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Comprehensive characterization via molecular imaging, longitudinal multisite sampling, and autoptic work-up in advanced small cell lung cancer undergoing SSTR-directed radiopharmaceutical therapy

  • Despite the addition of immune checkpoint blockade to first-line chemotherapy, the prognosis for patients with small cell lung cancer (SCLC) is still devastating. For the subset of SCLC with somatostatin receptor (SSTR) overexpression, radiopharmaceutical therapy (RPT) might be an effective future treatment option. Methods: Here, we present the case of a heavily pretreated stage IV SCLC patient showing an exceptional response to SSTR-directed RPT. A comprehensive translational work-up consisting of histopathologic, immunohistochemical, and molecular pathology analyses at different time points during treatment and especially of lesions with discordant tracer uptake was performed. Results: Besides a promising response to RPT, interesting signs of clonal dynamics under therapy and, most importantly, SSTR downregulation of some lesions as a potential evasion mechanism to SSTR-directed RPT could be identified. Conclusion: This unique investigation for a clinical–molecular understanding ofDespite the addition of immune checkpoint blockade to first-line chemotherapy, the prognosis for patients with small cell lung cancer (SCLC) is still devastating. For the subset of SCLC with somatostatin receptor (SSTR) overexpression, radiopharmaceutical therapy (RPT) might be an effective future treatment option. Methods: Here, we present the case of a heavily pretreated stage IV SCLC patient showing an exceptional response to SSTR-directed RPT. A comprehensive translational work-up consisting of histopathologic, immunohistochemical, and molecular pathology analyses at different time points during treatment and especially of lesions with discordant tracer uptake was performed. Results: Besides a promising response to RPT, interesting signs of clonal dynamics under therapy and, most importantly, SSTR downregulation of some lesions as a potential evasion mechanism to SSTR-directed RPT could be identified. Conclusion: This unique investigation for a clinical–molecular understanding of novel treatment paradigms in SCLC may provide the basis for future treatment designs.show moreshow less

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Metadaten
Author:Johanna S. EnkeORCiDGND, Nic G. ReitsamORCiDGND, Sebastian DintnerORCiDGND, Friederike Liesche-StarneckerORCiDGND, Tina SchallerGND, Josua A. DeckerORCiD, Angela Langer, Eva SiposORCiDGND, Ana Antic Nikolic, Thomas KrönckeORCiDGND, Martin TrepelGND, Constantin LapaORCiDGND, Rainer ClausORCiDGND, Bruno MärklORCiDGND, Ralph A. BundschuhORCiDGND
URN:urn:nbn:de:bvb:384-opus4-1205189
Frontdoor URLhttps://opus.bibliothek.uni-augsburg.de/opus4/120518
ISSN:0161-5505OPAC
ISSN:2159-662XOPAC
Parent Title (English):Journal of Nuclear Medicine
Publisher:Society of Nuclear Medicine
Place of publication:Reston, VA
Type:Article
Language:English
Year of first Publication:2025
Publishing Institution:Universität Augsburg
Release Date:2025/03/24
Volume:66
Issue:2
First Page:245
Last Page:249
DOI:https://doi.org/10.2967/jnumed.124.268513
Institutes:Medizinische Fakultät
Medizinische Fakultät / Universitätsklinikum
Medizinische Fakultät / Lehrstuhl für Allgemeine und Spezielle Pathologie
Medizinische Fakultät / Lehrstuhl für Diagnostische und Interventionelle Radiologie
Medizinische Fakultät / Lehrstuhl für Innere Medizin mit Schwerpunkt Hämatologie und Onkologie
Medizinische Fakultät / Lehrstuhl für Nuklearmedizin
Medizinische Fakultät / Professur für personalisierte Tumormedizin und molekulare Onkologie
Medizinische Fakultät / Lehrstuhl für Strahlentherapie
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Licence (German):License LogoCC-BY 4.0: Creative Commons: Namensnennung (mit Print on Demand)