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Download the ESMO 2012 Abstract Book - Oxford Journals

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Annals of Oncology<br />

Results: Between Dec 2010 and Apr <strong>2012</strong>, ∼1000 pts were enrolled from 35<br />

countries, predominantly Spain (n = 180), Italy (n = 110) and France (n = 101).<br />

Baseline characteristics were available from 677 pts as of 30 Jan <strong>2012</strong>. Most pts had<br />

stage III/IV OC (stage I/II/III/IV: 7%/11%/60%/18%). The majority (93%) received<br />

paclitaxel q3w and 94% received BEV at a dose of 15 mg/kg; 14% had received prior<br />

neoadjuvant CT. Baseline characteristics from <strong>the</strong> entire population of ∼1000 pts will<br />

be reported, toge<strong>the</strong>r with details of CT and BEV schedules selected.<br />

Conclusions: ROSiA should provide valuable new information on <strong>the</strong> safety of BEV<br />

for up to 36 cycles and in pts who have received neoadjuvant CT, as well as enabling<br />

extensive translational research.<br />

Disclosure: N. Colombo: NC has received honoraria for advisory boards and speaker<br />

engagements from Roche. F. Selle: FS acts as a Consultant for Roche and PharmaMar.<br />

P. Pautier: PP has served on Advisory Boards for Roche and Ipsen. D. Bollag: DB is an<br />

employee and holds stocks in F Hoffmann-La Roche Ltd. A.M. Oza: AO has received<br />

research funding from Roche. All o<strong>the</strong>r authors have declared no conflicts of interest.<br />

979P PREDICTIVE AND PROGNOSTIC ROLE OF SURVIVIN AND P53<br />

EXPRESSION IN PATIENTS WITH ADVANCED OVARIAN<br />

CANCER TREATED WITH NEOADJUVANT CHEMOTHERAPY<br />

A. Ga˛ sowska- Bodnar 1 , L. Bodnar 2 , M. Jerzak 3 , G. Wcisło 2 , M. Cichowicz 4 ,<br />

A. Da˛ bek 4 , W. Kozłowski 4 , C. Szczylik 2 , W. Baranowski 1<br />

1 Department of Gynecology and Gyneacology Oncology, MIlitary Institute of<br />

Medicine, Warsaw, POLAND, 2 Department of Oncology, Military Institute of<br />

Medicine, Warsaw, POLAND, 3 Department of Gyneacology and Gyneacology<br />

Oncology, MIlitary Institute of Medicine, Warsaw, POLAND, 4 Department of<br />

Pathology, Military Institute of Medicine, Warsaw, POLAND<br />

Background: Qualification of patients with advanced ovarian cancer (AOC) to<br />

treatment with primary or interval debulking surgery (IDS) is <strong>the</strong> subject of<br />

controversy. The aim of this study was to assess <strong>the</strong> expressions of selected proteins of<br />

apoptosis to <strong>the</strong> effects of neoadjuvant chemo<strong>the</strong>rapy (NAC) in patients with AOC.<br />

Material and methods: We evaluated 60 consecutive patients with AOS (FIGO stage<br />

IIIC-IV) treated with NAC, retrospectively. Formalin-fixed, paraffin-embedded tissue<br />

specimens were immunohistochemically stained for expression of p53 and survivin in<br />

patients given platinum-based NAC undergoing IDS. The expression of survivin was<br />

adopted dichotomization by <strong>the</strong> median expression of <strong>the</strong> protein found total score<br />

(TS) equals 2. For low expression of survivin was TS ≤ 2, while high total score TS> 2<br />

The positive and negative expression of p53 were used to dichotomization study group.<br />

Results: Median age of 60 patients was 60 years. The optimal IDS was achieved in<br />

69.1% (38/55). We observed significant difference in <strong>the</strong> percentage of stained nuclei<br />

(PS, p = 0.0002), <strong>the</strong> intensity of staining (IS, p = 0.0003) and TS (p = 0.0001) by<br />

comparing <strong>the</strong> expression of survivin in tumor tissue taken before and after NAC. The<br />

expression of p53 in tumor tissue before and after NAC was observed and significant<br />

difference was in PS, (p = 0.0424). There were no statistically significant difference in<br />

IS and <strong>the</strong> TS. Expression of survivin and p53 was not related to <strong>the</strong> results of IDS.<br />

Survivin expression was a prognostic factor in AOC patients treated with NAC (p =<br />

0.0484). Expression of survivin and p53 proteins was not a predictor factor in AOC<br />

patients. Adverse factors affecting <strong>the</strong> PFS for AOC patients treated with NAC were:<br />

lack of optimal IDS and <strong>the</strong> lack of an objective response by RECIST criteria<br />

(respectively HR was 3.93 (95% CI, 2.07-7.46, p

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