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Women’s Health Forum Ovarian cancer – not quite a ‘silent killer’ Ovarian cancer is often asymptomatic until the late stages, but there are certain signs to look out for, write Peter Hayes and Siobhan Carruthers Ovarian cancer is a serious disease. According to the Irish Cancer Society, there are 300 or so new diagnosed cases in Ireland per year and about 200 deaths. It often presents when a cure is no longer possible. There are few early warning signs; however, there are certain symptoms that GPs should be aware of. We want to highlight some of the few ‘warning shots’ that exist and follow on with a brief up-to-date review of many of the management issues. Main risk factors1-4 • Repeated ovulations (long menstrual lifetime, null parity, not breastfeeding, infertility) • G enetics (BRCA gene/breast-ovary syndrome, Lynch syndrome/colon-ovary syndrome, strong family history of ovarian cancer) • P ostmenopausal oestrogen (hormone replacement treatment) • Cigarettes and increased body mass index • E ndometriosis (2.5% lifetime risk of ovarian malignancy).6 Symptom watch for ovarian cancer7,9,10-12 • Abdominal/pelvic pain • Abdominal swell/bloating • Feeling unusually full post meals • Urinary urgency. If any of these symptoms are present in women, especially in those over 50 years, then the symptom index is positive. These symptoms, if present for less than one year and are present more than 12 times per month, give a sensitivity of 56% for early disease and 79.5% for late disease. The specificity is 86.7%-90%.14 If you combine the symptom index being positive with either a raised CA-125 or the new ovarian tumour marker HE-4, then the sensitivity becomes 84% and the specificity 98%.14 A new onset of irritable bowel disease-type symptoms in a woman over 50 years should also ring an alarm bell about ovarian cancer issues. Colonoscopy referral, while important, should maybe occur parallel to gynaecological referral. Signs5 The signs of ovarian cancer are notoriously silent until the late stages of the disease when a patient will often have: pelvic mass on exam and/or ascites/pelvic lymph nodes. Table 1 Detection of ovarian cancer in primary care* Woman presents to GP Physical examination identifies ascites and/or a pelvic or abdominal mass (not obviously uterine fibroids) Woman reports having any of the following symptoms persistently or frequently – particularly more than 12 times per month (especially if she is 50 years or over)5 • Persistent abdominal distension (’bloating’) • Feeling full (early satiety) and/or loss of appetite • Pelvic or abdominal pain • Increased urinary urgency and/or frequency OR: Woman is 50 years or over and has had symptoms within the last 12 months that suggest IBS6 Woman reports any of the following symptoms: • Unexplained weight loss • Fatigue • Changes in bowel habit Symptoms not suggestive of ovarian cancer Ovarian cancer suspected? Yes No Measure serum CA125 ≥ 35 IU/ml Arrange ultrasound of abdomen and pelvis Suggestive of ovarian cancer Refer urgently *Adapted from NICE 2011 www.nice.org.uk/cg122 < 35 IU/ml Normal Assess carefully: are other clinical causes of symptoms apparent? Yes Investigate No Advise her to return if symptoms become more frequent and/or persistent FORUM April 2012 53 WomensHealth/Ovarian cancerSS/NH 1 29/03/2012 10:52:45 Forum Women’s Health Treatment staging and survival rates15 Stage Treatment Outcome/five-year survival Stage 1a/1b Surgery removing the uterus, fallopian tubes and one or both ovaries. Conservative surgery spares the uterus and one ovary 90% survival Stage 1c/2 Surgery as above but with adjuvant chemotherapy 50% relapse within five years Stage 3/4 Pelvic de-bulking operations and adjuvant chemotherapy but with eventual palliation. Treatment is decided on a person-by-person basis Five-year survival low, 75% of cancers diagnosed here Diagnosis All cases with suspicious symptoms or signs should be referred from primary to secondary care for assessment. This will involve examination and imaging with ultrasound if not already performed. A CA-125 tumour marker should also be performed. Care pathway (adapted from NICE 2011) If a patient presents with the following symptoms they may be managed initially in primary care according to the skill level of the practitioner: • Positive symptom index (listed previously) • New irritable bowel type symptoms aged over 50 years • Anxiety about risk factors. GP with little experience in gynaecology: Refer all of the above groups to secondary care for opinion. GP with some training in gynaecology: Perform a CA-125 serum test and refer if higher than accepted limits. If the CA-125 is within normal limits, a careful re-evaluation of symptoms and re-assessment examination should take place. Further investigations to other organ systems can be organised if appropriate. GP with specialist interest in gynaecology: If CA-125 is elevated you may wish to order an ultrasound of pelvis. If the ultrasound does not show any suspicious signs of malignancy then a careful follow-up and monitoring process may take place. This should occur along with a careful re-evaluation of symptoms and re-examination to rule out the involvement of other organ systems. The patient with ‘clinical signs’ on exam such as ascites or pelvic lymph nodes should be referred to secondary care expediently in all cases. Screening without symptoms in the general population The Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial of the National Cancer Institute (2011)16 has recently published its findings. It performed yearly CA-125 blood tests on women for six years and annual ultrasound tests for four years. The effect of screening on this group’s mortality was dubious. Screening was felt to be unbeneficial. It was felt that screening probably causes harm, with far too many false positive patients being identified and operated on. The UKTOCS trial is ongoing and will have results in late 2014. This trial compares three screening possibilities: a no screening arm; an annual ultrasound screening arm; and a combined CA125 and ultrasound (if CA-125 raised) arm. The results are eagerly awaited. Many combined tumour marker groups have been used in studies of general population screening for ovarian cancer. These combine CA-125 with other tumour markers in an attempt to increase specificity and sensitivity in these blood markers diagnosing ovarian cancer. None are proven, but the latest ongoing studies are using a panel profile of circa 30 blood tumour markers.13 Staging Staging details are usually not of relevance to primary care providers but with patients who are diagnosed with ovarian cancer surviving longer than ever before, it is plausible that these types of patients may need a ‘chronic-care’ type model of care (see Table 2). Follow up for successful treatment of stage 1 and stage 215 Follow up every three months for two years, then every six months for a further three years and annually thereafter. Research/other treatment options Neo-adjuvant chemotherapy is also used in some centres for late stage disease where the chemotherapy happens before the de-bulking surgery. Radiotherapy is not an option for most patients as the problems with pelvic irradiation outweigh the benefits Intra-peritoneal chemotherapy is currently in trials. The port is a trans-abdominal opening and placed at laparotomy/laparoscopy. Peter Hayes is in practice in Limerick city and teaches at NUI Galway and Siobhan Carruthers is a tutor in obstetrics and gynaecology at NUI Galway References 1. Carlson, KJ, Skates, SJ, Singer, DE, Ann Intern Med 1994; 121:124 2. Whittemore AS, R Harris, J Intyre, and the Collaborative Ovarian Cancer Group. Am J Epidemiol 1992; 136: 1184 3. Gotlieb, WH, Baruch, GB, Friedman, E. Semin Surg Oncol 2000; 19:20 4. Ness, RB, Cramer, DW, Goodman, MT, et al. Infertility, fertility drugs, and ovarian cancer: a pooled analysis of case-control studies. Am J Epidemiol 2002; 155217 5. Gynaecology by ten teachers, Campbell and Monga. Hodder Education 2006 6. Van Gorp T, Amant F, Neven P et al. Endometriosis and the development of malignant tumours of the pelvis. A Review of literature. Best Pract.Res. Clin.Obstet.Gynaecol 2004 18-349 7. Symptoms associated with diagnosis of ovarian cancer: a systematic review. Bankhead CR, Kehoe ST, Austoker J ,BJOG. 2005;112(7):857. 8. Ultrasonography, computed tomography and magnetic resonance imaging for diagnosis of ovarian carcinoma. Liu J, Xu Y, Wang J, Eur J Radiol. 2007; 62(3): 328 9. Goff BA, Mandel LS, Drescher CW, et al. “Development of an ovarian cancer symptom index: possibilities for earlier detection”. Cancer 2007 109 (2): 221-7 10. Goff BA, Mandel LS, Melancon CH, Muntz HG “Frequency of symptoms of ovarian cancer in women presenting to primary care clinics”. JAMA June 2004 291 (22): 2705-12 11. Smith LH, Morris CR, Yasmeen S, Parikh-Patel A, et al. Ovarian cancer: can we make the clinical diagnosis earlier. Cancer 2005; 104(7): 1398-407 12. Goff BA,Mandal LS, Drescher CW,Urban N et al. Frequency of symptoms of ovarian cancer in women presenting to primary care clinics. JAMA 2004; 291(22): 2705-12 13. Bast RC Jr, Brewer M, Zou C, Hernandez MA. Prevention and early detection of ovarian cancer: mission impossible? Recent results cancer Res. 2007;174:91-100. Serail markers 14. Anderson MR, Goff BA, Lowe KA, Scholler N et al. Use of a Symptom Index, CA125, and HE4 to predict ovarian cancer. Gynecol Oncol 2010; 116(3): 378-83. Epub 2009 Nov 28. 15. SIGN guidelines. www.sign.ac.uk/pdf/sign75.pdf 16. Buys S, Black A, Johnson C, et al. Effect of screening on ovarian cancer mortality. PLCO Trial. JAMA 2011; 305(22): 2295-2303 54 FORUM April 2012 WomensHealth/Ovarian cancerSS/NH 2 29/03/2012 10:52:50