Evidence map›Paper›PMID 41866643›Full record

ArticleBreast cancer research and treatment2026

Risk of CNS relapse following pathological complete response to neoadjuvant chemotherapy in early breast cancer.

Luciana de Moura Leite, Guilherme Rossato de Almeida, Monique Celeste Tavares, Marcelle Goldner Cesca, Fernando Augusto Batista Campos, Fernanda Alves de Oliveira, Debora Maciel Santana Dornellas, Erick F Saldanha, Paula Tavares Guimarães, Daniella Dias Sá de Arruda and 10 more

Abstract read
In one paragraph

Article in Breast cancer research and treatment, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Luciana de Moura Leite *Department of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil. luciana.leite@accamargo.org.br.
Guilherme Rossato de Almeida *Department of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Monique Celeste TavaresDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Marcelle Goldner CescaDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Fernando Augusto Batista CamposDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Fernanda Alves de OliveiraDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Debora Maciel Santana DornellasDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Erick F SaldanhaDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Paula Tavares GuimarãesDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Daniella Dias Sá de ArrudaDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Maria Fernanda Simões Devides de HeldDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Rafael Lima VianaDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Francisca Giselle Rocha MouraDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Simone Klug LooseDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Sinara Figueiredo SilvaDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Rafaela PirolliDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Camilla Albina Zanco FogassaDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Bruna Raphaeli Silva MattosDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Solange Moraes SanchesDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.
Vladmir C Cordeiro de LimaDepartment of Medical Oncology, A.C. Camargo Cancer Center, São Paulo, SP, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePathological complete response (pCR) after neoadjuvant chemotherapy (NAC) improves outcomes in breast cancer (BC); however it may not prevent brain metastases. We evaluated central nervous system (CNS) recurrence patterns in early-stage BC following NAC according to pCR.

methodsAll consecutive stage I-III BC treated with NAC and surgery at a single center between 2007 and 2018 were analyzed. Endpoints included the impact of pCR on CNS recurrence across BC subtypes-hormone receptor-positive(HR)/HER2-negative, HER2-positive and triple-negative (TNBC), CNS recurrence patterns and overall survival (OS) after CNS relapse. Statistical comparisons included Fisher's Exact test, Chi-square, Kaplan-Meier, and regression analyses.

resultsAmong 1147 patients, 537 had HR-positive/HER2-negative, 301 HER2-positive, 309 TNBC, mostly stage III, treated with anthracycline + taxane NAC, and trastuzumab if HER2-positive. Three hundred sixty-five achieved pCR (59/537 HR-positive/HER2-negative, 158/301 HER2-positive, 148/309 TNBC). CNS recurrence occurred in 72 (6.2%) patients, with no difference between pCR and non-pCR (4.7 vs. 7.0%, p = 0.15). Across subtypes, there was no difference for HR-positive/HER2-negative (3.4 vs. 4%, p = 1.0), TNBC (5.4 vs. 9.3%, p = 0.2), however there was a reduction in HER2-positive (4.4 vs. 14.7%, p = 0.003) after pCR. Isolated CNS relapse was the predominant pattern of CNS metastasis (82.4%) in pCR, particularly in HER2-positive. Median OS after CNS relapse was 12 months. Multivariate analysis identified HER2-positive, TNBC, and cN2-3 status as independent predictors of CNS recurrence.

conclusionAlthough pCR was not associated with a lower overall risk of CNS recurrence, it predicted a reduced risk in HER2-positive disease. Isolated CNS relapse predominated, suggesting a sanctuary effect.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsCentral Nervous System NeoplasmsNeoadjuvant TherapyNeoplasm Recurrence, LocalAdultAgedChemotherapy, AdjuvantErb-b2 Receptor Tyrosine KinasesFemaleHumansMiddle AgedNeoplasm StagingPathologic Complete ResponseERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesCentral nervous system metastasesNeoadjuvant chemotherapyPathologic complete response

Identifiers

PMID41866643
PMCPMC13006468

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