Radiotherapy Chemotherapy

In radiation therapy, certain treatment plans require a water-equivalent material called a bolus to raise the maximum dose buildup (Dmax) closer to the surface of the skin. One of the most common materials used to create this more superficial treatment dose is a commercial product called Superflab. Superflab is a manufactured vinyl gel material that is uniform in thickness, easy to cut, and reusable (Radiation Products Inc, 2010). Therapists use other materials in clinical settings, but there is currently very little research available comparing alternative bolus materials and their respective Dmax values. The limited amount of research that is available look at different materials such as wet gauze and other similar materials for their easy,

It has targeted cells that work to kill and defend any pathogen or impurity that enters one’s body. In the case of cancers, a person’s cells grow abnormally forming a tumor. Unlike normal cells, cancer cells lose the ability to undergo apoptosis, cell death. Thus, one’s body harvests a tumor that most likely has a chance to spread and become deadly. Luckily, the biotech industry concocted innovative research that called for a new method of cancer treatment. Immunotherapy is designed to program one’s immune system to destroy and fight off the cancer. Originally, it has been mainly used for allergies. Dosages of medication or vaccinations are given to a patient to ensure that the immune system will not overreact to certain types of foreign substances. The therapy requires a drug that delivers an anticancer immune cell, specifically designed to attach on to the specific antigen that the tumor contains. According to scientist, immunotherapy gives patients “long term protection with reduced side effects against the cancer” (McGinley). The purpose of this treatment is to strengthen the immune system and specifically targets cancerous cells. Due to scientific research and the use of biotechnological methods, immunotherapy is able to prevent the threat of killing cells necessary to one’s body. Providing patients with a treatment that does not take a toll on their bodies, nor threaten to kill healthy cells is one relief the person

The research presented in Jedd D. Wolchok “Cancer’s Off Switch” examines two different forms of immunotherapy used to treat cancer cells by boosting the patient's own immune system defenses. The article provides a comprehensive history of the scientific discoveries and previous research that lead to the immunotherapy treatments, specifically the different levels of the immune system. In addition, the article addresses two different methods of immunotherapy currently in testing in clinical use. The research is educationally significant because it focuses on the body's internal defense system and attempts to disable the brakes cancer cells enforce on the immune system, which has shown progress in both tumor size regression and improvements in

Prof. Jonathan Bramson holds a BSc in Biochemistry and a PhD in Experimental Medicine from McGill University. He has published 96 research manuscripts, 11 review articles, and 2 book chapters. He has also submitted 3 patent applications in the area of immunotherapy. His research is focused on the mechanisms by which the adaptive immune system recognizes and responds to tumours and a specific interest is the development of immunological strategies to fight cancer. He is currently a tenured professor at the department of pathology and molecular medicine at McMaster University, since 2009 director of the McMaster Immunology Research Centre (MIRC) and holder of the John Bienenstock Chair in Molecular Medicine as well as the Tier I Canada Research

Cancer immunotheraphy is a concept that has been around for centuries. Back in the 1800s, a bone surgeon named William Coley injected his patients with a vaccine consisting of killed bacteria hoping it would stimulate the body's defense system. During the 1990s, physicians treated people with cancer with a cytokine treatment. This treatment involved high amounts of interleuken-2 (IL-2) and interferon-γ (IFNγ), also known as inflammatory cytokines. These inflammatory cytokines were released by white blood cells that fight infection (T cells). However, this treatment can have very dangerous side effects such as vascular leakage and kidney damage, but some people that received the cytokine treatment have lived for decades. In the year of 1996,

In other words, it specifically triggers immune responses pertaining to the mesothelioma malignancy or targets the cancer cells at hand. Active immunotherapy excites an immune response by presenting antigens to the immune system for a response against the malignancy itself. Although the mesothelioma malignancy has a unique set of cells, the tumor does not always produce antigens. This results in the use of an antigen precursor protein called Mesothelin, which allows these antigens to form around the tumor in hopes to specifically target the malignancy site. On the other hand, passive immunotherapy does just the opposite. Passive immunotherapy does not induce an immune response; it simply and directly targets the malignancy by injecting “immune compounds that attack the cancer such as antibodies, cytokines, T cells and macrophages” (Selby). Non-specific immunotherapy injects cells that inhibit the growth of the tumor cells, preventing those cells from constant reproduction. These cells that are injected cooperate directly with the malignancy and are known as cytokines, lymphokine-activated killer cells and macrophages. Immunotherapies such as active, passive and non-specific passive all are becoming effective therapies for mesothelioma and are indicative of improving the patient’s

Melanoma is a skin cancer derived from melanocytes and is considered to be the most common fatal malignancy of young adults. About 60% of melanomas harbor a mutation in BRAF, a serine/threonine protein kinase involved in promoting MAPK signaling and cellular proliferation. Of these, 90% harbor the BRAFV600E mutation. To combat this disease, the BRAF inhibitor, vemurafenib, was approved in 2011 to treat late-stage melanomas that are driven by the BRAFV600E mutation. Despite the immediate, positive clinical response to the drug, resistance develops after 7 months of vemurafenib treatment. Significant research effort has been devoted to understanding the origin of this drug resistance, but few studies have examined the fate of individual cells

According to Rosenberg (1988), the field of immunotherapy has become an area of significant and increasing interest within the field of medical science, prompted by the recent advances in knowledge of both biotechnology and cellular immunology. The field of immunology has produced revolutionary developments such as vaccines, which have prevented and decreased the occurrence of numerous infectious diseases over the past two centuries (Oviedo-Orta et al. 2013). Vaccine development has in turn combined immunology and drug design, resulting in a great deal of innovation over the last four decades endeavouring to expand the benefit of immunology past vaccines against foreign pathogens, and towards the treatment of chronic debilitating diseases.

Lymphoma is a cancer that starts in our cells and affects our immune system (“Lymphoma”). The natural killer cells in our bodies, also known as NK cells, can fight off the malignant lymphoma cells for our immune system. They are an important part of our immune system because they allow immunity of dangerous and altered structures. The only problem is, they lose their effect once they are within the vicinity of the tumor itself. With belief that natural killer cells are very therapeutic to killing lymphoma cells, scientists of Helmholtz Zentrum Munchen have discovered a way to fix this.

As the world continues to suffer from these devastating diseases, researchers continue to find alternative therapeutic ways of addressing cancer treatment. It is on this premise that various immunotherapeutic alternatives have emerged and currently garnering the greatest level of attention and already raising hope throughout the world in addressing the treatment of NSCLC. However, this can no longer be viewed as a discovery but a wave in the medicine world that began in the 20th century. Various researchers have found the importance of the role of immune systems in fighting the growth of tumor caused by cancer cells. A study by Huncharek (2000) stated that specific immune boosters are capable of eliminating preclinical cancers. In contrast, Jermal et al. (2011) found that immunotherapy is an effective approach for the treatment of tumors that have already turned into solid. Similarly, the researchers highlighted that immunotherapy can be an effective approach to the treatment of melanoma as well as renal cell cancers (Lasalvia-Prisco, 2008). However, Jemal et al. (2011) noted that immunotherapy cannot achieve much in cancer treatment due to limitation brought about by the emission of immunosuppressive cytokines and subsequent loss of antigen expressions. Recent development in research studies on the immunotherapy approach to cancer treatment continues to elicit mixed reactions among researchers of medicinal ecology (Jadad et al., 1996). However, recent development in

In contrast, internal radiation therapy uses a radioactive material that is is placed inside the tumor. Internal radiotherapy can be performed in several ways. Brachytherapy is a type of internal radiation treatment in which a solid radioactive source in placed in the tumor. This involves the patient staying in hospital for a few days or until the radioactive source has been removed from their body. Another form of internal radiotherapy is radionuclide, which uses a liquid source of radiation. This can either be taken through the patient's mouth or by an injection placed into a vein. For radionuclide, the patient would need to stay in hospital until the radioactivity has left the body. Internal radiation therapy allows a higher dosage of radiation

Adoptive cell transfer (ACT) is an immunotherapeutic strategy that takes advantage of tumor antigen-specific CD8+ T cells within tumor infiltrating lymphocyte (TIL) populations. Preclinical and clinical studies have proven the principle of ACT immunotherapy, in which TIL are isolated from tumors, stimulated to undergo massive in vitro proliferation, and infused into patients in hopes of causing immunological tumor regression [1-3]. ACT protocols typically depend on pre-transfer lymphodepletion to maximize the engraftment and persistence of ex vivo-expanded T cell populations [4,6]. Although clinical trials of melanoma ACT have demonstrated favorable response rates and cases of profound and durable disease regression, suboptimal response

Immunotherapy is a form of medical treatment intended to stimulate or restore the ability of the immune system to fight infection and disease. This can be by inducing, enhancing, or suppressing an immune response. Immunotherapies designed to elicit or amplify an immune response are classified as activation immunotherapies, while those that reduce or suppress immune response are suppression immunotherapies. Active immunotherapy has been effective against agents that normally cause acute self-limiting infectious disease. However, a more effective immunotherapy for chronic infectious diseases or cancer requires the use of appropriate target antigens; the

Cancer occurrs by the production of multiple mutations in a single cell that causes it to proliferate out of control. Cancer cells often different from their normal neighbors by a host of specific phenotypic changes, such as rapid division rate, invasion of new cellular territories, high metabolic rate, and altered shape. Some of those mutations may be transmitted from the parents through the germ line. Others arise de novo in the somatic cell lineage of a particular cell. Cancer-promoting mutations can be identified in a variety of ways. They can be cloned and studied to learn how they can be controlled.

In 2007, it is predicted that almost 1.5 million people will be diagnosed with cancer in the United States (Pickle et al., 2007). More than half of these cancer patients will undergo the use of radiation as a means for treating cancer at some point during the course of their disease (Perez and Brady, 1998). Cancer, a disease caused by an uncontrollable growth of abnormal cells, affects millions of people around the world. Radiotherapy is one of the well known various methods used to treat cancer, where high powered rays are aimed directly at the tumor from the outside of the body as external radiation or an instrument is surgically placed inside the body producing a result of internal radiation. Radiation is delivered to the cancerous regions of the body to damage and destroy the cells in that area, terminating the rapid growth and division of the cells. Radiation therapy has been used by medicine as a treatment for cancer from the beginning of the twentieth century, with its earliest beginnings coming from the discovery of x-rays in 1895 by Wilhelm Röntgen. With the advancements in physics and computer programming, radiation had greatly evolved towards the end of the twentieth century and made the radiation treatment more effective. Radiation therapy is a curative treatment approach for cancer because it is successful in killing cancerous tumor cells and stop them from regenerating.