Introduction
The most common cause of death from female reproductive
cancers is ovarian cancer. In addition to the lack of early-stage illness symptoms, there also are no reliable screening techniques,
which leaves two thirds of patients with advanced-stage ovarian
cancer when they are diagnosed. The development of efficient
screening tests and their implementation in a clinical setting are
of utmost importance to improve the prognosis of ovarian cancer
by prompt detection because the 5-year survival rate is up to 90%
in patients with early-stage disease while it is less than 20% in
those with advanced-stage disease [1]. A deadly form of gynecologic cancer that develops from an ovarian tumor is called ovarian
cancer. Initially, symptoms are typically subtle and may include
bloating, pelvic pain, and difficulty eating, and excessive urination, and they can be mistaken for other conditions. Ovarian cancers are categorized as «epithelial» and are thought to develop
from the ovary’s surface in the majority (>90%) of cases. However,
some data point to the possibility that certain ovarian malignancies may potentially originate in the fallopian tube. These ovarian cancer-mimicking fallopian cancer cells are believed to exist.
Some varieties (germ cell cancers) arise from supporting cells or
from egg cells. Gynecologic cancers, including ovarian cancers, fall
within this category [2]. According to Globocan http://globocan.
iarc.fr/Default.aspx), ovarian cancer had 238,619 incident cases
in 2012, making it the seventh most prevalent cancer overall and
the leading cause of death from gynecological cancers. It is listed
as the second most prevalent gynecological cancer in developing
nations with 17,755 incident cases in 2012 and the fourth most
prevalent cancer in women overall. Basically, industrialized nations have the highest ovarian cancer incidence rates. North America and Western Europe had the highest incidence rates (10.7 per
100,000 person-years and 13.3 per 100,000 person-years, respectively), whereas North Africa has the lowest incidence rates (2.6
per 100,000 person-years). However, in a hospital-based data
set from the National Cancer Institute, Gezira University, Central Sudan, and Radiation Isotopes Center in Khartoum, collected between 2000 and 2006, ovarian cancer accounted for 6.8%
(949) of all recorded cancers (n=226,652) and was ranked the
sixth most common cancer for both genders. The incidence rate
of ovarian cancer in the entire Sudan has not yet been determined. In addition, ovarian cancer ranked fourth among all female
cancers in a more recent data set (2009-2010) from the National
Cancer Registry for the Khartoum State alone, with an estimated
incidence rate of 188 per 100,000 people, a gender-specific rate
of 8.0 per 100,000 people, and an age-standardized rate (ASR)
of 7.0 per 100,000 people. Due to the lack of death certificates,
the survival rate for ovarian cancer in Sudan has also never been
reported, and the majority of patients who presented with advanced-stage disease did not receive complete examinations or
symptomatic treatment [3]. The precise cause of ovarian cancer
is still mostly unknown. There are various factors that seem to
influence the likelihood of getting ovarian cancer [4]. The risk is
higher for older women who have never given birth and for those
with first- or second-degree relatives who have the illness. Mutations in particular genes, most notably the BRCA1 and BRCA2
genes of hereditary nonpolyposis colorectal cancer, can result in
hereditary forms of ovarian cancer. Women who are infertile, suffer from endometriosis, or use postmenopausal estrogen replacement treatment are at higher risk [5]. The epithelial surface of the ovary accounts for around 90% of ovarian neoplasms, with the
remaining 10% coming from germ cells or stromal cells. Serous
(30-70%), endometrioid (10-20%), mucinous (5-20%), clear cell
(3-10%), and undifferentiated (1%), are the different categories
for epithelial neoplasms. For each of these subtypes, the 5-year
survival rates are 20-35%, 40-63%, 40-69%, 35-50%, and 11-29%,
respectively [6,7,8]. The ovarian, fallopian tube, and peritoneum
cancer classifications are combined in the updated, revised FIGO
staging system. It is founded on data gathered from exploratory
surgery [9]. Histological grading, which is connected with prognosis, is used to further subclassify epithelial malignancies of the
ovary and fallopian tube. This approach does not grade non-epithelial cancers. There are two grading schemes used. According
to an architecture with a one-step upgrade, if there is substantial
nuclear atypia, nonserous carcinomas (most endometrioid and
mucinous) are graded in the same way as uterine cancers. GX:
Grade not measurable G1 is a well-differentiated group, followed
by G2 and G3, which are moderately and poorly differentiated [9].
Materials and methods
Ethical considerations
The study protocol was reviewed and passed by the Ethics
Committee of the Institute of Endemic Diseases, University of
Khartoum. Written informed consent was obtained from enrolled
patients and apparently healthy volunteers.
Study design, sites, and duration
A prospective, hospital-based was conducted over two years
(January 2014-December 2015) at tertiary-referred hospitals.
Study population
One hundred and twelve women with histologically-confirmed
ovarian cancers (cases).
Statistical analysis
The collected data was analyzed using SPSS version 16; frequencies, t-test, correlation and significance for patients data. P
value of <0.05 was considered statistically significant.
Result
The average patient age, according to demographic statistics,
was 46.5 27.5 years. 90% of the women in this cohort ranged
in age from 30 to 70. (figure1). Ovarian cancer is not prevalent
(p=0.5) in women under the age of 30 (frequency=4.5%) or over
the age of 70 (frequency=1.7%), although the most common age
group is over 60. (Table1). In the previous six months, more than
40% (50/112, 44.6%) of the patients experienced symptoms of
abdominal discomfort, pelvic pain, and irregular bleeding (Table
2). 38/112 (33.9%) of the patients had symptoms for more than a
year, compared to 6.4% for two years and 14.3% for three years,
respectively (Table 3). Eighty percent of the patients (89/112)
were childless. A fifth (20.5%, 23/112) were married and had
children, whereas a third (44/112, 39.3%) were unmarried, 4and
0.2% (45/112) were married but had no children. Thus, women
without children and single women made up the bulk of patients
[79.5%] (Table 4). Breast and colon cancers were the most frequent concomitant cancers, whereas endometrial, colon, lung,
breast, and brain cancers were the least prevalent (6/112, 5.4%) among the patients (Table 5). The majority of patients in the research cohort (81.1%, 91/112) had serous adenocarcinoma of the
ovaries. More than half of the patients had advanced stages, with
stages III and IV present in 31.3% and 26.8% of patients, respectively. A minority (3.6%) of patients were diagnosed with the early
stages, or stage I, whereas a fifth (19.6%) of patients came with
stage II. With 1.8% at stage II, 4.5% at stage III, and 3.6% at stage
IV, mucinous types were observed in 11 patients (11/112, 9.9%).
10.7% (6/112) of the patients had the endometroid type, with
stage I patients having 3.6% and stage III patients having 1.8%. In
the minority, germinoma (1/112, 0.8%) and poorly differentiated
carcinomas (2.7%, 3/112) were detected (Tables 6 and 7).
Table 1: Distribution of the patients according to age group.
|
Frequency |
Percent |
Valid Percent |
Cumulative Percent |
p Value |
20-29 years |
5 |
4.5 |
4.5 |
4.5 |
0.507 |
30-39 |
years |
20 |
17.9 |
17.9 |
22.3 |
40-49 |
years |
28 |
25.0 |
25.0 |
47.3 |
50-59 |
years |
27 |
24.1 |
24.1 |
71.4 |
60 years and Above |
32 |
28.6 |
28.6 |
100.0 |
|
Total |
112 |
100.0 |
100.0 |
|
|
Table 2: Distribution of symptoms and signs among studied patients.
Sign and symptoms |
Frequencies and percentages
|
Ascites Abdominal
discomfort Pelvic pain
and swelling Irregular
bleeding
|
14/112 (12.5%) 52/112
(46%) 32/112 (29%) 14/112
(12.5)
|
Table 3: Duration of the symptoms of diseases among the study subjects.
Duration of disease |
No & frequency |
Less than 6 months |
50/112 (45%) |
6-12 months |
38/112 (34%) |
12-18 months |
2/112 (1.8%) |
18-24 months |
4/112 (3.6%) |
24-30 months |
2/112 (1.8%) |
30-36 months |
14/112 (12%) |
36-42 months |
2/112 (10.8%) |
Table 4: Marital status of the study women.
Variable |
Frequency |
Percent |
Valid Percent |
Cumulative Percent |
t-test |
p value |
Married with children |
23 |
20.5 |
20.5 |
20.5 |
|
|
Married without children
|
46 |
41.1 |
41.1 |
61.6 |
9.795 |
0.000 |
Single |
43 |
38.4 |
38.4 |
100.0 |
|
|
Total |
112 |
100.0 |
100.0 |
|
|
|
Table 5: Association of other tumors with ovarian cancer.
|
Frequency |
Percent |
Valid Percent |
Cumulative Percent |
P value |
correlation |
No |
106 |
94.6 |
94.6 |
94.6 |
|
|
Yes |
6 |
5.4 |
5.4 |
100.0 |
0.132 |
.143 |
Total |
112 |
100.0 |
100.0 |
|
|
|
Table 6: Histological distribution among the patients.
Histological type |
Frequency |
Percent |
Valid Percent |
Cumulative Percent |
Serious Adenocarcinoma |
91 |
81.2 |
81.2 |
81.2 |
Mucinous |
11 |
9.8 |
9.8 |
91.1 |
Endometroid |
6 |
5.4 |
5.4 |
96.4 |
Poorly Differenyiated
Carcinoma
|
3 |
2.7 |
2.7 |
99.1 |
Germinoma |
1 |
.9 |
.9 |
100.0 |
Total |
112 |
100.0 |
100.0 |
|
Table 7: Stages of different hispatternsal pattern of disease.
Disease Stage |
Frequency |
Percent |
3 |
42 |
37.5 |
4 |
34 |
30.4 |
2 |
23 |
20.5 |
1 |
11 |
9.8 |
Total |
110 |
98.2 |
Missing |
2 |
1.8 |
Total |
112 |
100.0 |
Discussion
Currently, ovarian cancer is the most fatal gynecologic malignancy affecting Sudanese women. Unfortunately, the subtle
symptoms of this disease cause the majority of cases to appear
late. It is worse because there are no sensitive and accurate testing for this cancer. In our study, the bulk of the patients were
older than 60, although it was far less frequent in people under 30
and older than 70. The findings concurred with those of a study
conducted in the United States, which found that women between
the ages of 60 and 64 had the highest prevalence (10). According
to this study, getting married and having kids greatly lowers the
risk of acquiring ovarian cancer. Most of the patients we saw had
never had children. This is in line with the U.S. Third National Cancer Survey [1969-1971], which found that women who had never
married were 60-70% more likely to get ovarian cancer than those
who did [11]. While irregular vaginal bleeding and ascites were
uncommon, the most prevalent symptoms were ambiguous (abdominal discomfort and pelvic pain), which explains the disease’s
late manifestation during the first year of development. This is
consistent with earlier findings from the area and around the
world [12]. A handful of our patients received an early diagnosis, but more than half of them had serous adenocarcinomas of
the ovaries that were in advanced stages. This is consistent with
earlier findings from the area and around the world [13]. Fewer
patients had other histological types visible. The findings did not
agree with those from the rest of the world, which indicated
that endometroid cancer predominated [14]. 6/112, or 5.4%, of
the patients also had endometrial, colon, lung, breast, or brain
tumors at the same time as their ovarian cancer. Compared to
other cancers, breast and colon cancer appear to occur more frequently together. This is consistent with earlier findings from the
area and around the world [15]. This could be explained by the
fact that BRCA1 and BRCA2 genes confer increased susceptibility
to cancer is more commonly seen in patients with breast, colon,
and ovarian cancers in agreement with the report of Wooster and
colleagues [16-18].
Conclusion
The majority of Sudanese women who get ovarian cancer are
childless and unmarried. Below 30 years old, it is less frequent,
and over 60 years old, it is more prevalent. Serous adenocarcinoma is the predominant histological type, with stage 3 being the
most frequent.
Declarations
Acknowledgments: The investigating team would like to thank
the staff of the Department of Immunology and Clinical Pathology, Institute of Endemic Diseases, and the University of Khartoum
for their great support. Full appreciation to the Department of
Obstetrics & Gynecology at Omdurman Military Hospital, for the
extra help, performed by their patients, and also many thanks to
Khartoum Radiation & Isotopes Centre, for making it possible to
conduct this research.
Funding: This research did not receive any specific grant from
funding agencies in the public, commercial or not-for-profit sectors.
Conflicts of interest: The authors declare no conflict of interest
of any sort, financial or otherwise.
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