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  <titleInfo>
    <title>Analysis File of Drug-Induced Lung Injury</title>
    <subTitle>Expert Opinion for Analysis of Big Data</subTitle>
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  <name type="personal">
    <namePart>Gemma, Akihiko.</namePart>
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    <dateIssued encoding="marc">2024</dateIssued>
    <edition>1st ed. 2024.</edition>
    <issuance>monographic</issuance>
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  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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  <physicalDescription>
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    <extent>XII, 116 p. 48 illus., 18 illus. in color. online resource.</extent>
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  <abstract>This book describes the pathologic conditions of drug-induced lung injuries, monitoring strategies, and guides on how to interpret the evidence. It also dives into particular drugs that caused the disorder, such as EGFR inhibitors, anti-EGFR antibodies, mTOR inhibitors, proteasome inhibitors, immune checkpoint inhibitors, neoangiogenesis inhibitors, and other molecular targeted drugs. It outlines the analysis and interpretation of the post-marketing survey on surveillance of each drug for inducing pulmonary lesions presenting diffuse haziness. The data and analysis from this survey are valuable since a guideline is yet to be established due to limited clinical evidence and cases. As new drugs are developed, establishing treatment and event management is crucial. Thus, Drug-induced Pulmonary Disorder in Medical Oncology - Expert Opinion to Decipher Big Data summarizes the accumulated information to provide a foundation for further research advancement. The book offers a refreshing alternative to current approaches to medical oncology and respiratory diseases professionals and will also attract medical affairs members in global pharmaceutical companies.</abstract>
  <tableOfContents>Part I Understanding Drug-Induced Lung Injuries -- 1 Understanding Drug-Induced Lung Injuries -- Part 2 Actual Practice in Drug-Induced Lung Injuries of Each Drug -- 2 EGFR inhibitors (gefitinib, erlotinib, afatinib, osimertinib) -- 3 Anti-EGFR antibodies (cetuximab, panitumumab, necitumumab) -- 4 mTOR inhibitors (temsirolimus, everolimus) -- 5 Proteasome inhibitor (bortezomib) -- 6 Immune checkpoint inhibitors (nivolumab, pembrolizumab, atezolizumab, durvalumab) -- 7 Neoangiogenesis inhibitors (sunitinib, sorafenib, bevacizumab) -- 8 Other molecular targeted drugs (crizotinib, alectinib, etc.) -- 9 Antibody-drug conjugates (ADC) (trastuzumab emtansine, trastuzumab deruxtecan) -- 10 Anti-cancer drugs (TS-1, taxanes, CPT-11, platinum-containing drugs, etc.).</tableOfContents>
  <note type="statement of responsibility">by Akihiko Gemma.</note>
  <subject authority="lcsh">
    <topic>Respiratory organs</topic>
    <topic>Diseases</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Medical genetics</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Diseases</topic>
    <topic>Causes and theories of causation</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Oncology</topic>
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  <subject authority="lcsh">
    <topic>Pharmacology</topic>
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  <subject authority="lcsh">
    <topic>Genetics</topic>
    <topic>Research</topic>
  </subject>
  <subject>
    <topic>Pneumology</topic>
  </subject>
  <subject>
    <topic>Clinical Genetics</topic>
  </subject>
  <subject>
    <topic>Pathogenesis</topic>
  </subject>
  <subject>
    <topic>Oncology</topic>
  </subject>
  <subject>
    <topic>Pharmacology</topic>
  </subject>
  <subject>
    <topic>Genetics Research</topic>
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  <classification authority="lcc">RC705-779</classification>
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  <identifier type="isbn">9789819734467</identifier>
  <identifier type="uri">https://doi.org/10.1007/978-981-97-3446-7</identifier>
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