SciELO - Scientific Electronic Library Online

vol.58 número2Avances en el diagnóstico y control de linfomasImportancia de los registros para el control del cáncer índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados




Links relacionados

  • No hay artículos similaresSimilares en SciELO


Salud Pública de México

versión impresa ISSN 0036-3634

Salud pública Méx vol.58 no.2 Cuernavaca mar./abr. 2016


Special articles

II: Advances in the diagnosis and treatment of cancer

Epidemiological overview, advances in diagnosis, prevention, treatment and management of epithelial ovarian cancer in Mexico

Panorama epidemiológico, avances diagnósticos, prevención, tratamiento y manejo de cáncer ovárico epitelial en México

Dolores Gallardo-Rincón, Oncol Med 1    

Raquel Espinosa-Romero, MC 2  

Wendy Rosemary Muñoz, Oncol Med 3  

Roberto Mendoza-Martínez, MC 1  

Susana del Villar-Álvarez, MC 1  

Luis Oñate-Ocaña, C Oncol 4  

David Isla-Ortiz, C Oncol 5  

Juan Pablo Márquez-Manríquez, Oncol Molec, Oncol Inmun 6  

Ángel Apodaca-Cruz, M Invest Clin 7  

Abelardo Meneses-García, MD, PhD 8  

1 Programa de Cáncer de Ovario, Instituto Nacional de Cancerología. Ciudad de México, México.

2 Departamento de Citopatología, Instituto Nacional de Cancerología. Ciudad de México, México.

3 Clínica de Tumores Mamarios, Instituto Nacional de Cancerología. Ciudad de México, México.

4 Subdirección de Investigación Clínica, Instituto Nacional de Cancerología. Ciudad de México, México.

5 Departamento de Ginecología Oncológica, Instituto Nacional de Cancerología. Ciudad de México, México.

6 Departamento de Oncología, Universidad de Washington. Seattle, USA.

7 Subdirector de Atención Hospitalaria y Consulta Externa, Instituto Nacional de Cancerología. Ciudad de México, México.

8 Dirección General, Instituto Nacional de Cancerología. Ciudad de México, México.


The epithelial ovarian cancer (EOC) has been underdiagnosed because it does not have a specific clinical presentation, and the signs and symptoms are similar to the irritable bowel syndrome and pelvic inflammatory disease. EOC is less common than breast and cervical cancer, but it is more lethal. On the whole, EOC has an early dissemination to peritoneal cavity, which delays a timely diagnosis and increases the rate of advanced diagnosed disease. The diagnosis usually surprises the women and the primary care physician. Therefore, it is necessary to count on prevention and early diagnosis programs. EOC has 80% response to surgical treatment, but nearly 70% of the patients may relapse in five years. The objectives of this document are presenting a summary of the EOC epidemiology and comment about advancements in prevention, diagnosis, and treatment of this cancer. That will raise awareness about the importance of this disease.

Keywords: ovarian cancer; epidemiology; risk factors; prevention; early detection; surgery; chemotherapy; antibody therapy; immune therapy


El cáncer ovárico epitelial (COE) ha sido subdiagnosticado debido a que no tiene presentación clínica específica y a que los signos y síntomas son similares al síndrome de colon irritable y a la enfermedad inflamatoria pélvica. Es menos común que el cáncer de mama o el cervicouterino, pero es más letal. En general, tiene diseminación temprana a cavidad peritoneal, lo cual retrasa un pronóstico oportuno e incrementa la tasa de diagnóstico de enfermedad avanzada. Usualmente, el diagnóstico sorprende a la mujer y al médico de primer contacto. Entonces, es necesario contar con programas de prevención y diagnóstico temprano. El COE tiene 80% de respuesta quirúrgica, pero cerca de 70% de las pacientes puede recaer en cinco años. Los objetivos de este documento son presentar un resumen de la epidemiología del COE y comentar los avances en prevención, diagnóstico y tratamiento de este cáncer. Esto despertará la conciencia acerca de la importancia de esta enfermedad.

Palabras clave: cáncer ovárico; epidemiología; factores de riesgo; prevención; detección oportuna; cirugía; quimioterapia; terapia con anticuerpos; terapia inmuno-oncológica

Ovarian cancer includes the epithelial cancer which develops on the ovary surface. It is the most common type of cancer and represents 85% of the cases, especially in women between 45 to 59 years old. The germ cell type which starts in the egg (immature germination cell) represents 10% and it is more frequent in less than 30 year old young women (figure 1).

Source: cases registry, "Programa Cáncer de Ovario 2011-2015", INCan * total of cases: 868 newly diagnosed

Figure I Distribution of patients with epithelial ovarian cancer by age* 

The stromal tumors are very scarce (barely 2-3%) and affect the ovarian tissue, but they can be functional and produce hormones. There can also be ovary sarcomas and neuroendocrine tumors, which are very rare malignancies.1,2

Epithelial ovarian cancer (EOC) develops from a complex cystic formation (solid and liquid) of the epithelial cells which cover the ovaries or from a cancer in situ of the Fallopian tube fimbria. The epithelial histology can be high-grade papillary serous, low-grade papillary serous, mucinous, endometrioid, and clear-cell. The most frequent subtype which causes the highest rate of mortality is the high-grade papillary serous type; followed by the endometrioid type.3 The risk of epithelial ovarian cancer is high, mostly during menopause.

EOC is the most common gynecologic neoplasia and the first gynecological cancer cause of death.4 Worldwide, 238 719 new cases are recorded every year; in Mexico around 4 000 new cases are estimated each year.5 This neoplasia is underestimated in comparison to other widely-known cancer, such as breast and cervical cancer.

EOC has non-specific symptoms which might be confused with irritable bowel syndrome or non-specific pelvic discomforts; many female patients go first to a gastroenterologist or a gynecologist not specialized in oncology,6,7 this means 6 to 12 months can pass before establishing an accurate diagnosis.8 Many of these patients may have incomplete and inappropriate surgeries; therefore, they must have a new one.9,10

If a patient undergoes a surgery performed by a doctor who is not an oncologist, she has an adverse prognosis factor of survival because her risk of having an incomplete surgery increases four times.10 Every patient with a complex cystic image (mixed with solid and liquid component) in one or both ovaries documented by ultrasonography (US), computed tomography (CT), or with an adnexal lump should be admitted in an institution with oncological attention suspecting cancer. Unfortunately, cancer centers in Mexico demand a pathology report which confirms diagnosis of cancer in order the patient to be admitted. This is not possible in the case of EOC because the diagnosis is surgical.

It is also essential the implementation of educational programs taken physically and on line, as well as radiology programs for evaluation of ovarian cystic images that examine the cyst size, the thickness of the capsule, presence or absence of papillary projections and presence of septa inside the cyst.11

The primary care physicians, general physicians, family physicians, general surgeons, and specially gynecologists must be supported by a radiologist with experience in transvaginal ultrasound (TVUS) in order to have a better evaluation of ovarian cysts.

Risk to develop EOC

The average risk to develop EOC in the general population is 1.8%. When there is an isolated family background of ovarian or breast cancer, this risk rises up to 5%, which is considered an intermediate risk.

When the hereditary pattern consists of two direct line family members with ovarian or breast cancer and it presents the BRCA gene 1 or 2 mutation, the risk in BRCA 1 case increases from 35% to 45% more than in general population; in BRCA 2, the risk of developing ovarian cancer increases from 15 to 25%. This is classified as high risk.12

If the patient has two direct line relatives with ovarian or breast cancer and the BRCA gene 1 and 2 mutations have not been determined or, if the test results have been negative for these mutations, the patient is considered high risk because there can be deletions and genes associated to BRCA 1 and 2 mutated that may not be shown.13

Other risk factors are infertility, which increases the relative risk 2.6 times more than general population;14 policystic ovary syndrome increases 2.56 times;15 endometriosis 2.04-3.05 times;16 hormone replacement therapy (for three years average or more) increases the relative risk (RR) in 1.41 times;17 smoking, 2.1 times more than the general population;18 and intrauterine device with a RR of 1.76.19

Protective factors

The use of oral contraceptives for three years decreases the risk 0.73 times more than in general population.20 Breastfeeding over twelve months has a protective factor of 0.72;21 pregnancy has 0.6; and bilateral tubal occlusion has a protective factor of 0.69.22

Prevention of EOC

The prevention applies to cases of family cancer, women who have BRCA 1 and 2 gene mutation, and who are considered in high risk to develop EOC. Nowadays, it is calculated that this mutation represents 10% of all EOC cases, although such figure may be higher; however a bilateral salpingo-oophorectomy (BSO) is recommended. Chemoprevention could be given in contraceptives, but it is not a universal recommendation.23

EOC early detection

Screening studies performed in ovarian cancer so far have been very controversial because they were designed twenty years ago. Then, there was scarce knowledge about the histological, molecular subtypes and their biological behavior. These studies include five histological types with different molecular behavior and cellular growth.3

Likewise, the pelvic and transvaginal ultrasound (PUS and TVUS, respectively) are also used, but the latter is more useful. There are numerous screening studies, but eight of them are the most important. PLCO (Program of Lung, Colon and Ovarian Cancer Screening) analyzed 7 237 women between 55 to 74 years old; 34 253 of them had CA 125 test for six years plus TVUS for four years; 34 304 were in observation with a 13-year follow up. This study revealed that the screening with CA 125 and TVUS does not achieve a mortality reduction, compared to the observation group. The negative result was obvious because its design was created over 20 years ago and the most common of these five types is the high-grade serous papillary. This type is known for presenting early clinical manifestations as well as cellomic dissemination to the peritoneum which covers the bowels. It can also appear within six months, so the performance of the TVUS study every year is useless.24

In spite of this, a Japanese trial followed the same methodology performing US every year (in this case was pelvic), but there was a bigger proportion of stage I with no statistical significance.25

The results of the University of Kentucky were positive for the screening group with TVUS every six months to find stages I, II with better survival (SV) for the screening group: 84.6 vs. 53.7%. Nevertheless, this trial comes from only one center which is very specialized in evaluation of ovary cysts and, therefore, is hard to reproduce.26

The NOCEDEP trial -focused on high-risk women to establish an early stage diagnosis- was negative.27 The UKFOKCS also analyzed high-risk women and suggests as performing a BSO, the BRCA 1 and 2 gene mutation test, and just a screening test on women who do not want surgery.28

ROC, UKCTOCS (not conclusive yet), and ROCA use algorithms to diagnose early ovarian cancer. They are based on the monitoring of CA 125 when its baseline value is 30 u/ml or higher. They check the values every 3 months, in addition to the performance of TVUS. However, ROC and ROCA are very promising.29-31

Keeping a record with a symptom index (non-specific abdominal pain, sensation of abdominal distention, constipation alternating with diarrhea, rectal tenesmus, pelvic sore, and feeling of early satiety) did not reach a predictive value of 10. Even so, it is suggested that the patient should have a TVUS every 6 months and the measuring of CA 125 in case of having these symptoms more than 12 times a month.32

Dr. Kurman stated that in order to identify ovarian cancer in early stages it is central to focus on the tumor size rather than on the clinical stage. Even though 75% of the patients are diagnosed in advanced stages (III and IV) around the world, that such figure may be higher in less developed countries. A patient in IIIa and IIIb is different from a patient in IIIC because the first two stages imply less tumor volume and higher possibilities of performing an exploratory laparotomy. That will also have a higher probability of achieving an optimal cytoreduction. This is strictly defined as the absence of visible macroscopic disease or, at least, disease with implants <.5 cm or <1cm, with a better prognosis, which may be performed in patients who, at the end, achieve implants > 1cm. Patients in IIIc have a shorter survival than patients in IIIa and IIIB; thus, the aim of establishing a diagnosis with advanced disease is preferable to try to establish an early diagnose, which is rather difficult to achieve, especially the papillary serous, high grade ovarian cancer, as well as the endometrioid with very early dissemination.33

Although, current evidence level to perform screening in ovarian cancer is weak; the National Comprehensive Cancer Network (NCCN) guidelines (2009) recommends applying to:

  • Women with high risk of developing ovarian cancer; that is to say, women with breast or ovarian cancer background or who have BRCA gene mutation, TVUS and CA 125 tests every six months;

  • Disease which began at 35 years or 5 to 10 years before the age the close relative was diagnosed with ovarian or breast cancer;

  • Women with BRCA mutation to whom are strongly recommended prophylactic BSO after meeting the desire of having a baby.34

Surgical staging of ovarian cancer, treatment with surgery, and chemotherapy

EOC is classified by stages:

  • Stages I and II, confined to the pelvis,

  • Stage III is sub-classified in IIIA (retroperitoneal lymph nodes and/or microscopic extra-pelvic peritoneal disease) and IIIB (microscopic extra-pelvic peritoneal disease with metastases < 2 cm; it is also possible to find retroperitoneal lymph nodes and disease disseminating to the liver capsule or spleen),

  • IIIC, macroscopic disease extra-pelvic peritoneal disease > 2cm, like in IIIB where it is possible to find retroperitoneal lymph nodes and extension to the liver capsule and spleen,

  • IVA, with pleural effusion and positive cytology,

  • IVB, metastases in hepatic, splenic parenchyma, in extra-abdominal organs, affection of inguinal nodes or affected nodes in another site35

Patients should be attended by a multidisciplinary team (gynecologist, oncology surgeon, medical oncologist, radiologist, and pathologist) in order to standardize the initial treatment (surgery or chemotherapy).

The diagnosis of advanced disease (stages III and IV) worldwide is 75%,36 but the survival for stage III is different, depending on the clinical stage IIIA, IIIB or IIIC. For stage IIIA, survival is 60% to five years; while for IIIB is 50 and 35% to IIIC.37

On the whole, our patients are at stages IIIc and IV. They represent 85% of all the patients who visit the doctor for the first time. They already have extensive disease in a clinical entity known as abdominal carcinomatosis, that is to say, disease in the abdominal wall and in the peritoneal surface (oment take), which makes impossible to perform a first surgery. Therefore, the patients are given induction chemotherapy (neoadjuvant chemotherapy) during three cycles; then, they will be submitted to a surgery known as interval debulking surgery, and then continue with three additional cycles of adjuvant chemotherapy, for a total of six cycles.38

Conversely, patients in stages I, IIa, IIb (and a few in IIIc) are treated with exploratory surgery known as exploratory laparotomy, which is cytoreductive and will stage the disease. It consists of performing panhysterectomy, omentectomy, pelvic and para-aortic lymphadenectomy, and cheking parietocolic gutters, pelvic floor, and diaphragmatic dome.

Surgery begins with an incision from the xiphoid appendix until the symphysis pubis. The purpose is to remove the visible disease from the abdominal and pelvic cavity where the prognosis is much more favorable. If that is not possible, the smaller the implants which remain, the better. The implants are measured in ≤.5 cm, >.5 cm, < 1cm, >1cm, and <2 cm.39

After surgery, patients receive six cycles of adjuvant chemotherapy. The standard chemotherapy is based on six cycles of carboplatin + paclitaxel. Every cycle is administered every three weeks.40,41 It is also possible to administer a weekly regimen of paclitaxel with the carboplatin administered every three weeks because this is a well-tolerated regimen.42 If the patient presents residual disease (implants) ≥1 cm, it is possible to add bevacizumab, a monoclonal antibody targeted to the vascular endothelial growth factor. This is administered during chemotherapy and it will be also indicated as maintenance treatment.43

As has been stated above, patients with EOC have a high relapse rate, even 75%, especially in the more advanced stages (IIIc and IV). Obviously, it is important to consider the disease free interval. Patients who relapse in less than six months or progress during chemotherapy are classified as resistant and refractory. They also have poor prognosis. The patients who relapse between 6 and 12 months have an intermediate prognosis; and the ones who relapse after 12 months have better prognosis. Overall, patients who relapse after 6 months may also be treated with the same regimen of carboplatin + paclitaxel. If the patient had neuropathy symptoms, secondary to paclitaxel, the rescue regimen may be carboplatin + gemcitabine.

Patients who have BRCA 1 and 2 mutations are considered more sensitive to chemotherapy; thus the use of PARP (Poly ADP-ribose Polymerase) inhibitors like olaparib may be assessed in their clinical condition, after chemotherapy as maintenance therapy for a year because PARP inhibitors have been approved for patients in the firs relapse occurred after six months.44

The issue is that patients with EOC and who relapse for the first time remain disease-free approximately for two years or more and relapse again in a shorter time; so, the time to relapse begin to diminish. The free-progression median is 2.5 years and the survival median with several treatment lines is four years.45

At Instituto Nacional de Cancerología we have a prevention, timely detection, and access to treatment program since 2011. We have received 1 758 women, 25% of them did not have cancer. There were 1 319 patients with ovarian cancer, 1 121 of them with epithelial type (EOC), 672 of them did not receive previous treatment. Although data is not accurate, we have estimated that the overall survival is 5.1 years. Nowadays, we want to run clinical trials including the use of immune action drugs like metformin, COX2 inhibitors, and antibodies like anti PDL1 and 2, anti CTLA4 targeted to proteins which are expressed on the surface of the tumor cells.

This is a very promising area to foster the immune response of the patient against the tumor or the sub-clinic disease in order to achieve more sustained responses with chemotherapy, avoid resistance to drugs, and prevent recurrence.


Since EOC is the most common of all the ovarian cancers, our efforts must be focused on the epithelial type. Thus, we have to consider it as a neoplasm whose clinical behavior is not only confined to the pelvis but to gastrointestinal symptoms like colitis, which now are more noticeable for primary care physicians, especially gastroenterologists, general surgeons, and gynecologists.

Thus, it is imperative to include the cancer diseases in women in the Secretaría de Salud prevention programs in order to make women to be aware that their ovaries may develop cancer, especially in women who are going through menopause or whose direct-lined female relatives have had breast or ovarian cancer.

Besides having a pap smear test, which women think identify any type of gynecological cancer, it is crucial to detect infertility, endometriosis, polycystic ovaries, and use of hormonal replacement therapy.

Women who have BRCA 1 and 2 mutations merit that their direct-lined female relatives receive genetic advice, be educated on preventive measures, and be attended by a multidisciplinary team which includes a genetist and a psychologist to discuss issues like satisfied parity and the acceptance of bilateral salpingo-oophorectomy.

Nevertheless, the early detection by TVUS plus CA 125 tests is not recognized as useful because the screening tests worldwide have been negative or not conclusive. Thus, women should be educated about the risk factors to develop this neoplasm, especially if they have breast or ovarian cancer family background. Likewise, if they have symptoms like persistent colitis; that is to say vague abdominal discomfort, abdominal distention sensation, constipation alternating with diarrhea, rectal tenesmus (frequently regarded as irritable bowel) and persistent urinary discomfort. All of those symptoms must be a reason to perform a TVUS plus CA 125 test.

CA 125 may have high values for different reasons, not only ovarian cancer. Nevertheless, women who have high levels of this antigen must be monitored preferably every three months, even if there is no visible disease at pelvis.

The objective in EOC is establishing a diagnosis of less advanced disease because its early dissemination towards peritoneum is the most common, even with adnexal cyst lesions, which may be small, especially in the serosa papillary type. Diagnosis reached even in the earliest stage III (IIIA or IIIB) is better than stage IIIC, where tumor burden and peritoneal carcinomatosis are generally found. It should be considered that more than clinical stage it is a matter of tumor volume, and that our aim is to diagnose it when there is less tumor volume in order to ensure successful surgeries which remove all the disease and only remain the microscopic disease or implants ≤5 cm, <1 cm, which is better than leaving implants of 2 cm or more. Identifying mucinous and clear cell type cancers are much more difficult to detect, even when they have not come up to the pelvis.

It is essential that if a patient goes to the pre-consultation services of the cancer institutions with an ultrasound or tomography which shows an adnexal (cyst and solid) tumor, she should be admitted without being required a neoplasm report. That would prevent that the patient be treated by non-oncologist surgeons and need to undergo a new surgery, not to mention the time wasted (from 6 to 12 months), while the disease progress towards an advanced stage.

It is also imperative to implement educative programs to identify the ovarian cyst lesions as well as gathering radiologic data by means of ultrasound which confirms the presence of cancer, based on the radiologists' expertise.

Surgery is the key treatment for EOC and includes the ovary, Fallopian tubes, and uterus resection (panhysterectomy), besides the pelvic nodes and para-aortic chains resection. Likewise, it includes the omentum resection, with an incision from the xiphoid appendix until the symphysis pubis which enables an appropriate vision of the abdominal cavity and a revision of the diaphragmatic domes, parietocolic gutters and pelvic floor.

Since EOC is a very sensitive neoplasm to chemotherapy is also treated with antibodies like bevacizumab as maintenance therapy for patients with residual disease (implants > 1 cm) after surgery and PARP inhibitors, such as olaparib. This is only recommended to women who have BRCA 1 and 2 mutations, responsible of the DNA reparation. However, its use is limited to patients who have experienced their first relapse.

Unfortunately, EOC has a very high recurrence pattern. The time to relapse is crucial for the prognosis; so it is better when it occurs after more than 12 months, when it may be capable of a new surgery, followed by chemotherapy.

Overall survival of advanced ovarian cancer has reached 4.9 years. During this time, it is possible that the patients have received several chemotherapy regimens (one to six lines). This may weaken the patient and shorten the free-disease intervals; thus, the disease may become more resistant.

As the relapse pattern is very high is imperative to implement protocols based on immune-oncologic treatments which are promising because they avoid the patients to undergo several lines of chemotherapy, which result in a higher resistant to drugs. Such drugs improve the immunologic response and enable that the cancer stem cell be identified by dendritic cells, by CD4 and CD8 T cells, and by T cell natural killer, where anti PLD1 and 2 as well as anti CTLA4 antibodies are used along with other drugs like metformin, COX2 inhibitors, among others, plus the conventional chemotherapy to achieve longer free-disease periods and relapses prevention.


The most common type of ovarian cancer is epithelial; thus, it deserves all our attention. Eight women die daily from it, so it is more lethal than the breast or cervical cancer. Therefore, women and physicians should be alert to identify persistent gastrointestinal symptoms, which are the most common in the clinical manifestation of the ovarian cancer.

Regarding its dissemination pattern, our objectives must be establishing a diagnosis in less advanced stages and warrantee that the patient be admitted in cancer centers only with and ultrasound or tomography which shows suspicion of ovarian cancer. This is important because as the diagnosis is surgical, we need to avoid the patient visit several hospitals and physicians before confirming the diagnosis, which also implies the disease progression (advanced stages and extensive tumor volume).

Even though the suitable surgical treatment, chemotherapy, and molecular therapy have achieved a 50% survival in five years, we believe we could obtained better results regarding the immunogenic nature of the ovarian cancer. In other words, as ovarian cancer is an immunogenic neoplasm is capable of being treated with a protocol based on immune-oncologic therapy.


We thank Dr. Alfredo Salmon Demongin for the editorial support for the preparation of this manuscript.


1. American Cancer Society. Global Cancer Fact & Figures 2011 (2nd Ed.). Atlanta: American Cancer Society, 2011. [ Links ]

2. Siegel R, Ma J, Zou Z, Jemal A. Cancer statistics, 2014. CA Cancer J Clin 2014;64(1):9-29. [ Links ]

3. Prat J. Ovarian carcinomas: five distinct diseases with different origins, genetic alterations, and clinicopathological features. Virchows Arch 2012;460(3):237-249. [ Links ]

4. Siegel R, Naishadham D, Jemal A. Cancer Statistics, 2012. CA Cancer J Clin 2012;62(1):10-29. [ Links ]

5. World Health Organization. Estimated cancer incidence, mortality and prevalence worldwide, Globocan 2012 [internet site]. Lyon: Globocan, 2016. Available at: [ Links ]

6. Goff BA, Mandel LS, Melancon CH, Muntz HG. Frequency of symptoms of ovarian cancer in woman presenting to primary care. JAMA 2004;291:2705-2712. [ Links ]

7. Olson SH, Mignone L, Nakraseive C, Caputo TA, Barakat RR, Harlap S. Symptoms of ovarian cancer. Obstet Gynecol 2001;98:212-217. [ Links ]

8. Goff BA, Mandel LS, Muntz HG Melancon CH. Ovarian carcinoma diagnosis. Cancer 2000;89:2068-2075. [ Links ]

9. American College of Obstetricians and Gynecologists Committee on Gynecologic Practice. Committee Opinion No. 477: the role of the obstetrician-gynecologist in the early detection of epithelial ovarian cancer. Obstet Gynecol 2011;117:742-746. [ Links ]

10. Chan JK, Kapp DS, Shin JY, Husain A, Teng NN, Berek JS, et al. Influence of the gynecologic oncologist on the survival of ovarian cancer patients. Obstet Gynecol 2007;109:1342-1350. [ Links ]

11. Clarke-Pearson DL. Screening for Ovarian Cancer. N Engl J Med 2009;361:170-177. [ Links ]

12. Lancaster JM, Powell CB, Kauff ND, Cass I, Chen LM, Lu KH, et al. Statement in risk assessment for inherited gynecologic cancer predispositions. Gynecol Oncol 2007;107:159-162. [ Links ]

13. Lee JS, John EM, McGuire V, Felberg A, Ostrow KL, DiCioccio RA, et al. Breast and ovarian cancer in relatives of cancer patients, with and without BRCA mutations. Cancer Epidemiol Biomarkers Prev 2006;15(2):359-363. [ Links ]

14. Bristow RE, Karlan BY Ovulation induction, infertility, and ovarian cancer risk. Fertil Steril 1996;66(4):499-507. [ Links ]

15. Chittenden BG, Fullerton G, Maheshwari A, Bhattacharya S. Polycystic ovary syndrome and the risk of gynecological cancer: a systematic review. Reprod Biomed Online 2009;19:398-405. [ Links ]

16. Pearce CL, Templeman C, Rossing MA, Lee A, Near AM, Webb PM, et al. Association between endometriosis and risk of histological subtypes of ovarian cancer: a pooled analysis of case-control studies. Lancet Oncol 2012;13:385-394. [ Links ]

17. Collaborative Group on Epidemiological Studies of Ovarian Cancer. Menopausal hormone use and ovarian cancer risk: individual participant meta-analysis of 52 epidemiological studies. Lancet 2015;385:1835-1842. [ Links ]

18. Jordan SJ, Whiteman DC, Purdie DM, Green AC, Webb PM. Does smoking increase risk of ovarian cancer? A systematic review. Gynecol Oncol 2006;103:1122-1129. [ Links ]

19. Tworoger SS, Fairfield KM, Colditz GA, Rosner BA, Hankinson SE. Association of oral contraceptive use, other contraceptive methods, and infertility with ovarian cancer risk. Am J Epidemiol 2007;166:894-901. [ Links ]

20. Beral V, Doll R, Collaborative Group on Epidemiological Studies of Ovarian Cancer. Ovarian cancer and oral contraceptives: Collaborative reanalysis of data from 45 epidemiological studies including 23,257 women with ovarian cancer and 87,303 controls. Lancet 2008;371:303-314. [ Links ]

21. Ip S, Chung M, Raman G, Trikalinos TA, Lau J. A summary of the Agency for Healthcare Research and Quality's evidence report on breastfeeding in developed countries. Breastfeed Med 2009; 4 Suppl 1:S17-S30. [ Links ]

22. Cibula D, Widschwendter M, Májek O, Dusek L. Tubal ligation and the risk of ovarian cancer: Review and meta-analysis. Hum Reprod Update 2011;17:55-67. [ Links ]

23. Hanna L. Prevention of ovarian cancer. Best Practice & Research Clinical Obstetrics & Gynaecology 2016;(30):1-12. [ Links ]

24. Buys SS, Partridge E, Black A, Johnson CC, Lamerato L, Isaacs C, et al. Effect of Screening on Ovarian Cancer Mortality: The Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening Randomized Controlled Trial. JAMA 2011;305(22):2295-2230. [ Links ]

25. Kobayashi H, Yamada Y, Sado T, Sakata M, Yoshida S, Kawaguchi R, et al. A randomized study of screening for ovarian cancer: a multicenter study in Japan. Int J Gynecol Cancer 2008;18(3):414-420. [ Links ]

26. van Nagell JR Jr, Higgins RV, Donaldson ES, Gallion HH, Powell DE, Pavlik EJ, et al. Transvaginal sonography as a screening method for ovarian cancer. Cancer 1990; 65(Issue 3):573-577. [ Links ]

27. Fishman DA, Cohen L, Blank SV, Shulman L, Singh D, Bozorgi K, et al. The role of ultrasound evaluation in the detection of early-stage epithelial ovarian cancer. Am J Obstet Gynecol 2005;(192):1214-1222. [ Links ]

28. Rosenthal AN. Ovarian Cancer Screening in the High Risk population -the UK Familial Ovarian ancer Screening Study (UKFOCSS). Int J Gynecol Cancer 2012;(22):S27-S28. [ Links ]

29. Menon U, Skates SJ, Lewis S, Rosenthal AN, Rufford B, Sibley K, et al. Prospective study using the risk of ovarian cancer algorithm to screen for ovarian cancer. J Clin Oncol 2005;23:7919-7926. [ Links ]

30. Menon U, Gentry-Maharaj A, Hallett R, Ryan A, Burnell M, Sharma A, et al. Sensitivity and specificity of multimodal and ultrasound screening for ovarian cancer, and stage distribution of detected cancers: results of the prevalence screen of the UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS). Lancet Oncology 2009;10(4):327-340. [ Links ]

31. Lu KH, Skates S, Hernandez MA, Bedi D, Bevers T, Leeds L, et al. A 2-stage ovarian cancer screening strategy using the Risk of Ovarian Cancer Algorithm (ROCA) identifies early-stage incident cancers and demonstrates high positive predictive value. Cancer 2013;119(19):3454-3461. [ Links ]

32. Rossing MA, Wicklund KG, Cushing-Haugen KL, Weiss NS. Predictive value of symptoms for early detection of ovarian cancer. J Nat Cancer Inst 2010;102(4):222-229. [ Links ]

33. Kurman RJ, Shih IeM. Pathogenesis of ovarian cancer: lessons from morphology and molecular biology and their clinical implications. Int J Gynecol Pathol 2008 Apr; 27(2):151-160. [ Links ]

34. National Comprehensive Cancer Network (NCCN). NCCN Guidelines for Ovarian Cancer 2009 [internet document]. Washington: NCNN, 2015. Available at: [ Links ]

35. Jonathan S. Berek, Christopher Crumb, Michael Friedlander. FIGO Cancer Report 2012, Cancer of the ovary, fallopian tube, and peritoneum. Int J Gynecol Obstet 2012;119S2:S118-S129. [ Links ]

36. American Joint Committee on Cancer. 8th Edition by the Numbers [internet document]. Chicago: AJCC, 2016.: Available from: [ Links ]

37. American Joint Committee on Cancer. Cancer Staging Manual, 7th Ed. New York: Springer, 2009. [ Links ]

38. Vergote I, Tropé CG, Kristensen GB, Neoadjuvant Chemotherapy or Primary Surgery in Stage IIIC or IV Ovarian Cancer, N Engl J Med 2010;363:943-953. [ Links ]

39. Young RC, Decker DG, Wharton JT, Piver MS, Sindelar WF, Edwards BK, et al, Staging Laparotomy in Early Ovarian Cancer. JAMA 1983;250(22):3072-3076. [ Links ]

40. Bookman MA, Brady MF, McGuire WP, Harper PG, Alberts DS, Friedlander M, et al. Evaluation of New Platinum-Based Treatment Regimens in Advanced-Stage Ovarian Cancer: A Phase III Trial of the Gynecologic Cancer Inter Group. J Clin Oncol 2009; 27(9):1419-1425. [ Links ]

41. Gallardo-Rincón D, Cantú-de-León D, Alanís-López P, Alvarez-Avitia MA, Bañuelos-Flores J, Herbert-Núñez GS, et al. Tercer Consenso Nacional de Cáncer de Ovario 2011. Grupo de Investigación de Cáncer de Ovario y Tumores Ginecológicos en México 'GICOM'. Rev Inv Clin 2011;63(6):665-702. [ Links ]

42. Katsumata N, Yasuda M, Takahashi F, Isonishi S, Jobo T, Aoki D, et al. Dose-dense paclitaxel once a week in combination with carboplatin every 3 weeks for advanced ovarian cancer a phase 3, open-label, randomized controlled trial. Lancet 2009;374: 1331-1338. [ Links ]

43. Perren TJ, Swart AM, Pfisterer J, Ledermann JA, Pujade-Lauraine E, Kristensen G, et al. Phase 3 Trial of Bevacizumab in ovarian cancer, ICON 7 study. N Engl J Med 2011;365:2484-2496. [ Links ]

44. Ledermann J, Harter P, Gourley CH. Olaparib Maintenance Therapy in Platinum-Sensitive Relapsed Ovarian Cancer. N Engl J Med 2012;366:1382-1392. [ Links ]

45. Ledermann JA, Raja FA, Fotopoulou C, Gonzalez-Martin A, Colombo N, Sessa C, et al. Newly diagnosed and relapsed epithelial ovarian carcinoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol 2013;24(Suppl 6):vi24-32.6:vi24-vi32. [ Links ]

Received: December 21, 2015; Accepted: February 08, 2016

Corresponding author: Dra. Dolores Gallardo Rincón. Departamento de Oncología Médica, Instituto Nacional de Cancerología. Av. San Fernando 22, col. Sección XVI. 040809 Tlalpan, Ciudad de México, México. Email:

Declaration of conflict of interests. The authors declare that they have no conflict of interests.

Creative Commons License This is an open-access article distributed under the terms of the Creative Commons Attribution License