?A75<23&3C7@N< .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H %#"%FIHKMXG<B:GH=B:@G_LMB<H>FHGBMH KBS:ZYHM>K:I]NMB<:=:I:MHEH@B:>G=_<KBG: <?>AC0=24>=3806=>B8B0=3<>=8C>A8I0 C8>=>54=3>2A8=438B40B4B &:<BGM:/:GMHL%L:;>E,:BO:"VMBF:(>BMYH):GN>E::KO:EA>BKH =C4A=0><?;4<4=C0A34=3>2A8=>;>680 BB8BC4=C4>B?8C0;0AA03D03034=3>2A8=>;>680 BB8BC4=C4 >B?8C0;0A A03D030 34 &0C>;>680 ;S=820 "01>A0CTA8> 34 >A<>=>;>680 )4AE8P> 34 &0C>;>680 ;S=820 3>B >B?8C08B 30 +=8E4AB8303434>8<1A0&>8<1A0 8A42C>A03>)4AE8P>34=3>2A8=>;>6808014C4B4#4C01>;8B<>3>B>B?8C08B30+=8E4AB8303434>8<1A0&>8<1A0 <??3@=<;2Q;17/!028=C0)0=C>BZ)4AE8P>34=3>2A8=>;>6808014C4B4#4C01>;8B<>+&Z&A024C0#>C0&8=C> >8<1A0 Z90B0=C>B6<08;2>< 137A/ON<AC86>A424183>4< A4E8BC>4< 40248C4?0A0?D1;820PO>4< &')!# A Hormona de Crescimento (GH) exerce efeitos directos nos tecidos periféricos, assim como efeitos indirectos através da IGF-1. Devido à capacidade de ligação a proteínas de alta afinidade (IGFBPs), a IGF-1 possui uma semi-vida mais duradoura que a maioria das hormonas polipeptídicas. A sua concentração sérica depende sobretudo do estado nutricional e da secreção de GH, embora factores como a idade, sexo, factores genéticos e patologias crónicas associadas tenham alguma influência. Devido à pulsatilidade da secreção de GH, a avaliação da sua produção é uma tarefa complexa. Os testes de estimulação, nomeadamente a prova da hipoglicemia insulínica e a prova da clonidina, são considerados os métodos de eleição para estabelecer o diagnóstico de deficiência de GH. Devido à estabilidade da IGF-1, o seu doseamento assume extrema relevância como adjuvante no diagnóstico desta patologia. Em crianças, a eficácia da terapêutica com GH é avaliada através do crescimento linear. Na população adulta, os estudos revelam efeitos benéficos na qualidade de vida, composição corporal, densidade mineral óssea e risco cardiovascular. A monitorização dos valores da IGF1 permite avaliar a adesão à terapêutica. A titulação da dose de GH de acordo com os valores de IGF-1 previne elevações da IGF-1 acima dos valores de referência, reduzindo a possibilidade de efeitos adversos do tratamento. Na acromegalia, o valor da IGF-1 correlaciona-se com a hipersecreção de HC, constituindo o método com maior sensibilidade e especificidade no diagnóstico, uma vez que o seu nível se encontra persistentemente elevado. A eficácia da terapêutica médica ou cirúrgica da acromegalia está associada à normalização da GH e IGF-1 sérica, embora possa ocorrer discordância entre a GH e a IGF-1 em alguns doentes. A manutenção de valores elevados de IGF-1 está associada a um aumento da taxa de mortalidade. Este facto justifica a importância das terapêuticas instituídas com o objectivo de normalizar a IGF-1, o que permitirá reduzir a mortalidade. $ *&'* Hipófise; Eixo Somatotrófico; IGF-1; Deficiência de Hormona de Crescimento; Acromegalia; Diagnóstico; Monitorização do Tratamento da Acromegália. fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ ?A75<23&3C7@N< .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H '(&( Growth Hormone (GH) has direct and indirect effects at the peripheral tissues, through the action of IGF-1. Because of its ability to bind to high affinity proteins (IGFBPs), IGF-1 has a substantially longer half-life than many polypeptide hormones. Serum IGF-1 concentration depends primarily on nutritional status and GH secretion, although other factors such as age, gender, genetic factors and associated chronic diseases have also some influence. The stimulation tests, namely the insulin tolerance test and the clonidine test, are considered the gold standard used to diagnose GH deficiency. Due to the pulsatility of the GH secretion, assessment of whether GH production is insufficient is a complex task. Because of IGF-1 stability, it’s measurement presents great relevance as adjuvant to the diagnosis of the situation. In children, the efficacy of GH therapy is evaluated through the linear growth. In the adult population, this evaluation is performed by indirect effects: improvement in the quality of life, body composition, bone density and cardiovascular risk factors. In theses cases, IGF-1 monitoring allows the evaluation of patient’s compliance to the treatment. GH dose titration according to IGF-1 levels prevents its elevation above the reference range, which could increase the adverse effects. In acromegaly, IGF-1 correlates well with GH hypersecretion, and is considered the most sensitive and specific test in diagnosis, since it’s measurement is persistently elevated. Successful medical or surgical treatment of acromegaly is usually associated with normalisation of serum IGF-1, but in some patients there is discordance between GH and IGF-1. The maintenance of high levels of IGF1 is associated with excess mortality. This fact justifies the importance of the therapeutic measures aiming at normalising IGF-1 and reducing the mortality rate. -+#&' Pituitary; Somatotropic Axis; IGF-1; Growth Hormone Deficiency; Acromegaly; Diagnosis; Monitoring of Acromegaly Treatment. 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IHBL G:L FNEA>K>L I:K: L> :E<:GZ: K>F O:EHK>L => %#" L>F>EA:GM>L :HL =HL AHF>GL [ G><>LLVKB: NF: L><K>ZYH => #$ LB@GB?B<:MBO:F>GM> F:BHK +L >LMKH@[GBHL M]FNF>?>BMH=BK><MHG>@:MBOHG:IKH=NZYH => %#" K>@NE:=: I>E: #$ >GJN:GMH JN> HL :G=KH@[GBHL M]F >?>BMHL IHM>G<B:EF>GM> fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ BGO>KLHL ,HK b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b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a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bK@B<H =::<KHF>@:EB:>G:FHGBMHKBS:ZYH=:M>K: I]NMB<:F[=B<:=>LM:I:MHEH@B: + =HL>:F>GMH =: %#" :LLNF> :BG=: F:BHKBFIHKMXG<B:GHL=H>GM>LLN;F>MB=HL : M>K:I]NMB<: F[=B<: <HF H :GM:@HGBLM: =HL K><>IMHK>L =: #$ I>@OBLHF:GM> !LM> ?VKF:<H :<MN: : G^O>E I>KB?[KB<H GYH BGB ;BG=H:L><K>ZYH=>#$I>EHMNFHK=:^JN> :FHGBMHKBS:ZYH=:>?B<V<B:=>LM:M>K:I]NMB <: L_ [ IHLL^O>E :MK:O[L =H =HL>:F>GMH =: %#" +I>@OBLHF:GM><HGL>@N>:GHKF:EB S:ZYH=:%#"GNF:I>K<>GM:@>FLNI>KBHK fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ ?A75<23&3C7@N< .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H #& 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. Clemmons DR. IGF-1 assays: current assay methodologies and their limitation. Pituitary 2007; 10: 121-128. Boguszewski CL. O laboratório no diagnóstico e seguimento da acromegalia. Arq Bras Endocrinol Metab 2002; 46 (1): 34-44. Brabant G, Wallaschofski. Normal levels of serum IGF-1: determinants and validity of current reference ranges. Pituitary 2007; 10: 129-133. Casagrande A, Czepielewski. Ensaios para a medida de GH e IGF-1: aspectos metodológicos e suas implicações no diagnóstico e seguimento da acromegalia. Arq Bras Endocrinol Metab 2007; 51 (4): 511-519. Frystyk J. Utility of free IGF-1 measurements. Pituitary 2007; 10: 181-187. Barkan AL. Defining normalcy of the somatotropic axis: an attainable goal? Pituitary 2007; 10: 135-139. Sherlock M, Toogood A. Aging and the growth hormone / insulin like growth factor-I axis. Pituitary 2007; 10: 189-203. Kwan AYM, Hartman ML. IGF-1 measurements in the diagnosis of adult growth hormone deficiency. Pituitary 2007; 10: 151-157. Roberts B, Katznelson L. Approach to the evaluation of the GH/IGF-1 axis in patients with pituitary disease: which test to order. Pituitary 2007; 10: 205-211. Toogood AA, Stewart PM. Hypopituitarism: Clinical features, diagnosis and management. Endocrinol Metab Clin N Am 2008; 37: 235-261. Higham CE, Jostel A, Trainer PJ. IGF-1 measurements in the monitoring of GH therapy. Pituitary 2007; 10: 159-163. Vance ML, Mauras N. Growth hormone therapy in adults and children. N Engl J Med 1999; 341 (16): 1206-1216. Abucham J, Vieira TCA, Barbosa ER, Ribeiro RS, Martins MRA. Terapia de reposição hormonal no hipopituitarismo. Arq Bras Endocrinol Metab 2003; 47 (4): 492-508. Brooke AM, Drake WM. Serum IGF-1 levels in the diagnosis and monitoring of acromegaly. Pituitary 2007; 10: 173-179. Taboada GF, Haute FR, Corrêa LL, Casini AF, Gadelha MR. Etiologic aspects and management of acromegaly. Arq Bras Endocrinol Metab 2005; 49 (5): 626-640. 16. Bem-Shlomo A, Melmed S. Acromegaly. Endocrinol Metab Clin N Am 2008; 37: 101-122. 17. Colao A, Ferone D, Marzullo P, Lombardi G. Systemic complications of acromegaly: epidemiology, pathogenesis and management. Endocrine Reviews 2004; 25 (1): 102-152. 18. Melmed S, Colao A, Barkan A, Molitch M, Grossman AB, et al. Guidelines for acromegaly management: an update. J Clin Endocrinol Metab 2009; 94 (5): 1509-1517. 19. Alexopoulou O, Bex M, Abs R, T’Sjoen GT, Velkeniers B, Maiter Dominique. Divergence between Growth Hormone and Insulin-Like Growth Factor-I concentrations in the followup of acromegaly. J Clin Endocrinol Metab 2008; 93 (4): 1324-1330. 20. Melmed S. Acromegaly. N Engl J Med 2006; 355 (24): 2558-2573. fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ ?A75<23&3C7@N< .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H :K<BGHF:=:@EXG=NE:LNIK:K>G:E:LI><MHL ?NG=:F>GM:BLIKH@K>LLHL>BG<>KM>S:L 3A4=>2>AC820;20A28=><05D=30<4=C0;8BBD4B 03E0=24<4=CB0=3D=24AC08=C84B $>E=>K/BFa>L&H:G:HLM::KEHL2:L<HG<>EHL(N^L.:IHLH%L:;>E,:BO:/>JN>BK: N:KM>):<A:=H/:K:BO: #Q382> =C4A=>34=3>2A8=>;>680)4AE8P>34=3>2A8=>;>6808014C4B4#4C01>;8B<>4=CA>>B?8C0;0A34"8B1>0%2834=C0;)#Y"% BB8BC4=C4>B?8C0;0A34=3>2A8=>;>680)4AE8P>34=3>2A8=>;>6808014C4B4#4C01>;8B<>4=CA>>B?8C0;0A34"8B1>0%2834=C0;)#Y"% 745434)4AE8P>34=3>2A8=>;>680)4AE8P>34=3>2A8=>;>6808014C4B4#4C01>;8B<>4=CA>>B?8C0;0A34"8B1>0%2834=C0;)#Y"% BB8BC4=C4 >B?8C0;0A A03D03> 34 =3>2A8=>;>680 )4AE8P> 34 =3>2A8=>;>680 8014C4B 4 #4C01>;8B<> 4=CA> >B?8C0;0A 34 "8B1>0 %2834=C0;)#Y"% BB8BC4=C4>B?8C0;0AA03D03034=3>2A8=>;>680)4AE8P>34=3>2A8=>;>6808014C4B4#4C01>;8B<>>B?8C08B30+=8E4AB8303434>8<1A0 8A42C>A34)4AE8P>34=3>2A8=>;>680)4AE8P>34=3>2A8=>;>6808014C4B4#4C01>;8B<>4=CA>>B?8C0;0A34"8B1>0%2834=C0;)#Y"% AD?>34BCD3>B3>B*D<>A4B30;N=3D;0)D?A0A4=0;)>2843034&>ACD6D4B034=3>2A8=>;>6804#4C01>;8B<> <??3@=<;2Q;17/ 4;34A )8<U4B Z )4AE8P> 34 =3>2A8=>;>680 8014C4B 4 #4C01>;8B<> Z 4=CA> >B?8C0;0A 34 "8B1>0 %2834=C0; )#Y"%Z(D030!D=@D48A0 "8B1>0Z74;34A55B6<08;2>< 137A/ON<AC86>A424183>4< A4E8BC>4< 40248C4?0A0?D1;820PO>4< &')!# Objectivos: rever os aspectos fundamentais e os últimos progressos no que respeita à etiopatogenia, diagnóstico, tratamento e seguimento do carcinoma do córtex da glândula supra-renal. Métodos: pesquisa de bibliografia original ou de revisão publicada até Agosto de 2009. Conclusões: Da escassez de evidência científica sólida sobre o assunto têm resultado várias incertezas. Persistem dúvidas acerca da definição dos estádios III e IV, está por estabelecer o lugar exacto das terapêuticas adjuvantes, assim como quais os esquemas de citotóxicos mais eficazes. Os estádios avançados de doença associam-se a mau prognóstico, sendo a sobrevida global aos cinco anos baixa. A remoção cirúrgica de toda a massa tumoral constitui a única hipótese de cura. O mitotano, alguns citotóxicos e até a radioterapia parecem ter um papel importante como terapêutica adjuvante na doença avançada, e também nas recidivas. Os últimos anos têm acrescentado novidades interessantes no tratamento, mas cujo papel definitivo está por estabelecer. $ *&'* Carcinoma; Supra-renal; Estadiamento; Suprarrenalectomia; Quimioterapia; Radioterapia. '(&( Objectives: to review the principal issues and recent progress in the pathogenesis, diagnosis, treatment and follow-up of adrenocortical carcinoma. Methods: Search of original and review data published until August of 2009. Conclusions: The uncertainty in the management of adrenocortical carcinoma is a result of the lack of solid scientific evidence in the field. Uncertainty persists in the definition of disease stages III and IV, in the exact place of adjuvant therapy, and in establishing the most efficient cytotoxic protocol. Advanced disease stages have a poor prognosis, and the five year survival rate is low. The complete surgical removal of all tumoral tissue is the only chance of cure. Mitotane, cytotoxic fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ ?A75<23&3C7@N< .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H agents and radiotherapy may have an important role as adjuvant therapy in advanced disease and recurrences. Recently some interesting discoveries in treatment have been published witch definitive role is yet to be established. -+#&' Carcinoma; Adrenocortical; Staging; Adrenalectomy; Chemotherapy; Radiotherapy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a>L>=:>QM>GLYH =:=H>GZ: K>FHZYH<BKbK@B<:=:MHM:EB=: =>=HM><B=HMNFHK:E<HGLMBMNB:bGB<:ABI_ M>L>=><NK: >OB=H :H GbF>KH EBFBM:=H => =H>GM>L H;L>KO:=HL G: F:BHK I:KM> =HL L>KOBZHL F[=B<HL :L L[KB>L IN;EB<:=:L LYH :BG=: K>=NSB=:L +L <E^GB<HL =>;:M>FL> :BG=: <HF BGbF>K:L BG<>KM>S:L LH;K> H /. JN> OYH=>L=>H=B:@G_LMB<H:HMK:M:F>GMHI:L L:G=H I>EH >LM:=B:F>GMH > L>@NBF>GMH 0H=:OB:GHLbEMBFHL:GHLM>FL>:LLBLMB=H WIN;EB<:ZYH=>BFIHKM:GM>>OB=]G<B:<B>G M^?B<: > => :E@NF:L M>GM:MBO:L => <HGL>GLH LH;K>>LM:I:MHEH@B: ,:K:I>LJNBL:;B;EBH@KV?B<:K><HKK>NL>W ;:L>=>=:=HL,N;)>=>FAMMIPPP G<;B GEF GBA @HOIN;F>= 1MBEBS:K:FL> >F <HF;BG:Za>L =BO>KL:L HL L>@NBGM>L M>KFHL => I>LJNBL: :=K>GH<HKMB<:E :=K>G:E <:K<B GHF:MNFHKLG>HIE:LF<:G<>K=B:@GHLBL LM:@BG@ MK>:MF>GM LNK@>KR K:=BHMA>K:IR BF:@BG@ FBMHM:G> "HK:F <HGLB=>K:=HL HL :KMB@HLHKB@BG:BLHN=>K>OBLYHLH;K>HM>F: >FANF:GHLIN;EB<:=HL>FE^G@N:BG@E>L: :M[@HLMH=> "HK:FB@N:EF>GM>MB=:L >F<HGM:?HGM>L<HFHEBOKHL=>M>QMH:KMB@HL <BM:=HL IHK HNMK:L IN;EB<:Za>L >G<HGMK:=:L =NK:GM> : I>LJNBL: > HNMK:L <HFNGB<:Za>L <B>GM^?B<:L <HFH IHK >Q>FIEH <HFNGB<: Za>LHK:BL:IK>L>GM:=:L>FK>NGBa>L<B>GM^?B <:L LH;K> H :LLNGMH />E><<BHG:K:FL> HL :KMB@HL>IN;EB<:Za>LJN>=>:<HK=H<HF: :GVEBL> =HL :NMHK>L =>LM: K>OBLYH FHLMK: K:FF:BHKK>E>OXG<B:<E^GB<:G::;HK=:@>F =>LM:I:MHEH@B: $(#J"' !QBLM>F IHN<:L <>KM>S:L :<>K<: =: >MBH I:MH@>GB:=H/. :=HL=HL>@NBF>GMH=> BG<B=>GM:EHF:L =: @EXG=NE: LNIK:K>G:E <HF <:K:<M>K^LMB<:L BGB<B:BL LN@>LMBO:L => :=>GHF: BG=B<:F JN> IKHO:O>EF>GM> HL /. GYH L> HKB@BG:F : I:KMBK =>LM:L F:L L:L *H>GM:GMH>LMYHIN;EB<:=HL<:LHL K:KHL => :I:K>GM> F:EB@GBS:ZYH => :=>GH F:LHJN>IH=>KVH<HKK>K=>:<HK=H<HFH I:K:=B@F: =:L =N:L FNM:Za>L L>JN]G<B:BL >F@>G>LLNIK>LLHK>LMNFHK:BL EBLM:=> fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ ?A75<23&3C7@N< .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H :EM>K:Za>L FHE><NE:K>L IKHIHLM: [ >QM>GL: -N:=KH% LF:BL<HFNGL=BS>FK>LI>BMH :FNM:Za>LBG:<MBO:=HK:LGH,>>QIK>L LYH>Q:@>K:=:=H%#"%%:<MN:G=HOB:K><>I MHK=H%#"% !LM:I:K><>M:F;[FL>K::EM> K:ZYHFHE><NE:KBFIEB<:=:GHL<:LHL=>L<KB MHL >F <KB:GZ:L G: K>@BYH /NE =H K:LBE >F;HK: GYH L> M>GA:F =>FHGLMK:=H ?HK F:L=>MK:GLFBLLYH?:FBEB:K QUADRO I: Alterações moleculares mais implicadas na etiopatogenia do CSR15 Expressão exagerada de IGF-II actuando via receptor IGF-I Mutações do P53 Activação da B-catenina Mutações no oncogene RAS Inactivação da subunidade R1A da proteína Cinase A Mutações do receptor da ACTH Mutações no gene MEN 1 $&'"(IW# _" # &(#& !# `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a>L<E^ GB<:L F:BL ?K>JN>GM>L :LLH<B:=:L : <:=: ?HKF:=>ABI>KL><K>ZYH>G=_<KBG: L?HKF:L>G=_<KBGHBG:<MBO:LIH=>FL>K =>L<H;>KM:L => ?HKF: :<B=>GM:E HN F:GB?>L M:KL> IHK =HK GVNL>:L ?>;K> >G?:KM:F>GMH HN>F:@K><BF>GMH=>I>G=>G=H=:L=BF>G La>L=:E>LYH>HN=:>QM>GLYH=:=H>GZ: fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ QUADRO II: Manifestações clínicas associadas a cada tipo de hipersecreção hormonal no CSR. Hiperandrogenismo (Testosterona, DHEAs) Hirsutismo, virilização, voz grave, alopécia andrógena, oligomenorreia Estrogénio Ginecomastia, atrofia testicular, disfunção eréctil, infertilidade. Aldosterona HTA, Hipocaliémia Hipercortisolismo Síndrome de Cushing, hipocaliémia 17-OHprogesterona, $4-androstenediona Podem apresentar-se como endócrino-inactivo =BF>GLYH F[=B: =HL /. KHG=: HL <FF:LM]FLB=HLN<>LLBO:F>GM>K>IHKM:=HL <:LHL => E>La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n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aracterísticas histológicas constituintes do Score de Weiss. Elevada taxa mitótica (>50 / CGA) Mitoses Atípicas (r 6 / CGA) Invasão venosa Elevado padrão nuclear (grau 3 e 4) Baixa % de células claras (b 25%) QUADRO III: Doseamentos a requisitar perante o achado de uma lesão da glândula SR. Testosterona total 17-OHprogesterona, $4-androstenediona DHEAs B-estradiol em homens e mulheres pós-menopausa Metanefrinas e normetanefrinas plasmáticas fraccionadas ou Metanefrinas totais e catecolaminas fraccionadas na urina das 24h Aldosterona Renina Rácio aldosterona/ renina ou actividade da renina plasmática Ionograma Prova de dexametasona com 1 mg ACTH e cortisol plasmático ou cortisol salivar nocturno e cortisol Livre na Urina de 24h (se suspeita elevada de Cushing) Adaptado a partir de 2 e 24. +LF[MH=HL=>F>=B<BG:GN<E>:KIH=>F =>L>FI>GA:KNFI:I>EBFIHKM:GM>GH>LMN =H =HL MNFHK>L =: /. MHFH@K:?B: IHK >FBLLYH=>IHLBMKa>L,!0<HF?ENHKH=> LHQB@EN<HL> " # IH=> I>KFBMBK =BLMBG @NBK>GMK>E>La>L;>GB@G:L>F:EB@G:L=:/. ;:L>:G=HL>GNF:F:BHK:<MBOB=:=>F>M: ;_EB<: > <HGL>JN>GM> F:BHK <:IM:ZYH =H K:=BH?VKF:<H IHK >LM:L bEMBF:L ,!0 <HF F>MHFB=:MH NF EB@:G=H =: B AB=KHQBE:L><HGLMBMNBNF>Q<>E>GM>F[MH=H I:K:<HG?BKF:K:HKB@>F/.=>E>La>L>I:K: B=>GMB?B<:KF>MVLM:L>L=>/. + =B:@G_LMB<H => /. [ ABLMHI:MHEH@B<H =B?>K>G<B:ZYH >GMK> F:EB@GB=:=> > ;>GB@ GB=:=>[;:L>:=:G:L<:K:<M>K^LMB<:LF:<KH > FB<KHL<_IB<:L =H MNFHK *: H;L>KO:ZYH F:<KHL<_IB<: =H MNFHK : =>GLB=:=> >E>O: =::>QM>GLYH>QMK:<:ILNE:K>:>QBLM]G<B: =>?H<HLA>FHKKV@B<HLLYH<:K:<M>K^LMB<:L=> F:EB@GB=:=> *:FB<KHL<HIB::IK>L>GZ:=> FBMHL>L :M^IB<:L => BGO:LYH O:L<NE:K > NF GbF>KH :NF>GM:=H => FBMHL>L LNI>KBHK : Necrose Arquitectura tumoral difusa (>33%) Invasão capsular Invasão sinusoidal A cada item é atribuída a pontuação de 1, caso esteja presente, e 0, caso não se observe. CGA: campo de grande ampliação. <:FIH=>QLYH:L<:K:<M>K^LMB<:L<HF F:BHK O:EHK IK>=BMBOH => F:EB@GB=:=> 0]F LB=H =>L>GOHEOB=HL LBLM>F:L => IHGMN:ZYH <HF ;:L> G: H;L>KO:ZYH => OVKB:L <:K:<M> K^LMB<:LABLMHE_@B<:L +L<HK>=>3>BLLO:KB: >GMK> [ H F:BL IHINE:K > NF: >E>O:=: :<NB=:=> =B:@G_LMB<: IK>L>GZ: => HN F:BL<:K:<M>K^LMB<:LM>F>E>O:=HO:EHKIK>=B MBOH IHLBMBOH I:K: F:EB@GB=:=> 0>F GH >GM:GMH:LEBFBM:Za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fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ ?A75<23&3C7@N< .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H =::FHLMK:HN=>LNLI>BM:=>F>MVLM:L>LG: /. => MNFHK>L <HF HKB@>F =BO>KL: !Q<EN^=HL HL <:LHL => :FHLMK:L BG:=>JN: =:LJN>K>IK>L>GM:F>GMK>n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a>L<HKK>LIHG=>KV=> ?:<MH:/. BG=::LLBF:M>G=>G=H:HF:N IKH@G_LMB<H@EH;:E=:=H>GZ:>WBG?EN]G<B: ;>G[?B<:=>NF:<BKNK@B:<NK:MBO:G:LH;K> OB=:=>O>FF:GM>KL>:LK><HF>G=:Za>L=> HI>K:KF:LL:L=:/.JN>:IK>L>GM>F:LK>?> KB=:L<:K:<M>K^LMB<:L=>LNLI>BZYH '(!"(#'#&* <E:LLB?B<:ZYH=>)<":KE:G>IKHIHLM:>F >FH=B?B<:=:IHK/NEEBO:G>FM>F LB=H:M[:JNB:F:BLNMBEBS:=: "HB:=HIM:=: I>E: 1GBYH %GM>KG:<BHG:E HGMK: H :G<KH 1% > I>E: +)/ >F JN:=KH 2 + JN:=KH 2% FHLMK: : LH;K>OB=: :HL :GHL :LLH<B:=: : <:=: >LMV=BH =: <E:LLB?B<:ZYH 1% >F =N:L <HHKM>L =B?>K>GM>L *H >GM:GMHHO:EHKIKH@G_LMB<H=:LOVKB:L<E:LLB fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ QUADRO V: Classificação de McFarlane modificada. Estádio Sullivan et al. 1978 I T1, N0, M0 II T2, N0, M0 III T3, N0 M0 ou T1-2, N1,M0 IV T4, N0, M0 ou T3, N1, M0 ou T3-4, N0-1,M1 T1: Tumor < 5 cm T2: Tumor > 5 cm T3: Infiltração tumoral local alcançando órgãos vizinhos T4: Invasão tumoral de órgãos vizinhos N1: Gânglios linfáticos positivos M1: Metástases distantes QUADRO VI: Sobrevida associada a cada Estádio da classificação da UICC. Estádio Sobrevida aos 5 anos I 60 - 82% II 58 - 61% III 24 - 50% IV 0 - 13% ?B<:Za>L>QBLM>GM>LIK><BL:=>L>KO:EB=:=HIHK L[KB>L<HFF:BHKGbF>KH=>=H>GM>L .><>GM>F>GM> : !NKHI>:G *>MPHKD ?HK MA> /MN=R H? =K>G:E 0NFHKL !*/0 > H =K>G:E :K<BGHF: .>@BLMKR #KHNI .# IN;EB<:K:F =:=HL => NF: <HHKM> =>=H>GM>LJN>FHLMK:FNFO:EHKIKH@ G_LMB<H EBFBM:=H =: <E:LLB?B<:ZYH 1% *>LM> MK:;:EAH : LH;K>OB=: >LI><B?B<: =: =H>GZ: L_ [ LB@GB?B<:MBO:F>GM> =B?>K>GM> >GMK>HL>LMV=BHL%%%>%2L>G>LM>b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lassificação proposta pela ENSAT com base na sobrevida especifica de doença da coorte de doentes ACCRG. Invasão local inclui gânglios linfáticos, a veia cava inferior, veia renal ou órgãos adjacentes. Estádio Dimensão Nódulos positivos Invasão local Metástases TNM I < 5 cm - - - T1, N0, M0 II > 5 cm - - - T2, N0, M0 III qualquer + + - T1-2, N1,M0 IV qualquer + + + T 1-2, N1, M1 (&(!"(# &)& + MK:M:F>GMH <BKb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h<F=BF>GLYHF[=B:OL<F >FI:K>EA:=HL JN:GMH : B=:=> L>QH :<MB OB=:=> >G=_<KBG: >LM:=B:F>GMH > M>K: I]NMB<: :=CNO:GM> + L>@NBF>GMH F[=BH ?HB=>F>L>L *YHL>>G<HGMKHN=B?>K>G Z:LB@GB?B<:MBO:>GMK>HL@KNIHLJN:GMH:H M>FIH=>K><HKK]G<B:>LH;K>OB=:@EH;:E M:Q: => <HGO>KLYH I:K: E:I:KHMHFB: ?HB <HGMN=H >E>O:=: => !LM>L > HNMKHL =:=HL :IHGM:F I:K: JN> : :;HK=:@>F E:I:KHL<_IB<: IHLL: L>K <HGLB=>K:=: >F /. F>GHK>L HN B@N:BL : <F bGB<HL > <BK<NGL<KBMHL >LMV=BHL % > %% >F <>GMKHL <HF >QI>KB]G<B: >F LNIK:KK>G:E><MHFB:L IHK >LM: OB: BG=: :LLBF : F:BHKB: =HL <BKNK@Ba>L>G=_<KBGHLIK>?>K>::=K>G:E>< MHFB:IHKOB::;>KM::<BF:=HL<FIHBL IHLLB;BEBM: :FIE: >QIHLBZYH => >LMKNMNK:L >K>LL><Za>L>QM>GL:LL>G><>LLVKBH -N:GMH W >QM>GLYH =: K>LL><ZYH [ ?K> JN>GM> : G><>LLB=:=> => >Q><NM:K EBG?:=> G><MHFB:L:@K>LLBO:L>>F<:LHL=>=H>GZ: EH<:EF>GM> :O:GZ:=: IH=> L>K G><>LLVKBH K><HKK>K : K>LL><Za>L :E:K@:=:L >HN >F ;EH<H + EBFB:K I:K: K>LL><:K >LMKNMNK:L :=C:<>GM>L=>O>L>K;:BQHA:O>G=HBG=B<: ZYH I:K: G>?K><MHFB: BILBE:M>K:E I>K:GM> LNLI>BM:=>BGO:LYH=HKBFHN=:O>B:K>G:E )>MVLM:L>L A>IVMB<:L bGB<:L > :<>LL^O>BL IH=>F L>K IKHIHLM:L I:K: <BKNK@B: L> >LM: K>IK>L>GM:KNF:IHLLB;BEB=:=>=><NK: + >FIK>@H =: <BKNK@B: G: K>=NZYH MNFHK:E GH >LMV=BH %2 341D;:8=6 [ <HGMKH O>KLHI>EHL>N>?>BMHEBFBM:=HG:LH;K>OB=: *H>GM:GMHI>KFBM>K>=NSBKHL>?>BMHLG>?:L MHL=:ABI>KL><K>ZYHAHKFHG:E>IHLLB;BEBM:K : NMBEBS:ZYH => HNMK:L HIZa>L M>K:I]NMB<:L *>LM> <HGM>QMH IH=> L>K <HGLB=>K:=: F:L :I>G:LL>?HKIK>OBL^O>ENF:K>FHZYHLNI> KBHK:=HM><B=HMNFHK:E %)!#(&$%( >OB=H :H >LMV=BH :O:GZ:=H >F JN> FNBM:L O>S>L L> >G<HGMK:F HL =H>GM>L > W BFIHLLB;BEB=:=>=>NF:<BKNK@B:<NK:MBO:: JNBFBHM>K:IB::LLNF>NFI:I>EBFIHKM:G M> GH MK:M:F>GMH =: =H>GZ: > GH <HGMKHEH =HABI>KL><K>ZYHAHKFHG:E fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ ?A75<23&3C7@N< .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H QUADRO VIII: Efeitos adversos devidos ao mitotano. Sistema / órgão Efeito adverso Frequência Leucopenia, tempo de coagulação prolongado Muito comum Anemia, trombocitopenia Comum Ataxia, parestesias, vertigens, miastenia, sonolência, confusão Muito comum Alterações cognitivas polineuropatia, cefaleias Comum Anorexia, mucosite, vómito, diarreia, náusea, dispepsia, elevação de enzimas hepáticas Muito comum Hepatites tóxicas ou autoimunes Comum Insuficiência supra-renal, ginecomastia. Elevação de colesterol, triglicéridos, SHBG, CBG e TBG. Indução da metabolização hepática via microssoma. Muito comum Disfunção tiroideia, hipogonadismo masculino Comuns Rash Muito comum Cistite hemorrágica, proteinúria, hematúria Desconhecida HTA, hipotensão ortostática, flushing Desconhecida Micoses oportunistas Desconhecida Hematologia Sistema nervoso Gastrointestinal Endócrino e metabólico Pele Uro-genital Cardiovascular Infecções Adaptado de informação disponível em http://www.ema.europa.eu/. Muito comum (r1/10), Comum (r1/100 to <1/10), Invulgar, (r1/1,000 to <1/100), Raro (r1/10,000 to <1/1,000), Muito raro (<1/10,000), Desconhecida (dados indisponíveis). SHBG – sex hormone binding globulin. CBG – cortisol binding globulin. TBG - thyroid binding globulin. + +Iq 7=B<EHKH><EHKH?>GBE ?>M:GH8 <HGA><B=H IHK FBMHM:GH [ => EHG@>H?VKF:<HF:BL>LMN=:=HGH/. "HB NMBEBS:=HI>E:IKBF>BK:O>S>FANF:GHLG: =[<:=: => 0K:M:L> => NF :=K>GHE^MB<H LH;K>MN=HI:K::SHG:K>MB<NE:K=:/.F:L M:F;[F<HF:<MBOB=:=>G:SHG:?:L<B<NE:K L>G=H F>M:;HEBS:=H G>LM:L K>@Ba>L >F ?HK F:LM_QB<:LJN><:NL:F=>@>G>K:ZYHFBMH <HG=KB:E > HKB@BG:F K:=B<:BL EBOK>L 0>F :BG=:NF>?>BMHBGB;BM_KBHLH;:BAB=KH QBE:L> > G: <EBO:@>F =H <HE>LM>KHE H JN> >QIEB<: : LN: <:I:<B=:=> => <HGMKHE:K H ABI>K<HKMBLHEBLFH :;LHKZYH BGM>LMBG:E [ O:KBVO>E +?VKF:<H>QBLM>LH;=N:L?HKFN E:Za>L <HFIKBFB=H ERLH=K>Ge > FB<KHGB S:=H >F <VILNE: <NC: :;LHKZYH [ F>GHK G><>LLBM:G=H IHK BLLH => =HL>L :M[ =N:L O>S>L LNI>KBHK>L + +Iq [ :EM:F>GM> EBIH?^EB<H > IH=> L>K =>M><M:=H G: <HKK>GM> L:G@N^G>: :M[ F>L>L =>IHBL =: LN: :=FBGBLMK:ZYH + ?VKF:<H >LMV BG=B<:=H GHL <:LHL => K>LL><ZYH.BFIHLL^O>EHN=H>GZ::O:GZ: =:>LMV=BHL%%%>%2 LN:>?B<V<B:G:K>L IHLM: MNFHK:E ?HB K>OBLM: IHK EEHEBH > fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ ":LLG:<AM >F =BO>KLHL >LMN=HL IKHLI><MBOHL <HF F:BL => =H>GM>L *H MHM:E <>K<: => =HL =H>GM>L :IK>L>GM: :E@NF @K:N => K>LIHLM: MNFHK:E :IK>L>GM: NF: K>L IHLM:I:K<B:E><>K<:=>NF:K>LIHLM: <HFIE>M: LN:NMBEBS:ZYHM>F:BG=:EN@:K GHL>LMV=BHL%>%%I>K:GM>:BFIHLLB;BEB=:=> <BKb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n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`LNF L>@NG=H >LJN>F: :LLH<B:G=H <BLIE:MBG: OBG<KBLMBG: M>GBIHLB=H > <B<EH?HL?:FB=: <HFH M>K:I]NMB<: L><NG=VKB: >F =H>G M>L:I_L?:E]G<B::Hk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a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fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ ?A75<23&3C7@N< .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H EH<:E=:=H>GZ:?HB=> +F>LFH@KNIH => BGO>LMB@:=HK>L GNF >LMN=H <HGMKHE:=H :G:EBLHN H >?>BMH =: .0 :=CNO:GM> >F =H>GM>L >F >LMV=BH %%%% I>KM>G<>GM>L :H #>KF:G K>@BLMKR + M>FIH => L>@NB F>GMH F[=BH ?HB => F>L>L 2>KB?B<HNL> NF GbF>KH LB@GB?B<:MBO:F>GM> F>GHK => K><HKK]G<B:LEH<:BLGHL=H>GM>LLN;F>MB=HL: .0:=CNO:GM>EB >:<HK=H<HF >LM>L =:=HL : .0 :=CNO:GM> IH=>KV <HGLMB MNBKNF:F:BLO:EB:I:K:<BKNK@B:L=>IHM>G <B:E<NK:MBOHBG=>M>KFBG:=H.>.QHJN> LN<>=> JN:L> L>FIK> >F <:LHL => MNFHK>L OHENFHLHL F:BHK>L JN> <F F:N IKH@ G_LMB<H ABLMHE_@B<H =BLL>FBG:ZYH EH<:E BGMK:HI>K:M_KB: =BLL>FBG:ZYH EBG?VMB<: > BGO:LYH EH<:E .0 :=CNO:GM> =>O>KV L>K :=FBGBLMK:=::M[F>L>L:I_L:<BKNK@B:> ?K:<<BHG:=:>F=HL>L=BVKB:L=>:#R =NK:GM> =B:LL>F:G: :H EHG@H => : L>F:G:L =HL>MHM:E=>K:=B:ZYHIKHIHLM: I:K:HE>BMHMNFHK:EO:KB:>GMK>#R !QBLM>F>L<:LLHLMK:;:EAHLLH;K>:>?B<V <B:=:.0G>H:=CNO:GM>JN>IHLL:F?:OHK> <>K:LN:NMBEBS:ZYH UF:BL<HGL>GLN:E:NMBEBS:ZYH=:.0G: =H>GZ: >F >LMV=BH %2 I:EB:MBO: HN G:L K><B=BO:LEH<HKK>@BHG:BL *:K>OBLYH>?><MN: =: IHK ,HE:M >M :E : I:KMBK =: :GVEBL> => >LMN=HL =B?>K>GM>L GNF MHM:E => BG=BO^ =NHL BG<ENBG=H I:<B>GM>L <HF F>MVLM:L>L _LL>:LEBG?VMB<:LINEFHG:K>L>K><HKK]G<B:L EH<:BLHN=BLM:GM>LLN;F>MB=HL:.0I:EB:MB O:I:K::E^OBHLBGMHFVMB<H=HL=H>GM>L H;M>O>;>G>?B<BHLBGMHFVMB<H<HF:.0 !LM> >?>BMH IHLBMBOH [ F:BL >OB=>GM> :H G^O>E =H <HGMKHEH=:=HK>=>LBGMHF:LG>NKHE_@B<HL +L IKHMH<HEHL F:BL >LMN=:=HL I:K: : .0 I:EB:MBO:<HGLBLM>F>F=HL>bGB<:=>#R HN#R=BLMKB;N^=HLIHK=HL>L?K:<<BHG: =:LI:K><>G=HGYH>QBLMBK=B?>K>GZ:LLB@GB ?B<:MBO:L >GMK> :F;HL I:K: :E[F => F:BHK G><>LLB=:=> => K>I>MBZYH =H IKH<>=BF>GMH GHIKBF>BKH<:LH NK:GM>:.0[?NG=: F>GM:EIKHM>@>KHKBF<HGMK:E:M>K:E>OB@B:K :?NGZYHK>G:E F:BHKB: =HL =H>GM>L BG=B<:=HL I:K: .0M>KVBG=B<:ZYH<HG<HFBM:GM>I:K:MK:M: fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ F>GMH <HF FBMHM:GH +L =HBL :@>GM>L IHM>G<B:FL>IH=>G=HM:F;[F:@K:O:KHL ?>BMHL :=O>KLHL L>G=H H F:BHK KBL<H H => A>I:MBM> M_QB<: *H <:LH => >E>O:ZYH =:L MK:GL:FBG:L>LLNI>KBHK:O>S>LHGHKF:E HFBMHM:GH=>O>KVL>KLNLI>GLH NK:GM>: .0 :L =HL>L => FBMHM:GH GYH =>O>F NEMK: I:LL:KHL@=B: M>G=>G=HW?:EM:=> =:=HLLH;K>:L>@NK:GZ:=HNLHLBFNEMXG>H =:.0>=:-0<HF<BMHM_QB<HL>LM>L:@>GM>L GYH=>O>FL>K>FIK>@N>L>FI:K:E>EH "#*'&!'(&$])(' l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k !LM: M[<GB<: [ NL:=: I:K: =>LMKNBK F>MVLM:L>L HN K><HKK]G<B:L EH<:BL => OVKBHL MNFHK>LG><>LLBM:G=H=><HGMKHEHBF:@BHE_ @B<H A:;BMN:EF>GM> IHK ><H@K:?B: HN 0 /YH >L<:LL:L :L L[KB>L K>IHKM:G=H : >?B<V<B: $?K1A71/9R;71/ .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H =:M[<GB<:GH/. 3HH=>M:E IN;EB <:K:FK>LNEM:=HL=HMK:M:F>GMH<HF."=> =H>GM>L<HF/.:O:GZ:=H>>F:E@NGL <:LHL<HFK><HKK]G<B:L +MK:M:F>GMHH;M>O> LN<>LLH>F=HL=H>GM>L ."I:K> <>M:F;[FL>K>?B<:SGH:E^OBH=:=HK<:NL: =: IHK F>MVLM:L>L _LL>:L :H =>LMKNBK :L I>JN>G:L M>KFBG:Za>L G>KOHL:L K>LIHGLV O>BL I>E: MK:GLFBLLYH =: =HK 1F >GL:BH FNEMB<]GMKB<H NMBEBSHN : ." >F =H>GM>L <HF F>MVLM:L>L _LL>:L > =HK <HF L<HK> F[=BH=>=>:K>?K:<MVKB:W.0 +L =H>GM>L H;MBO>K:F K>=NZYH => IHGMHL G: >L<:E:=:=HK>F=HL<:LHL:H?BF=> NF:L>F:G:>F:H?BF=>L>F:G:L > H;MBO>K:F :E^OBH LBGMHFVMB<H >F :E@NF::EMNK::HEHG@H=HL>@NBF>GMH JNBFBH>F;HEBS:ZYH MK:GL:KM>KB:E => F>MVLM:L>LA>IVMB<:L[NF:HIZYHI:EB:MBO: I:K:E>La>LABI>KO:L<NE:KBS:=:L>F=H>GM>L GYH <:G=B=:MHL : <BKNK@B: HN ." :>K> >M :EK>IHKM:K:FHLK>LNEM:=HL=HMK:M:F>GMH> L>@NBF>GMH => =H>GM>L <HF F>MVLM:L>L A>IVMB<:L => /. I_L : L>LLa>L ?HB H;MB=:K>LIHLM:I:K<B:E>F=H>GM>L>LM:;B EBS:ZYH=:=H>GZ:?HBIHLL^O>E>F<:LHL> : IKH@K>LLYH GYH I`=> L>K >OBM:=: >F =H>GM>L =NK:ZYH =: >LM:;BEBS:ZYH ?HB >F F[=B: => F>L>L F^GBFH > FVQBFH => F>L>L K>LI><MBO:F>GM> +L <:LHL => K>LIHLM:<HFIE>M:H<HKK>K:F>FF>MVLM:L>L BG?>KBHK>L : <F "HB :BG=: H;L>KO:=H NF =><K[L<BFH=>GHLG^O>BLAHKFHG:BL>F =><:LHL=>MNFHK>L>G=_<KBGH:<MBOHL + IKBG<BI:E>?>BMH:=O>KLH[NF:LN;B=:MK:GLB M_KB:=:LMK:GL:FBG:L>L:O>S>LHGHK F:E>LBGMHF:L=>F:E>LM:K@>K:E 1FIKBF>BKH>GL:BH>LMN=HN:NMBEBS:ZYH FIGURA 1: Esquema de tratamento e Follow-up Tx – terapêutica. QT engloba mitotano isolado ou associado a EDP ou a S. * O mitotano ou a RT adjuvantes devem ser considerados mesmo após ressecções R0 nos tumores de maiores dimensões, de pior prognóstico histológico e no estádio III. (Os doentes em estádio IV, mesmo após cirurgia curativa, têm elevado risco de recorrência e devem sempre ser submetidos a terapia adjuvante, pelo menos, com mitotano). Adaptado a partir de 15 e 24. fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ ?A75<23&3C7@N< .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H => %%H=HF>MHFB=:MH %%)0+ >F =H>GM>L <HF /. F>M:LMVMB<H > :IK>L>GMHN K>LNEM:=HL=HL>@NBF>GMH=>=>E>L HL>L :M[#J?HK:FNMBEBS:=:LH;L>KO:G=HL> >E>O:=: <:IM:ZYH > :?BGB=:=> =H K:=BH?VK F:<HI>E:LE>La>L !F=H>GM>LO>KB?B<HNL> K>=NZYH HN >LM:;BEBS:ZYH =:L E>La>L + ?VK F:<H [ >F @>K:E ;>F MHE>K:=H F:L H =>L>GOHEOBF>GMH => E>N<H > MKHF;H<BMHI> GB:MK:GLBM_KB:LLYH>?>BMHL:=O>KLHLK>IHKM: =HLG:F:BHKB:=HL=H>GM>L ')!"(# <NK: %G<>KM>S:L:<>K<:=:=>?BGBZYH=HLbEMB FHL>LMV=BHL=:NMBEBS:ZYH:IKHIKB:=:=> -0 > .0 I>KF:G><>F <HFH H;LMV<NEHL *H >GM:GMH :L M>GM:MBO:L => <HGL>GLHL <HF> Z:F:LNK@BK>HLIKBF>BKHL>GL:BHL<HFI:K: MBOHL K:G=HFBS:=HL >LMYH >F F:K<A: +L b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bK@B<: L>FIK> JN> IHLL^O>E > H >FIK>@H => -0 >HN.0=><HGLB=>K:K>F:LLH<B:ZYHW<BKNK @B:HN>F:EM>KG:MBO::>LM: #" )'W# +/.[NF:=H>GZ:K:K:<NCH=B:@G_LMB <H<HGMBGN:=B?^<BE>HLMK:M:F>GMHL=BLIHG^ O>BL GYH M]F :E<:GZ:=H H LN<>LLH =>L>C:=H =>?HKF::<HGMK:KB:KHF:NIKH@G_LMB<H@EH ;:E +L =HL>:F>GMHL AHKFHG:BL > HL F[MH =HL=>BF:@BHEH@B:<:=:O>SF:BLL>GL^O>BL> =BLIHG^O>BLM]FI>KFBMB=H=B:@G_LMB<HLF:BL IK><H<>L >QBLM]G<B: => >JNBI:L <BKbK@B<:L =>=B<:=:LWK>FHZYH<HFIE>M:=>LM>LMNFH K>L>:NMBEBS:ZYH:=>JN:=:=:-0>.0=BL IHG^O>BL <HGLMBMN>F :L bGB<:L ABI_M>L>L => fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ $?K1A71/9R;71/ .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H &&]"' #&^' 1. 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Oral communication presented in11th European Congress of Endocrinology Symposia, Istambul, 2009, April. fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ ?A75<23&3C7@N< .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H !?>BMHL,E>BHMK_IB<HL=:L!LM:MBG:L n-N:E:>OB=]G<B: &;48>CA>?8245542CB>5BC0C8=B Y-70C8BC744E834=24 G:/H?B:.B;>BKH&HK@> HK>L =C4A=0><?;4<4=C0A34#43828=04A0;40<8;80A30+=8303434)0V340<8;80A,8E4A#08BY)#080 BB8BC4=C4>B?8C0;0AA03D03>3>)4AE8P>34=3>2A8=>;>6808014C4B4#4C01>;8B<>3>4=CA>>B?8C0;0A3>&>AC>Y>B?8C0;34)0=C> =CT=8> <??3@=<;2Q;17/=0)>580(8148A>Z+=8303434)0V340<8;80A,8E4A#08BZ(D0&A>54BB>A"050H4C4(>3A86D4B,848A0340BCA> Y)0=C0#0A803>E8>B># Z0=0B>580A8148A>6<08;2>< 137A/ON<AC86>A424183>4< A4E8BC>4< 40248C4?0A0?D1;820PO>4< &')!# Introdução: Os efeitos das estatinas sobre a redução dos níveis de colesterol LDL são amplamente conhecidos e cientificamente comprovados. Recentemente, vários ensaios clínicos têm levantado a questão das estatinas possuírem efeitos ditos pleiotrópicos, isto é, independentes de qualquer alteração/diminuição dos níveis de colesterol. Objectivo: Rever a evidência clínica dos benefícios da terapêutica com estatinas, distintos dos seus efeitos sobre o perfil lipídico. Metodologia: Pesquisa de artigos na Pubmed e sítios de Medicina Baseada na Evidência, publicados entre 2001 e 2009, nas línguas portuguesa, inglesa, francesa e espanhola. Para avaliação do nível de evidência, foi aplicada a Escala SORT (Strength of Recommendation Taxonomy) da American Academy of Family Physicians. Resultados: As estatinas apresentam efeitos pleiotrópicos a nível vascular, cardíaco e extra-cardiovascular secundários, na sua maioria, à inibição da síntese de isoprenóides. Existe evidência científica da melhoria da função endotelial e da diminuição da inflamação vascular (SORT A) com redução dos níveis séricos dos marcadores de inflamação aguda. Estudos sugerem efeitos positivos na hipertensão arterial, resposta trombogénica e estabilidade da placa aterosclerótica (SORT B). Recentemente têm sido atribuídas propriedades imunomoduladoras, anti-demenciais, antiosteoporóticas e anti-neoplásicas que carecem de evidência clínica (SORT C). Conclusão: A redução do colesterol LDL continua a ser o mecanismo primário na base da redução do risco cardiovascular atribuído às estatinas. São necessários mais estudos com enfoque nos efeitos pleiotrópicos das estatinas como end points primários. $ *&'* Estatina; Efeito pleiotrópico. '(&( Introduction: The effects of statins on reducing levels of LDL cholesterol are widely known and scientifically proven. Recently, several clinical trials have raised the issue of statins have pleiotropic effects, ie independent of any change/decrease in cholesterol levels. fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ ?A75<@23&3C7@N< .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H Aim: Review the clinical evidence of the benefits of statin therapy, as distinct from its effects on the lipid profile. Methodology: Research articles in Pubmed and sites of Evidence Based Medicine, published between 2001 and 2009, in Portuguese, English, French and Spanish. To assess the level of evidence was applied to scale SORT (Strength of Recommendation Taxonomy) of the American Academy of Family Physicians. Results: Statins have pleiotropic effects at the vascular, cardiac and extra-cardiovascular side, mostly due to the inhibition of isoprenoid synthesis. There is scientific evidence of improved endothelial function and decreasing vascular inflammation (SORT A) with decreases in serum markers of acute inflammation. Studies suggest positive effects on hypertension, thrombogenic response and stability of atherosclerotic plaque (SORT B). Recently there have been ascribed immunomodulatory properties, anti-dementia, anti-osteoporotic and anti-neoplastic that lack of clinical evidence (SORT C). Conclusion: The reduction of LDL cholesterol remains the primary mechanism at the base of cardiovascular risk reduction attributed to statins. Further studies are needed focusing on the pleiotropic effects of statins as primary end points. -+#&' Statins; Pleiotropic effects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n : OB: =H V<B=H F>O:E_GB<H "B@NK:n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bL<NEHEBLHO:L<NE:K>=HLFB_ <BMHL <:K=^:<HL !LM> ?:<MH ?HKG><>N : ;:L> fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ ?A75<@23&3C7@N< .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H FIGURA 1: Via do ácido mevalónico e mecanismo de acção das estatinas (PP: Pirofosfato). 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BGM>K E>N<BG:%(>?:<MHK=>G><KHL>MNFHK:E:E?: 0*"A ;>F <HFH FH=NE:ZYH =: IKH=NZYH =>HNMK:L<BMH<BG:L +L >?>BMHL :GMBHQB=:GM>L :MKB;N^=HL WL >LM:MBG:L M]F G: ;:L> : G>NMK:EBS:ZYH => >LI[<B>L K>:<MBO:L => HQB@[GBH FBGBFBS:G =H :L E>La>L IHK K:=B<:BL EBOK>L L><NG=VKB: :H:NF>GMH=:;BH=BLIHGB;BEB=:=>=H*+> W =BFBGNBZYH =: I>KHQB=:ZYH =HL E^IB=HL IHK BGB;BZYH =: L^GM>L> =HL BGM>KF>=BVKBHL BLHIK>G_B=>L M>K:I]NMB<:<HF>LM:MBG:L>LMV:LLH<B: =::NF:NF>GMH=:>LM:;BEB=:=>=:IE:<: :M>KHL<E>K_MB<: 0:;>E: %% JN> L> K>E:<BHG: <HF:=BFBGNBZYH=:<HG<>GMK:ZYH=>F>M: EHIKHM>:L>L<HE>LM>KHE( (HQB=:=H>=H<HG M>b=H <>GMK:E => E^IB=HL > F:<K_?:@HL =: F:MKBS=:IE:<:LN;LMBMN^=HIHK<HE:@[GBH fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ ?A75<@23&3C7@N< .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H TABELA I: Artigos de revisão centrados nos efeitos pleiotrópicos das estatinas. Efeito Artigo Metodologia Resultado/Conclusão Microalbuminúria Estatinas e Microalbuminúria5 Dias P et al, 2003 Artigo de revisão 13 ensaios clínicos 1991 – 2002 (9 em DM1 ou 2) 5 ensaios: diminuição estatisticamente significativa da microalbuminúria - Parece haver tendência para n na microalbuminúria com a terapêutica hipolipemiante Estenose aórtica O Papel das Estatinas Revisão de 6 estudos na Estenose Valvular retrospectivos não aleatoAórtica Calcificada. rizados Mito ou Realidade?14 (2001 – 2004) Moura et al, 2007 Are statins effective for simultaneously treating dyslipidemias Antiand hypertension?7 hipertensor Kwang K K et al, 2008 Fibrilhação auricular Imunomodulador Diabetogénico Vasoespasmo cerebral Uso no pré-operatório Artigo de Revisão É perceptível a utilidade e a eficácia da terapêutica com estatinas em doentes com estenose aórtica ligeira a moderada (<1.5 cm2) e com valores de LDL > 100 mg/dl. - Estatinas estão associadas a n modesta da TA em pacientes HTA, independentemente dos níveis de colesterol - Uso combinado de estatina com IECAs ou antagonistas da AT como prevenção de arteriosclerose e DC em pacientes HTA controlados Nível de evidência 3 (Grande heterogeneidade nos resultados dos ensaios; Estudos pequenos) 3 2 3 Pleiotropic effects of statins in atrial fibrillation patients: the evidence15 Hadi AR et al, 2009 Revisão 4 meta-análises 5 estudos randomizados 27 estudos prospectivos Relativa efectividade do uso de estatinas na 3 prevenção de FA após cardioversão electrica, inserção de pacemaker ou CDI e na ICC; (Estudos com metodologias e objectivos dispares) Uso perioperatório associado com outcome pos-operatório favoravel. Statins – are they potentially useful in rheumatology?16 Bielinska A et al, 2007 Artigo de revisão Spotlight on statins17 Weber M S, 2007 Artigo de revisão 7 ensaios clínicos (2002 – 2006) LES – n proteinúria e deposição glomerular de imunoglobulina AR – n parâmetros inflamatórios EM – n nº e volume de lesões de novo na ressonância magnética 3 Statin Therapy and Risk of Developing Type 2 Diabetes: A Meta-Analysis12 Rajpathak S et al, 2009 Meta-análise 57 593 pacientes 3 anos e 9 meses Estudo WOSCOPS – l 6% Risco relativo 2 Statins and risk of incident diabetes: a collaborative metaanalysis of randomised statin trials11 Sattar N et al, 2010 Meta-análise 91 140 pacientes 4 anos (1994 – 2009) l 9% Risco relativo - Em ensaios com indivíduos>65 anos - Independentes do IMC e do LDL > Tratamento de 255 pacientes em 4 anos – 1 caso de DM2 Role of statins in cerebral vasospasm18 Sugawara T et al, 2008 Artigo de revisão Uso de estatinas após uma hemorragia subaracnoideia é seguro e melhora o vasospasmo cerebral. Perioperative statins: More than lipidlowering?19 Feldman L S, 2008 Artigo de Revisão 10 estudos (2003 – 2007) n Progressão da aterosclerose - Efeito positivo na AR e LES (?) 3 (Não há estudos exclusivos) Uso aceitável em pacientes que se irão submeter a cirurgia cardíaca ou vascular (ACC/AHA 2007) Efeitos benéficos CV cessam após paragem da toma, com possível efeito rebound 2 3 (Estudos limitados) 2 Legenda: n- diminuição; l- aumento; TA – tensão arterial; FA – fibrilação auricular; HTA - hipertensão arterial; IECA -inibidores da enzima de conversão da angiotensina; AT - angiotensina; DC - doença coronária; CDI - cardiodesfibrilador implantável; ICC - insuficiência cardíaca congestiva; IMC - índice de massa corporal; DM2 - diabetes mellitus tipo 2; DM1 – diabetes mellitus tipo 1; LES – lúpus eritematoso sistémico; AR – artrite reumatóide; EM – esclerose múltipla. BGB;BZYH =: K>LIHLM: MKHF;H@[GB<: 0:;>E:%%=>O>L>:H:NF>GMH=:;BH=BLIH GB;BEB=:=>=H*+>G=HM>EB:E<HFBGB;BZYH=: fn/+%! !,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ :@K>@:ZYHIE:JN>MVKB:>:NF>GMH=:>QIK>L LYH=>MKHF;HFH=NEBG:BGB;BZYH=:>QIK>L LYH=H?:<MHKM><B=N:E>=HBGB;B=HK=H:<MBO: ?A75<@23&3C7@N< .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H =HK =H IE:LFBGH@[G>H <HF <HGL>JN>GM> :NF>GMH =H :<MBO:=HK =H IE:LFBGH@[G>H M><B=N:E=BFBGNBZYH=::@K>@:ZYHIE:JN>MV KB:>=::<MBO:ZYHIE:JN>MVKB:M>FIH>=HL> TABELA II: Ensaios clínicos nos quais foram observados efeitos pleiotrópicos das estatinas. Efeito Antiinflamatório Metodologia Myocardial Ischemia Reduction with Aggressive Cholesterol Lowering20 (MIRACL) Schwartz et al, 2001 n=2 402– Prevenção Secundária – 24 semanas Atorvastatina 80 mg/dia vs. placebo nn PCR (p<0,001) - n 86% em EAM - n 71% Angina instável - n 60% LDL - n 37% triglicerídeos Pravastatin Inflammation CRP Evaluation21 (PRINCE) Albert et al, 2001 n1=1702 – Prevenção Primária – 24 semanas n2=1182 – Prevenção Secundária – 12 semanas Pravastatina 40mg/dia vs placebo n1: n16,9% PCR (p<0,001) n2: n14,7% PCR (p<0,001) Ø associação entre os níveis basais de PCR e de LDL Atorvastatin vs. Simvastatin on Atherosclerosis Progression22 (ASAP) Van Wissen et al, 2002 n=325 com hipercolesterolémia familiar – 2 anos Atorvastatina 80 mg/dia vs. Sinvastatina 40mg/dia nn PCR (p<0,02) - n 34% Atorvastatina - n 9% Sinvastatina nn Espessura da intima-média carotidea - n 40,1% Atorvastatina - n 19,7% Sinvastatina 1 n=133 diabéticos tipo 2 sem DCV – 30 semanas Atorvastatina 10 mg vs. 80 mg/dia 10mg – n 15% PCR (p=0,012) 80mg – n 47% PCR (p<0,001) 2 Atorvastatin and thrombogenicity of the carotid atherosclerotic plaque24 (ATROCAP) Cortellaro et al, 2002 n=59 com estenose carotídea bilateral elegíveis para endarterectomia em 2 passos – 5 meses Atorvastatina 20 mg/dia vs. placebo nn Atorvastatina (p<0,02) na placa de ateroma de: - Macrofagos - Antigénio e actividade do factor tecidual > nFenótipo inflam./trombogénico das placas ateroma 2 Reversing Atherosclerosis with Aggressive Lipid Lowering25 (REVERSAL) Nissen, 2004 n1=654 com doença coronária sintomática e estenose r 20% na angiografia coronária – 18 meses Pravastatina 40mg/dia vs Atorvastatina 80mg/dia nn LDL (p<0,001) -25,2% Pravastatina -46,3% Atorvastatina Volume do ateroma (p=0,02) - l 2,7% Pravastatina - n 0,4% Atorvastatina nn PCR (p<0,001) -5,2% Pravastatina -36,4% Atorvastatina 2 Increase in circulating endothelial pro- n=15 com doença coronária – 4 genitor cells by statin therapy in semanas patients with stable coronary artery Atorvastatina 40 mg/dia disease26 Vasa M et al, 2001 l Células endoteliais progenitoras derivadas da medula óssea vermelha (p<0.05) - 1,5x após 1 semana - 3x após 4 semanas 3 Effects of atorvastatin on bone in postmenopausal women with dyslipidemia: a double-blind, placebo-controlled, dose-ranging trial13 Bone HG et al, 2007 n= 626 Mulheres pós-menopausa com dislipidémia – 1 ano Atorvastatina 10, 20, 40, ou 80 mg/dia vs placebo Não houve diferença significativa na densidade mineral óssea entre os grupos com atorvastatina ou placebo, independentemente dos efeitos anti-dislipidémicos 2 n=40 com SOP e hiperandrogenemia – 12 semanas Atorvastatina 20mg/dia vs placebo n n n n n n 2 Diabetes Atorvastatin Lipid Intervention Study23 (DALI) Van de Ree et al, 2003 Anticoagulante Placa arterios-clerótica Neovascularização miocárdica Anti-osteoporótico Síndrome do Ovário Policístico The Effect os Atorvastatin in Patients with Polycystic Ovary Syndrome: A Randomized Double Blind Placebo Controlled Study27 Sathyapalan T et al, 2008 Resultado Nível de evidência Ensaio Clínico Colesterol total (p<0,01) LDL (p<0,01) Triglicerídeos (p<0,01) PCR (p=0,04) Testosterona (p<0,01) Resistência à insulina 1 1 Legenda: n - amostra; n - diminuição; l - aumento; PCR - proteína C reactiva; EAM – enfarte agudo do miocárdio; Ø – ausência; DCV – doença cardiovascular; SOP – síndrome do ovário poliquístico. fn/+%! 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!,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+ ?A75<@23&3C7@N< .!2%/0,+.01#1!/ !!* +.%*+(+#% %!0!/!)!0+(%/)+H H &&]"' #&^' 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 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