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The effect of denosumab on disseminated tumor cells (DTCs) of breast cancer patients with neoadjuvant treatment: a GeparX translational substudy

BACKGROUND: Disseminated tumor cells (DTCs) in the bone marrow are observed in about 40% at primary diagnosis of breast cancer and predict poor survival. While anti-resorptive therapy with bisphosphonates was shown to eradicate minimal residue disease in the bone marrow, the effect of denosumab on D...

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Autores principales: Wimberger, Pauline, Blohmer, Jens-Uwe, Krabisch, Petra, Link, Theresa, Just, Marianne, Sinn, Bruno Valentin, Simon, Eike, Solbach, Christine, Fehm, Tanja, Denkert, Carsten, Kühn, Cristin, Rhiem, Kerstin, Tesch, Hans, Kümmel, Sherko, Petzold, Andrea, Stötzer, Oliver, Meisel, Cornelia, Kuhlmann, Jan Dominik, Nekljudova, Valentina, Loibl, Sibylle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045108/
https://www.ncbi.nlm.nih.gov/pubmed/36978142
http://dx.doi.org/10.1186/s13058-023-01619-2
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author Wimberger, Pauline
Blohmer, Jens-Uwe
Krabisch, Petra
Link, Theresa
Just, Marianne
Sinn, Bruno Valentin
Simon, Eike
Solbach, Christine
Fehm, Tanja
Denkert, Carsten
Kühn, Cristin
Rhiem, Kerstin
Tesch, Hans
Kümmel, Sherko
Petzold, Andrea
Stötzer, Oliver
Meisel, Cornelia
Kuhlmann, Jan Dominik
Nekljudova, Valentina
Loibl, Sibylle
author_facet Wimberger, Pauline
Blohmer, Jens-Uwe
Krabisch, Petra
Link, Theresa
Just, Marianne
Sinn, Bruno Valentin
Simon, Eike
Solbach, Christine
Fehm, Tanja
Denkert, Carsten
Kühn, Cristin
Rhiem, Kerstin
Tesch, Hans
Kümmel, Sherko
Petzold, Andrea
Stötzer, Oliver
Meisel, Cornelia
Kuhlmann, Jan Dominik
Nekljudova, Valentina
Loibl, Sibylle
author_sort Wimberger, Pauline
collection PubMed
description BACKGROUND: Disseminated tumor cells (DTCs) in the bone marrow are observed in about 40% at primary diagnosis of breast cancer and predict poor survival. While anti-resorptive therapy with bisphosphonates was shown to eradicate minimal residue disease in the bone marrow, the effect of denosumab on DTCs, particularly in the neoadjuvant setting, is largely unknown. The recent GeparX clinical trial reported that denosumab, applied as an add-on treatment to nab-paclitaxel based neoadjuvant chemotherapy (NACT), did not improve the patient’s pathologic complete response (pCR) rate. Herein, we analyzed the predictive value of DTCs for the response to NACT and interrogated whether neoadjuvant denosumab treatment may eradicate DTCs in the bone marrow. METHODS: A total of 167 patients from the GeparX trial were analyzed for DTCs at baseline by immunocytochemistry using the pan-cytokeratin antibody A45-B/B3. Initially DTC-positive patients were re-analyzed for DTCs after NACT ± denosumab. RESULTS: At baseline, DTCs were observed in 43/167 patients (25.7%) in the total cohort, however their presence did not predict response to nab-paclitaxel based NACT (pCR rates: 37.1% in DTC-negative vs. 32.6% DTC-positive; p = 0.713). Regarding breast cancer subtypes, the presence of DTCs at baseline was numerically associated with response to NACT in TNBC patients (pCR rates: 40.0% in DTC-positive vs. 66.7% in DTC-negative patients; p = 0.16). Overall, denosumab treatment did not significantly increase the given DTC-eradication rate of NACT (NACT: 69.6% DTC-eradication vs. NACT + denosumab: 77.8% DTC-eradication; p = 0.726). In TNBC patients with pCR, a numerical but statistically non-significant increase of DTC-eradication after NACT + denosumab was observed (NACT: 75% DTC-eradication vs. NACT + denosumab: 100% DTC-eradication; p = 1.00). CONCLUSION: This is the first study worldwide, demonstrating that neoadjuvant add-on denosumab over a short-term period of 24 months does not increase the DTC-eradication rate in breast cancer patients treated with NACT. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13058-023-01619-2.
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spelling pubmed-100451082023-03-29 The effect of denosumab on disseminated tumor cells (DTCs) of breast cancer patients with neoadjuvant treatment: a GeparX translational substudy Wimberger, Pauline Blohmer, Jens-Uwe Krabisch, Petra Link, Theresa Just, Marianne Sinn, Bruno Valentin Simon, Eike Solbach, Christine Fehm, Tanja Denkert, Carsten Kühn, Cristin Rhiem, Kerstin Tesch, Hans Kümmel, Sherko Petzold, Andrea Stötzer, Oliver Meisel, Cornelia Kuhlmann, Jan Dominik Nekljudova, Valentina Loibl, Sibylle Breast Cancer Res Research BACKGROUND: Disseminated tumor cells (DTCs) in the bone marrow are observed in about 40% at primary diagnosis of breast cancer and predict poor survival. While anti-resorptive therapy with bisphosphonates was shown to eradicate minimal residue disease in the bone marrow, the effect of denosumab on DTCs, particularly in the neoadjuvant setting, is largely unknown. The recent GeparX clinical trial reported that denosumab, applied as an add-on treatment to nab-paclitaxel based neoadjuvant chemotherapy (NACT), did not improve the patient’s pathologic complete response (pCR) rate. Herein, we analyzed the predictive value of DTCs for the response to NACT and interrogated whether neoadjuvant denosumab treatment may eradicate DTCs in the bone marrow. METHODS: A total of 167 patients from the GeparX trial were analyzed for DTCs at baseline by immunocytochemistry using the pan-cytokeratin antibody A45-B/B3. Initially DTC-positive patients were re-analyzed for DTCs after NACT ± denosumab. RESULTS: At baseline, DTCs were observed in 43/167 patients (25.7%) in the total cohort, however their presence did not predict response to nab-paclitaxel based NACT (pCR rates: 37.1% in DTC-negative vs. 32.6% DTC-positive; p = 0.713). Regarding breast cancer subtypes, the presence of DTCs at baseline was numerically associated with response to NACT in TNBC patients (pCR rates: 40.0% in DTC-positive vs. 66.7% in DTC-negative patients; p = 0.16). Overall, denosumab treatment did not significantly increase the given DTC-eradication rate of NACT (NACT: 69.6% DTC-eradication vs. NACT + denosumab: 77.8% DTC-eradication; p = 0.726). In TNBC patients with pCR, a numerical but statistically non-significant increase of DTC-eradication after NACT + denosumab was observed (NACT: 75% DTC-eradication vs. NACT + denosumab: 100% DTC-eradication; p = 1.00). CONCLUSION: This is the first study worldwide, demonstrating that neoadjuvant add-on denosumab over a short-term period of 24 months does not increase the DTC-eradication rate in breast cancer patients treated with NACT. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13058-023-01619-2. BioMed Central 2023-03-28 2023 /pmc/articles/PMC10045108/ /pubmed/36978142 http://dx.doi.org/10.1186/s13058-023-01619-2 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/) . 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
Wimberger, Pauline
Blohmer, Jens-Uwe
Krabisch, Petra
Link, Theresa
Just, Marianne
Sinn, Bruno Valentin
Simon, Eike
Solbach, Christine
Fehm, Tanja
Denkert, Carsten
Kühn, Cristin
Rhiem, Kerstin
Tesch, Hans
Kümmel, Sherko
Petzold, Andrea
Stötzer, Oliver
Meisel, Cornelia
Kuhlmann, Jan Dominik
Nekljudova, Valentina
Loibl, Sibylle
The effect of denosumab on disseminated tumor cells (DTCs) of breast cancer patients with neoadjuvant treatment: a GeparX translational substudy
title The effect of denosumab on disseminated tumor cells (DTCs) of breast cancer patients with neoadjuvant treatment: a GeparX translational substudy
title_full The effect of denosumab on disseminated tumor cells (DTCs) of breast cancer patients with neoadjuvant treatment: a GeparX translational substudy
title_fullStr The effect of denosumab on disseminated tumor cells (DTCs) of breast cancer patients with neoadjuvant treatment: a GeparX translational substudy
title_full_unstemmed The effect of denosumab on disseminated tumor cells (DTCs) of breast cancer patients with neoadjuvant treatment: a GeparX translational substudy
title_short The effect of denosumab on disseminated tumor cells (DTCs) of breast cancer patients with neoadjuvant treatment: a GeparX translational substudy
title_sort effect of denosumab on disseminated tumor cells (dtcs) of breast cancer patients with neoadjuvant treatment: a geparx translational substudy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045108/
https://www.ncbi.nlm.nih.gov/pubmed/36978142
http://dx.doi.org/10.1186/s13058-023-01619-2
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