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2019, International Journal of Current Medical Sciences
https://doi.org/10.24327/ijcmes2019.09010064…
3 pages
1 file
Chemotherapy is a therapy used for the treatment of cancer, particularly since the 1940s. This essay aims to be a contribution to the study of this subject, namely in the description of its history, indicating the main types of regimens and treatments in chemotherapy.
2000
The use of chemotherapy to treat cancer began at the start of the 20th century with attempts to narrow the universe of chemicals that might affect the disease by developing methods to screen chemicals using transplantable tumors in rodents. It was, however, four World War II-related programs, and the effects of drugs that evolved from them, that provided the impetus
2018
At the beginning of the 20th century, attempts to use chemotherapy for the treatment of cancer were started, and the first four decades of the 20th century were mainly dedicated to model development. There existed a dominant doubt regarding the capacity of drugs to treat advanced cancers until the success of combination of chemotherapy in treatment of acute childhood leukemia and advanced Hodgkin's disease in the 1960s and the early 1970s. Chemotherapy has undergone a lot of changes until the date, and nowadays molecular abnormalities are intensely studied to screen for potential new drugs and targeted treatments as well. The article highlights the major milestones in chemotherapy through the years. Key Words-Chemotherapy-cancer-leukemia -NCI-lymphoma-monoclonal antibodies-Rituximabvinca alkaloidsbreast cancer -targeted therapyTKIimatinibCisplatinCarboplatin -mechlorethaminevincristinemethotrexateprednisone INTRODUCTION In 1910, the German chemist Paul Ehrlic started the age of ...
During the first two decades of the 20th century, drug production changed with the coming together of tropical medicine, pharmaceutical industries, parasites and philanthropic capital. Chemical methods gained prominence in 'European' hegemonic medicine, and medical research became an industry. These processes gave birth to modern chemotherapy, an emblem of (neo)colonial claims to hegemony that arose with drugs like salvarsan as an allegedly European invention. This paper is based on my PhD thesis titled 'The Production of a Pharmacon: A Cartography of the Kala-Azar and the Antimonials' in which I analyse the history of kala-azar, a deadly 'tropical disease' that was described in Assam for the first time, and of the antimonials, organic and inorganic compounds that contain the chemical element antimony and became a landmark for modern chemotherapy during the 1920s. The linear teleological narrative that prevails is quite simple: The disease was described through colonial medicine in the late 19 th century. In 1903, its causative agent, the Leishman-Donovan bodies, later Leishmania donovani, was 'discovered' by two British physicians, William Leishman and Charles Donovan, and in the 1910s and 1920s, modern chemotherapy, i.e. pharmaceutical companies like Bayer and Burroughs Wellcome & Co., but also single persons like Upendranath Brahmachari, successfully invented suitable drugs. My period of interest is from the late 19th century to the late 1920s, and my cartography particularly focuses on the excluding power relations that constituted cognitive processes. The history of kala-azar is closely tied to British India and to the history of modern chemotherapeutics, i.e. drugs for infectious diseases.
International Journal of Gynecology & Obstetrics, 2015
Chemotherapy is a common treatment for cancer that uses drugs to destroy cancer cells. It worksby targeting rapidly dividing cells in the body, which includes cancer cells. Chemotherapy drugscan be administered in a variety of ways, including intravenously, orally, or through injections.Chemotherapy can be used to treat many types of cancer, including leukemia, lymphoma, breastcancer, lung cancer, and many others. It can be used in combination with other treatments, suchas surgery or radiation therapy, or it may be used as the primary treatment for certain types ofcancer. Chemotherapy drugs work by targeting the DNA or RNA of cancer cells, which preventsthem from dividing and growing.
Veterinary Clinics of North America: Small Animal Practice, 2007
T he range of chemotherapeutic drug options available to veterinarians continues to expand as we learn how to translate them from human oncology to the treatment of our patients. Newer drugs, such as gemcitabine [1], ifosfamide [2], and vinorelbine [3], are just a few examples. In addition to this are different approaches that evaluate alternate ways to use chemotherapeutics. Examples include intracavitary applications that aid in malignant effusion control by pleurodesis or radiation therapy sensitization , in which the benefits of the drugs are not necessarily restricted to their individual cancer cell cytotoxicity per se. Another approach that is emerging in the era of targeted cancer treatment is termed metronomic chemotherapy. This terminology was coined by Dr. Doug Hanahan and his colleagues in an editorial [6] regarding the publication of two preclinical studies in rodent models in which there was a treatment advantage for chemotherapeutics delivered in a low-dose continuous manner, even in tumors previously made resistant to the same drug given in a more traditional schedule . Other popular names for this approach include low-dose continuous chemotherapy or antiangiogenic chemotherapy. Regardless of the chosen terminology, this form of treatment is receiving increased attention in human and veterinary oncology circles. The use of drugs that we are already familiar with, plus the low cost, ease of application, and generally nontoxic nature of the dose and schedules chosen, make this approach attractive for application to veterinary oncology practice. The aim of this article is to outline the origin of and rationale for metronomic chemotherapy, explain what is known about the mechanism(s) responsible for its potential benefit, and highlight some of the clinical trial evaluations taking place. Although most metronomic clinical trials are taking place in human beings, veterinary oncology trials are also ongoing; thus, contacting a veterinary oncologist regarding the results of these trials, cases that may benefit, and specific protocols is advised.
Cancer, 1984
Progress in the treatment of cancer with drugs has radically altered the clinical approach to patients with malignancy. Not only have new drugs produced promising results in hitherto untreatable tumors, but they have extended and enhanced the effectiveness of other modalities, including surgery and radiotherapy. In this article, the authors consider avenues of research that likely to aid in the discovery of new anticancer drugs and improve the effectiveness of established agents. Promising new efforts in drug development include the use of new screening systems, particularly those employing human tumor material; the development of improved analogs of existing active agents particularly those of the anthracycline and platinum complex types; and the search for agents that which promote differentiation or prevent metastasis. In an effort to improve the effectiveness of established agents, the authors consider the application of pharmacokinetic principles in developing regional perfusion routes, intraperitoneal chemotherapy, and central nervous system penetration. Finally, the contribution of biochemical pharmacology to the current understanding of drug action, mechanisms of resistance, and drug interactions are considered, and the impact of this knowledge on clinical protocol design is assessed.
Journal of Clinical Investigation, 1986