Ovarian cancer is expected to occur in 22,000 women and cause 14,030 deaths in the United States. This fatality rate makes this tumor the leading cause of gynecologic cancer mortality. Epithelial ovarian cancer typically spreads in a logical fashion to involve the peritoneal cavity and lymph nodes as well as outside the abdomen. The most common site of extra-abdominal spread is the pleural space and thought to occur through the lymphatics. Hematologic also spreads to the liver, spleen, or lung occurs.
Most patients with ovarian cancer experience no signs or symptoms of the disease until it spreads to the upper abdomen—approximately 70% of patients with this tumor present with advanced stage III or stage IV. Abdominal discomfort, bloating, and early satiety are the most common symptoms, occasionally found as a pelvic mass during physical examination.
The tumor marker CA 125 is only elevated in approximately 50% of patients presenting with ovarian cancer. This limits this test as a screening tool. Postoperatively it is a useful screening tool. Transvaginal ultrasound is an essential diagnostic: Transvaginal ultrasound is more sensitive than screening by CAT scanning. New genomic analysis and evaluation of peripheral blood circulating cancer cells can make an early diagnosis which allows for advanced treatment and eradication.
Management of advanced-stage disease is by debulking surgery, which includes the removal of large, necrotic tumors with the inadequate blood supply that might lead to impaired chemotherapy delivery. Primary debulking surgery is surgery before chemotherapy and is the standard of care. Postoperatively we use systemic chemotherapy and intraperitoneal chemotherapy.
Most patients with advanced ovarian cancer will recur after first-line chemotherapy. Over 50% of newly diagnosed advanced ovarian cancers will achieve complete clinical remission after the platinum chemotherapy drugs. The problem is in many patients; it returns a few years later. We now know that the tumors secrete circulating cancer cells, which can remain in the blood for years after the initial chemotherapy dose and cause metastasis and new tumor growth. We now have advanced genomic, molecular testing to improve our outcomes.
We are now able to profile through genomic testing to evaluate the “tumor drivers,” which are the pathways causing cancer to multiply and divide. These factors include genetic mutations, growth factors, hormone factors, and other factors causing new blood vessel growth and the metastasis of cancer. Various pathways are blocked to stop the growth of the tumor. By evaluating the circulating cancer cells, we can predict remission prognosis and recurrence. New chemosensitivity testing to find out which chemotherapy will be most effective in your cancer as well as testing for natural substances performed. The patient’s underlying immune system is of critical importance and is evaluated and optimized in all cases.
Low dose metronomic chemotherapy does not have toxic side effects as seen in traditional high-dose maximum tolerated dose chemotherapy. In addition, low-dose chemotherapy does not suppress the patient’s immune system and cause chemotherapy resistance. Natural targeted therapies are nontoxic and can reverse chemotherapy resistance and can improve the patient’s underlying immune status. Combination therapy with synergism is more effective.
The recent approval of immunotherapy with checkpoint inhibitors have changed the management of advanced ovarian cancer. Anti-PD–1, anti-PD–L1 and CT LA–4 checkpoint inhibitors currently used. They are synergistic with other treatments. The patient’s tumor mutational burden and microsatellite instability are assessed before treatment. Also, before treatment, the patient’s underlying immune function is of critical importance and is optimized.
Personalized Vaccines are currently made for your stage 4 ovarian cancer. These vaccines have taken from the patient’s circulating cancer cell in their blood and made in the laboratory. They are injected directly back into the bloodstream to attack cancer and administered several times a year. Optimization of your immune function is critical to their effectiveness.
Through new personalized genomic testing, we now have genuinely customized cancer care. By evaluating your “biomarkers,” we can see which cancer pathways are causing cancer to be more aggressive and spread. We can block those pathways. Low dose metronomic chemotherapy does not have the associated toxic side effects, as seen with traditional dose chemotherapy. Low-dose chemotherapy does not cause chemotherapy resistance and does not cause immunosuppression. The addition of natural substances is synergistic, and nontoxic always indicated. Various forms of immunotherapy, including the checkpoint inhibitors, autologous cancer vaccines, dendritic cell vaccines, and supportive oligonucleotides (SOT), are a combination solution for the Treatment of Ovarian Cancer.
If you would like more information on stage IV ovarian cancer, please call us at 727-330-3844.
- Personalized Genomic Molecular Profiling
- Low-dose Chemotherapy
- Natural Synergistic Substance
- Immunotherapy w/ Checkpoint inhibitors
- Immunotherapy w/ Autologous Whole Tumor Vaccine
- Dendritic Cell Vaccine
- Supportive Oligonucleotides (SOT)