Litcius/Paper detail

Survival predictors of 177Lu-Dotatate peptide receptor radionuclide therapy (PRRT) in patients with progressive well-differentiated neuroendocrine tumors (NETS)

Mina Swiha, Duncan E. K. Sutherland, Golmehr Sistani, Alireza Khatami, Rami M. Abazid, Amol Mujoomdar, Daniele Wiseman, Jonathan Romsa, Robert H. Reid, David Laidley

2021Journal of Cancer Research and Clinical Oncology29 citationsDOIOpen Access PDF

Abstract

Abstract Purpose 177 Lu-Dotatate is an emerging treatment modality for patients with unresectable or metastatic well-differentiated NETs. This study examines survival predictors in patients who received 177 Lu-Dotatate. Methods A retrospective single-center review was conducted, examining 47 individuals with progressive well-differentiated NETs treated with 177 Lu-Dotatate (four induction cycles of 5.5 GBq at 10-week intervals followed by eight maintenance cycles of 3.7 GBq at 6-month intervals). Results Median follow-up was 63.1 months with a median progression-free survival (PFS) of 34.1 months. However, median overall survival (OS) was not reached at the time of analysis. The presence of ≥ 5 bone metastases (hazard ratio HR 4.33; p = 0.015), non-gastroenteropancreatic (non-GEP) NETs (HR 3.22; p = 0.025) and development of interim ascites (HR 3.15; p = 0.047) independently predicted a worse OS. Patients with chromogranin A of ≥ 4 × upper limit of normal (ULN) had shorter OS ( p < 0.001) and PFS ( p = 0.004). Similarly, those with pre-existing ascites demonstrated a worse OS ( p = 0.009) and PFS ( p = 0.026). Liver metastases involving greater than 50% liver volume and the existence of unusual metastatic locations had a negative impact on OS ( p = 0.033) and PFS ( p = 0.026), respectively. Conclusion High burden of skeletal and hepatic metastases, non-GEP-NETs, chromogranin A of ≥ 4 × ULN, unusual metastatic sites, pre-existing and interim ascites are predictors of poor outcomes in patients treated with 177 Lu-Dotatate. These common indicators can be used for the risk stratification and identification of patients most likely to benefit from PRRT. Trial registration ClinicalTrials.gov identifier: NCT02236910, Retrospectively registered on September, 2014.

Topics & Concepts

Radionuclide therapyMedicineInternal medicineHazard ratioNeuroendocrine tumorsChromogranin AAscitesProportional hazards modelGastroenterologyOncologyProgression-free survivalConfidence intervalChemotherapyImmunohistochemistryNeuroendocrine Tumor Research AdvancesRadiopharmaceutical Chemistry and ApplicationsThyroid Cancer Diagnosis and Treatment