On-treatment biopsies to predict response to neoadjuvant chemotherapy for breast cancer.


Journal

Breast cancer research : BCR
ISSN: 1465-542X
Titre abrégé: Breast Cancer Res
Pays: England
ID NLM: 100927353

Informations de publication

Date de publication:
24 Sep 2024
Historique:
received: 27 05 2024
accepted: 19 08 2024
medline: 25 9 2024
pubmed: 25 9 2024
entrez: 24 9 2024
Statut: epublish

Résumé

Patients with pathologic complete response (pCR) to neoadjuvant chemotherapy for invasive breast cancer (BC) have better outcomes, potentially warranting less extensive surgical and systemic treatments. Early prediction of treatment response could aid in adapting therapies. On-treatment biopsies from 297 patients with invasive BC in three randomized, prospective neoadjuvant trials were assessed (GeparQuattro, GeparQuinto, GeparSixto). BC quantity, tumor-infiltrating lymphocytes (TILs), and the proliferation marker Ki-67 were compared to pre-treatment samples. The study investigated the correlation between residual cancer, changes in Ki-67 and TILs, and their impact on pathologic complete response (pCR) and disease-free survival (DFS). Among the 297 samples, 138 (46%) were hormone receptor-positive (HR+)/human epidermal growth factor 2-negative (HER2-), 87 (29%) were triple-negative (TNBC), and 72 (24%) were HER2+. Invasive tumor cells were found in 70% of on-treatment biopsies, with varying rates across subtypes (HR+/HER2-: 84%, TNBC: 62%, HER2+: 51%; p < 0.001). Patients with residual tumor on-treatment had an 8% pCR rate post-treatment (HR+/HER2-: 3%, TNBC: 19%, HER2+: 11%), while those without any invasive tumor had a 50% pCR rate (HR+/HER2-: 27%; TNBC: 48%, HER2+: 66%). Sensitivity for predicting residual disease was 0.81, with positive and negative predictive values of 0.92 and 0.50, respectively. Increasing TILs from baseline to on-treatment biopsy (if residual tumor was present) were linked to higher pCR likelihood in the overall cohort (OR 1.034, 95% CI 1.013-1.056 per % increase; p = 0.001) and with a longer DFS in TNBC (HR 0.980, 95% CI 0.963-0.997 per % increase; p = 0.026). Persisting or increased Ki-67 was associated with with lower pCR probability in the overall cohort (OR 0.957, 95% CI 0.928-0.986; p = 0.004) and shorter DFS in TNBC (HR 1.023, 95% CI 1.001-1.047; p = 0.04). On-treatment biopsies can predict patients unlikely to achieve pCR post-therapy. This could facilitate therapy adjustments for TNBC or HER2 + BC. They also might offer insights into therapy resistance mechanisms. Future research should explore whether standardized or expanded sampling enhances the accuracy of on-treatment biopsy procedures. Trial registration GeparQuattro (EudraCT 2005-001546-17), GeparQuinto (EudraCT 2006-005834-19) and GeparSixto (EudraCT 2011-000553-23).

Sections du résumé

BACKGROUND BACKGROUND
Patients with pathologic complete response (pCR) to neoadjuvant chemotherapy for invasive breast cancer (BC) have better outcomes, potentially warranting less extensive surgical and systemic treatments. Early prediction of treatment response could aid in adapting therapies.
METHODS METHODS
On-treatment biopsies from 297 patients with invasive BC in three randomized, prospective neoadjuvant trials were assessed (GeparQuattro, GeparQuinto, GeparSixto). BC quantity, tumor-infiltrating lymphocytes (TILs), and the proliferation marker Ki-67 were compared to pre-treatment samples. The study investigated the correlation between residual cancer, changes in Ki-67 and TILs, and their impact on pathologic complete response (pCR) and disease-free survival (DFS).
RESULTS RESULTS
Among the 297 samples, 138 (46%) were hormone receptor-positive (HR+)/human epidermal growth factor 2-negative (HER2-), 87 (29%) were triple-negative (TNBC), and 72 (24%) were HER2+. Invasive tumor cells were found in 70% of on-treatment biopsies, with varying rates across subtypes (HR+/HER2-: 84%, TNBC: 62%, HER2+: 51%; p < 0.001). Patients with residual tumor on-treatment had an 8% pCR rate post-treatment (HR+/HER2-: 3%, TNBC: 19%, HER2+: 11%), while those without any invasive tumor had a 50% pCR rate (HR+/HER2-: 27%; TNBC: 48%, HER2+: 66%). Sensitivity for predicting residual disease was 0.81, with positive and negative predictive values of 0.92 and 0.50, respectively. Increasing TILs from baseline to on-treatment biopsy (if residual tumor was present) were linked to higher pCR likelihood in the overall cohort (OR 1.034, 95% CI 1.013-1.056 per % increase; p = 0.001) and with a longer DFS in TNBC (HR 0.980, 95% CI 0.963-0.997 per % increase; p = 0.026). Persisting or increased Ki-67 was associated with with lower pCR probability in the overall cohort (OR 0.957, 95% CI 0.928-0.986; p = 0.004) and shorter DFS in TNBC (HR 1.023, 95% CI 1.001-1.047; p = 0.04).
CONCLUSION CONCLUSIONS
On-treatment biopsies can predict patients unlikely to achieve pCR post-therapy. This could facilitate therapy adjustments for TNBC or HER2 + BC. They also might offer insights into therapy resistance mechanisms. Future research should explore whether standardized or expanded sampling enhances the accuracy of on-treatment biopsy procedures. Trial registration GeparQuattro (EudraCT 2005-001546-17), GeparQuinto (EudraCT 2006-005834-19) and GeparSixto (EudraCT 2011-000553-23).

Identifiants

pubmed: 39317942
doi: 10.1186/s13058-024-01883-w
pii: 10.1186/s13058-024-01883-w
doi:

Substances chimiques

Receptor, ErbB-2 EC 2.7.10.1
Ki-67 Antigen 0
Biomarkers, Tumor 0
ERBB2 protein, human EC 2.7.10.1
Receptors, Progesterone 0
Receptors, Estrogen 0

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

138

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Bruno Valentin Sinn (BV)

Department of Pathology, Charité - Universitätsmedizin Berlin, 10117, Berlin, Germany. bruno.sinn@web.de.

Katharina Sychra (K)

Department of Pathology, Charité - Universitätsmedizin Berlin, 10117, Berlin, Germany.

Michael Untch (M)

Department of Gynecology, Helios Kliniken Berlin-Buch, Berlin, Germany.

Thomas Karn (T)

Department of Gynecology and Obstetrics, Goethe-University, Frankfurt, Germany.
UCT-University Cancer Center, Frankfurt-Marburg, Germany.

Marion van Mackelenbergh (M)

Department of Gynecology and Obstetrics, Universitätsklinikum Schleswig-Holstein, Kiel, Germany.

Jens Huober (J)

Breast Center St. Gallen, Kantonsspital St. Gallen, St. Gallen, Switzerland.

Wolfgang Schmitt (W)

Department of Pathology, Charité - Universitätsmedizin Berlin, 10117, Berlin, Germany.

Frederik Marmé (F)

Department of Gynecologic Oncology, Medical Faculty Mannheim, Heidelberg University, University Hospital Mannheim, Mannheim, Germany.

Christian Schem (C)

Mammazentrum Hamburg, Hamburg, Germany.

Christine Solbach (C)

Breast Center, Universitätsklinikum Frankfurt, Frankfurt, Germany.
UCT-University Cancer Center, Frankfurt-Marburg, Germany.

Elmar Stickeler (E)

Department of Gynecology, Uniklinik RWTH Aachen, Aachen, Germany.

Hans Tesch (H)

Centrum für Hämatologie und Onkologie Bethanien, Frankfurt am Main, Germany.

Peter A Fasching (PA)

Department of Gynecology and Obstetrics, University Hospital Erlangen, Erlangen, Germany.

Andreas Schneeweiss (A)

Universitätsfrauenklinik Heidelberg, Heidelberg, Germany.

Volkmar Müller (V)

Department of Gynecology, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.

Johannes Holtschmidt (J)

German Breast Group, Neu-Isenburg, Germany.

Valentina Nekljudova (V)

German Breast Group, Neu-Isenburg, Germany.

Sibylle Loibl (S)

German Breast Group, Neu-Isenburg, Germany.
UCT-University Cancer Center, Frankfurt-Marburg, Germany.

Carsten Denkert (C)

Department of Pathology, Philipps-University Marburg and University Hospital Marburg (UKGM), Marburg, Germany.
UCT-University Cancer Center, Frankfurt-Marburg, Germany.

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