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Identification of a new prognostic score for patients with high-grade metastatic GEP-NEN treated with palliative chemotherapy

PURPOSE: High-grade gastroenteropancreatic neuroendocrine neoplasms (GEP-NEN G3) are rare and heterogeneous malignancies with poor prognosis. Aim of this study was to develop prognosticators identifying those patients that derive the most benefit from currently available systemic therapies. METHODS:...

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Autores principales: Rosery, Vivian, Mika, Stephan, Schmid, Kurt Werner, Reis, Henning, Stuschke, Martin, Treckmann, Jürgen, Markus, Peter, Schumacher, Brigitte, Albers, David, Mende, Bastian, Lahner, Harald, Wiesweg, Marcel, Schuler, Martin, Siveke, Jens T., Kasper, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349702/
https://www.ncbi.nlm.nih.gov/pubmed/36071236
http://dx.doi.org/10.1007/s00432-022-04314-5
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author Rosery, Vivian
Mika, Stephan
Schmid, Kurt Werner
Reis, Henning
Stuschke, Martin
Treckmann, Jürgen
Markus, Peter
Schumacher, Brigitte
Albers, David
Mende, Bastian
Lahner, Harald
Wiesweg, Marcel
Schuler, Martin
Siveke, Jens T.
Kasper, Stefan
author_facet Rosery, Vivian
Mika, Stephan
Schmid, Kurt Werner
Reis, Henning
Stuschke, Martin
Treckmann, Jürgen
Markus, Peter
Schumacher, Brigitte
Albers, David
Mende, Bastian
Lahner, Harald
Wiesweg, Marcel
Schuler, Martin
Siveke, Jens T.
Kasper, Stefan
author_sort Rosery, Vivian
collection PubMed
description PURPOSE: High-grade gastroenteropancreatic neuroendocrine neoplasms (GEP-NEN G3) are rare and heterogeneous malignancies with poor prognosis. Aim of this study was to develop prognosticators identifying those patients that derive the most benefit from currently available systemic therapies. METHODS: This retrospective analysis included 78 patients with metastatic GEP-NEN G3. For patients with imaging data available (n = 52), the overall response rate (ORR) and disease control rate (DCR) were evaluated according to the Response Evaluation Criteria in Solid Tumors 1.1 (RECIST 1.1). A Cox proportional hazard model was used to analyze the prognostic value of selected clinical and blood-based biomarkers. The impact of palliative chemotherapy regimens on time-to-treatment-failure (TTF) and overall survival (OS) was assessed. RESULTS: Median OS of the study cohort was 9.0 months (95% CI 7.0–11.1). The majority of patients received first-line treatment with platinum plus etoposide (83.3%). The ORR and DCR of the RECIST-evaluable subgroup were 34.6% and 76.9%. Median TTF upon first-line treatment was 4.9 months (95% CI 3.4–6.4). Multivariate analysis identified the Eastern Cooperative Oncology Group performance status (ECOG PS), lactate dehydrogenase (LDH) and absolute lymphocyte count as independent prognostic factors. A prognostic score based on these parameters discriminated patients with favorable and unfavorable outcomes. CONCLUSION: Outcomes of patients with GEP-NEN G3 are still limited. A new prognostic score identifying those patients benefitting from current platinum/etoposide-based chemotherapy protocols may help as stratification factor in future trial design. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00432-022-04314-5.
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spelling pubmed-103497022023-07-17 Identification of a new prognostic score for patients with high-grade metastatic GEP-NEN treated with palliative chemotherapy Rosery, Vivian Mika, Stephan Schmid, Kurt Werner Reis, Henning Stuschke, Martin Treckmann, Jürgen Markus, Peter Schumacher, Brigitte Albers, David Mende, Bastian Lahner, Harald Wiesweg, Marcel Schuler, Martin Siveke, Jens T. Kasper, Stefan J Cancer Res Clin Oncol Research PURPOSE: High-grade gastroenteropancreatic neuroendocrine neoplasms (GEP-NEN G3) are rare and heterogeneous malignancies with poor prognosis. Aim of this study was to develop prognosticators identifying those patients that derive the most benefit from currently available systemic therapies. METHODS: This retrospective analysis included 78 patients with metastatic GEP-NEN G3. For patients with imaging data available (n = 52), the overall response rate (ORR) and disease control rate (DCR) were evaluated according to the Response Evaluation Criteria in Solid Tumors 1.1 (RECIST 1.1). A Cox proportional hazard model was used to analyze the prognostic value of selected clinical and blood-based biomarkers. The impact of palliative chemotherapy regimens on time-to-treatment-failure (TTF) and overall survival (OS) was assessed. RESULTS: Median OS of the study cohort was 9.0 months (95% CI 7.0–11.1). The majority of patients received first-line treatment with platinum plus etoposide (83.3%). The ORR and DCR of the RECIST-evaluable subgroup were 34.6% and 76.9%. Median TTF upon first-line treatment was 4.9 months (95% CI 3.4–6.4). Multivariate analysis identified the Eastern Cooperative Oncology Group performance status (ECOG PS), lactate dehydrogenase (LDH) and absolute lymphocyte count as independent prognostic factors. A prognostic score based on these parameters discriminated patients with favorable and unfavorable outcomes. CONCLUSION: Outcomes of patients with GEP-NEN G3 are still limited. A new prognostic score identifying those patients benefitting from current platinum/etoposide-based chemotherapy protocols may help as stratification factor in future trial design. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00432-022-04314-5. Springer Berlin Heidelberg 2022-09-08 2023 /pmc/articles/PMC10349702/ /pubmed/36071236 http://dx.doi.org/10.1007/s00432-022-04314-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Rosery, Vivian
Mika, Stephan
Schmid, Kurt Werner
Reis, Henning
Stuschke, Martin
Treckmann, Jürgen
Markus, Peter
Schumacher, Brigitte
Albers, David
Mende, Bastian
Lahner, Harald
Wiesweg, Marcel
Schuler, Martin
Siveke, Jens T.
Kasper, Stefan
Identification of a new prognostic score for patients with high-grade metastatic GEP-NEN treated with palliative chemotherapy
title Identification of a new prognostic score for patients with high-grade metastatic GEP-NEN treated with palliative chemotherapy
title_full Identification of a new prognostic score for patients with high-grade metastatic GEP-NEN treated with palliative chemotherapy
title_fullStr Identification of a new prognostic score for patients with high-grade metastatic GEP-NEN treated with palliative chemotherapy
title_full_unstemmed Identification of a new prognostic score for patients with high-grade metastatic GEP-NEN treated with palliative chemotherapy
title_short Identification of a new prognostic score for patients with high-grade metastatic GEP-NEN treated with palliative chemotherapy
title_sort identification of a new prognostic score for patients with high-grade metastatic gep-nen treated with palliative chemotherapy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349702/
https://www.ncbi.nlm.nih.gov/pubmed/36071236
http://dx.doi.org/10.1007/s00432-022-04314-5
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