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Early stage breast cancer follow-up in real-world clinical practice: the added value of cell free circulating tumor DNA
PURPOSE: Physical examinations and annual mammography (minimal follow-up) are as effective as laboratory/imaging tests (intensive follow-up) in detecting breast cancer (BC) recurrence. This statement is now challenged by the availability of new diagnostic tools for asymptomatic cases. Herein, we ana...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9114063/ https://www.ncbi.nlm.nih.gov/pubmed/35396978 http://dx.doi.org/10.1007/s00432-022-03990-7 |
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author | La Rocca, E. De Santis, M. C. Silvestri, M. Ortolan, E. Valenti, M. Folli, S. de Braud, F. G. Bianchi, G. V. Scaperrotta, G. P. Apolone, G. Daidone, M. G. Cappelletti, V. Pruneri, G. Di Cosimo, S. |
author_facet | La Rocca, E. De Santis, M. C. Silvestri, M. Ortolan, E. Valenti, M. Folli, S. de Braud, F. G. Bianchi, G. V. Scaperrotta, G. P. Apolone, G. Daidone, M. G. Cappelletti, V. Pruneri, G. Di Cosimo, S. |
author_sort | La Rocca, E. |
collection | PubMed |
description | PURPOSE: Physical examinations and annual mammography (minimal follow-up) are as effective as laboratory/imaging tests (intensive follow-up) in detecting breast cancer (BC) recurrence. This statement is now challenged by the availability of new diagnostic tools for asymptomatic cases. Herein, we analyzed current practices and circulating tumor DNA (ctDNA) in monitoring high-risk BC patients treated with curative intent in a comprehensive cancer center. PATIENTS AND METHODS: Forty-two consecutive triple negative BC patients undergoing neoadjuvant therapy and surgery were prospectively enrolled. Data from plasma samples and surveillance procedures were analyzed to report the diagnostic pattern of relapsed cases, i.e., by symptoms, follow-up procedures and ctDNA. RESULTS: Besides minimal follow-up, 97% and 79% of patients had at least 1 non-recommended imaging and laboratory tests for surveillance purposes. During a median follow-up of 5.1(IQR, 4.1–5.9) years, 13 events occurred (1 contralateral BC, 1 loco-regional recurrence, 10 metastases, and 1 death). Five recurrent cases were diagnosed by intensive follow-up, 5 by symptoms, and 2 incidentally. ctDNA antedated disseminated disease in all evaluable cases excepted two with bone-only and single liver metastases. The mean time from ctDNA detection to suspicious findings at follow-up imaging was 3.81(SD, 2.68), and to definitive recurrence diagnosis 8(SD, 2.98) months. ctDNA was undetectable in the absence of disease and in two suspected cases not subsequently confirmed. CONCLUSIONS: Some relapses are still symptomatic despite the extensive use of intensive follow-up. ctDNA is a specific test, sensitive enough to detect recurrence before other methods, suitable for clarifying equivocal imaging, and exploitable for salvage therapy in asymptomatic BC survivors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00432-022-03990-7. |
format | Online Article Text |
id | pubmed-9114063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-91140632022-05-19 Early stage breast cancer follow-up in real-world clinical practice: the added value of cell free circulating tumor DNA La Rocca, E. De Santis, M. C. Silvestri, M. Ortolan, E. Valenti, M. Folli, S. de Braud, F. G. Bianchi, G. V. Scaperrotta, G. P. Apolone, G. Daidone, M. G. Cappelletti, V. Pruneri, G. Di Cosimo, S. J Cancer Res Clin Oncol Article PURPOSE: Physical examinations and annual mammography (minimal follow-up) are as effective as laboratory/imaging tests (intensive follow-up) in detecting breast cancer (BC) recurrence. This statement is now challenged by the availability of new diagnostic tools for asymptomatic cases. Herein, we analyzed current practices and circulating tumor DNA (ctDNA) in monitoring high-risk BC patients treated with curative intent in a comprehensive cancer center. PATIENTS AND METHODS: Forty-two consecutive triple negative BC patients undergoing neoadjuvant therapy and surgery were prospectively enrolled. Data from plasma samples and surveillance procedures were analyzed to report the diagnostic pattern of relapsed cases, i.e., by symptoms, follow-up procedures and ctDNA. RESULTS: Besides minimal follow-up, 97% and 79% of patients had at least 1 non-recommended imaging and laboratory tests for surveillance purposes. During a median follow-up of 5.1(IQR, 4.1–5.9) years, 13 events occurred (1 contralateral BC, 1 loco-regional recurrence, 10 metastases, and 1 death). Five recurrent cases were diagnosed by intensive follow-up, 5 by symptoms, and 2 incidentally. ctDNA antedated disseminated disease in all evaluable cases excepted two with bone-only and single liver metastases. The mean time from ctDNA detection to suspicious findings at follow-up imaging was 3.81(SD, 2.68), and to definitive recurrence diagnosis 8(SD, 2.98) months. ctDNA was undetectable in the absence of disease and in two suspected cases not subsequently confirmed. CONCLUSIONS: Some relapses are still symptomatic despite the extensive use of intensive follow-up. ctDNA is a specific test, sensitive enough to detect recurrence before other methods, suitable for clarifying equivocal imaging, and exploitable for salvage therapy in asymptomatic BC survivors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00432-022-03990-7. Springer Berlin Heidelberg 2022-04-09 2022 /pmc/articles/PMC9114063/ /pubmed/35396978 http://dx.doi.org/10.1007/s00432-022-03990-7 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 | Article La Rocca, E. De Santis, M. C. Silvestri, M. Ortolan, E. Valenti, M. Folli, S. de Braud, F. G. Bianchi, G. V. Scaperrotta, G. P. Apolone, G. Daidone, M. G. Cappelletti, V. Pruneri, G. Di Cosimo, S. Early stage breast cancer follow-up in real-world clinical practice: the added value of cell free circulating tumor DNA |
title | Early stage breast cancer follow-up in real-world clinical practice: the added value of cell free circulating tumor DNA |
title_full | Early stage breast cancer follow-up in real-world clinical practice: the added value of cell free circulating tumor DNA |
title_fullStr | Early stage breast cancer follow-up in real-world clinical practice: the added value of cell free circulating tumor DNA |
title_full_unstemmed | Early stage breast cancer follow-up in real-world clinical practice: the added value of cell free circulating tumor DNA |
title_short | Early stage breast cancer follow-up in real-world clinical practice: the added value of cell free circulating tumor DNA |
title_sort | early stage breast cancer follow-up in real-world clinical practice: the added value of cell free circulating tumor dna |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9114063/ https://www.ncbi.nlm.nih.gov/pubmed/35396978 http://dx.doi.org/10.1007/s00432-022-03990-7 |
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