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		<title>Honest Straightforward Fact Around The Succimer Victory - Історія редагувань</title>
		<link rel="self" type="application/atom+xml" href="http://istoriya.soippo.edu.ua/index.php?action=history&amp;feed=atom&amp;title=Honest_Straightforward_Fact_Around_The_Succimer_Victory"/>
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		<updated>2026-05-12T15:38:03Z</updated>
		<subtitle>Історія редагувань цієї сторінки в вікі</subtitle>
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		<id>http://istoriya.soippo.edu.ua/index.php?title=Honest_Straightforward_Fact_Around_The_Succimer_Victory&amp;diff=120975&amp;oldid=prev</id>
		<title>Animal13neck: Створена сторінка: Mean age at diagnosis among BRCA mutation carriers is reported to range from 45 to 48 years old in the literature [14, 16]. In our series, median age at diagnos...</title>
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				<updated>2016-12-13T05:52:56Z</updated>
		
		<summary type="html">&lt;p&gt;Створена сторінка: Mean age at diagnosis among BRCA mutation carriers is reported to range from 45 to 48 years old in the literature [14, 16]. In our series, median age at diagnos...&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Нова сторінка&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Mean age at diagnosis among BRCA mutation carriers is reported to range from 45 to 48 years old in the literature [14, 16]. In our series, median age at diagnosis was 54 years old both for sporadic and for HBOC ovarian cancer. HBOC ovarian tumours are generally diagnosed at a higher stage and grade as compared to sporadic cancers [1, 4]. On the contrary, in our study, a significant higher proportion of patients in the BRCA+ group was diagnosed at stage II when compared [https://en.wikipedia.org/wiki/Succimer Succimer] to the sporadic group. Furthermore, HBOC ovarian tumours are typically of serous histology [1, 2, 16] Generally, among HBOC ovarian cancers, no borderline or mucinous cancers are reported [4]. Consistent with the literature, in the present series, most of the HBOC ovarian tumours (70%) were high-grade serous and 25% were undifferentiated tumours. On the contrary, among the sporadic tumours, only around 50% of tumours were high-grade serous and endometrioid; clear cells, and mucinous tumours were observed as well. In our series, radical primary surgery was performed in more than 70% of patients in both groups. In one-third of the patients, both in BRCA+ and in control groups, a neoadjuvant chemotherapy was administered. In our series, in patients who underwent surgery after neoadjuvant chemotherapy, optimal cytoreduction was achieved in all BRCA+ and in 70% of controls. According to many studies, patients carrying BRCA mutation have a higher response rate to platinum-based chemotherapy [2, 5, 6, 7, 9, 10, 17]. In the study of Cass et al., a significantly greater [http://www.selleckchem.com/products/rsl3.html RSL3 chemical structure] response to first-line platinum-based chemotherapy and a longer disease-free interval was observed among patients with BRCA+ ovarian cancer [5]. Also, in the study of Tan et al., in BRCA+ patients, a significantly higher response rate to first-, second-, and third-line platinum-based chemotherapy as compared to controls was observed [10]. In the study of Gorodnova et al., complete clinical response was documented in 34% of BRCA mutation carriers versus 4% of non-carriers (p [http://www.selleckchem.com/products/ag-221-enasidenib.html AG-221 manufacturer] BRCA1/2 function, there is a deficiency in the homologous-recombination repair, resulting in an impaired ability of tumour cells to repair platinum-induced double-strand breaks [2, 6]. Whether the superior response to platinum-based chemotherapy translates into a better outcome is unclear. Tan et al. described the ��BRCAness�� phenotype, with superior outcomes following platinum-based therapy in patients with BRCA mutations [10, 18], with survival advantage demonstrated by other retrospective studies [3, 5, 8, 12, 13, 19].&lt;/div&gt;</summary>
		<author><name>Animal13neck</name></author>	</entry>

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