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O Linfoma de Hodgkin (LH) Ă© uma neoplasia hematolinfoide rara que constitui cerca de 0,2% dos novos casos de cancros a nĂvel mundial, sendo mais comum nos jovens adultos entre os 20-34 anos, representando a doença oncolĂłgica mais recorrente nesta faixa etĂĄria.
A patologia divide-se em dois grupos, o Linfoma de Hodgkin ClĂĄssico (LHC), que se encontra subdividido em quatro histologias e o Linfoma de Hodgkin Nodular de PredomĂnio LinfocitĂĄrio (LHNPL), correspondendo a cerca de 90% e 10% dos casos reportados, respetivamente. Estas duas apresentaçÔes da doença distinguem-se pela presença de cĂ©lulas caracterĂsticas de cada uma, como as cĂ©lulas de Reed-Sternberg no LHC, e as cĂ©lulas predominantemente linfocĂticas no LHNPL.
O diagnĂłstico patolĂłgico do LH Ă© realizado, preferencialmente, atravĂ©s da biĂłpsia excisional e avaliação imunohistoquĂmica. O correto diagnĂłstico, estadiamento baseado na classificação de Ann Arbor e avaliação de fatores de risco sĂŁo fundamentais para a escolha de um tratamento correto.
Atualmente, a tomografia por emissĂŁo de positrĂ”es com tomografia computorizada Ă© a tĂ©cnica imagiolĂłgica (PET/CT) mais importante na avaliação da doença. Este exame complementar permite avaliar a resposta Ă terapĂȘutica atravĂ©s de um re-estadiamento. Mediante esta abordagem permite-se realizar uma terapĂȘutica personalizada e dirigida Ă resposta dos doentes.
A terapĂȘutica do LH recorre maioritariamente ao regime combinado de radioterapia e quimioterapia, destacando-se os protocolos ABVD e BEACOPPesc. Com uma abordagem mediada pela resposta ao tratamento com a utilização da PET/CT, o LH Ă© atualmente uma das doenças oncolĂłgicas com maiores taxas de sucesso, apresentando como o seu objetivo terapĂȘutico final a cura da doença.
No entanto, apesar da terapĂȘutica clĂĄssica combinada apresentar Ăłtimos resultados, 10% a 30% dos doentes apresentam recidiva ou sĂŁo refratĂĄrios ao tratamento. Existe assim uma necessidade de estender o arsenal terapĂȘutico de modo a dar resposta a estes doentes.
Surgem assim as novas abordagens terapĂȘuticas, nĂŁo sĂł no Ăąmbito de novos fĂĄrmacos, mas tambĂ©m na otimização das terapĂȘuticas jĂĄ existentes e em combinação com estas novas alternativas terapĂȘuticas. Destacam-se assim as abordagens maioritariamente pertencentes Ă terapĂȘutica dirigida como conjugados anticorpo-fĂĄrmaco, inibidores dos checkpoints imunitĂĄrios, inibidores das vias de sinalização oncogĂ©nicas e imunomoduladores, jĂĄ implementadas na prĂĄtica clĂnica.
Hodgkin's Lymphoma (HL) is a rare hematolymphoid neoplasm that accounts for approximately 0.2% of new cancer cases worldwide, being more common in young adults between the ages of 20-34 years. It represents the most recurring oncological disease in this age group. The pathology is divided into two groups: Classic Hodgkin Lymphoma (CHL), which is further subdivided into four histologies, and Nodular Lymphocyte Predominant Hodgkin Lymphoma (NLPHL), accounting for approximately 90% and 10% of the reported cases, respectively. These two disease presentations are distinguished by the presence of characteristic cells, such as Reed-Sternberg cells in CHL and predominantly lymphocytic cells in NLPHL. The pathological diagnosis of HL is preferably performed through excisional biopsy and immunohistochemical evaluation. The accurate diagnosis, staging based on the Ann Arbor classification, and evaluation of risk factors are essential for choosing the correct treatment. Currently, positron emission tomography with computed tomography (PET/CT) is the most important imaging technique for assessing the disease. This complementary examination allows for evaluating the response to therapy through restaging. This approach enables personalized and response-directed treatment for patients. The therapy for HL mainly involves a combined regimen of radiation therapy and chemotherapy, with ABVD and BEACOPPesc being the most used protocols. With an approach guided by treatment response using PET/CT, HL is currently one of the oncological diseases with the highest success rates, aiming for disease cure as the ultimate therapeutic goal. However, despite the excellent results of the combined classical therapy, 10% to 30% of patients experience relapse or are refractory to treatment. Therefore, there is a need to expand the therapeutic arsenal in order to provide a response for these patients. New therapeutic approaches emerge, not only in terms of new drugs but also in the optimization of existing therapies and in combination with these new therapeutic alternatives. Notable approaches include those mainly belonging to targeted therapy, such as antibody-drug conjugates, immune checkpoint inhibitors, inhibitors of oncogenic signaling pathways, and immunomodulators, which have already been implemented in clinical practice.
Hodgkin's Lymphoma (HL) is a rare hematolymphoid neoplasm that accounts for approximately 0.2% of new cancer cases worldwide, being more common in young adults between the ages of 20-34 years. It represents the most recurring oncological disease in this age group. The pathology is divided into two groups: Classic Hodgkin Lymphoma (CHL), which is further subdivided into four histologies, and Nodular Lymphocyte Predominant Hodgkin Lymphoma (NLPHL), accounting for approximately 90% and 10% of the reported cases, respectively. These two disease presentations are distinguished by the presence of characteristic cells, such as Reed-Sternberg cells in CHL and predominantly lymphocytic cells in NLPHL. The pathological diagnosis of HL is preferably performed through excisional biopsy and immunohistochemical evaluation. The accurate diagnosis, staging based on the Ann Arbor classification, and evaluation of risk factors are essential for choosing the correct treatment. Currently, positron emission tomography with computed tomography (PET/CT) is the most important imaging technique for assessing the disease. This complementary examination allows for evaluating the response to therapy through restaging. This approach enables personalized and response-directed treatment for patients. The therapy for HL mainly involves a combined regimen of radiation therapy and chemotherapy, with ABVD and BEACOPPesc being the most used protocols. With an approach guided by treatment response using PET/CT, HL is currently one of the oncological diseases with the highest success rates, aiming for disease cure as the ultimate therapeutic goal. However, despite the excellent results of the combined classical therapy, 10% to 30% of patients experience relapse or are refractory to treatment. Therefore, there is a need to expand the therapeutic arsenal in order to provide a response for these patients. New therapeutic approaches emerge, not only in terms of new drugs but also in the optimization of existing therapies and in combination with these new therapeutic alternatives. Notable approaches include those mainly belonging to targeted therapy, such as antibody-drug conjugates, immune checkpoint inhibitors, inhibitors of oncogenic signaling pathways, and immunomodulators, which have already been implemented in clinical practice.
Descrição
Trabalho Final de Mestrado Integrado, CiĂȘncias FarmacĂȘuticas, 2023, Universidade de Lisboa, Faculdade de FarmĂĄcia.
Palavras-chave
Linfoma de Hodgkin Quimioterapia TerapĂȘutica dirigida PET/CT Mestrado Integrado - 2023
