A Medical Device Strategy to Inhibit HER2+ Breast Cancer Progression

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1. A Medical Device Strategy To Inhibit HER2+ Breast Cancer Progression September 27, 2011 James A. Joyce Chairman & CEO, Aethlon Medical, Inc…
  • 1. A Medical Device Strategy To Inhibit HER2+ Breast Cancer Progression September 27, 2011 James A. Joyce Chairman & CEO, Aethlon Medical, Inc jj@aethlonmedical.comLast week, we introduced HER2osome™ as a therapeutic strategy to maximize the abilityof the immune system and established drug therapies to combat HER2+ breast cancer,which is characterized by aggressive growth and poor prognosis resulting from the over-expression of HER2 protein. HER2osome™ is a novel medical device, whose goal is toinhibit HER2+ breast cancer progression by reducing the circulatory presence of HER2protein and breast cancer exosomes, which increasingly have become recognized asplaying a pivotal role in the development and progression of breast cancer. Researchershave reported that breast cancer exosomes suppress the immune response, stimulateangiogenesis, contribute to the spread of metastasis, and inhibit the therapeutic benefit ofHerceptin® (trastuzumab), a leading monoclonal antibody treatment against the HER2+breast cancer. As an adjunct therapeutic candidate, HER2osome™ offers to fill an unmetmedical need and enhance the benefit of Herceptin and standard of care chemotherapieswithout adding drug toxicity or interaction risks.HER2some™ therapy has evolved from our Aethlon ADAPT™ system, which is anadaptable dialysis-like affinity platform technology that provides the foundation for anentirely new class of device-based therapeutics. Products developed from the AethlonADAPT™ system target the selective clearance of harmful agents from the entire bloodvolume within clinically relevant time frames and without the loss of essential bloodcomponents. The Aethlon ADAPT™ system overcomes the historic limitation ofextracorporeal strategies that indiscriminately adsorb or remove particles solely by
  • 2. molecule size. In function, the device platform allows the immobilization of single ormultiple affinity agents in the outer-capillary space of plasma filtration membranetechnology as a means to provide rapid real-time clearance of corresponding targets. Inthe case of HER2osome™, the immobilization of a HER2 antibody and an exosometargeted affinity agent provides a mechanism to clear both targets from the circulatorysystem of HER2+ breast cancer patients. Like all ADAPT™ derived therapies,HER2osome™ will operate dialysate free, will not require replacement fluids, and can beutilized on dialysis machines or CRRT systems already located in hospitals and clinicsworldwide.The multi-faceted pro-cancer mechanisms of tumor-secreted exosomes and disappointingresponse rates to HER2+ drug therapy provide a compelling rationale for the clinicaladvancement of HER2osome™. In this regard, the therapeutic objective ofHER2osome™ will be to address three unmet medical needs. 1. To provide a synergistic device mechanism that works in concert with drug therapies to improve HER2 protein clearance. 2. To reduce drug resistance associated with exosome proliferation. 3. To eliminate immunosuppressive and pro-cancer exosomes from circulation.The following sections entitled; HER2 Protein and Breast Cancer; The Implication ofBreast Cancer Exosomes in Drug Resistance; and The Role of Exosomes in BreastCancer Progression detail supporting scientific rationale for HER2osome™ therapy.HER2 Protein and Breast CancerBreast cancer is the most common form of cancer in women, accounting for 20% ofcancer deaths with approximately 180,000 women diagnosed annually in the UnitedStates (Merrill, R. M., and A. Sloan. 2011. Risk-adjusted female breast cancer incidencerates in the United States. Cancer Epidemiol.). Over-expression of the human epidermalgrowth factor receptor 2 (HER2; ErbB2) gene occurs in approximately 25% of breastcancers and has been linked to poor prognosis (Slamon, D. J., G. M. Clark, S. G. Wong,
  • 3. W. J. Levin, A. Ullrich, and W. L. McGuire. 1987. Human breast cancer: correlation ofrelapse and survival with amplification of the HER-2/neu oncogene. Science 235:177-182).HER2 is a receptor tyrosine kinase, member of the EGF receptor family, which possessesproliferative and anti-apoptotic activities. The standard of treatment for womendiagnosed with HER2+ breast cancer includes the humanized monoclonal antibodytrastuzumab (marketed as Herceptin®) directed against the extracellular domain ofHER2. Trastuzumab binding to HER2 mediates direct growth inhibition of tumor cellsand induces antibody-dependent cell cytotoxicity (ADCC), a major anti-cancermechanism by which natural killer (NK) cells lyse antibody-coated tumor cells (Nahta,R., D. Yu, M. C. Hung, G. N. Hortobagyi, and F. J. Esteva. 2006. Mechanisms of disease:understanding resistance to HER2-targeted therapy in human breast cancer. Nat ClinPract Oncol 3:269-280).In patients with metastatic breast cancer undergoing chemotherapy, treatment withtrastuzumab augments overall response rates and increases median survival time by 25%(Baselga, J. 2001. Clinical trials of Herceptin® (trastuzumab). Eur J Cancer 37 Suppl1:18-24). However, response rates to trastuzumab range from 12% to 34% with medianduration of 9 months due to development of resistance. Despite co-treatment with otherHER2 targeting therapies (e.g. the tyrosine kinase inhibitor lapatinib) and chemotherapy,patients with metastatic breast cancer experience a limited duration of benefit; therefore,novel treatment strategies that act synergistically or overcome drug resistance areurgently needed (Sachdev, J. C., and M. Jahanzeb. 2011. Blockade of the HER Family ofReceptors in the Treatment of HER2-Positive Metastatic Breast Cancer. Clin BreastCancer).The Implication of Breast Cancer Exosomes in Drug ResistanceAlthough trastuzumab (Herceptin®) has significantly altered the standard of care forHER2 over-expressing breast cancer, resistance remains a significant obstacle, with only30% responses achieved on monotherapy and average responses lasting 9 months (Nahta,R., D. Yu, M. C. Hung, G. N. Hortobagyi, and F. J. Esteva. 2006. Mechanisms of disease:
  • 4. understanding resistance to HER2-targeted therapy in human breast cancer. Nat ClinPract Oncol 3:269-280.). Tumor-secreted exosomes play a role in directly acceleratingtumor progression through stimulation of angiogenesis and ECM remodeling, as well asindirectly by causing immune suppression (Taylor, D. D., and C. Gercel-Taylor. 2011.Exosomes/microvesicles: mediators of cancer-associated immunosuppressivemicroenvironments. Semin Immunopathol.). Exosomes have been shown to directly bindagents such as trastubuzumab and rituximab, potentially decreasing efficacy (Ciravolo,V., V. Huber, G. C. Ghedini, E. Venturelli, F. Bianchi, M. Campiglio, D. Morelli, A.Villa, P. D. Mina, S. Menard, P. Filipazzi, L. Rivoltini, E. Tagliabue, and S. M. Pupa.2011. Potential role of HER2-overexpressing exosomes in countering Trastuzumab-basedtherapy. J Cell Physiol; and Aung, T., B. Chapuy, D. Vogel, D. Wenzel, M. Oppermann,M. Lahmann, T. Weinhage, K. Menck, T. Hupfeld, R. Koch, L. Trumper, and G. G.Wulf. 2011. Exosomal evasion of humoral immunotherapy in aggressive B-celllymphoma modulated by ATP-binding cassette transporter A3. Proc Natl Acad Sci U S A108:15336-15341).The Role of Exosomes in Breast Cancer ProgressionExosomes are 30-100 nm microvesicles shed by many cell types, serving as“messengers” that mediate intercellular transport of proteins and genetic material orinteract directly with target cells. Tumor-derived exosomes express tumor antigens andimmune inhibitory molecules that mirror their tumor of origin and are produced inincreasing quantities during tumor progression (Taylor, D. D., K. S. Lyons, and C.Gercel-Taylor. 2002. Shed membrane fragment-associated markers for endometrial andovarian cancers. Gynecol Oncol 84:443-448). Tumor-derived exosomes bind andsequester tumor-reactive antibodies, thereby potentially inhibiting the ability of immuneeffector cells to mediate ADCC (Battke, C., R. Ruiss, U. Welsch, P. Wimberger, S. Lang,S. Jochum, and R. Zeidler. 2011. Tumour exosomes inhibit binding of tumour-reactiveantibodies to tumour cells and reduce ADCC. Cancer Immunol Immunother 60:639-648).Exosomes secreted by breast cancer cells express HER2 and effectively sequestertrastuzumab. Functional assays revealed that HER2+ exosomes suppress trastuzumab’s
  • 5. ability to inhibit tumor cell proliferation. Cancer exosomes release ECM remodelingenzymes that promote metastasis, and pro-angiogenic factors for tumor growth. Hence,breast cancer patients can benefit from therapeutic strategies that counter the systemicimmune suppression and tumor growth-promoting activities of exosomes.ConclusionHER2osome™ therapy provides a novel strategy to improve treatment outcomes ofHER2+ breast cancer through the improved clearance of HER2 protein and removal ofcirculating exosomes that contribute to cancer progression and drug resistance. TheHER2osome™ mechanism of action offers to improve patient responsiveness to currentand future drug therapies without adding drug toxicity or interaction risks.About Aethlon MedicalThe Aethlon Medical mission is to create innovative medical devices that address unmetmedical needs in cancer, infectious disease, and other life-threatening conditions.Aethlon’s ADAPT™ platform provides the technology foundation for a new class oftherapeutics that target the selective removal of disease enabling particles from the entirecirculatory system. The Aethlon ADAPT™ product pipeline includes the Hemopurifier®,a first-in-class medical device with broad-spectrum capabilities against exosomes thatcontribute to the progression of cancer and infectious viral pathogens such as HIV andHepatitis C. For more information, please visit www.aethlonmedical.com.Certain of the statements within this report may be forward-looking and involve risks and uncertainties.Such forward-looking statements involve assumptions, known and unknown risks, uncertainties and otherfactors which may cause the actual results, performance or achievements of Aethlon Medical, Inc to bematerially different from any future results, performance, or achievements expressed or implied by theforward-looking statements. Such potential risks and uncertainties include, without limitation, theCompany’s ability to raise capital when needed, the Company’s ability to complete the development of itsplanned products, the ability of the Company to obtain FDA and other regulatory approvals permitting thesale of its products, the Company’s ability to manufacture its products and provide its services, the impactof government regulations, patent protection on the Company’s proprietary technology, product liabilityexposure, uncertainty of market acceptance, competition, technological change, and other risk factors. Insuch instances, actual results could differ materially as a result of a variety of factors, including the risksassociated with the effect of changing economic conditions and other risk factors detailed in theCompany’s Securities and Exchange Commission filings which can be accessed at www.SEC.gov.
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