<div class="elementor-post__thumbnail elementor-fit-height imagem_injetada" style="margin-bottom:7px; display:none;"><img width="300" height="168" src="https://www.femama.org.br/site_old/_files/noticia/3696/5d37447307c52.jpg" class="attachment-medium size-medium" alt=""></div><div class="elementor-post__thumbnail elementor-fit-height imagem_injetada" style="margin-bottom:7px; display:none;"><img width="300" height="168" src="https://www.femama.org.br/site_old/_files/noticia/3696/5d37447307c52.jpg" class="attachment-medium size-medium" alt=""></div>{"id":19967,"date":"2019-07-23T00:00:00","date_gmt":"2019-07-23T03:00:00","guid":{"rendered":"https:\/\/femama.org.br\/site_novo\/noticias-recentes\/anvisa-aprova-t-dm1-para-pacientes-com-cancer-de-mama-her2-em-estagio-inicial\/"},"modified":"2019-07-23T00:00:00","modified_gmt":"2019-07-23T03:00:00","slug":"anvisa-aprova-t-dm1-para-pacientes-com-cancer-de-mama-her2-em-estagio-inicial","status":"publish","type":"post","link":"https:\/\/femama.org.br\/site\/noticias-recentes\/anvisa-aprova-t-dm1-para-pacientes-com-cancer-de-mama-her2-em-estagio-inicial\/","title":{"rendered":"ANVISA aprova T-DM1 para pacientes com c\u00e2ncer de mama HER2+ em est\u00e1gio inicial"},"content":{"rendered":"<p style=\"text-align: justify;\">A Ag&ecirc;ncia Nacional de Vigil&acirc;ncia Sanit&aacute;ria (ANVISA) acaba de aprovar um novo tratamento para pacientes com c&acirc;ncer de mama do tipo HER2-positivo em est&aacute;gio inicial que apresentam doen&ccedil;a residual invasiva mesmo depois de ter passado por terapia medicamentosa pr&eacute;via &agrave; cirurgia. O medicamento j&aacute; estava dispon&iacute;vel para c&acirc;ncer de mama metast&aacute;tico, o &uacute;ltimo est&aacute;gio, e agora chega para tratar a doen&ccedil;a no est&aacute;gio inicial.<\/p>\n<p style=\"text-align: justify;\">O medicamento injet&aacute;vel chamado T-DM1 reduziu em 50% o risco de recorr&ecirc;ncia do c&acirc;ncer ou morte nessas pacientes, de acordo com os dados do estudo Katherine, publicados em dezembro no New England Journal of Medicine e que embasaram a decis&atilde;o da ag&ecirc;ncia regulat&oacute;ria brasileira. A novidade &eacute; considerada pela comunidade cient&iacute;fica o maior avan&ccedil;o em 15 anos para essas pacientes.<\/p>\n<p style=\"text-align: justify;\">Ao contr&aacute;rio da quimioterapia convencional administrada de forma sist&ecirc;mica e que pode agir em todas as c&eacute;lulas do organismo, a quimioterapia do T-DM1 &eacute; liberada seletivamente no interior das c&eacute;lulas cancer&iacute;genas.<\/p>\n<p style=\"text-align: justify;\">A precis&atilde;o desse mecanismo de a&ccedil;&atilde;o permite que as pacientes apresentem menos efeitos colaterais, como a queda de cabelo, em compara&ccedil;&atilde;o com a quimioterapia tradicional. No estudo Katherine, em tr&ecirc;s anos, 88,3% das pacientes tratadas n&atilde;o tiveram retorno do c&acirc;ncer de mama ou morte comparados a 77% tratadas com a terapia padr&atilde;o anterior.<\/p>\n<p style=\"text-align: justify;\">&#8220;Esta &eacute; a primeira terapia anti-HER2 aprovada especificamente para essas pacientes, que possuem maior risco de recorr&ecirc;ncia do tumor. Os resultados s&atilde;o promissores e colocam o T-DM1 como o novo padr&atilde;o de tratamento para esses casos. &Eacute; a principal mudan&ccedil;a na pr&aacute;tica cl&iacute;nica em face da doen&ccedil;a HER2 superexpressa desde o lan&ccedil;amento do trastuzumabe no contexto adjuvante (ap&oacute;s a cirurgia), h&aacute; quase 15 anos&#8221;, ressalta o oncologista cl&iacute;nico Max Mano, do Hospital S&iacute;rio-Liban&ecirc;s, que participou do estudo.<\/p>\n<p style=\"text-align: justify;\">Segundo o Instituto Nacional de C&acirc;ncer (Inca), cerca de 60 mil novos casos de tumores de mama s&atilde;o diagnosticados ao ano no Brasil. O tipo HER2-positivo &eacute; uma forma particularmente agressiva da doen&ccedil;a, quando n&atilde;o tratada adequadamente, e afeta em torno de 15% a 20% das pacientes.<\/p>\n<p style=\"text-align: justify;\">&nbsp;<\/p>\n<p style=\"text-align: justify;\"><a href=\"https:\/\/www.folhavitoria.com.br\/saude\/noticia\/07\/2019\/novo-tratamento-para-pacientes-com-cancer-de-mama-invasivo\" target=\"_blank\" rel=\"noopener\"><strong>Fonte: Folha Vit&oacute;ria, 22\/07\/2019<\/strong><\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p align=\"center\"><em>Precis&atilde;o desse mecanismo de a&ccedil;&atilde;o permite que as pacientes apresentem menos efeitos colaterais, como diminui&ccedil;&atilde;o da queda de cabelo.<\/em><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[18,13],"tags":[],"class_list":["post-19967","post","type-post","status-publish","format-standard","hentry","category-cancer-de-mama","category-noticias-recentes"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>ANVISA aprova T-DM1 para pacientes com c\u00e2ncer de mama HER2+ em est\u00e1gio inicial | FEMAMA<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/femama.org.br\/site\/noticias-recentes\/anvisa-aprova-t-dm1-para-pacientes-com-cancer-de-mama-her2-em-estagio-inicial\/\" \/>\n<meta property=\"og:locale\" content=\"pt_BR\" \/>\n<meta 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