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A pooled analysis evaluating prognostic significance of Residual Cancer Burden in invasive lobular breast cancer.

Rita A Mukhtar ,
Soumya Gottipati ,
Christina Yau ,
Sara López-Tarruella ,
Helena Earl ,
Larry Hayward ,
Louise Hiller ,
Marie Osdoit ,
Marieke van der Noordaa ,
Diane de Croze ,
Anne-Sophie Hamy ,
Marick Laé ,
Fabien Reyal ,
Gabe S Sonke ,
Tessa G Steenbruggen ,
Maartje van Seijen ,
Jelle Wesseling ,
Miguel Martín ,
Maria Del Monte-Millán ,
Judy C Boughey ,
Matthew P Goetz ,
Tanya Hoskin ,
Vicente Valero ,
Stephen B Edge ,
Jean E Abraham ,
John M S Bartlett ,
Carlos Caldas ,
Janet Dunn ,
Elena Provenzano ,
Stephen-John Sammut ,
Jeremy S Thomas ,
Ashley Graham ,
Peter Hall ,
Lorna Mackintosh ,
Fang Fan ,
Andrew K Godwin ,
Kelsey Schwensen ,
Priyanka Sharma ,
Angela M DeMichele ,
Kimberly Cole ,
Lajos Pusztai ,
Mi-Ok Kim ,
Laura J van 't Veer ,
David Cameron ,
Laura J Esserman ,
W Fraser Symmans

Abstract

Residual Cancer Burden (RCB) after neoadjuvant chemotherapy (NAC) is validated to predict event-free survival (EFS) in breast cancer but has not been studied for invasive lobular carcinoma (ILC). We studied patient-level data from a pooled cohort across 12 institutions. Associations between RCB index, class, and EFS were assessed in ILC and non-ILC with mixed effect Cox models and multivariable analyses. Recursive partitioning was used in an exploratory model to stratify prognosis by RCB components. Of 5106 patients, the diagnosis was ILC in 216 and non-ILC in 4890. Increased RCB index was associated with worse EFS in both ILC and non-ILC (p = 0.002 and p < 0.001, respectively) and remained prognostic when stratified by receptor subtype and adjusted for age, grade, T category, and nodal status. Recursive partitioning demonstrated residual invasive cancer cellularity as most prognostic in ILC. These results underscore the utility of RCB for evaluating NAC response in those with ILC.

More about this publication

NPJ breast cancer

Volume 11
Issue nr. 1
Pages 14
Publication date 13-02-2025

Full text links

Publisher website (DOI) 10.1038/s41523-025-00720-3
Europe PubMed Central 39948079
Pubmed 39948079

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