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Three weekly versus weekly concurrent cisplatin: safety propensity score analysis on 166 head and neck cancer patients
BACKGROUND: Radio-chemotherapy with CDDP is the standard for H&N squamous cell cancer. CDDP 100 mg/m(2)/q3 is the standard; alternative schedules are used to reduce toxicity, mostly 40 mg/m(2)/q1. METHODS: Patients were treated from 1/2010 to 1/2017 in two Radiation Oncology Centres. Propensity...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686550/ https://www.ncbi.nlm.nih.gov/pubmed/34930353 http://dx.doi.org/10.1186/s13014-021-01966-4 |
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author | Buglione, Michela Alterio, Daniela Maddalo, Marta Greco, Diana Gerardi, Marianna Alessandra Tomasini, Davide Pegurri, Ludovica Augugliaro, Matteo Marvaso, Giulia Turturici, Irene Guerini, Andrea Ansarin, Mohssen Spiazzi, Luigi Costa, Loredana Cossu Rocca, Maria Magrini, Stefano Maria Jereczek-Fossa, Barbara Alicja |
author_facet | Buglione, Michela Alterio, Daniela Maddalo, Marta Greco, Diana Gerardi, Marianna Alessandra Tomasini, Davide Pegurri, Ludovica Augugliaro, Matteo Marvaso, Giulia Turturici, Irene Guerini, Andrea Ansarin, Mohssen Spiazzi, Luigi Costa, Loredana Cossu Rocca, Maria Magrini, Stefano Maria Jereczek-Fossa, Barbara Alicja |
author_sort | Buglione, Michela |
collection | PubMed |
description | BACKGROUND: Radio-chemotherapy with CDDP is the standard for H&N squamous cell cancer. CDDP 100 mg/m(2)/q3 is the standard; alternative schedules are used to reduce toxicity, mostly 40 mg/m(2)/q1. METHODS: Patients were treated from 1/2010 to 1/2017 in two Radiation Oncology Centres. Propensity score analysis (PS) was retrospectively used to compare these two schedules. RESULTS: Patients analyzed were 166. Most (114/166) had 1w-CDDP while 52 had 3w-CDDP. In the 3w-CDDP group, patients were younger, with better performance status, smaller disease extent and a more common nodal involvement than in the 1w-CDDP. Acute toxicity was similar in the groups. Treatment compliance was lower in the w-CCDP. Overall survival before PS was better for female, for oropharyngeal disease and for 3w-CDDP group. After PS, survival was not related to the CDDP schedule. CONCLUSIONS: 3w-CDDP remains the standard for fit patients, weekly schedule could be safely used in selected patients. |
format | Online Article Text |
id | pubmed-8686550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86865502021-12-20 Three weekly versus weekly concurrent cisplatin: safety propensity score analysis on 166 head and neck cancer patients Buglione, Michela Alterio, Daniela Maddalo, Marta Greco, Diana Gerardi, Marianna Alessandra Tomasini, Davide Pegurri, Ludovica Augugliaro, Matteo Marvaso, Giulia Turturici, Irene Guerini, Andrea Ansarin, Mohssen Spiazzi, Luigi Costa, Loredana Cossu Rocca, Maria Magrini, Stefano Maria Jereczek-Fossa, Barbara Alicja Radiat Oncol Research BACKGROUND: Radio-chemotherapy with CDDP is the standard for H&N squamous cell cancer. CDDP 100 mg/m(2)/q3 is the standard; alternative schedules are used to reduce toxicity, mostly 40 mg/m(2)/q1. METHODS: Patients were treated from 1/2010 to 1/2017 in two Radiation Oncology Centres. Propensity score analysis (PS) was retrospectively used to compare these two schedules. RESULTS: Patients analyzed were 166. Most (114/166) had 1w-CDDP while 52 had 3w-CDDP. In the 3w-CDDP group, patients were younger, with better performance status, smaller disease extent and a more common nodal involvement than in the 1w-CDDP. Acute toxicity was similar in the groups. Treatment compliance was lower in the w-CCDP. Overall survival before PS was better for female, for oropharyngeal disease and for 3w-CDDP group. After PS, survival was not related to the CDDP schedule. CONCLUSIONS: 3w-CDDP remains the standard for fit patients, weekly schedule could be safely used in selected patients. BioMed Central 2021-12-20 /pmc/articles/PMC8686550/ /pubmed/34930353 http://dx.doi.org/10.1186/s13014-021-01966-4 Text en © The Author(s) 2021 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Buglione, Michela Alterio, Daniela Maddalo, Marta Greco, Diana Gerardi, Marianna Alessandra Tomasini, Davide Pegurri, Ludovica Augugliaro, Matteo Marvaso, Giulia Turturici, Irene Guerini, Andrea Ansarin, Mohssen Spiazzi, Luigi Costa, Loredana Cossu Rocca, Maria Magrini, Stefano Maria Jereczek-Fossa, Barbara Alicja Three weekly versus weekly concurrent cisplatin: safety propensity score analysis on 166 head and neck cancer patients |
title | Three weekly versus weekly concurrent cisplatin: safety propensity score analysis on 166 head and neck cancer patients |
title_full | Three weekly versus weekly concurrent cisplatin: safety propensity score analysis on 166 head and neck cancer patients |
title_fullStr | Three weekly versus weekly concurrent cisplatin: safety propensity score analysis on 166 head and neck cancer patients |
title_full_unstemmed | Three weekly versus weekly concurrent cisplatin: safety propensity score analysis on 166 head and neck cancer patients |
title_short | Three weekly versus weekly concurrent cisplatin: safety propensity score analysis on 166 head and neck cancer patients |
title_sort | three weekly versus weekly concurrent cisplatin: safety propensity score analysis on 166 head and neck cancer patients |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686550/ https://www.ncbi.nlm.nih.gov/pubmed/34930353 http://dx.doi.org/10.1186/s13014-021-01966-4 |
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