TY - JOUR
T1 - Nuklearmedizinische Theranostik
T2 - Update Nuklearmedizin 2021
AU - Eiber, Matthias
AU - Kratochwil, Clemens
AU - Lapa, Constantin
AU - Brenner, Winfried
N1 - Publisher Copyright:
© 2021, Springer Medizin Verlag GmbH, ein Teil von Springer Nature.
PY - 2021/8
Y1 - 2021/8
N2 - Background: Theranostic approaches increasingly define the combined diagnostic and therapeutic patient management in nuclear medicine. Three novel approaches in different clinical stages are presented. Methods: The manuscript is based on a literature and guideline compilation on the current status of selected radiopharmaceuticals. Results: For prostate cancer, radiolabeled ligands to prostate-specific membrane antigen (PSMA) have been available for several years. 68Ga-PSMA PET/CT is currently used under the rules of „Ambulante Spezialärztliche Versorgung“ (ASV) for diagnosis of early biochemical recurrences. Recent studies also demonstrate clear advantages in the initial staging of high-risk patients. For therapy of metastatic castration-resistant prostate cancer (mCRPC), 177Lu-PSMA is available and can be used in accordance with the current German S3 guideline. Moreover, a phase III study was recently reported to meet the primary endpoints indicating an early drug approval. The chemokine receptor 4 (CXCR4) ligands 68Ga-pentixafor and 90Y/177Lu-pentixather provide a pair of theranostics for the receptor-specific detection and therapy of tumors expressing chemokine receptor 4. Results of first clinical studies in hematological neoplasms such as non-Hodgkin’s lymphoma, CNS lymphoma and multiple myeloma suggest an increased use of these radiopharmaceuticals in the future. Radiolabeled inhibitors against fibroblast activation protein (FAP) are currently opening completely new diagnostic and therapeutic aspects in tumors with a high stromal proportion and immune involvement, such as colon, pancreatic, and ovarian cancer. Although data are still limited, the central role of FAP-positive tumor fibroblasts in neoangiogenesis and immune response suggests significant contributions to in vivo image-based phenotyping and combined tumor therapy. Conclusion: Following the approval of Lutathera® (Lutetium[177Lu]-Oxodotreotid), three new theranostic approaches for the systemic treatment of tumors are currently under clinical investigation, with PSMA ligands for diagnosis and treatment of prostate cancer already having found their way into the current S3 guideline.
AB - Background: Theranostic approaches increasingly define the combined diagnostic and therapeutic patient management in nuclear medicine. Three novel approaches in different clinical stages are presented. Methods: The manuscript is based on a literature and guideline compilation on the current status of selected radiopharmaceuticals. Results: For prostate cancer, radiolabeled ligands to prostate-specific membrane antigen (PSMA) have been available for several years. 68Ga-PSMA PET/CT is currently used under the rules of „Ambulante Spezialärztliche Versorgung“ (ASV) for diagnosis of early biochemical recurrences. Recent studies also demonstrate clear advantages in the initial staging of high-risk patients. For therapy of metastatic castration-resistant prostate cancer (mCRPC), 177Lu-PSMA is available and can be used in accordance with the current German S3 guideline. Moreover, a phase III study was recently reported to meet the primary endpoints indicating an early drug approval. The chemokine receptor 4 (CXCR4) ligands 68Ga-pentixafor and 90Y/177Lu-pentixather provide a pair of theranostics for the receptor-specific detection and therapy of tumors expressing chemokine receptor 4. Results of first clinical studies in hematological neoplasms such as non-Hodgkin’s lymphoma, CNS lymphoma and multiple myeloma suggest an increased use of these radiopharmaceuticals in the future. Radiolabeled inhibitors against fibroblast activation protein (FAP) are currently opening completely new diagnostic and therapeutic aspects in tumors with a high stromal proportion and immune involvement, such as colon, pancreatic, and ovarian cancer. Although data are still limited, the central role of FAP-positive tumor fibroblasts in neoangiogenesis and immune response suggests significant contributions to in vivo image-based phenotyping and combined tumor therapy. Conclusion: Following the approval of Lutathera® (Lutetium[177Lu]-Oxodotreotid), three new theranostic approaches for the systemic treatment of tumors are currently under clinical investigation, with PSMA ligands for diagnosis and treatment of prostate cancer already having found their way into the current S3 guideline.
KW - Chemokine receptor 4 (CXCR4)
KW - Fibroblast activation protein inhibitor (FAPI)
KW - Positron emission tomography (PET)
KW - Prostate-specific membrane antigen (PSMA)
KW - Radionuclide therapy
UR - http://www.scopus.com/inward/record.url?scp=85106228267&partnerID=8YFLogxK
U2 - 10.1007/s00761-021-00956-1
DO - 10.1007/s00761-021-00956-1
M3 - Übersichtsartikel
AN - SCOPUS:85106228267
SN - 0947-8965
VL - 27
SP - 809
EP - 819
JO - Onkologe
JF - Onkologe
IS - 8
ER -