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Can MASCC and CISNE scores predict delays of lung cancer chemotherapy after febrile neutropenia?

BACKGROUND: Febrile neutropenia (FN) during cancer chemotherapy can lead to morbidity and mortality. The Multinational Association of Supportive Care in Cancer (MASCC) and clinical index of stable febrile neutropenia (CISNE) scores have been widely used to predict the risk of severe medical complica...

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Autores principales: Ono, Yoshitaka, Hayama, Naoki, Hattori, Shigeaki, Ito, Yoko, Oguma, Tsuyoshi, Sakamaki, Fumio, Asano, Koichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9750814/
https://www.ncbi.nlm.nih.gov/pubmed/36330990
http://dx.doi.org/10.1111/1759-7714.14720
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author Ono, Yoshitaka
Hayama, Naoki
Hattori, Shigeaki
Ito, Yoko
Oguma, Tsuyoshi
Sakamaki, Fumio
Asano, Koichiro
author_facet Ono, Yoshitaka
Hayama, Naoki
Hattori, Shigeaki
Ito, Yoko
Oguma, Tsuyoshi
Sakamaki, Fumio
Asano, Koichiro
author_sort Ono, Yoshitaka
collection PubMed
description BACKGROUND: Febrile neutropenia (FN) during cancer chemotherapy can lead to morbidity and mortality. The Multinational Association of Supportive Care in Cancer (MASCC) and clinical index of stable febrile neutropenia (CISNE) scores have been widely used to predict the risk of severe medical complications in patients with FN; however, there are few tools for predicting chemotherapy delays or discontinuation after FN. METHODS: Patients admitted to two university hospitals between 2014 and 2018 with a FN diagnosis during the first cycle of chemotherapy for lung cancer were reviewed retrospectively. RESULTS: Among 539 patients who received 813 courses of chemotherapy for lung cancer, 49 (9%) developed FN during the first treatment cycle. Although all the patients recovered from their primary infection, 19 patients (38.8%) developed serious medical complications, 11 (22.4%) were unable to resume chemotherapy and one (2.0%) declined to resume chemotherapy, and nine (18.4%) died within 90 days. Patients who failed to resume chemotherapy had a lower MASCC score (median 8.5 vs. 17, p < 0.01) and a higher CISNE score (median 3 vs. 1, p < 0.01) at the onset of FN. The specificity to predict the patient who failed to resume chemotherapy was 90% or more with MASCC score ≤9 or CISNE score ≥3, with the sensitivity of 61%. MASCC score ≤ 16 can also be a sensitive indicator with the sensitivity and specificity of 89 and 52%, respectively. CONCLUSION: The MASCC and CISNE scores are useful in identifying lung cancer patients who are unable to resume chemotherapy as scheduled after the onset of FN.
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spelling pubmed-97508142022-12-15 Can MASCC and CISNE scores predict delays of lung cancer chemotherapy after febrile neutropenia? Ono, Yoshitaka Hayama, Naoki Hattori, Shigeaki Ito, Yoko Oguma, Tsuyoshi Sakamaki, Fumio Asano, Koichiro Thorac Cancer Original Articles BACKGROUND: Febrile neutropenia (FN) during cancer chemotherapy can lead to morbidity and mortality. The Multinational Association of Supportive Care in Cancer (MASCC) and clinical index of stable febrile neutropenia (CISNE) scores have been widely used to predict the risk of severe medical complications in patients with FN; however, there are few tools for predicting chemotherapy delays or discontinuation after FN. METHODS: Patients admitted to two university hospitals between 2014 and 2018 with a FN diagnosis during the first cycle of chemotherapy for lung cancer were reviewed retrospectively. RESULTS: Among 539 patients who received 813 courses of chemotherapy for lung cancer, 49 (9%) developed FN during the first treatment cycle. Although all the patients recovered from their primary infection, 19 patients (38.8%) developed serious medical complications, 11 (22.4%) were unable to resume chemotherapy and one (2.0%) declined to resume chemotherapy, and nine (18.4%) died within 90 days. Patients who failed to resume chemotherapy had a lower MASCC score (median 8.5 vs. 17, p < 0.01) and a higher CISNE score (median 3 vs. 1, p < 0.01) at the onset of FN. The specificity to predict the patient who failed to resume chemotherapy was 90% or more with MASCC score ≤9 or CISNE score ≥3, with the sensitivity of 61%. MASCC score ≤ 16 can also be a sensitive indicator with the sensitivity and specificity of 89 and 52%, respectively. CONCLUSION: The MASCC and CISNE scores are useful in identifying lung cancer patients who are unable to resume chemotherapy as scheduled after the onset of FN. John Wiley & Sons Australia, Ltd 2022-11-04 2022-12 /pmc/articles/PMC9750814/ /pubmed/36330990 http://dx.doi.org/10.1111/1759-7714.14720 Text en © 2022 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Ono, Yoshitaka
Hayama, Naoki
Hattori, Shigeaki
Ito, Yoko
Oguma, Tsuyoshi
Sakamaki, Fumio
Asano, Koichiro
Can MASCC and CISNE scores predict delays of lung cancer chemotherapy after febrile neutropenia?
title Can MASCC and CISNE scores predict delays of lung cancer chemotherapy after febrile neutropenia?
title_full Can MASCC and CISNE scores predict delays of lung cancer chemotherapy after febrile neutropenia?
title_fullStr Can MASCC and CISNE scores predict delays of lung cancer chemotherapy after febrile neutropenia?
title_full_unstemmed Can MASCC and CISNE scores predict delays of lung cancer chemotherapy after febrile neutropenia?
title_short Can MASCC and CISNE scores predict delays of lung cancer chemotherapy after febrile neutropenia?
title_sort can mascc and cisne scores predict delays of lung cancer chemotherapy after febrile neutropenia?
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9750814/
https://www.ncbi.nlm.nih.gov/pubmed/36330990
http://dx.doi.org/10.1111/1759-7714.14720
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