<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Stenner-Liewen F</dc:creator>
  <dc:creator>Zippelius A</dc:creator>
  <dc:creator>Pestalozzi BC</dc:creator>
  <dc:creator>Knuth A</dc:creator>
  <dc:date>2006</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Until recently, cancer therapy was based on three modalities: surgery, radiotherapy, and cytostatic chemotherapy. In most instances treatment of solid tumors was a surgical domain. For patients with incomplete resection or relapse after surgery, radiotherapy and chemotherapy usually offered only partial response and mostly of limited duration. By the mid-1990s visions of antibody-based therapies, vaccination strategies, and even gene-specific therapies existed but seemed far from clinical practice. United States Federal Drug Administration approval of the humanized antibody rituximab (1997) and the tyrosine kinase inhibitor imatinib (2001) has changed perceptions of oncologic treatment. These drugs turned visions into reality and led the pharmaceutical industry, clinicians, and patients to new perspectives. This article gives an overview of the development of this fourth modality in cancer therapy, so-called targeted therapy.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/4272</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1007/s00104-006-1262-8</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/17109101</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen. - 2006</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Animals</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Antibodies, Monoclonal</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Antibodies, Monoclonal, Humanized</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Antibodies, Monoclonal, Murine-Derived</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Antineoplastic Agents</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Benzamides</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Cancer Vaccines</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Cell Survival</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Clinical Trials as Topic</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Drug Delivery Systems</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Humans</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Imatinib Mesylate</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">Neoplasms</dc:subject>
  <dc:subject xmlns:ns14="xml" ns14:lang="en">Piperazines</dc:subject>
  <dc:subject xmlns:ns15="xml" ns15:lang="en">Protein Kinase Inhibitors</dc:subject>
  <dc:subject xmlns:ns16="xml" ns16:lang="en">Pyrimidines</dc:subject>
  <dc:subject xmlns:ns17="xml" ns17:lang="en">Rituximab</dc:subject>
  <dc:subject xmlns:ns18="xml" ns18:lang="en">Trastuzumab</dc:subject>
  <dc:title xmlns:ns19="xml" ns19:lang="en">[Molecular targeted therapy].</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
