TY - JOUR
T1 - Parameters to Predict Progression-Free and Overall Survival After Peptide Receptor Radionuclide Therapy
T2 - A Multivariate Analysis in 782 Patients
AU - Aalbersberg, Else A.
AU - Huizing, Daphne M. V.
AU - Walraven, Iris
AU - de Wit-van der Veen, Berlinda J.
AU - Kulkarni, Harshad R.
AU - Singh, Aviral
AU - Stokkel, Marcel P. M.
AU - Baum, Richard P.
N1 - Publisher Copyright:
COPYRIGHT © 2019 by the Society of Nuclear Medicine and Molecular Imaging.
PY - 2019/9/1
Y1 - 2019/9/1
N2 - Peptide receptor radionuclide therapy (PRRT) is an effective treatment for patients with neuroendocrine neoplasms. The aim of this study was to identify clinical and treatment parameters associated with progression-free survival (PFS) and overall survival (OS). Methods: All patients treated from October 2002 until March 2016 at the Zentralklinik Bad Berka with at least 3 administrations of PRRT (maximal interval of 6 mo between consecutive administrations) were included. Data were collected in 5 categories: general patient characteristics, tumor characteristics, prior treatments, radioisotope used for PRRT, and blood chemistry. Survival was analyzed using Kaplan-Meier curves. Univariate and multivariate Cox regression analyses were performed to identify parameters associated with PFS and OS. Results: In total, 782 patients were included, with a median follow-up of 36 mo. The median PFS and OS were 22 and 53 mo, respectively. Parameters associated with lower PFS in the multivariate analysis were a Ki-67 of more than 5%, previous treatment with interferon-alpha and chemotherapy, presence of diabetes, and chromogranin-A (CgA) levels higher than 336 mu g/L. Parameters associated with lower OS were a Ki-67 of more than 10%, performance status of at least 1, previous chemotherapy and ablation, and CgA levels higher than 112 mu g/L. Conclusion: Higher Ki-67 values, as well as higher CgA levels and previous chemotherapy, had a negative outcome on both PFS and OS. Furthermore, PFS was negatively associated with previous interferon-alpha treatment and diabetes, whereas lower OS was related to prior ablation and higher performance status.
AB - Peptide receptor radionuclide therapy (PRRT) is an effective treatment for patients with neuroendocrine neoplasms. The aim of this study was to identify clinical and treatment parameters associated with progression-free survival (PFS) and overall survival (OS). Methods: All patients treated from October 2002 until March 2016 at the Zentralklinik Bad Berka with at least 3 administrations of PRRT (maximal interval of 6 mo between consecutive administrations) were included. Data were collected in 5 categories: general patient characteristics, tumor characteristics, prior treatments, radioisotope used for PRRT, and blood chemistry. Survival was analyzed using Kaplan-Meier curves. Univariate and multivariate Cox regression analyses were performed to identify parameters associated with PFS and OS. Results: In total, 782 patients were included, with a median follow-up of 36 mo. The median PFS and OS were 22 and 53 mo, respectively. Parameters associated with lower PFS in the multivariate analysis were a Ki-67 of more than 5%, previous treatment with interferon-alpha and chemotherapy, presence of diabetes, and chromogranin-A (CgA) levels higher than 336 mu g/L. Parameters associated with lower OS were a Ki-67 of more than 10%, performance status of at least 1, previous chemotherapy and ablation, and CgA levels higher than 112 mu g/L. Conclusion: Higher Ki-67 values, as well as higher CgA levels and previous chemotherapy, had a negative outcome on both PFS and OS. Furthermore, PFS was negatively associated with previous interferon-alpha treatment and diabetes, whereas lower OS was related to prior ablation and higher performance status.
KW - DISEASE
KW - EFFICACY
KW - ENETS CONSENSUS GUIDELINES
KW - LU-177-OCTREOTATE
KW - METASTATIC NICHE
KW - NEOPLASMS
KW - NEUROENDOCRINE TUMORS
KW - PRRT
KW - TOLERABILITY
KW - TRACERS
KW - multivariate analysis
KW - neuroendocrine tumor
KW - CRITERIA
U2 - 10.2967/jnumed.118.224386
DO - 10.2967/jnumed.118.224386
M3 - Article
C2 - 30850483
SN - 0161-5505
VL - 60
SP - 1259
EP - 1265
JO - Journal of Nuclear Medicine
JF - Journal of Nuclear Medicine
IS - 9
ER -