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Sabato 27 ottobre 2012 - Pacini Editore

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COmuNiCaziONi ORali<br />

patients who had undergone cystoprostatectomy for bladder cancer<br />

(controls). Immunostainings and confocal microscopy were<br />

used to visualize SLUG expression at the protein level.<br />

Results. SLUG gene expression levels were significantly<br />

(P < 0.05) lower in the neoplastic (with no appreciable difference<br />

between low and high-grade PCa) versus normal prostatic<br />

epithelia (~12 times in low grade, ~16 times in high grade) and in<br />

neoplastic versus normal stroma (~4 times in both grades).<br />

SLUG was predominantly expressed in the stromal rather than<br />

the epithelial compartment, with higher levels in the neoplastic<br />

stroma. The mean expression level of SLUG in normal samples<br />

from the untreated patients was not significantly different to that<br />

obtained in normal samples from controls.<br />

Immunostainings showed that, in the normal prostate glands,<br />

both basal and luminal secretory cells strongly expressed SLUG<br />

in their nuclei, whereas SLUG staining ranged from very weak<br />

to moderate in the neoplastic glands. SLUG expression was inversely<br />

related to that of the cell cycle regulator cyclin D1, and<br />

the proliferation marker Ki-67.<br />

Lastly, ADT generally enhanced SLUG expression in the stroma,<br />

particularly in that of low-grade PCa.<br />

Conclusions. These preliminary findings suggest that, as observed<br />

in PCa cell lines (3), in the human prostate tissues, SLUG<br />

may inhibit neoplastic epithelial cell proliferation rather than act<br />

as an EMT promoter. It may also have a different role in the PCaassociated<br />

stroma, whose response to ADT may have important<br />

clinical and pathological implications. All these issues are the<br />

subject of ongoing investigation in our laboratories.<br />

references<br />

1 Nieto MA, Sargent MG, Wilkinson DG, et al. Control of cell behavior<br />

during vertebrate development by Slug, a zinc finger gene. Science<br />

1994;264:835-9.<br />

2 Barrallo-Gimeno A, Nieto MA. The Snail genes as inducers of cell<br />

movement and survival: implications in development and cancer.<br />

Development 2005;132:3151-61.<br />

3 Liu J, Uygur B, Zhang Z, et al. Slug inhibits proliferation of human<br />

prostate cancer cells via downregulation of cyclin D1 expression.<br />

Prostate 2010;70:1768-77.<br />

Pathological staging of uterine cervical carcinoma<br />

after neoadjuvant chemotherapy: a predictor<br />

of survival<br />

V.G. Vellone1 , D. Lorusso2 , V. Masciullo2 , G. Amodio2 , G. Chiarello1<br />

, E.D. Rossi1 , G. Fadda1 , G. Scambia1 , G.F. Zannoni2 1 Istituto di Anatomia ed Istologia Patologica, Policlinico A. Gemelli, Università<br />

Cattolica S.Cuore, Roma; 2 Istituto di Ostetricia e Ginecologia,<br />

Policlinico A. Gemelli, Università Cattolica S.Cuore, Roma<br />

Background. Radio-chemotherapy represents a relevant therapeutic<br />

option for cervical carcinoma. Surgical removal of uterus,<br />

ovaries, lymph nodes and peritoneal sampling after the neoadjuavant<br />

treatment give us the unique opportunity to evaluate the real<br />

ammount of the residual, its anatomic location and its impact on<br />

overall survival. A staging method is proposed and its implication<br />

in prognosis is investigated.<br />

Materials and methods. Study population: 114 cervical cancer<br />

patients (stage IB-IV FIGO)<br />

Treatment: platinum based chemotherapy with concomitant<br />

external beam radioterapy and then radical hysterectomy, lyphadenectomy<br />

and peritoneal sampling<br />

Local response classificated as follow 1 2 :<br />

pR0: Pathological Complete Response<br />

pR1: Pathological Partial Response<br />

pR2: Pathological No Response.<br />

325<br />

All patients were re-staged according to ypTNM and FIGO staging<br />

and then combined with pR as follow:<br />

No Residual Disease (NRD): pR0 Stage 0<br />

Minimal Residual Disease (MRD): pR1 Stage IA and IB; pR2<br />

Stage IA<br />

Local Residual Disease (LRD): pR1 Stage IIA and IIB; pR2<br />

Stage IB, IIA, IIB<br />

Metastatic Disease (MD): any pR Stage III and IV<br />

Mean follow-up: 39 months<br />

Results. 46 patients resulted NRD; 25 MRD; 23 LRD; 20 MD.<br />

NRD patients showed a significant advantage in suvival if compared<br />

to LRD (p < 0,001) and MD (p < 0,001). No significant<br />

difference were observed with MRD<br />

LRD showed a slight better survival if compared to MD (p = 0,1).<br />

Conclusions. A complete pathological staging confirmed its crucial<br />

role in risk stratification. Furthermore it could be useful for planning<br />

a second line treatment after surgery in patient with residual.<br />

referencies<br />

1 Zannoni GF, Vellone VG, Carbone A. Morphological effects of radiochemotherapy<br />

on cervical carcinoma: a morphological study of<br />

50 cases of hysterectomy specimens after neoadjuvant treatment. Int J<br />

Gynecol Pathol 2008;<strong>27</strong>:<strong>27</strong>4-81.<br />

2 Zannoni GF, Vellone VG. Accuracy of Papanicolaou smears in cervical<br />

cancer patients treated with radiochemotherapy followed by radical<br />

surgery. Am J Clin Pathol 2008;130:787-94.<br />

Clinical, pathological and molecular prognostic<br />

factors for non-endometrioid (type II) endometrial<br />

carcinoma<br />

V.G. Vellone1 , A. Fagotti2 , D. Gallo2 , C. Bottoni2 , L. Santoro1 ,<br />

E.D. Rossi1 , G. Fadda1 , G. Scambia1 , G.F. Zannoni2 1 Istituto di Anatomia ed Istologia Patologica, Policlinico A.Gemelli, Università<br />

Cattolica S.Cuore, Roma; 2 Istituto di Ostetricia e Ginecologia,<br />

Policlinico A.Gemelli, Università Cattolica S.Cuore, Roma<br />

Background. Non Endometrioid Endometrial Carcinoma (NEC)<br />

are an heterogeneus group of neoplasms with a notorius highly<br />

malignant behaviour, with different features and a worse prognosis<br />

if compared to conventional endometrioid carcinomas 1 .<br />

The impact in prognosis of a series of clinical, pathological and<br />

molecular markers is investigated.<br />

Materials and methods. Study population: 28 non endometrioid<br />

endometrial carcinoma patients treated withradical hysterectomy,<br />

lymph adenectomy and peritoneal sampling.<br />

Mean Follow up duration: 32 months<br />

Impact in overall survivall of Patients age, Tumor size, % of<br />

Myometrial Invasion, Lymph nodes metastases, extralimphonodal<br />

metastases, Stage, ER, PR, Her2/neu, Ki67, p53, bcl-2 is<br />

investigated<br />

Results. NEC confirmed its fame of deadly disease: half of the<br />

patients died of the disease. We found no prognostic significance<br />

for Age, Tumor size, % of Myometrial Invasion, Lymph nodes<br />

metastases, extralimphonodal metastases, Stage, ER, PR, Ki67,<br />

p53, bcl-2 (p > 0,05).<br />

Only positivity for Her2/neu (2+ FISH+ or 3+) identified a sub<br />

population of cases with a worse prognosis (p = 0,03).<br />

Conclusions. This finding confirm the aggressiveness of these<br />

neoplasms but rise new opportunities in target terapies for these<br />

unlucky patients.<br />

references<br />

1 Zannoni GF, Vellone VG, Arena V, et al. Does high-grade endometrioid<br />

carcinoma (grade 3 FIGO) belong to type I or type II endometrial<br />

cancer? A clinical-pathological and immunohistochemical study. Virchows<br />

Arch 2010;457:<strong>27</strong>-34.

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