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Targeted radiotherapy in metastatic neuroendocrine tumours: clinical and experimental studies

Författare Anna-Karin Elf
Datum för examination 2018-11-23
ISBN 978-91-7833-188-8
Publiceringsår 2018
Publicerad vid Institutionen för kliniska vetenskaper, Avdelningen för kirurgi
Språk en
Länkar https://gupea.ub.gu.se/handle/2077/...
Ämnesord neuroendocrine tumour, peptide receptor radionuclide therapy, somatostatin receptor 2 expression, radiosensitization, radioembolization, diffusion weighted imaging
Ämneskategorier Kirurgi


ABSTRACT Neuroendocrine tumours (NET) often present at a metastatic stage, which diminishes the possibility for curative surgery. Peptide receptor radiotherapy (PRRT) with 177Lu-DOTATATE targets somatostatin receptors, which are overexpressed on NET cells. PRRT results in symptom relief and often tumour control of NETs, but rarely cure. Tumour response is variable and renal and haematological toxicity are dose-limiting side effects. In metastatic small intestinal NET (SI-NET) hepatic metastases are often a clinical problem. Several treatment options exist and radioembolization (RE) of the liver is a recently introduced therapy. Diffusion weighted MRI (DWI) is a new imaging technique reflecting the microenvironment of tumours and is maybe useful for treatment response evaluation. Aims of the thesis project were to identify predictive factors for response and long-term outcome after PRRT, and investigate a possibility for radiosensitization. Further, RE was compared to hepatic artery embolization (HAE) for SI-NET hepatic metastases, and the utility of DWI as a predictor for morphologic treatment response was investigated. A retrospective study of 51 NET patients treated with 177Lu-DOTATATE revealed an objective response rate of 13%, however most patients responded with halted tumour growth. High tumour proliferation rate, but not diagnosis, was associated with shorter survival. Overall long-term toxicity was low. The absorbed tumour dose varied considerably within and between patients, but the median absorbed tumour dose was correlated with tumour shrinkage. In a retrospective study on stage IV SI-NET, patients with low somatostatin receptor 2 (SSTR2) expression did not have an inferior outcome after PRRT. In contrast, a tendency was found towards both higher activity uptake after PRRT and longer survival. In an experimental animal study, the NAMPT inhibitor GMX1778 enhanced the efficacy of 177Lu-DOTATATE and almost eradicated all tumours. In a clinical prospective study on SI-NET hepatic metastases, HAE resulted in earlier tumour shrinkage than RE, and the response at 3 months was correlated with DWI after 1 month. A low baseline apparent diffusion was correlated with a larger tumour shrinkage at 6 months. In conclusion, tumour grade can predict long-term outcome after PRRT in metastatic NET and tumour dosimetry can be useful for response prediction. Low SSTR2 expression should not exclude patients from PRRT. GMX1778 might be used as a radiosensitizer in PRRT for SI-NET. DWI can be useful for prediction and early evaluation of treatment response after RE and HAE for liver metastasized SI-NET.

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