Evidence map›Paper›PMID 38601755›Full record

ArticleFrontiers in oncology2024

Case report: Primary CDK4/6 inhibitor and endocrine therapy in locally advanced breast cancer and its effect on gut and intratumoral microbiota.

Guilherme Vilhais, Diogo Alpuim Costa, Mário Fontes-Sousa, Pedro Casal Ribeiro, Filipa Martinho, Carolina Botelho de Sousa, Catarina Rodrigues Santos, Ida Negreiros, Ana Canastra, Paula Borralho and 7 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
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

17 authors at 7 institutions in 4 countries.

Guilherme Vilhais *Haematology and Oncology Department, CUF Oncologia, Lisbon, Portugal.
Diogo Alpuim Costa *Haematology and Oncology Department, CUF Oncologia, Lisbon, Portugal.
Mário Fontes-SousaHaematology and Oncology Department, CUF Oncologia, Lisbon, Portugal.
Pedro Casal RibeiroBioinformatics Department, Centro de Medicina Laboratorial Germano de Sousa, Lisbon, Portugal.
Filipa MartinhoBreast Unit, CUF Oncologia, Lisbon, Portugal.
Carolina Botelho de SousaBreast Unit, CUF Oncologia, Lisbon, Portugal.
Catarina Rodrigues SantosBreast Unit, CUF Oncologia, Lisbon, Portugal.
Ida NegreirosBreast Unit, CUF Oncologia, Lisbon, Portugal.
Ana CanastraAnatomic Pathology Department, CUF Oncologia, Lisbon, Portugal.
Paula BorralhoBreast Unit, CUF Oncologia, Lisbon, Portugal.
Ana Guia PereiraGenetics Laboratory, Centro de Medicina Laboratorial Germano de Sousa, Lisbon, Portugal.
Cristina MarçalClinical Pathology Department, Centro de Medicina Laboratorial Germano de Sousa, Lisbon, Portugal.
José Germano SousaClinical Pathology Department, Centro de Medicina Laboratorial Germano de Sousa, Lisbon, Portugal.
Renata ChaleiraPsychology Department, CUF Descobertas Hospital, Lisbon, Portugal.
Júlio César RochaNOVA Medical School (NMS), Faculdade de Ciências Médicas (FCM), Universidade NOVA de Lisboa (UNL), Lisbon, Portugal.
Conceição CalhauNOVA Medical School (NMS), Faculdade de Ciências Médicas (FCM), Universidade NOVA de Lisboa (UNL), Lisbon, Portugal.
Ana FariaNOVA Medical School (NMS), Faculdade de Ciências Médicas (FCM), Universidade NOVA de Lisboa (UNL), Lisbon, Portugal.
CUF Porto Hospital · PTUniversidade Nova de Lisboa · PTCentro de Genética Clínica · PTBreast Center · CHInstituto Português de Oncologia Francisco Gentil · PTHospital do Desterro · PTInstitute of Bioinformatics · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Locally advanced breast cancer poses significant challenges to the multidisciplinary team, in particular with hormone receptor (HR) positive, HER2-negative tumors that classically yield lower pathological complete responses with chemotherapy. The increasingly significant use of CDK 4/6 inhibitors (CDK4/6i) plus endocrine therapy (ET) in different breast cancer settings has led to clinical trials focusing on this strategy as a primary treatment, with promising results. The impact of the microbiota on cancer, and vice-versa, is an emerging topic in oncology. The authors report a clinical case of a postmenopausal female patient with an invasive breast carcinoma of the right breast, Luminal B-like, staged as cT4cN3M0 (IIIB). Since the lesion was considered primarily inoperable, the patient started letrozole and ribociclib. Following 6 months of systemic therapy, the clinical response was significant, and surgery with curative intent was performed. The final staging was ypT3ypN2aM0, R1, and the patient started adjuvant letrozole and radiotherapy. This case provides important insights on primary CDK4/6i plus ET in locally advanced unresectable HR+/HER2- breast cancer and its potential implications in disease management further ahead. The patient's gut microbiota was analyzed throughout the disease course and therapeutic approach, evidencing a shift in gut microbial dominance from Firmicutes to Bacteroidetes and a loss of microbial diversity following 6 months of systemic therapy. The analysis of the intratumoral microbiota from the surgical specimen revealed high microbial dissimilarity between the residual tumor and respective margins.

Indexed as

breast cancerCDK 4/6 inhibitorsgut microbiomegut microbiotaintratumoral microbiotamicrobiomemicrobiota

Identifiers

PMID38601755
PMCPMC11004348
OpenAlexW4393229285

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.