Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2 Suppl 1
pubmed:dateCreated
2007-5-3
pubmed:abstractText
There are few approved therapies for cutaneous T-cell lymphoma (CTCL). The retinoids are the major biologic response modifiers used in CTCL, producing good response rates but few complete responses. For patients with early-stage disease, the oral retinoids can be combined with other therapies, such as psoralen plus ultraviolet A or interferon alpha, to improve response rates. Combined-modality therapy with oral retinoids, combined chemotherapy, electron-beam therapy, and topical mustargen has also proved effective. For the treatment of advanced-stage disease, the targeted therapy denileukin diftitox (Ontak) provides a nonimmunosuppressive alternative to conventional chemotherapy or radiation therapy. Of the conventional chemotherapies that have been tested in CTCL, gemcitabine (Gemzar) has demonstrated good efficacy in producing responses, particularly in patients with tumors. This agent can be used in combination with a maintenance therapy of bexarotene (Targretin) to manage the plaques and patches of mycosis fungoides. Several other targeted therapies are now also in testing, for example, alemtuzumab (CamPath), HuMax-CD4, several histone deacetylase inhibitors, and the transition-state inhibitor forodesine. These drugs, in combination with currently used therapies, may increase the number and combinations of therapies available for the treatment of this chronic condition to optimize long-lasting responses in CTCL.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal, http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal, Humanized, http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Neoplasm, http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents, http://linkedlifedata.com/resource/pubmed/chemical/Diphtheria Toxin, http://linkedlifedata.com/resource/pubmed/chemical/Hydroxamic Acids, http://linkedlifedata.com/resource/pubmed/chemical/Immunologic Factors, http://linkedlifedata.com/resource/pubmed/chemical/Interferon-alpha, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2, http://linkedlifedata.com/resource/pubmed/chemical/Mechlorethamine, http://linkedlifedata.com/resource/pubmed/chemical/Purine Nucleosides, http://linkedlifedata.com/resource/pubmed/chemical/Pyrimidinones, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Retinoids, http://linkedlifedata.com/resource/pubmed/chemical/alemtuzumab, http://linkedlifedata.com/resource/pubmed/chemical/denileukin diftitox, http://linkedlifedata.com/resource/pubmed/chemical/immucillin H, http://linkedlifedata.com/resource/pubmed/chemical/vorinostat
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0890-9091
pubmed:author
pubmed:issnType
Print
pubmed:volume
21
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
33-40
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:17474358-Antibodies, Monoclonal, pubmed-meshheading:17474358-Antibodies, Monoclonal, Humanized, pubmed-meshheading:17474358-Antibodies, Neoplasm, pubmed-meshheading:17474358-Antineoplastic Agents, pubmed-meshheading:17474358-Antineoplastic Combined Chemotherapy Protocols, pubmed-meshheading:17474358-Chemotherapy, Adjuvant, pubmed-meshheading:17474358-Diphtheria Toxin, pubmed-meshheading:17474358-Dose-Response Relationship, Drug, pubmed-meshheading:17474358-Humans, pubmed-meshheading:17474358-Hydroxamic Acids, pubmed-meshheading:17474358-Immunologic Factors, pubmed-meshheading:17474358-Interferon-alpha, pubmed-meshheading:17474358-Interleukin-2, pubmed-meshheading:17474358-Lymphoma, T-Cell, Cutaneous, pubmed-meshheading:17474358-Mechlorethamine, pubmed-meshheading:17474358-Purine Nucleosides, pubmed-meshheading:17474358-Pyrimidinones, pubmed-meshheading:17474358-Radiotherapy, Adjuvant, pubmed-meshheading:17474358-Recombinant Fusion Proteins, pubmed-meshheading:17474358-Retinoids, pubmed-meshheading:17474358-Sezary Syndrome, pubmed-meshheading:17474358-Skin Neoplasms
pubmed:year
2007
pubmed:articleTitle
Systemic monotherapy vs combination therapy for CTCL: rationale and future strategies.
pubmed:affiliation
Department of Dermatology, The University of Texas, M.D. Anderson Cancer Center, Houston, Texas 77030, USA. mduvic@mdanderson.org
pubmed:publicationType
Journal Article, Review