Predicting the survival probability of functional neuroendocrine tumors treated with peptide receptor radionuclide therapy: Serbian experience

Peptide receptor radionuclide therapy (PRRT) is a treatment option for well-differentiated, somatostatin receptor positive, unresectable or/and metastatic neuroendocrine tumors (NETs). Although high disease control rates seen with PRRT a significant number NET patients have a short progression-free...

Celý popis

Uložené v:
Podrobná bibliografia
Vydané v:Frontiers in endocrinology (Lausanne) Ročník 14; s. 1270421
Hlavní autori: Vukomanovic, Vladimir, Nedic, Katarina Vuleta, Radojevic, Marija Zivkovic, Dagovic, Aleksandar, Milosavljevic, Neda, Markovic, Marina, Ignjatovic, Vladimir, Simic Vukomanovic, Ivana, Djukic, Svetlana, Sreckovic, Marijana, Backovic, Milena, Vuleta, Marko, Djukic, Aleksandar, Vukicevic, Verica, Ignjatovic, Vesna
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: Switzerland Frontiers Media S.A 04.01.2024
Predmet:
ISSN:1664-2392, 1664-2392
On-line prístup:Získať plný text
Tagy: Pridať tag
Žiadne tagy, Buďte prvý, kto otaguje tento záznam!
Abstract Peptide receptor radionuclide therapy (PRRT) is a treatment option for well-differentiated, somatostatin receptor positive, unresectable or/and metastatic neuroendocrine tumors (NETs). Although high disease control rates seen with PRRT a significant number NET patients have a short progression-free interval, and currently, there is a deficiency of effective biomarkers to pre-identify these patients. This study is aimed at determining the prognostic significance of biomarkers on survival of patients with NETs in initial PRRT treatment. We retrospectively analyzed 51 patients with NETs treated with PRRT at the Department for nuclear medicine, University Clinical Center Kragujevac, Serbia, with a five-year follow-up. Eligible patients with confirmed inoperable NETs, were retrospectively evaluated hematological, blood-based inflammatory markers, biochemical markers and clinical characteristics on disease progression. In accordance with the progression og the disease, the patients were divided into two groups: progression group (n=18) and a non-progression group (n=33). Clinical data were compared between the two groups. A total of 51 patients (Md=60, age 25-75 years) were treated with PRRT, of whom 29 (56.86%) demonstrated stable disease, 4 (7.84%) demonstrated a partial response, and 14 (27.46%) demonstrated progressive disease and death was recorded in 4 (7.84%) patients. The mean PFS was a 36.22 months (95% CI 30.14-42.29) and the mean OS was 44.68 months (95% CI 37.40-51.97). Univariate logistic regression analysis displayed that age (p<0.05), functional tumors (p<0.05), absolute neutrophil count (p<0.05), neutrophil-lymphocyte ratio-NLR (p<0.05), C-reactive protein-CRP (p<0.05), CRP/Albumin (p<0.05), alanine aminotransferase-ALT (p<0.05), were risk factors for disease progression. Multivariate logistic regression analysis exhibited that functional tumors (p<0.001), age (p<0.05), CRP (p<0.05), and ALT (p<0.05), were independent risk factors for the disease progression in patients with NETs. Tumor functionality was the most powerful prognostic factor. The median PFS (11.86 ± 1.41 vs. 43.38 ± 3.16 months; p=0.001) and OS (21.81 ± 2.70 vs 53.86 ± 3.70, p=0.001) were significantly shorter in patients with functional than non-functional NETs respectively. The study's results suggest that tumor functionality, and certain biomarkers may serve as prognostic survival indicators for patients with NETs undergoing PRRT. The findings can potentially help to identify patients who are at higher risk of disease progression and tailor treatment strategies accordingly.
AbstractList Peptide receptor radionuclide therapy (PRRT) is a treatment option for well-differentiated, somatostatin receptor positive, unresectable or/and metastatic neuroendocrine tumors (NETs). Although high disease control rates seen with PRRT a significant number NET patients have a short progression-free interval, and currently, there is a deficiency of effective biomarkers to pre-identify these patients. This study is aimed at determining the prognostic significance of biomarkers on survival of patients with NETs in initial PRRT treatment. We retrospectively analyzed 51 patients with NETs treated with PRRT at the Department for nuclear medicine, University Clinical Center Kragujevac, Serbia, with a five-year follow-up. Eligible patients with confirmed inoperable NETs, were retrospectively evaluated hematological, blood-based inflammatory markers, biochemical markers and clinical characteristics on disease progression. In accordance with the progression og the disease, the patients were divided into two groups: progression group (n=18) and a non-progression group (n=33). Clinical data were compared between the two groups. A total of 51 patients (Md=60, age 25-75 years) were treated with PRRT, of whom 29 (56.86%) demonstrated stable disease, 4 (7.84%) demonstrated a partial response, and 14 (27.46%) demonstrated progressive disease and death was recorded in 4 (7.84%) patients. The mean PFS was a 36.22 months (95% CI 30.14-42.29) and the mean OS was 44.68 months (95% CI 37.40-51.97). Univariate logistic regression analysis displayed that age (p<0.05), functional tumors (p<0.05), absolute neutrophil count (p<0.05), neutrophil-lymphocyte ratio-NLR (p<0.05), C-reactive protein-CRP (p<0.05), CRP/Albumin (p<0.05), alanine aminotransferase-ALT (p<0.05), were risk factors for disease progression. Multivariate logistic regression analysis exhibited that functional tumors (p<0.001), age (p<0.05), CRP (p<0.05), and ALT (p<0.05), were independent risk factors for the disease progression in patients with NETs. Tumor functionality was the most powerful prognostic factor. The median PFS (11.86 ± 1.41 vs. 43.38 ± 3.16 months; p=0.001) and OS (21.81 ± 2.70 vs 53.86 ± 3.70, p=0.001) were significantly shorter in patients with functional than non-functional NETs respectively. The study's results suggest that tumor functionality, and certain biomarkers may serve as prognostic survival indicators for patients with NETs undergoing PRRT. The findings can potentially help to identify patients who are at higher risk of disease progression and tailor treatment strategies accordingly.
Peptide receptor radionuclide therapy (PRRT) is a treatment option for well-differentiated, somatostatin receptor positive, unresectable or/and metastatic neuroendocrine tumors (NETs). Although high disease control rates seen with PRRT a significant number NET patients have a short progression-free interval, and currently, there is a deficiency of effective biomarkers to pre-identify these patients. This study is aimed at determining the prognostic significance of biomarkers on survival of patients with NETs in initial PRRT treatment.IntroductionPeptide receptor radionuclide therapy (PRRT) is a treatment option for well-differentiated, somatostatin receptor positive, unresectable or/and metastatic neuroendocrine tumors (NETs). Although high disease control rates seen with PRRT a significant number NET patients have a short progression-free interval, and currently, there is a deficiency of effective biomarkers to pre-identify these patients. This study is aimed at determining the prognostic significance of biomarkers on survival of patients with NETs in initial PRRT treatment.We retrospectively analyzed 51 patients with NETs treated with PRRT at the Department for nuclear medicine, University Clinical Center Kragujevac, Serbia, with a five-year follow-up. Eligible patients with confirmed inoperable NETs, were retrospectively evaluated hematological, blood-based inflammatory markers, biochemical markers and clinical characteristics on disease progression. In accordance with the progression og the disease, the patients were divided into two groups: progression group (n=18) and a non-progression group (n=33). Clinical data were compared between the two groups.MethodologyWe retrospectively analyzed 51 patients with NETs treated with PRRT at the Department for nuclear medicine, University Clinical Center Kragujevac, Serbia, with a five-year follow-up. Eligible patients with confirmed inoperable NETs, were retrospectively evaluated hematological, blood-based inflammatory markers, biochemical markers and clinical characteristics on disease progression. In accordance with the progression og the disease, the patients were divided into two groups: progression group (n=18) and a non-progression group (n=33). Clinical data were compared between the two groups.A total of 51 patients (Md=60, age 25-75 years) were treated with PRRT, of whom 29 (56.86%) demonstrated stable disease, 4 (7.84%) demonstrated a partial response, and 14 (27.46%) demonstrated progressive disease and death was recorded in 4 (7.84%) patients. The mean PFS was a 36.22 months (95% CI 30.14-42.29) and the mean OS was 44.68 months (95% CI 37.40-51.97). Univariate logistic regression analysis displayed that age (p<0.05), functional tumors (p<0.05), absolute neutrophil count (p<0.05), neutrophil-lymphocyte ratio-NLR (p<0.05), C-reactive protein-CRP (p<0.05), CRP/Albumin (p<0.05), alanine aminotransferase-ALT (p<0.05), were risk factors for disease progression. Multivariate logistic regression analysis exhibited that functional tumors (p<0.001), age (p<0.05), CRP (p<0.05), and ALT (p<0.05), were independent risk factors for the disease progression in patients with NETs. Tumor functionality was the most powerful prognostic factor. The median PFS (11.86 ± 1.41 vs. 43.38 ± 3.16 months; p=0.001) and OS (21.81 ± 2.70 vs 53.86 ± 3.70, p=0.001) were significantly shorter in patients with functional than non-functional NETs respectively.ResultsA total of 51 patients (Md=60, age 25-75 years) were treated with PRRT, of whom 29 (56.86%) demonstrated stable disease, 4 (7.84%) demonstrated a partial response, and 14 (27.46%) demonstrated progressive disease and death was recorded in 4 (7.84%) patients. The mean PFS was a 36.22 months (95% CI 30.14-42.29) and the mean OS was 44.68 months (95% CI 37.40-51.97). Univariate logistic regression analysis displayed that age (p<0.05), functional tumors (p<0.05), absolute neutrophil count (p<0.05), neutrophil-lymphocyte ratio-NLR (p<0.05), C-reactive protein-CRP (p<0.05), CRP/Albumin (p<0.05), alanine aminotransferase-ALT (p<0.05), were risk factors for disease progression. Multivariate logistic regression analysis exhibited that functional tumors (p<0.001), age (p<0.05), CRP (p<0.05), and ALT (p<0.05), were independent risk factors for the disease progression in patients with NETs. Tumor functionality was the most powerful prognostic factor. The median PFS (11.86 ± 1.41 vs. 43.38 ± 3.16 months; p=0.001) and OS (21.81 ± 2.70 vs 53.86 ± 3.70, p=0.001) were significantly shorter in patients with functional than non-functional NETs respectively.The study's results suggest that tumor functionality, and certain biomarkers may serve as prognostic survival indicators for patients with NETs undergoing PRRT. The findings can potentially help to identify patients who are at higher risk of disease progression and tailor treatment strategies accordingly.ConclusionThe study's results suggest that tumor functionality, and certain biomarkers may serve as prognostic survival indicators for patients with NETs undergoing PRRT. The findings can potentially help to identify patients who are at higher risk of disease progression and tailor treatment strategies accordingly.
IntroductionPeptide receptor radionuclide therapy (PRRT) is a treatment option for well-differentiated, somatostatin receptor positive, unresectable or/and metastatic neuroendocrine tumors (NETs). Although high disease control rates seen with PRRT a significant number NET patients have a short progression-free interval, and currently, there is a deficiency of effective biomarkers to pre-identify these patients. This study is aimed at determining the prognostic significance of biomarkers on survival of patients with NETs in initial PRRT treatment.MethodologyWe retrospectively analyzed 51 patients with NETs treated with PRRT at the Department for nuclear medicine, University Clinical Center Kragujevac, Serbia, with a five-year follow-up. Eligible patients with confirmed inoperable NETs, were retrospectively evaluated hematological, blood-based inflammatory markers, biochemical markers and clinical characteristics on disease progression. In accordance with the progression og the disease, the patients were divided into two groups: progression group (n=18) and a non-progression group (n=33). Clinical data were compared between the two groups.ResultsA total of 51 patients (Md=60, age 25-75 years) were treated with PRRT, of whom 29 (56.86%) demonstrated stable disease, 4 (7.84%) demonstrated a partial response, and 14 (27.46%) demonstrated progressive disease and death was recorded in 4 (7.84%) patients. The mean PFS was a 36.22 months (95% CI 30.14-42.29) and the mean OS was 44.68 months (95% CI 37.40-51.97). Univariate logistic regression analysis displayed that age (p<0.05), functional tumors (p<0.05), absolute neutrophil count (p<0.05), neutrophil-lymphocyte ratio-NLR (p<0.05), C-reactive protein-CRP (p<0.05), CRP/Albumin (p<0.05), alanine aminotransferase-ALT (p<0.05), were risk factors for disease progression. Multivariate logistic regression analysis exhibited that functional tumors (p<0.001), age (p<0.05), CRP (p<0.05), and ALT (p<0.05), were independent risk factors for the disease progression in patients with NETs. Tumor functionality was the most powerful prognostic factor. The median PFS (11.86 ± 1.41 vs. 43.38 ± 3.16 months; p=0.001) and OS (21.81 ± 2.70 vs 53.86 ± 3.70, p=0.001) were significantly shorter in patients with functional than non-functional NETs respectively.ConclusionThe study’s results suggest that tumor functionality, and certain biomarkers may serve as prognostic survival indicators for patients with NETs undergoing PRRT. The findings can potentially help to identify patients who are at higher risk of disease progression and tailor treatment strategies accordingly.
Author Djukic, Svetlana
Sreckovic, Marijana
Vukicevic, Verica
Radojevic, Marija Zivkovic
Djukic, Aleksandar
Dagovic, Aleksandar
Vukomanovic, Vladimir
Simic Vukomanovic, Ivana
Backovic, Milena
Ignjatovic, Vesna
Nedic, Katarina Vuleta
Ignjatovic, Vladimir
Milosavljevic, Neda
Markovic, Marina
Vuleta, Marko
AuthorAffiliation 7 Department of Social Medicine, Faculty of Medical Sciences, University of Kragujevac , Kragujevac , Serbia
3 Department for Radiotherapy, University Clinical Center Kragujevac , Kragujevac , Serbia
4 Department for Medical Oncology, University Clinical Center Kragujevac , Kragujevac , Serbia
9 Clinic for Hematology, University Clinical Center Kragujevac , Kragujevac , Serbia
11 Department for Pathology, Faculty of Medicine, University of Belgrade , Belgrade , Serbia
12 Department for Cardiology, Clinical Hospital Center “Dr Dragisa Misovic Dedinje” , Belgrade , Serbia
8 Department of Health Promotion, Institute of Public Health , Kragujevac , Serbia
15 Emergency Medical Institute , Belgrade , Serbia
2 Department for Nuclear Medicine, University Clinical Center Kragujevac , Kragujevac , Serbia
13 Department of Pathophysiology, Faculty of Medical Sciences, University of Kragujevac , Kragujevac , Serbia
14 Clinic for Endocrinology, Diabetes and Metabolic Diseases, University Clinical Center Kragu
AuthorAffiliation_xml – name: 15 Emergency Medical Institute , Belgrade , Serbia
– name: 14 Clinic for Endocrinology, Diabetes and Metabolic Diseases, University Clinical Center Kragujevac , Kragujevac , Serbia
– name: 2 Department for Nuclear Medicine, University Clinical Center Kragujevac , Kragujevac , Serbia
– name: 4 Department for Medical Oncology, University Clinical Center Kragujevac , Kragujevac , Serbia
– name: 6 Clinic for Cardiology, University Clinical Center Kragujevac , Kragujevac , Serbia
– name: 7 Department of Social Medicine, Faculty of Medical Sciences, University of Kragujevac , Kragujevac , Serbia
– name: 10 Department of Medical and Business-Technological, Academy of Professional Studies Sabac , Sabac , Serbia
– name: 3 Department for Radiotherapy, University Clinical Center Kragujevac , Kragujevac , Serbia
– name: 11 Department for Pathology, Faculty of Medicine, University of Belgrade , Belgrade , Serbia
– name: 8 Department of Health Promotion, Institute of Public Health , Kragujevac , Serbia
– name: 5 Department of Internal Medicine, Faculty of Medical Sciences, University of Kragujevac , Kragujevac , Serbia
– name: 12 Department for Cardiology, Clinical Hospital Center “Dr Dragisa Misovic Dedinje” , Belgrade , Serbia
– name: 13 Department of Pathophysiology, Faculty of Medical Sciences, University of Kragujevac , Kragujevac , Serbia
– name: 9 Clinic for Hematology, University Clinical Center Kragujevac , Kragujevac , Serbia
– name: 1 Department of Nuclear Medicine and Clinical Oncology, Faculty of Medical Sciences, University of Kragujevac , Kragujevac , Serbia
Author_xml – sequence: 1
  givenname: Vladimir
  surname: Vukomanovic
  fullname: Vukomanovic, Vladimir
– sequence: 2
  givenname: Katarina Vuleta
  surname: Nedic
  fullname: Nedic, Katarina Vuleta
– sequence: 3
  givenname: Marija Zivkovic
  surname: Radojevic
  fullname: Radojevic, Marija Zivkovic
– sequence: 4
  givenname: Aleksandar
  surname: Dagovic
  fullname: Dagovic, Aleksandar
– sequence: 5
  givenname: Neda
  surname: Milosavljevic
  fullname: Milosavljevic, Neda
– sequence: 6
  givenname: Marina
  surname: Markovic
  fullname: Markovic, Marina
– sequence: 7
  givenname: Vladimir
  surname: Ignjatovic
  fullname: Ignjatovic, Vladimir
– sequence: 8
  givenname: Ivana
  surname: Simic Vukomanovic
  fullname: Simic Vukomanovic, Ivana
– sequence: 9
  givenname: Svetlana
  surname: Djukic
  fullname: Djukic, Svetlana
– sequence: 10
  givenname: Marijana
  surname: Sreckovic
  fullname: Sreckovic, Marijana
– sequence: 11
  givenname: Milena
  surname: Backovic
  fullname: Backovic, Milena
– sequence: 12
  givenname: Marko
  surname: Vuleta
  fullname: Vuleta, Marko
– sequence: 13
  givenname: Aleksandar
  surname: Djukic
  fullname: Djukic, Aleksandar
– sequence: 14
  givenname: Verica
  surname: Vukicevic
  fullname: Vukicevic, Verica
– sequence: 15
  givenname: Vesna
  surname: Ignjatovic
  fullname: Ignjatovic, Vesna
BackLink https://www.ncbi.nlm.nih.gov/pubmed/38317712$$D View this record in MEDLINE/PubMed
BookMark eNp9UstuEzEUHaEiWkp_gAXykk2CXzO22SBU8ahUCSRgbflxJ3E1sQePJyU_wTfjNClqWeCNr-49j8U5z5uTmCI0zUuCl4xJ9aaH6NOSYsqWhArMKXnSnJGu4wvKFD15MJ82F9N0g-vjmCglnzWnTDIiBKFnze-vGXxwJcQVKmtA05y3YWsGNOZkjQ1DKDuUetTPsYJSrJcIc057d5dDBFTmTcoTKhlMAY9uQ1mjEcYSPKAMrk4po2x8Jc9u2G-rTzbj7i36BtkGExH8GiEHiA5eNE97M0xwcfzPmx8fP3y__Ly4_vLp6vL99cLxTpWFEJz2LWNOKOU7ZoH2zHJqsO86wR0m3DMpeo9x74UUbYs7KVtPuKXeSkfYeXN10PXJ3Ogxh43JO51M0HeLlFfa5BLcANpJaVrnOHOYcSw72YkeW25Vb51y1lStdwetcbYb8A5iyWZ4JPr4EsNar9JWEyxrIqytCq-PCjn9nGEqehMmB8NgIqR50lRRqrgStKvQVw_N_rrcJ1oB8gBwOU1Thl67UMw-uuodhmqq9_3Rd_3R-_7oY38qlf5DvVf_D-kP8lXOGw
CitedBy_id crossref_primary_10_1016_j_remn_2025_500138
crossref_primary_10_3390_ijms26178526
Cites_doi 10.12659/MSM.907182
10.31557/APJCP.2018.19.12.3597
10.1186/s13045-021-01187-y
10.21037/gs.2017.10.08
10.1001/jamanetworkopen.2021.24750
10.1016/j.canep.2019.101598
10.1016/j.esmoop.2021.100171
10.1245/s10434-018-6518-2
10.3389/fendo.2021.657698
10.1016/j.lanepe.2022.100510
10.3390/cancers13246290
10.22034/APJCP.2018.19.8.2177
10.1016/j.asjsur.2022.01.094
10.2967/jnumed.118.224386
10.1097/SLA.0000000000003162
10.1530/ERC-16-0538
10.21037/jtd.2017.09.82
10.1007/s00432-021-03672-w
10.3390/diagnostics11030504
10.1016/j.neo.2017.09.002
10.1016/S1470-2045(21)00572-6
10.1097/00000421-198212000-00014
10.3892/ol.2018.8413
10.1080/07435800.2020.1870234
10.1200/OP.21.00240
10.1089/cbr.2021.0053
10.3389/fendo.2022.861434
10.3390/biology10100950
10.1210/jc.2018-01214
10.1210/jc.2015-3114
10.2967/jnumed.119.236935
10.3389/fonc.2019.00906
10.1210/clinem/dgab588
10.3390/diagnostics12030737
10.3390/ijms24021418
ContentType Journal Article
Copyright Copyright © 2024 Vukomanovic, Nedic, Radojevic, Dagovic, Milosavljevic, Markovic, Ignjatovic, Simic Vukomanovic, Djukic, Sreckovic, Backovic, Vuleta, Djukic, Vukicevic and Ignjatovic.
Copyright © 2024 Vukomanovic, Nedic, Radojevic, Dagovic, Milosavljevic, Markovic, Ignjatovic, Simic Vukomanovic, Djukic, Sreckovic, Backovic, Vuleta, Djukic, Vukicevic and Ignjatovic 2024 Vukomanovic, Nedic, Radojevic, Dagovic, Milosavljevic, Markovic, Ignjatovic, Simic Vukomanovic, Djukic, Sreckovic, Backovic, Vuleta, Djukic, Vukicevic and Ignjatovic
Copyright_xml – notice: Copyright © 2024 Vukomanovic, Nedic, Radojevic, Dagovic, Milosavljevic, Markovic, Ignjatovic, Simic Vukomanovic, Djukic, Sreckovic, Backovic, Vuleta, Djukic, Vukicevic and Ignjatovic.
– notice: Copyright © 2024 Vukomanovic, Nedic, Radojevic, Dagovic, Milosavljevic, Markovic, Ignjatovic, Simic Vukomanovic, Djukic, Sreckovic, Backovic, Vuleta, Djukic, Vukicevic and Ignjatovic 2024 Vukomanovic, Nedic, Radojevic, Dagovic, Milosavljevic, Markovic, Ignjatovic, Simic Vukomanovic, Djukic, Sreckovic, Backovic, Vuleta, Djukic, Vukicevic and Ignjatovic
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
5PM
DOA
DOI 10.3389/fendo.2023.1270421
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE
MEDLINE - Academic

Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: 7X8
  name: MEDLINE - Academic
  url: https://search.proquest.com/medline
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1664-2392
ExternalDocumentID oai_doaj_org_article_c88a5cc43c034086867f0b4b9fbc9cba
PMC10840135
38317712
10_3389_fendo_2023_1270421
Genre Journal Article
GeographicLocations Serbia
GeographicLocations_xml – name: Serbia
GroupedDBID 53G
5VS
9T4
AAFWJ
AAKDD
AAYXX
ACGFO
ACGFS
ADBBV
ADRAZ
AFPKN
ALMA_UNASSIGNED_HOLDINGS
AOIJS
BAWUL
BCNDV
CITATION
DIK
EMOBN
GROUPED_DOAJ
GX1
HYE
KQ8
M48
M~E
OK1
PGMZT
RPM
ACXDI
CGR
CUY
CVF
ECM
EIF
IPNFZ
NPM
RIG
7X8
5PM
ID FETCH-LOGICAL-c469t-7742f533c799d63be2f3b42a0d6674c014d387fd00fd7875506885d14b2db8c13
IEDL.DBID DOA
ISICitedReferencesCount 2
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=001143669500001&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 1664-2392
IngestDate Fri Oct 03 12:45:01 EDT 2025
Thu Aug 21 18:35:31 EDT 2025
Thu Sep 04 17:49:10 EDT 2025
Thu Apr 03 07:06:48 EDT 2025
Sat Nov 29 03:00:11 EST 2025
Tue Nov 18 21:25:43 EST 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Keywords overall survival
PRRT
functional tumors
NET
progression free survival
Language English
License Copyright © 2024 Vukomanovic, Nedic, Radojevic, Dagovic, Milosavljevic, Markovic, Ignjatovic, Simic Vukomanovic, Djukic, Sreckovic, Backovic, Vuleta, Djukic, Vukicevic and Ignjatovic.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c469t-7742f533c799d63be2f3b42a0d6674c014d387fd00fd7875506885d14b2db8c13
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Edited by: Aviral Singh, GenesisCare Australia Pty Ltd, Australia
Reviewed by: Vineet Pant, Royal Liverpool University Hospital, United Kingdom
These authors have contributed equally to this work and share first authorship
Osborn Jiang, University of New South Wales, Australia
Manoj Gupta, Rajiv Gandhi Cancer Institute and Research Centre, India
OpenAccessLink https://doaj.org/article/c88a5cc43c034086867f0b4b9fbc9cba
PMID 38317712
PQID 2922949726
PQPubID 23479
ParticipantIDs doaj_primary_oai_doaj_org_article_c88a5cc43c034086867f0b4b9fbc9cba
pubmedcentral_primary_oai_pubmedcentral_nih_gov_10840135
proquest_miscellaneous_2922949726
pubmed_primary_38317712
crossref_citationtrail_10_3389_fendo_2023_1270421
crossref_primary_10_3389_fendo_2023_1270421
PublicationCentury 2000
PublicationDate 2024-01-04
PublicationDateYYYYMMDD 2024-01-04
PublicationDate_xml – month: 01
  year: 2024
  text: 2024-01-04
  day: 04
PublicationDecade 2020
PublicationPlace Switzerland
PublicationPlace_xml – name: Switzerland
PublicationTitle Frontiers in endocrinology (Lausanne)
PublicationTitleAlternate Front Endocrinol (Lausanne)
PublicationYear 2024
Publisher Frontiers Media S.A
Publisher_xml – name: Frontiers Media S.A
References Zhou (B21) 2017; 23
Black (B24) 2019; 104
Gheorghișan-Gălățeanu (B12) 2023; 24
Wiese (B23) 2016; 101
Genç (B33) 2018; 25
Kalligeros (B28) 2021; 10
Zhu (B27) 2018; 19
Zhang (B2) 2022; 18
Shyr (B31) 2022; 45
Pauwels (B25) 2020; 61
Strosberg (B7) 2021; 22
Oronsky (B1) 2017; 19
Theiler (B18) 2021; 13
Xiong (B22) 2021; 14
Calissendorff (B35) 2021; 12
Sakin (B30) 2018; 19
Aalbersberg (B32) 2019; 60
Hayes (B6) 2021; 106
Puliani (B9) 2022; 13
Zandee (B34) 2017; 24
Ohlendorf (B8) 2021; 11
Oh (B10) 2022; 12
Wang (B16) 2019; 9
Chen (B26) 2018; 15
Xu (B3) 2021; 4
Satapathy (B11) 2022; 37
Swiha (B29) 2022; 148
Bodei (B4) 2017; 9
Severi (B5) 2021; 6
Oken (B14) 1982; 5
Solak (B20) 2021; 46
Vinault (B17) 2020; 272
Wyld (B19) 2019; 63
White (B15) 2022; 23
Öberg (B13) 2018; 7
References_xml – volume: 23
  year: 2017
  ident: B21
  article-title: Prognostic significance of preoperative neutrophil-to-lymphocyte ratio in surgically resectable pancreatic neuroendocrine tumors
  publication-title: Med Sci Monit
  doi: 10.12659/MSM.907182
– volume: 19
  year: 2018
  ident: B30
  article-title: Factors affecting survival in neuroendocrine tumors: A 15-year single center experience
  publication-title: Asian Pac. J Cancer Prev
  doi: 10.31557/APJCP.2018.19.12.3597
– volume: 14
  start-page: 173
  year: 2021
  ident: B22
  article-title: Neutrophils in cancer carcinogenesis and metastasis
  publication-title: J Hematol Oncol
  doi: 10.1186/s13045-021-01187-y
– volume: 7
  year: 2018
  ident: B13
  article-title: Management of functional neuroendocrine tumors of the pancreas
  publication-title: Gland Surg
  doi: 10.21037/gs.2017.10.08
– volume: 4
  year: 2021
  ident: B3
  article-title: Epidemiologic trends of and factors associated with overall survival for patients with gastroenteropancreatic neuroendocrine tumors in the United States
  publication-title: JAMA Netw Open
  doi: 10.1001/jamanetworkopen.2021.24750
– volume: 63
  year: 2019
  ident: B19
  article-title: Epidemiological trends of neuroendocrine tumours over three decades in Queensland, Australia
  publication-title: Cancer Epidemiol
  doi: 10.1016/j.canep.2019.101598
– volume: 6
  year: 2021
  ident: B5
  article-title: Peptide receptor radionuclide therapy in patients with metastatic progressive pheochromocytoma and paraganglioma: long-term toxicity, efficacy and prognostic biomarker data of phase II clinical trials
  publication-title: ESMO Open
  doi: 10.1016/j.esmoop.2021.100171
– volume: 25
  year: 2018
  ident: B33
  article-title: Recurrence of pancreatic neuroendocrine tumors and survival predicted by ki67
  publication-title: Ann Surg Oncol
  doi: 10.1245/s10434-018-6518-2
– volume: 12
  year: 2021
  ident: B35
  article-title: Characteristics, treatment, outcomes, and survival in neuroendocrine G1 and G2 pancreatic tumors: experiences from a single tertiary referral center
  publication-title: Front Endocrinol (Lausanne)
  doi: 10.3389/fendo.2021.657698
– volume: 23
  year: 2022
  ident: B15
  article-title: Incidence and survival of neuroendocrine neoplasia in England 1995–2018: A retrospective, population-based study
  publication-title: Lancet Regional Health - Europe
  doi: 10.1016/j.lanepe.2022.100510
– volume: 13
  start-page: 6290
  year: 2021
  ident: B18
  article-title: Safety and efficacy of peptide-receptor radionuclide therapy in elderly neuroendocrine tumor patients
  publication-title: Cancers (Basel)
  doi: 10.3390/cancers13246290
– volume: 19
  year: 2018
  ident: B27
  article-title: Impaired liver function implied shorter progression free survival for EGFR tyrosine kinase inhibitors
  publication-title: Asian Pac J Cancer Prev
  doi: 10.22034/APJCP.2018.19.8.2177
– volume: 45
  year: 2022
  ident: B31
  article-title: Impact of tumor grade on pancreatic neuroendocrine tumors
  publication-title: Asian J Surg
  doi: 10.1016/j.asjsur.2022.01.094
– volume: 60
  year: 2019
  ident: B32
  article-title: Parameters to predict progression-free and overall survival after peptide receptor radionuclide therapy: A multivariate analysis in 782 patients
  publication-title: J Nucl Med
  doi: 10.2967/jnumed.118.224386
– volume: 272
  year: 2020
  ident: B17
  article-title: Metastatic Potential and Survival of Duodenal and Pancreatic Tumors in Multiple Endocrine Neoplasia Type 1: A GTE and AFCE Cohort Study(Groupe d’etude des Tumeurs Endocrines and Association Francophone de Chirurgie Endocrinienne)
  publication-title: Ann Surger
  doi: 10.1097/SLA.0000000000003162
– volume: 24
  year: 2017
  ident: B34
  article-title: Effect of hormone secretory syndromes on neuroendocrine tumor prognosis
  publication-title: Endocr Relat Cancer.
  doi: 10.1530/ERC-16-0538
– volume: 9
  year: 2017
  ident: B4
  article-title: The role of peptide receptor radionuclide therapy in advanced/metastatic thoracic neuroendocrine tumors
  publication-title: J Thorac Dis
  doi: 10.21037/jtd.2017.09.82
– volume: 148
  year: 2022
  ident: B29
  article-title: Survival predictors of 177Lu-Dotatate peptide receptor radionuclide therapy (PRRT) in patients with progressive well-differentiated neuroendocrine tumors (NETS)
  publication-title: J Cancer Res Clin Oncol
  doi: 10.1007/s00432-021-03672-w
– volume: 11
  year: 2021
  ident: B8
  article-title: Predictive and prognostic impact of blood-based inflammatory biomarkers in patients with gastroenteropancreatic neuroendocrine tumors commencing peptide receptor radionuclide therapy
  publication-title: Diagnostics (Basel)
  doi: 10.3390/diagnostics11030504
– volume: 19
  start-page: 991
  year: 2017
  ident: B1
  article-title: Nothing but NET: A review of neuroendocrine tumors and carcinomas
  publication-title: Neoplasia
  doi: 10.1016/j.neo.2017.09.002
– volume: 22
  year: 2021
  ident: B7
  article-title: 177Lu-Dotatate plus long-acting octreotide versus high-dose long-acting octreotide in patients with midgut neuroendocrine tumours (NETTER-1): final overall survival and long-term safety results from an open-label, randomised, controlled, phase 3 trial
  publication-title: Lancet Oncol
  doi: 10.1016/S1470-2045(21)00572-6
– volume: 5
  year: 1982
  ident: B14
  article-title: Toxicity and response criteria of the Eastern Cooperative Oncology Group
  publication-title: Am J Clin Oncol
  doi: 10.1097/00000421-198212000-00014
– volume: 15
  year: 2018
  ident: B26
  article-title: Analysis of the clinicopathological features and prognostic factors of primary hepatic neuroendocrine tumors
  publication-title: Oncol Lett
  doi: 10.3892/ol.2018.8413
– volume: 46
  year: 2021
  ident: B20
  article-title: Croatian ACC study group. Neutrophil-lymphocyte ratio as a prognostic marker in adrenocortical carcinoma
  publication-title: Endocr Res
  doi: 10.1080/07435800.2020.1870234
– volume: 18
  year: 2022
  ident: B2
  article-title: Making sense of a complex disease: A practical approach to managing neuroendocrine tumors
  publication-title: JCO Oncol Pract
  doi: 10.1200/OP.21.00240
– volume: 37
  year: 2022
  ident: B11
  article-title: Hematological markers as predictors of treatment outcomes with lutetium 177 (177Lu)-DOTATATE in patients with advanced neuroendocrine tumors
  publication-title: Cancer BiotherRadiopharm
  doi: 10.1089/cbr.2021.0053
– volume: 13
  year: 2022
  ident: B9
  article-title: New insights in PRRT: lessons from 2021
  publication-title: Front Endocrinol (Lausanne)
  doi: 10.3389/fendo.2022.861434
– volume: 10
  year: 2021
  ident: B28
  article-title: Biomarkers in small intestine NETs and carcinoid heart disease: A comprehensive review
  publication-title: Biol (Basel)
  doi: 10.3390/biology10100950
– volume: 104
  year: 2019
  ident: B24
  article-title: The inflammation-based index can predict response and improve patient selection in NETs treated with PRRT: A pilot study
  publication-title: J Clin Endocrinol Metab
  doi: 10.1210/jc.2018-01214
– volume: 101
  year: 2016
  ident: B23
  article-title: C-reactive protein as a new prognostic factor for survival in patients with pancreatic neuroendocrine neoplasia
  publication-title: JCEM
  doi: 10.1210/jc.2015-3114
– volume: 61
  year: 2020
  ident: B25
  article-title: Inflammation-based index and 68Ga-DOTATOC PET-derived uptake and volumetric parameters predict outcome in neuroendocrine tumor patients treated with 90Y-DOTATOC
  publication-title: J Nucl Med
  doi: 10.2967/jnumed.119.236935
– volume: 9
  year: 2019
  ident: B16
  article-title: Consideration of age is necessary for increasing the accuracy of the AJCC TNM staging system of pancreatic neuroendocrine tumors
  publication-title: Front Oncol
  doi: 10.3389/fonc.2019.00906
– volume: 106
  year: 2021
  ident: B6
  article-title: Metastatic medullary thyroid cancer: the role of 68Gallium-DOTA-somatostatin analogue PET/CT and peptide receptor radionuclide therapy
  publication-title: J Clin Endocrinol Metab
  doi: 10.1210/clinem/dgab588
– volume: 12
  year: 2022
  ident: B10
  article-title: The predicting role of the neutrophil-to-lymphocyte ratio for the tumor grade and prognosis in pancreatic neuroendocrine tumors
  publication-title: Diagnostics (Basel).
  doi: 10.3390/diagnostics12030737
– volume: 24
  year: 2023
  ident: B12
  article-title: The complex histopathological and immunohistochemical spectrum of neuroendocrine tumors-an overview of the latest classifications
  publication-title: Int J Mol Sci
  doi: 10.3390/ijms24021418
SSID ssj0000401998
Score 2.3359847
Snippet Peptide receptor radionuclide therapy (PRRT) is a treatment option for well-differentiated, somatostatin receptor positive, unresectable or/and metastatic...
IntroductionPeptide receptor radionuclide therapy (PRRT) is a treatment option for well-differentiated, somatostatin receptor positive, unresectable or/and...
SourceID doaj
pubmedcentral
proquest
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage 1270421
SubjectTerms Adult
Aged
Biomarkers
Disease Progression
Endocrinology
functional tumors
Humans
Middle Aged
NET
Neuroendocrine Tumors - drug therapy
Octreotide - therapeutic use
overall survival
progression free survival
PRRT
Radioisotopes - therapeutic use
Receptors, Peptide - therapeutic use
Retrospective Studies
Serbia - epidemiology
Title Predicting the survival probability of functional neuroendocrine tumors treated with peptide receptor radionuclide therapy: Serbian experience
URI https://www.ncbi.nlm.nih.gov/pubmed/38317712
https://www.proquest.com/docview/2922949726
https://pubmed.ncbi.nlm.nih.gov/PMC10840135
https://doaj.org/article/c88a5cc43c034086867f0b4b9fbc9cba
Volume 14
WOSCitedRecordID wos001143669500001&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVAON
  databaseName: DOAJ Directory of Open Access Journals
  customDbUrl:
  eissn: 1664-2392
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0000401998
  issn: 1664-2392
  databaseCode: DOA
  dateStart: 20100101
  isFulltext: true
  titleUrlDefault: https://www.doaj.org/
  providerName: Directory of Open Access Journals
– providerCode: PRVHPJ
  databaseName: ROAD: Directory of Open Access Scholarly Resources
  customDbUrl:
  eissn: 1664-2392
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0000401998
  issn: 1664-2392
  databaseCode: M~E
  dateStart: 20100101
  isFulltext: true
  titleUrlDefault: https://road.issn.org
  providerName: ISSN International Centre
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9QwELagQogL4k14VEbihpY6jhPb3AC14kCrHgDtzfJTVCpJld0g9cJP4DczY6erXYTgwiWyEluxPGN7vvH4G0JeKq6VahNIwKLrxlu5cE60i-C0DkxI2ebMc18-ypMTtVzq061UXxgTVuiBy8AdeKVs671oPGsE2N-qk4k54XRyXnuXTSOwerbAVF6DATYAkCi3ZACF6YMU-4CX_XjzGg9bBa93dqJM2P8nK_P3YMmt3efoDrk9m430benuXXIt9vfIzeP5YPw--Xk6YhljmCmYdHQ1wRIASkQxYUyh4r6kQ6K4jRXvH81MlthdjxcA6Xr6NowrmgPPY6Don6UXGPISIoVVEUrDSEcboPHkz_Ftubp1-YbCeoPM5TRuaJMfkM9Hh5_ef1jMqRYWHvDxGmxswRNYfl6CiLrGRZ4aJ7hloeuk8ICjQqNkCoylAFMcYE0HIg61cDw45evmIdnrhz4-JrRx3oVaO2UtE7X1ykZkCbQqATZjiVWkvhp242ceckyHcW4Aj6CoTBaVQVGZWVQVebVpc1FYOP5a-x1Kc1MTGbTzC9ArM-uV-ZdeVeTFlS4YmHF4jGL7OEwrwzXnWmjJu4o8Krqx-RXg_VrKmldE7WjNTl92v_RnXzOrd80UYt32yf_o_VNyC0ZEZF-ReEb21uMUn5Mb_vv6bDXuk-tyqfbzjIHn8Y_DXwx6IGQ
linkProvider Directory of Open Access Journals
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Predicting+the+survival+probability+of+functional+neuroendocrine+tumors+treated+with+peptide+receptor+radionuclide+therapy%3A+Serbian+experience&rft.jtitle=Frontiers+in+endocrinology+%28Lausanne%29&rft.au=Vukomanovic%2C+Vladimir&rft.au=Nedic%2C+Katarina+Vuleta&rft.au=Radojevic%2C+Marija+Zivkovic&rft.au=Dagovic%2C+Aleksandar&rft.date=2024-01-04&rft.pub=Frontiers+Media+S.A&rft.eissn=1664-2392&rft.volume=14&rft_id=info:doi/10.3389%2Ffendo.2023.1270421&rft.externalDocID=PMC10840135
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1664-2392&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1664-2392&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1664-2392&client=summon