Existing literature supports the role of signaling protein vascular endothelial growth factor (VEGF) in tumor growth and metastasis and furthers its involvement in recurrence. In both experimental and clinical studies, VEGF has been shown to be a significant factor involved for aberrant blood vessel growth, and in fact is the target of several classes of antineoplastic drugs [1] [2] [3] [4]. That said, the current standard of care for estrogen receptor positive breast cancer (although improved over the last decade), has not provided a “meaningful preventive shift” since the discovery of angiogenesis and its role in induction of recurrence. In this article, we discuss an anti angiogenic therapy implementing natural compounds to inhibit the production of VEGF. We applied our preclinical data to justify the predicted effect on VEGF. We used liquid biopsy to monitor patients response to therapy as a surrogate for recurrence. We hypothesize that by inhibition of angiogenesis through this protocol, we are able to positively impact tumor recurrence. It is our experience that patients in our sample even with high recurrence scores (based on Oncotype Dx testing) had a major reduction in recurrence when estrogen blockers were combined with this protocol. We also propose longitudinal studies to compare outcomes with combinational therapies with estrogen blockers in highly expected to recur disease.
Invasive breast cancer is a disease that affects 1 in every 8 women [
15 cases of Stage I-III breast cancer patients in whom tumors were estrogen receptor (ER) positive were randomly selected, and their biological cancer markers were assessed prior to, and after intervention. Most patients had undergone lumpectomy or mastectomy, and started hormonal blockade prior to the intervention. None of these patients received neoadjuvant chemotherapy or radiation.
Hormonal blockade was defined by intake of tamoxifen (dosed at least 10 mg per day, all had extensive metabolizer profile identified), or an aromatase inhibitor of physician’s choice. Several of these patients’ breast cancer assays performed by Oncotype Dx, and were given high recurrence scores (however, none of these patients chose to receive chemotherapy). The maximum Oncotype Dx score was reported at 50%. A liquid biopsy (circulating tumor DNA) was obtained when available. These were obtained prior to therapy, and performed again after therapy.
The antiangiogenic therapy was introduced by intravenous injections of a polyphenols including Quercetin, per multitargeted epigenetic therapy (MTET) protocol. The patients’ tumor markers, (such as CA 15-3 and CA 27.29), along with growth factors, and serum/plasma VEGF were monitored before, during, and after therapy. The hormonal blockade drug of choice in each patient was not changed. These patients did not receive any other mode of therapy, and were instructed not to change their diet or lifestyle.
100 percent of patients had reduced and/or normalized growth factors following treatment with the MTET protocol. These markers included fibroblast growth factor 2 (FGF-2), insulin-like growth factors 1 (IGF-1) and VEGF. In cases where liquid biopsy was available, there was complete resolution of circulating tumor DNA (ctDNA) post-therapy. There was direct correlation between the frequency of therapy and reduction in the biomarkers, specifically serum/plasma VEGF. The frequency of therapy was determined by elevations in these biomarkers prior to administration of the therapy. Patients with dramatically elevated biomarkers had treatment as often as ten treatments in a two-week period, while those slightly abnormal biomarkers were given treatment as infrequently as once a month. Since every individual’s biomarkers were measured and reported abnormal prior to therapy, every case represented their own control. There were no side effects reported from the therapy. None of the patients were found to have recurrence over the monitoring time, which so far has been between 6 months to 5 years. Here we include a case, with a summary of the results.
A 68-year-old female with a history of left lobular invasive breast cancer, presented to our clinic treatment. She was first diagnosed in June 2016, and was status post biopsy of the left breast. The pathology showed ER and progesterone receptor (PR) positive, human epidermal growth factor receptor 2 (HER2) negative. A PET scan was done for staging, which was negative for distant metastasis. She had a remote history of thyroid carcinoma insitu, and was status-post thyroidectomy. She also had a history of laryngeal squamous cell carcinomain 2011, status-post radiation and cetuximab, which she responded to.
She was referred to us for second opinion, and was evaluated through BioFocus labs for circulating tumor cells (CTCs), Guardant 360 for ctDNA, and Caris Target Now for molecular profiling. Her molecular profiling revealed several mutations, including somatic mutations at BRCA (breast cancer susceptibility gene), CDH1 (cadherin-1), CSF1R (colony stimulating factor 1 receptor), IDH1 (Isocitrate dehydrogenase 1), and PI3k (phosphoinositide 3-Kinase) were detected by these labs. A BRCA germ line test was ordered and it came back negative. Tumor markers were drawn through LabCorp and were reported normal, although her serum HER2 was borderline normal at 14 (ng/mL). The CTC was also negative. Her ctDNA was positive for BRAF, AR, FGFR, and ERBB2.
She was started on Tamoxifen at 10 mg per day, as her Cytochrome P450 2D6showed an extensive metabolizer profile. She was started on daily IV epigenetic therapies (MTET protocol), which she received for 10 days over a two week period. Her serum Her2/Neu Quant level dropped from 14.6 ng/mL down to 11.7 ng/mL, post therapy. After 10 treatments, second ctDNA assay showed marked reduction of the mutant allele fraction (MAF), (see
This is an interesting case of successful response in a patient with no detectable distant metastases, but positive ctDNA. This demonstrates the concept of secondary prevention and reduced angiogenesis and heterogeneity of the tumor in response to MTET protocol, which consists of epigenetic therapies, as all ctDNA disappeared with the protocol. It is worth noting that neither tamoxifen nor mastectomy could positively impact the ctDNA, and in fact there was an increase in ctDNA post-mastectomy.
Our treatment protocol, which uses multitargeted epigenetic therapies, has generated interest in the use of combinational therapy to reduce recurrence, through a safe and effective method of treatment using natural compounds. We believe that such approach could change the current standard of care. Further research is needed to conclude whether this research would translate to improved progression free survival on a large scale, and to determine whether overall survival and cure rates are improved in the setting of hormonally sensitive breast cancer. Further trials are needed to optimize the therapy schedule and protocols.
Nezami, M.A. and Garner, J. (2017) Role of Anti Angiogenic Therapy in Prevention of Recurrence in Hormonal Positive Breast Cancer: A Secondary Prevention Strategy and Method of Therapy. Journal of Cancer Therapy, 8, 546-552. https://doi.org/10.4236/jct.2017.86046