematologia/Hemoterapia1,04 MBAdobe PDFVisualizar/Abrir
Mostrar registro simples do item Visualizar estatísticas


Os itens no repositório estão protegidos por copyright, com todos os direitos reservados, salvo quando é indicado o contrário.