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Minimally Invasive Breast Biopsy After Neoadjuvant Systemic Treatment to Identify Breast Cancer Patients with Residual Disease for Extended Neoadjuvant Treatment: A New Concept.
Pfob, André; Cai, Lie; Schneeweiss, Andreas; Rauch, Geraldine; Thomas, Bettina; Schaefgen, Benedikt; Kuemmel, Sherko; Reimer, Toralf; Hahn, Markus; Thill, Marc; Blohmer, Jens-Uwe; Hackmann, John; Malter, Wolfram; Bekes, Inga; Friedrichs, Kay; Wojcinski, Sebastian; Joos, Sylvie; Paepke, Stefan; Degenhardt, Tom; Rom, Joachim; Rody, Achim; van Mackelenbergh, Marion; Banys-Paluchowski, Maggie; Große, Regina; Reinisch, Mattea; Karsten, Maria Margarete; Sidey-Gibbons, Chris; Wallwiener, Markus; Golatta, Michael; Heil, Joerg.
Afiliação
  • Pfob A; Department of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg University, Heidelberg, Germany. Andre.pfob@med.uni-heidelberg.de.
  • Cai L; MD Anderson Center for INSPiRED Cancer Care (Integrated Systems for Patient-Reported Data), The University of Texas MD Anderson Cancer Center, Houston, TX, USA. Andre.pfob@med.uni-heidelberg.de.
  • Schneeweiss A; National Center for Tumor Diseases, Heidelberg University Hospital and German Cancer Research Center, Heidelberg, Germany. Andre.pfob@med.uni-heidelberg.de.
  • Rauch G; Department of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg University, Heidelberg, Germany.
  • Thomas B; National Center for Tumor Diseases, Heidelberg University Hospital and German Cancer Research Center, Heidelberg, Germany.
  • Schaefgen B; Institute of Biometry and Clinical Epidemiology, Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Kuemmel S; Coordination Centre for Clinical Trials (KKS), University Heidelberg, Heidelberg, Germany.
  • Reimer T; Department of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg University, Heidelberg, Germany.
  • Hahn M; Breast Unit, Kliniken Essen-Mitte, Essen, Germany.
  • Thill M; Department of Gynecology with Breast Center, Charité - Universitätsmedizin Berlin, Freie Universität Berlin and Humboldt Universität zu Berlin, Berlin, Germany.
  • Blohmer JU; Department of Gynecology/Breast Unit, University Hospital Rostock, Rostock, Germany.
  • Hackmann J; Department of Gynecology/Breast Unit, University Hospital Tuebingen, Tübingen, Germany.
  • Malter W; Department of Gynecology and Gynecological Oncology/Breast Unit, Agaplesion Markus Hospital Frankfurt, Frankfurt, Germany.
  • Bekes I; Department of Gynecology with Breast Center, Charité - Universitätsmedizin Berlin, Freie Universität Berlin and Humboldt Universität zu Berlin, Berlin, Germany.
  • Friedrichs K; Department of Gynecology/Breast Unit, Marienhospital, Witten, Germany.
  • Wojcinski S; Department of Gynecology and Obstetrics, Medical Faculty, Breast Cancer Center, University of Cologne, Cologne, Germany.
  • Joos S; Department of Gynecology/Breast Unit, University Hospital Ulm, Ulm, Germany.
  • Paepke S; Department of Gynecology/Breast Unit, Jerusalem Hospital Hamburg, Hamburg, Germany.
  • Degenhardt T; Department of Gynecology and Obstetrics, Breast Cancer Center, Klinikum Bielefeld Mitte GmbH, Bielefeld, Germany.
  • Rom J; Radiologische Allianz Hamburg, Hamburg, Germany.
  • Rody A; Frauenklinik, Interdisziplinäres Brustzentrum des Klinikums rechts der Isar der Technischen Universität München, Munich, Germany.
  • van Mackelenbergh M; Department of Gynecology/Breast Unit, University Hospital Munich, Munich, Germany.
  • Banys-Paluchowski M; Department of Gynecology/Breast Unit, Klinikum Frankfurt-Höchst, Frankfurt, Germany.
  • Große R; Department of Gynecology/Breast Unit, University Hospital Schleswig-Holstein, Lübeck, Germany.
  • Reinisch M; Department of Gynecology/Breast Unit, University Hospital Schleswig-Holstein, Kiel, Germany.
  • Karsten MM; Department of Gynecology/Breast Unit, University Hospital Schleswig-Holstein, Lübeck, Germany.
  • Sidey-Gibbons C; Department of Gynecology/Breast Unit, University Hospital Halle, Halle, Germany.
  • Wallwiener M; Breast Unit, Kliniken Essen-Mitte, Essen, Germany.
  • Golatta M; Department of Gynecology with Breast Center, Charité - Universitätsmedizin Berlin, Freie Universität Berlin and Humboldt Universität zu Berlin, Berlin, Germany.
  • Heil J; MD Anderson Center for INSPiRED Cancer Care (Integrated Systems for Patient-Reported Data), The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Ann Surg Oncol ; 31(2): 957-965, 2024 Feb.
Article em En | MEDLINE | ID: mdl-37947974
BACKGROUND: Breast cancer patients with residual disease after neoadjuvant systemic treatment (NAST) have a worse prognosis compared with those achieving a pathologic complete response (pCR). Earlier identification of these patients might allow timely, extended neoadjuvant treatment strategies. We explored the feasibility of a vacuum-assisted biopsy (VAB) after NAST to identify patients with residual disease (ypT+ or ypN+) prior to surgery. METHODS: We used data from a multicenter trial, collected at 21 study sites (NCT02948764). The trial included women with cT1-3, cN0/+ breast cancer undergoing routine post-neoadjuvant imaging (ultrasound, MRI, mammography) and VAB prior to surgery. We compared the findings of VAB and routine imaging with the histopathologic evaluation of the surgical specimen. RESULTS: Of 398 patients, 34 patients with missing ypN status and 127 patients with luminal tumors were excluded. Among the remaining 237 patients, tumor cells in the VAB indicated a surgical non-pCR in all patients (73/73, positive predictive value [PPV] 100%), whereas PPV of routine imaging after NAST was 56.0% (75/134). Sensitivity of the VAB was 72.3% (73/101), and 74.3% for sensitivity of imaging (75/101). CONCLUSION: Residual cancer found in a VAB specimen after NAST always corresponds to non-pCR. Residual cancer assumed on routine imaging after NAST corresponds to actual residual cancer in about half of patients. Response assessment by VAB is not safe for the exclusion of residual cancer. Response assessment by biopsies after NAST may allow studying the new concept of extended neoadjuvant treatment for patients with residual disease in future trials.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama Limite: Female / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama Limite: Female / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article