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Biological response modifiers agents

Agents which enhance the host s response against neoplasias or force them to differentiate are termed biological response modifiers. Examples include interleukin 2 which is used to treat renal cell carcinoma, interferon a which is active against hematologic neoplasias, and tretinoin (all-trans retinoic acid) which is a powerful inducer of differentiation in certain leukemia cells by acting on retinoid receptors. Side effects include influenza like symptoms, changes in blood pressure and edema. [Pg.156]

Cytokines and biological response modifiers represent a broad class of therapeutic agents that modify the hosts response to cancer or cancer therapies. The enormous body information about their clinical uses and their side effects is beyond the scope of this essay that can only give illustrative examples. For an up-to-date information the reader can resort to reference [5]. As many as 33 different interleukins are known and the list continues to grow IL-2 used in the treatment of kidney cancer is one example. Interferon alpha is used for chronic myelogenous leukeia, hairy cell leukaemia and Kaposi s sarcoma. Interferons are also used in the treatment of chronic infections such as viral hepatitis. Tumor necrosis factor (alpha), G/GM/M-CSF, and several other cellular factors are used in treatment of various cancers. Many of these cytokines produce serious side effects that limit their use. [Pg.268]

Biologic response modifiers (BRMs) are indicated in patients who have failed an adequate trial of DMARD therapy.1 BRMs may be added to DMARD monotherapy (i.e., methotrexate) or replace ineffective DMARD therapy.22 The decision to select a particular agent generally is based on the prescriber s comfort level with monitoring the safety and efficacy of the medications, the frequency and route of administration, the patient s comfort level or manual dexterity to self-administer subcutaneous injections, the cost, and the availability of insurance coverage.23 In general, BRMs should be avoided in patients with serious infections, demyelinating disorders (e.g., multiple sclerosis or optic neuritis) or heart failure.21... [Pg.874]

Pharmacologic alternatives for psoriasis include topical agents, phototherapy, and systemic agents including the use of biologic response modifiers. [Pg.949]

Systemic therapies are seldom used for mild to moderate psoriasis, and are generally reserved for patients with moderate to severe psoriasis.17 29 Oral agents include sulfasalazine, acitretin, methotrexate, cyclosporine, mycophenolate mofetil, azathioprine, tacrolimus, and hydroxyurea. Parenteral agents include the biologic response modifiers alefacept, efalizumab, etanercept, infliximab, and many others, currently at various stages of research or approval for psoriasis. [Pg.955]

Begun in 1972, the Biological Response Modifiers Program supports intramural and extramural research (including some clinical investigation) on agents or... [Pg.311]

Hait WN, Rubin E, Goodin S. Tubulin-targeting agents. In Giaconne G, Schilsky R, Sondel P, eds. Cancer Chemotherapy and Biological Response Modifiers, Annual 21. Amsterdam Elsevier BV,... [Pg.1846]

Recently, NCI has established a "disease-oriented" approach to antitumor activity screening [5,15,16], the biological response modifiers (BRM) [17,18] program, which takes into account the diversity and specificity of tumor, and the requirements of novel structure types and novel action-mechanistic types of anticancer agents. [Pg.275]


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Biologic response modifiers

Biological modifier

Biological response modifier

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Modifying agents

Responsive biological

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