Evidence map›Paper›PMID 36139688›Full record

ArticleCancers2022

Primary Chemoradiotherapy Treatment (PCRT) for HER2+ and Triple Negative Breast Cancer Patients: A Feasible Combination.

Raquel Ciérvide, Ángel Montero, Eduardo García-Rico, Mariola García-Aranda, Mercedes Herrero, Jessica Skaarup, Leticia Benassi, Maria José Barrera, Estela Vega, Beatriz Rojas and 22 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Preoperative accelerated hypofractionated radiotherapy (PHYPORT): state of art and potential clinical application.Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology · 2025
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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

32 authors at 2 institutions in 1 country.

Raquel CiérvideDepartment of Radiation Oncology, HM Hospitales, 28050 Madrid, Spain.ORCID 0000-0003-0130-878X
Ángel MonteroDepartment of Radiation Oncology, HM Hospitales, 28050 Madrid, Spain.ORCID 0000-0001-5566-0493
Eduardo García-RicoDepartment of Medical Oncology, HM Hospitales, 28050 Madrid, Spain.ORCID 0000-0003-0697-5952
Mariola García-ArandaDepartment of Radiation Oncology, HM Hospitales, 28050 Madrid, Spain.
Mercedes HerreroDepartment of Gynecology and Obstetrics, HM Hospitales, 28050 Madrid, Spain.
Jessica SkaarupDepartment of Gynecology and Obstetrics, HM Hospitales, 28050 Madrid, Spain.
Leticia BenassiDepartment of Gynecology and Obstetrics, HM Hospitales, 28050 Madrid, Spain.
Maria José BarreraDepartment of Gynecology and Obstetrics, HM Hospitales, 28050 Madrid, Spain.
Estela VegaDepartment of Medical Oncology, HM Hospitales, 28050 Madrid, Spain.
Beatriz RojasDepartment of Medical Oncology, HM Hospitales, 28050 Madrid, Spain.
Raquel BratosDepartment of Medical Oncology, HM Hospitales, 28050 Madrid, Spain.
Ana LunaDepartment of Medical Oncology, HM Hospitales, 28050 Madrid, Spain.
Manuela ParrasDepartment of Radiology, HM Hospitales, 28050 Madrid, Spain.
María LópezDepartment of Radiology, HM Hospitales, 28050 Madrid, Spain.
Ana DelgadoDepartment of Radiology, HM Hospitales, 28050 Madrid, Spain.ORCID 0000-0002-8412-3221
Paloma QuevedoDepartment of Radiology, HM Hospitales, 28050 Madrid, Spain.ORCID 0000-0001-7414-0397
Silvia CastillaDepartment of Radiology, HM Hospitales, 28050 Madrid, Spain.
Margarita FeyjooDepartment of Medical Oncology, Hospital Sanitas La Moraleja, 28050 Madrid, Spain.
Ana HiguerasDepartment of Gynecology and Obstetrics, Hospital Sanitas La Moraleja, 28050 Madrid, Spain.
Mario PrietoDepartment of Pathology, HM Hospitales, 28050 Madrid, Spain.
Ana Suarez-GauthierDepartment of Pathology, HM Hospitales, 28050 Madrid, Spain.
Lina Garcia-CañamaqueDepartment of Nuclear Medicine, HM Hospitales, 28050 Madrid, Spain.
Nieves EscolánDepartment of Plastic Surgery, HM Hospitales, 28050 Madrid, Spain.
Beatriz ÁlvarezDepartment of Radiation Oncology, HM Hospitales, 28050 Madrid, Spain.
Xin ChenDepartment of Radiation Oncology, HM Hospitales, 28050 Madrid, Spain.
Rosa AlonsoDepartment of Radiation Oncology, HM Hospitales, 28050 Madrid, Spain.
Mercedes LópezDepartment of Radiation Oncology, HM Hospitales, 28050 Madrid, Spain.
Ovidio HernandoDepartment of Radiation Oncology, HM Hospitales, 28050 Madrid, Spain.
Jeannette ValeroDepartment of Radiation Oncology, HM Hospitales, 28050 Madrid, Spain.
Emilio SánchezDepartment of Radiation Oncology, HM Hospitales, 28050 Madrid, Spain.
Eva CiruelosDepartment of Medical Oncology, HM Hospitales, 28050 Madrid, Spain.
Carmen RubioDepartment of Radiation Oncology, HM Hospitales, 28050 Madrid, Spain.
HM Hospitales · ESHospital General de La Rioja · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary systemic treatment (PST) downsizes the tumor and improves pathological response. The aim of this study is to analyze the feasibility and tolerance of primary concurrent radio−chemotherapy (PCRT) in breast cancer patients. Patients with localized TN/HER2+ tumors were enrolled in this prospective study. Radiation was delivered concomitantly during the first 3 weeks of chemotherapy, and it was based on a 15 fractions scheme, 40.5 Gy/2.7 Gy per fraction to whole breast and nodal levels I-IV. Chemotherapy (CT) was based on Pertuzumab−Trastuzumab−Paclitaxel followed by anthracyclines in HER2+ and CBDCA-Paclitaxel followed by anthracyclines in TN breast cancers patients. A total of 58 patients were enrolled; 25 patients (43%) were TN and 33 patients HER2+ (57%). With a median follow-up of 24.2 months, 56 patients completed PCRT and surgery. A total of 35 patients (87.5%) achieved >90% loss of invasive carcinoma cells in the surgical specimen. The 70.8% and the 53.1% of patients with TN and HER-2+ subtype, respectively, achieved complete pathological response (pCR). This is the first study of concurrent neoadjuvant treatment in breast cancer in which three strategies were applied simultaneously: fractionation of RT (radiotherapy) in 15 sessions, adjustment of CT to tumor phenotype and local planning by PET. The pCR rates are encouraging.

Indexed as

breast cancerchemoradiationneoadjuvantpathological responsepreoperativeTN/HER-2+ phenotype

Identifiers

PMID36139688
PMCPMC9496977
OpenAlexW4296462505

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.