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Early skeletal muscle mass decline is a prognostic factor in patients receiving gemcitabine plus nab-paclitaxel for unresectable pancreatic cancer: a retrospective observational study

PURPOSE: Patients with pancreatic cancer often have cancer cachexia at diagnosis. Recent studies suggested that loss of skeletal muscle mass was related to cancer cachexia, which hindered continuance of chemotherapy and could be one of prognostic factors in pancreatic cancer, however the association...

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Autores principales: Suzuki, Yukari, Saito, Kei, Nakai, Yousuke, Oyama, Hiroki, Kanai, Sachiko, Suzuki, Tatsunori, Sato, Tatsuya, Hakuta, Ryunosuke, Ishigaki, Kazunaga, Saito, Tomotaka, Hamada, Tsuyoshi, Takahara, Naminatsu, Tateishi, Ryosuke, Fujishiro, Mitsuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981495/
https://www.ncbi.nlm.nih.gov/pubmed/36862196
http://dx.doi.org/10.1007/s00520-023-07659-w
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author Suzuki, Yukari
Saito, Kei
Nakai, Yousuke
Oyama, Hiroki
Kanai, Sachiko
Suzuki, Tatsunori
Sato, Tatsuya
Hakuta, Ryunosuke
Ishigaki, Kazunaga
Saito, Tomotaka
Hamada, Tsuyoshi
Takahara, Naminatsu
Tateishi, Ryosuke
Fujishiro, Mitsuhiro
author_facet Suzuki, Yukari
Saito, Kei
Nakai, Yousuke
Oyama, Hiroki
Kanai, Sachiko
Suzuki, Tatsunori
Sato, Tatsuya
Hakuta, Ryunosuke
Ishigaki, Kazunaga
Saito, Tomotaka
Hamada, Tsuyoshi
Takahara, Naminatsu
Tateishi, Ryosuke
Fujishiro, Mitsuhiro
author_sort Suzuki, Yukari
collection PubMed
description PURPOSE: Patients with pancreatic cancer often have cancer cachexia at diagnosis. Recent studies suggested that loss of skeletal muscle mass was related to cancer cachexia, which hindered continuance of chemotherapy and could be one of prognostic factors in pancreatic cancer, however the association remains unclear in patients receiving gemcitabine and nab-paclitaxel (GnP). METHODS: We retrospectively studied 138 patients with unresectable pancreatic cancer receiving first-line GnP at the University of Tokyo from January 2015 to September 2020. We calculated body composition in CT images before chemotherapy and at initial evaluation, and evaluated the association of both body composition before chemotherapy and its changes at initial evaluation. RESULTS: Compared by skeletal muscle mass index (SMI) change rate between pre-chemotherapy and initial evaluation, there were statistically significantly differences in the median OS: 16.3 months (95%CI 12.3–22.7) and 10.3 months (95%CI 8.3–18.1) between SMI change rate ≥ -3.5% and < -3.5% groups (P = 0.01). By multivariate analysis for OS, CA19-9 (HR 3.34, 95%CI 2.00–5.57, P < 0.01), PLR (HR 1.68, 95%CI 1.01–2.78, P = 0.04), mGPS (HR 2.32, 95%CI 1.47–3.65, P < 0.01) and relative dose intensity (HR 2.21, 95%CI 1.42–3.46, P < 0.01) were significantly poor prognostic factors. SMI change rate (HR 1.47, 95%CI 0.95–2.28, P = 0.08) showed a trend to poor prognosis. Sarcopenia before chemotherapy was not significantly associated with PFS or OS. CONCLUSION: Early skeletal muscle mass decline was associated with poor OS. Further investigation is warranted whether the maintenance of skeletal muscle mass by nutritional support would improve prognosis.
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spelling pubmed-99814952023-03-04 Early skeletal muscle mass decline is a prognostic factor in patients receiving gemcitabine plus nab-paclitaxel for unresectable pancreatic cancer: a retrospective observational study Suzuki, Yukari Saito, Kei Nakai, Yousuke Oyama, Hiroki Kanai, Sachiko Suzuki, Tatsunori Sato, Tatsuya Hakuta, Ryunosuke Ishigaki, Kazunaga Saito, Tomotaka Hamada, Tsuyoshi Takahara, Naminatsu Tateishi, Ryosuke Fujishiro, Mitsuhiro Support Care Cancer Research PURPOSE: Patients with pancreatic cancer often have cancer cachexia at diagnosis. Recent studies suggested that loss of skeletal muscle mass was related to cancer cachexia, which hindered continuance of chemotherapy and could be one of prognostic factors in pancreatic cancer, however the association remains unclear in patients receiving gemcitabine and nab-paclitaxel (GnP). METHODS: We retrospectively studied 138 patients with unresectable pancreatic cancer receiving first-line GnP at the University of Tokyo from January 2015 to September 2020. We calculated body composition in CT images before chemotherapy and at initial evaluation, and evaluated the association of both body composition before chemotherapy and its changes at initial evaluation. RESULTS: Compared by skeletal muscle mass index (SMI) change rate between pre-chemotherapy and initial evaluation, there were statistically significantly differences in the median OS: 16.3 months (95%CI 12.3–22.7) and 10.3 months (95%CI 8.3–18.1) between SMI change rate ≥ -3.5% and < -3.5% groups (P = 0.01). By multivariate analysis for OS, CA19-9 (HR 3.34, 95%CI 2.00–5.57, P < 0.01), PLR (HR 1.68, 95%CI 1.01–2.78, P = 0.04), mGPS (HR 2.32, 95%CI 1.47–3.65, P < 0.01) and relative dose intensity (HR 2.21, 95%CI 1.42–3.46, P < 0.01) were significantly poor prognostic factors. SMI change rate (HR 1.47, 95%CI 0.95–2.28, P = 0.08) showed a trend to poor prognosis. Sarcopenia before chemotherapy was not significantly associated with PFS or OS. CONCLUSION: Early skeletal muscle mass decline was associated with poor OS. Further investigation is warranted whether the maintenance of skeletal muscle mass by nutritional support would improve prognosis. Springer Berlin Heidelberg 2023-03-02 2023 /pmc/articles/PMC9981495/ /pubmed/36862196 http://dx.doi.org/10.1007/s00520-023-07659-w Text en © The Author(s) 2023 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
Suzuki, Yukari
Saito, Kei
Nakai, Yousuke
Oyama, Hiroki
Kanai, Sachiko
Suzuki, Tatsunori
Sato, Tatsuya
Hakuta, Ryunosuke
Ishigaki, Kazunaga
Saito, Tomotaka
Hamada, Tsuyoshi
Takahara, Naminatsu
Tateishi, Ryosuke
Fujishiro, Mitsuhiro
Early skeletal muscle mass decline is a prognostic factor in patients receiving gemcitabine plus nab-paclitaxel for unresectable pancreatic cancer: a retrospective observational study
title Early skeletal muscle mass decline is a prognostic factor in patients receiving gemcitabine plus nab-paclitaxel for unresectable pancreatic cancer: a retrospective observational study
title_full Early skeletal muscle mass decline is a prognostic factor in patients receiving gemcitabine plus nab-paclitaxel for unresectable pancreatic cancer: a retrospective observational study
title_fullStr Early skeletal muscle mass decline is a prognostic factor in patients receiving gemcitabine plus nab-paclitaxel for unresectable pancreatic cancer: a retrospective observational study
title_full_unstemmed Early skeletal muscle mass decline is a prognostic factor in patients receiving gemcitabine plus nab-paclitaxel for unresectable pancreatic cancer: a retrospective observational study
title_short Early skeletal muscle mass decline is a prognostic factor in patients receiving gemcitabine plus nab-paclitaxel for unresectable pancreatic cancer: a retrospective observational study
title_sort early skeletal muscle mass decline is a prognostic factor in patients receiving gemcitabine plus nab-paclitaxel for unresectable pancreatic cancer: a retrospective observational study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981495/
https://www.ncbi.nlm.nih.gov/pubmed/36862196
http://dx.doi.org/10.1007/s00520-023-07659-w
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