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Search: onr:"swepub:oai:lup.lub.lu.se:ab89be12-9718-4381-a3b3-1fc2d055fa46" > Clinical insights i...

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Clinical insights into small cell lung cancer : Tumor heterogeneity, diagnosis, therapy, and future directions

Megyesfalvi, Zsolt (author)
Medical University of Vienna,National Institute of Oncology, Budapest,National Korányi Institute for Tuberculosis and Pulmonology, Hungary
Gay, Carl M. (author)
University of Texas
Popper, Helmut (author)
Medical University of Graz
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Pirker, Robert (author)
Medical University of Vienna
Ostoros, Gyula (author)
National Korányi Institute for Tuberculosis and Pulmonology, Hungary
Heeke, Simon (author)
University of Texas
Lang, Christian (author)
Medical University of Vienna
Hoetzenecker, Konrad (author)
Medical University of Vienna
Schwendenwein, Anna (author)
Medical University of Vienna
Boettiger, Kristiina (author)
Medical University of Vienna
Bunn, Paul A. (author)
University of Colorado School of Medicine
Renyi-Vamos, Ferenc (author)
National Korányi Institute for Tuberculosis and Pulmonology, Hungary,National Institute of Oncology, Budapest
Schelch, Karin (author)
Medical University of Vienna
Prosch, Helmut (author)
Vienna General Hospital / University Hospital Vienna
Byers, Lauren A. (author)
University of Texas
Hirsch, Fred R. (author)
University of Colorado,Icahn School of Medicine at Mount Sinai
Dome, Balazs (author)
Lund University,Lunds universitet,Klinisk kemi, Malmö,Forskargrupper vid Lunds universitet,Clinical Chemistry, Malmö,Lund University Research Groups,National Korányi Institute for Tuberculosis and Pulmonology, Hungary,Semmelweis University,Medical University of Vienna
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 (creator_code:org_t)
2023
2023
English.
In: CA: a cancer journal for clinicians. - 0007-9235. ; 73:6, s. 620-652
  • Research review (peer-reviewed)
Abstract Subject headings
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  • Small cell lung cancer (SCLC) is characterized by rapid growth and high metastatic capacity. It has strong epidemiologic and biologic links to tobacco carcinogens. Although the majority of SCLCs exhibit neuroendocrine features, an important subset of tumors lacks these properties. Genomic profiling of SCLC reveals genetic instability, almost universal inactivation of the tumor suppressor genes TP53 and RB1, and a high mutation burden. Because of early metastasis, only a small fraction of patients are amenable to curative-intent lung resection, and these individuals require adjuvant platinum-etoposide chemotherapy. Therefore, the vast majority of patients are currently being treated with chemoradiation with or without immunotherapy. In patients with disease confined to the chest, standard therapy includes thoracic radiotherapy and concurrent platinum-etoposide chemotherapy. Patients with metastatic (extensive-stage) disease are treated with a combination of platinum-etoposide chemotherapy plus immunotherapy with an anti-programmed death-ligand 1 monoclonal antibody. Although SCLC is initially very responsive to platinum-based chemotherapy, these responses are transient because of the development of drug resistance. In recent years, the authors have witnessed an accelerating pace of biologic insights into the disease, leading to the redefinition of the SCLC classification scheme. This emerging knowledge of SCLC molecular subtypes has the potential to define unique therapeutic vulnerabilities. Synthesizing these new discoveries with the current knowledge of SCLC biology and clinical management may lead to unprecedented advances in SCLC patient care. Here, the authors present an overview of multimodal clinical approaches in SCLC, with a special focus on illuminating how recent advancements in SCLC research could accelerate clinical development.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

chemotherapy
diagnosis
immunotherapy
molecular subtypes
small cell lung cancer

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