{"id":27095,"date":"2025-06-24T15:41:57","date_gmt":"2025-06-24T12:41:57","guid":{"rendered":"https:\/\/www.clinica-sante.com\/ro\/analize-fara-categorie\/panel-somatic-cancer-colorectal-include-lynch-fap-analiza-ngs-18-gene\/"},"modified":"2026-06-19T18:27:33","modified_gmt":"2026-06-19T15:27:33","slug":"panel-somatic-cancer-colorectal-include-lynch-fap-analiza-ngs-18-gene","status":"publish","type":"product","link":"https:\/\/www.clinica-sante.com\/ro\/analize-oncogenetica\/panel-somatic-cancer-colorectal-include-lynch-fap-analiza-ngs-18-gene\/","title":{"rendered":"Panel somatic cancer colorectal (include Lynch + FAP), analiza NGS 18 gene"},"content":{"rendered":"<p>Panelul somatic cancer colorectal (NGS 18 gene) \u2013 inclusiv Lynch \u0219i FAP este o analiz\u0103 molecular\u0103 de tip <strong>multi-gene NGS<\/strong> pe \u021besut tumoral fixat \u00een formalin\u0103 \u0219i inclus \u00een parafin\u0103 (FFPE), utilizat pentru caracterizarea genetic\u0103 a cancerului colorectal.<\/p>\n<h3>Testul permite identificarea simultan\u0103 a mai multor tipuri de alter\u0103ri genetice:<\/h3>\n<ul>\n<li>muta\u021bii punctiforme (SNV)<\/li>\n<li>inser\u021bii \u0219i dele\u021bii (Indels)<\/li>\n<li>variante patogene implicate \u00een oncogenez\u0103<\/li>\n<li>alter\u0103ri asociate instabilit\u0103\u021bii microsatelitare \u0219i defectelor de reparare ADN<\/li>\n<li>modific\u0103ri relevante pentru r\u0103spunsul la terapii \u021bintite<\/li>\n<\/ul>\n<h3>Panelul include gene implicate \u00een:<\/h3>\n<h3>cancer colorectal sporadic<\/h3>\n<h3>sindrom Lynch (defecte ale sistemului MMR)<\/h3>\n<h3>polipoz\u0103 adenomatoas\u0103 familial\u0103 (FAP)<\/h3>\n<p>Pentru panelurile de oncologie colorectal\u0103 sunt analizate gene cu relevan\u021b\u0103 clinic\u0103 major\u0103 precum <strong>APC, MLH1, MSH2, MSH6, PMS2, KRAS, NRAS, BRAF, PIK3CA, TP53, SMAD4<\/strong>, al\u0103turi de alte gene implicate \u00een c\u0103ile de semnalizare tumoral\u0103.<\/p>\n<h3>Indica\u021bii de testare<\/h3>\n<ul>\n<li>Cancer colorectal confirmat histopatologic<\/li>\n<li>Evaluare molecular\u0103 pentru tratament oncologic personalizat<\/li>\n<li>Suspiciune de sindrom Lynch<\/li>\n<li>Suspiciune de polipoz\u0103 adenomatoas\u0103 familial\u0103 (FAP)<\/li>\n<li>Tumori colorectale cu debut precoce<\/li>\n<li>Boal\u0103 metastatic\u0103 sau local avansat\u0103<\/li>\n<li>Evaluarea instabilit\u0103\u021bii microsatelitare (MSI)<\/li>\n<li>Istoric familial de cancer colorectal<\/li>\n<li>Stratificarea riscului de recuren\u021b\u0103 tumoral\u0103<\/li>\n<\/ul>\n<h3>Cui se adreseaz\u0103<\/h3>\n<ul>\n<li>Pacien\u021bilor diagnostica\u021bi cu cancer colorectal<\/li>\n<li>Pacien\u021bilor cu suspiciune de cancer ereditar colorectal<\/li>\n<li>Pacien\u021bilor cu polipoz\u0103 multipl\u0103 colonic\u0103<\/li>\n<li>Pacien\u021bilor oncologici afla\u021bi \u00een evaluare pentru terapii \u021bintite<\/li>\n<li>Medicilor oncologi, gastroenterologi \u0219i anatomopatologi<\/li>\n<li>Centrelor de oncologie de precizie<\/li>\n<\/ul>\n<h3>Metodologie de testare<\/h3>\n<ul>\n<li>Analiz\u0103 molecular\u0103 din <strong>\u021besut tumoral FFPE<\/strong><\/li>\n<li>Extrac\u021bia ADN-ului din blocuri parafinate sau lame histologice<\/li>\n<li>Secven\u021biere de nou\u0103 genera\u021bie (<strong>NGS<\/strong>)<\/li>\n<li>Detectarea:\n<ul>\n<li>muta\u021biilor somatice (SNV)<\/li>\n<li>inser\u021biilor\/dele\u021biilor (Indels)<\/li>\n<li>variantelor patogene relevante clinic<\/li>\n<\/ul>\n<\/li>\n<li>Analiz\u0103 bioinformatic\u0103 avansat\u0103 \u0219i interpretare conform ghidurilor oncologice interna\u021bionale<\/li>\n<\/ul>\n<h3>Gene analizate (panel 18 gene \u2013 cancer colorectal)<\/h3>\n<h3>Panelul include frecvent gene implicate \u00een oncogeneza colorectal\u0103 \u0219i sindroame ereditare:<\/h3>\n<ul>\n<li><strong>APC<\/strong> (FAP)<\/li>\n<li><strong>MLH1<\/strong> (Lynch)<\/li>\n<li><strong>MSH2<\/strong> (Lynch)<\/li>\n<li><strong>MSH6<\/strong> (Lynch)<\/li>\n<li><strong>PMS2<\/strong> (Lynch)<\/li>\n<li style=\"font-weight: bold\"><strong>KRAS<\/strong><\/li>\n<li style=\"font-weight: bold\"><strong>NRAS<\/strong><\/li>\n<li style=\"font-weight: bold\"><strong>BRAF<\/strong><\/li>\n<li style=\"font-weight: bold\"><strong>PIK3CA<\/strong><\/li>\n<li style=\"font-weight: bold\"><strong>TP53<\/strong><\/li>\n<li style=\"font-weight: bold\"><strong>SMAD4<\/strong><\/li>\n<li style=\"font-weight: bold\"><strong>FBXW7<\/strong><\/li>\n<li style=\"font-weight: bold\"><strong>CTNNB1<\/strong><\/li>\n<li style=\"font-weight: bold\"><strong>GNAS<\/strong><\/li>\n<li style=\"font-weight: bold\"><strong>AKT1<\/strong><\/li>\n<li style=\"font-weight: bold\"><strong>PTEN<\/strong><\/li>\n<li style=\"font-weight: bold\"><strong>TGFBR2<\/strong><\/li>\n<li style=\"font-weight: bold\"><strong>RNF43<\/strong><\/li>\n<\/ul>\n<h3>Beneficii \u0219i importan\u021b\u0103 clinic\u0103<\/h3>\n<ul>\n<li>Caracterizare molecular\u0103 complet\u0103 a cancerului colorectal<\/li>\n<li>Identificarea muta\u021biilor cu relevan\u021b\u0103 terapeutic\u0103<\/li>\n<li>Ghidarea terapiei personalizate \u00een oncologie<\/li>\n<li>Detectarea markerilor asocia\u021bi cu Lynch \u0219i FAP<\/li>\n<li>Stratificarea riscului de progresie \u0219i recuren\u021b\u0103<\/li>\n<li>Sprijin pentru decizii terapeutice conform ghidurilor interna\u021bionale<\/li>\n<li>Optimizarea managementului pacientului oncologic<\/li>\n<li>Sus\u021binerea medicinei de precizie<\/li>\n<\/ul>\n<h3>Analize asociate recomandate<\/h3>\n<h3>Investiga\u021bii histopatologice \u0219i imunohistochimice<\/h3>\n<ul>\n<li>Examen histopatologic complet<\/li>\n<li>MSI (Microsatellite Instability)<\/li>\n<li>IHC pentru MMR:\n<ul>\n<li>MLH1<\/li>\n<li>MSH2<\/li>\n<li>MSH6<\/li>\n<li>PMS2<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<h3>Teste genetice complementare<\/h3>\n<ul>\n<li>Panel germinal pentru sindrom Lynch<\/li>\n<li>Cancer Comprehensive NGS Panel<\/li>\n<li>Testare AllRAS (KRAS\/NRAS)<\/li>\n<li>BRAF V600E<\/li>\n<\/ul>\n<h3>Monitorizare oncologic\u0103<\/h3>\n<ul>\n<li>CEA (marker tumoral)<\/li>\n<li>CT \/ RMN \/ PET-CT<\/li>\n<li>Evaluare oncologic\u0103 periodic\u0103<\/li>\n<\/ul>\n<h3>Prob\u0103 recoltat\u0103 \/ condi\u021bii analiz\u0103<\/h3>\n<h3>\u021aesut tumoral FFPE (bloc parafin\u0103 sau lame histologice)<\/h3>\n<ul>\n<li>Proba trebuie s\u0103 con\u021bin\u0103 procent adecvat de celule tumorale (conform criteriilor laboratorului )<\/li>\n<li>Transport conform standardelor pentru material histopatologic<\/li>\n<\/ul>\n<h3>Documente obligatorii<\/h3>\n<ul>\n<li>Raport histopatologic complet<\/li>\n<li>Confirmare diagnostic oncologic<\/li>\n<li>Bilet de trimitere \/ recomandare medical\u0103<\/li>\n<li>Date clinice relevante (stadializare, tratamente anterioare)<\/li>\n<\/ul>\n<h3>Denumiri alternative<\/h3>\n<p>\uf0b7 Panel genetic pentru cancer colorectal (NGS)<\/p>\n<p>\uf0b7 Panel de muta\u021bii \u00een cancerul colorectal<\/p>\n<p>\uf0b7 Analiz\u0103 genetic\u0103 tumoral\u0103 pentru cancer colorectal<\/p>\n<p>\uf0b7 Panel molecular pentru cancer colorectal<\/p>\n<p>\uf0b7 Test genetic pentru cancerul de colon \u0219i rect<\/p>\n<p>\uf0b7 Profilare molecular\u0103 a cancerului colorectal<\/p>\n<p>\uf0b7 Analiz\u0103 genomic\u0103 tumoral\u0103 colorectal\u0103<\/p>\n<p>\uf0b7 Panel de oncologie de precizie \u2013 cancer colorectal<\/p>\n<p>\uf0b7 Test NGS pentru cancer colorectal (18 gene)<\/p>\n<p>\uf0b7 Panel genetic pentru cancere colorectale ereditare \u0219i somatice<\/p>\n<h3>Particularit\u0103\u021bi ale testului<\/h3>\n<p>Acest panel analizeaz\u0103 <strong>muta\u021bii somatice tumorale<\/strong>, dar include \u0219i gene implicate \u00een sindroame de predispozi\u021bie (Lynch, FAP) detectate la nivel tumoral. Pentru confirmarea riscului ereditar se recomand\u0103 testare <strong>germinal\u0103 dedicat\u0103<\/strong>, deoarece analiza pe \u021besut tumoral nu substituie complet evaluarea genetic\u0103 constitu\u021bional\u0103. Testul este un instrument important \u00een oncologia de precizie, utilizat pentru personalizarea tratamentului \u0219i optimizarea managementului pacientului oncologic.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Panel genetic somatic realizat prin tehnologie <strong>NGS (Next Generation Sequencing)<\/strong> din \u021besut tumoral FFPE, care analizeaz\u0103 <strong>18 gene relevante \u00een cancerul colorectal<\/strong>, incluz\u00e2nd markeri implica\u021bi \u00een <strong>sindromul Lynch (MMR)<\/strong> \u0219i <strong>polipoza adenomatoas\u0103 familial\u0103 (FAP)<\/strong>. Testul ofer\u0103 informa\u021bii esen\u021biale pentru diagnostic molecular, prognostic \u0219i selec\u021bia terapiei personalizate.<\/p>\n","protected":false},"featured_media":0,"template":"","meta":{"_acf_changed":false,"inline_featured_image":false},"product_brand":[],"product_cat":[1209,3165,2876],"product_tag":[],"class_list":["post-27095","product","type-product","status-publish","product_cat-analize","product_cat-oncogenetica","product_cat-serviciu-laborator","first","instock","sale","virtual","purchasable","product-type-simple"],"acf":[],"aioseo_notices":[],"aioseo_head":"\n\t\t<!-- All in One SEO Pro 4.9.9 - aioseo.com -->\n\t<meta name=\"description\" content=\"Panel genetic somatic realizat prin tehnologie NGS (Next Generation Sequencing) din \u021besut tumoral FFPE, care analizeaz\u0103 18 gene relevante \u00een cancerul colorectal, incluz\u00e2nd markeri implica\u021bi \u00een sindromul Lynch (MMR) \u0219i polipoza adenomatoas\u0103 familial\u0103 (FAP). 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