Ovarian cancer is a complex disease that requires knowledge of its biology and clinical course in order to select necessary diagnostic tests and to embark upon an appropriate treatment course. It is a disease of the elderly population and generally produces no specific signs or symptoms. Most patients are in their mid 60s when they are diagnosed, after a prolonged period of having vague abdominal complaints. Patients frequently undergo extensive radiologic studies unnecessarily, since a definitive diagnosis usually requires surgery, most frequently a laparotomy . A careful laparotomy is mandatory to stage the disease and to remove as much disease as possible.
At the time of diagnosis, most patients already have advanced-stage disease such that the disease has spread throughout the peritoneal cavity to involve multiple sites on peritoneal surfaces. About 75% of all patients will present with stage III disease. Stage IV disease, in which there is spread to the pleural or extraperitoneal sites such as the liver, has an even worse prognosis and, like stage III disease, is not curable by surgery. Subsequently, the vast majority of patients with ovarian cancer are treated immediately with chemotherapy following their initial surgery. Appropriate chemotherapy for ovarian cancer remains controversial. However, it appears that paclitaxel (Taxol) has made a significant impact upon the survival of patients with advanced disease, and the investigators in the Gynecologic Oncology Group (GOG) have now adopted the combination of paclitaxel plus a platinum compound as their standard therapy for ovarian cancer patients.
Such a combined modality approach using surgery and chemotherapy produces an approximately 70% to 85% response rate in patients with advanced disease . Unfortunately, the vast majority of these patients will ultimately recur, and 5-year survival rates for patients with advanced disease are somewhere around 25% to 30%. The appropriate treatment of patients at the time of recurrence and the follow-up of patients who do undergo a complete remission are also areas of controversy.
Because ovarian cancer has a markedly superior survival rate in patients who present with early-stage disease, a major effort has been underway to diagnose the disease in asymptomatic women with appropriate screening tests. However, this too has led to controversy: Some investigators are strong advocates of screening while others are concerned about its cost and potential deleterious effects.
Critical quality of life studies and outcomes analyses have not been frequently performed in ovarian cancer patients. This review points out those areas where such studies are needed. Clinical pathways need to be developed that give the patient the greatest opportunity for long-term survival and, at the same time, produce acceptable morbidity. Furthermore, outcomes analyses must be linked with economic studies to determine the cost effectiveness of practices and procedures used in the management of ovarian cancer patients.
This review examines current approaches to diagnosis, screening, initial treatment, follow-up, and management of recurrent disease, to focus on those areas that require further outcomes analyses and quality of life studies.
As noted, most patients with ovarian cancer are elderly with a protracted history of vague abdominal complaints. Unfortunately, many of these patients do not undergo pelvic examination at the time of their first visit to a physician or caregiver. When the patient does present with an adnexal mass, an upper abdominal mass, ascites, and/or pleural effusion, often an expensive diagnostic work-up is begun. Patients frequently undergo CT scans, ultrasound examinations, cystoscopies, barium enemas, and colonoscopies . The justification often given is to help the surgeon define the extent of normal tissue invasion prior to debulking surgery. Since most of these patients will go to surgery, it is unclear exactly how these preoperative studies are routinely beneficial. In addition, if there is any question about the diagnosis, a CA 125 test done in the presence of a pelvic mass in a postmenopausal woman has a high degree of specificity in correctly diagnosing epithelial ovarian cancer [3,4].
Most physicians would, at a minimum, require a chest x-ray and a CT scan of the abdomen prior to surgery, and reserve barium studies and in-depth examinations of the bowel for those patients in whom there is suspected involvement of the gastrointestinal tract.
Since patients who are diagnosed with early-stage ovarian cancer (ie, the disease has not spread beyond the pelvis) have a markedly higher survival rate, screening has been proposed to decrease morbidity and mortality from this disease [5,6]. The current screening tests being studied include transvaginal ultrasound, serum CA 125, and pelvic palpation. It should be emphasized that screening does not diagnose ovarian cancer. It only identifies patients who are at potential high risk for the disease, in whom a surgical procedure such as laparotomy is required to determine if they indeed have ovarian cancer.
The primary requirement for any screening procedure for ovarian cancer is that it have a high specificity, to avoid an excess of false-positive results leading to numerous unnecessary laparotomies. Although perhaps somewhat arbitrary, a minimum criterion for an acceptable screening procedure is a positive predictive value of 10% . (Positive predictive value is the ratio of true positives to true positives plus false negatives.) Even such a low positive predictive value means that there will be nine false-positive laparotomies for each diagnosed case of ovarian cancer.
Several large screening studies have been done [8-10], and these have recently been reviewed at the National Institutes of Health Consensus Conference on ovarian cancer . Due to the inadequate sensitivity and specificity of available screening tests, the current recommendation is that screening not be employed for the general population. This decision reflects three major factors:
1. The high rate of false-positive test results would lead to unnecessary operations and has the potential for doing harm in the screened population . Among patients undergoing unnecessary laparotomies, some would experience complications, and some, however small the number, might die from an unnecessary procedure. These deaths would likely outweigh any possible benefit from identifying a few patients with early-stage ovarian cancer in the screening protocol.
2. An elevated CA 125 level induces a great deal of anxiety in the patient and consequently leads to an unnecessary and expensive diagnostic workup, which often results in a negative laparotomy.
3. The cost of screening has been estimated to be about $15 billion if applied to the general US population . Consequently, while there may be a role for screening in patients with hereditary familial syndrome, women who are desirous of screening should participate in the ongoing National Cancer Institute PLCO trial in which 75,000 women will be randomized to screening with ovarian palpation, transvaginal ultrasound, and serum CA 125 or to routine follow-up. The study began in 1993, and initial results will be presented by the end of 1995. Dr. John Gohagan is coordinating the trial at the NCI.
The accepted surgical approach when the diagnosis of ovarian cancer is expected is a comprehensive laparotomy with a large midline incision that extends above the umbilicus. This will allow the gynecologic oncologist to adequately stage the cancer and at the same time perform cytoreduction. The standard operation includes a bilateral salpingo-oophorectomy and omentectomy as well as removal of any masses in the upper abdomen. The goal of cytoreductive surgery is to leave no tumor mass greater than 1 cm in diameter; if this is achieved, it is termed an optimal cytoreductive procedure.
Approximately 50% to 60% of all patients with advanced disease can undergo effective cytoreduction. However, controversy remains regarding the impact of cytoreductive surgery on the overall survival of these patients [14,15]. Nevertheless, it is accepted practice, since patients who undergo successful cytoreduction have a subsequently improved quality of life with decreased symptoms from large masses, and also respond more favorably to postoperative chemotherapy.
There has been substantial recent progress made in defining more effective chemotherapy for advanced ovarian cancer. Until recently, the combination of cyclophosphamide (Cytoxan, Neosar) and a platinum compound was considered standard care. This type of combination produced a response rate of approximately 55% to 60% in patients with suboptimal stage III and IV disease, and in this group of patients, median survival usually was 21 to 22 months. Carboplatin (Paraplatin) is a less toxic analog of cisplatin (Platinol), and many investigators have used carboplatin instead of cisplatin in combination with cyclophosphamide. A series of randomized trials and a metaanalysis have failed to demonstrate any significant difference in survival between patients treated with cisplatin or carboplatin [16-18]. Patients treated with carboplatin have a better quality of life due to decreased nausea and vomiting, less neurotoxicity, and less anorexia.
The taxanes represent a new family of antineoplastic agents that have altered the standard approach to ovarian cancer. The greatest clinical experience available is with paclitaxel (Taxol). This drug was initially derived from bark of the Western yew (Taxus brevifolia). Interest in this compound was heightened by its marked in vitro and in vivo activity in preclinical models of human cancer and by its novel mechanism of cytotoxicity . In contrast to other drugs that interfere with tubulin, paclitaxel leads to a polymerization of the microtubules, thereby disrupting mitoses.
Initial phase I trials with this agent were hampered by hypersensitivity reactions. Subsequently, by increasing the length of infusion to 24 hours and by premedicating the patients with steroids, diphenhydramine, and cimetidine (Tagamet), hypersensitivity reactions became infrequent .
In early phase II trials, paclitaxel was shown to induce a high response rate (approximately 30% to 40%) in previously untreated patients with advanced ovarian cancer [21,22]. Of particular note in these trials was the finding that even cisplatin-resistant patients were responding to paclitaxel. A subsequent phase I trial demonstrated that paclitaxel could be combined with cisplatin at full doses, and this led to a prospective randomized trial in untreated patients .
The GOG protocol 111 is a pivotal study in ovarian cancer in which patients with suboptimal stage III and IV disease were randomized to receive either six cycles of standard cisplatin plus cyclophosphamide or six cycles of cisplatin plus paclitaxel . After the completion of chemotherapy, patients were reassessed clinically, and those patients in a clinical complete remission underwent a second-look procedure to surgically assess their response to therapy. The patients randomized to the paclitaxel combination had a higher overall response rate (77% vs 62%), a higher clinical complete remission rate (54% vs 33%), a higher negative second-look or microscopic positive second-look rate (26% vs 41%), a longer time to disease progression (18 months vs 14 months), and, most important, a marked prolongation in median survival (37 months vs approximately 23 months). On the basis of these results, the GOG has accepted paclitaxel plus cisplatin as the standard chemotherapy regimen.
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