Evidence map›Paper›PMID 37441419›Full record

ArticleFrontiers in oncology2023

Pathologic response and survival after neoadjuvant chemotherapy with or without pertuzumab in patients with HER2-positive breast cancer: the Neopearl nationwide collaborative study.

Agnese Fabbri, Fabrizio Nelli, Andrea Botticelli, Diana Giannarelli, Eleonora Marrucci, Cristina Fiore, Antonella Virtuoso, Simone Scagnoli, Simona Pisegna, Daniele Alesini and 16 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. 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

26 authors at 11 institutions in 1 country.

Agnese FabbriDepartment of Oncology and Hematology, Medical Oncology and Breast Unit, Central Hospital of Belcolle, Viterbo, Italy.
Fabrizio NelliDepartment of Oncology and Hematology, Medical Oncology and Breast Unit, Central Hospital of Belcolle, Viterbo, Italy.
Andrea BotticelliDepartment of Radiological, Oncological and Pathological Science, Sapienza University of Rome, Rome, Italy.
Diana GiannarelliBiostatistics Unit, Scientific Directorate, Fondazione Policlinico Universitario A. Gemelli, IRCCS, Rome, Italy.
Eleonora MarrucciDepartment of Oncology and Hematology, Medical Oncology and Breast Unit, Central Hospital of Belcolle, Viterbo, Italy.
Cristina FioreDepartment of Oncology and Hematology, Medical Oncology and Breast Unit, Central Hospital of Belcolle, Viterbo, Italy.
Antonella VirtuosoDepartment of Oncology and Hematology, Medical Oncology and Breast Unit, Central Hospital of Belcolle, Viterbo, Italy.
Simone ScagnoliDepartment of Radiological, Oncological and Pathological Science, Sapienza University of Rome, Rome, Italy.
Simona PisegnaDepartment of Radiological, Oncological and Pathological Science, Sapienza University of Rome, Rome, Italy.
Daniele AlesiniUOSD Centro Oncologico S. Spirito e Nuovo Regina Margherita (SS-NRM), Ospedale Santo Spirito in Sassia, Rome, Italy.
Valentina SiniUOSD Centro Oncologico S. Spirito e Nuovo Regina Margherita (SS-NRM), Ospedale Santo Spirito in Sassia, Rome, Italy.
Armando OrlandiDepartment of Medical Oncology, Comprehensive Cancer Center, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Alessandra FabiPrecision Medicine Breast Unit, Scientific Directorate, Department of Women, Children and Public Health Sciences, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Federico PiacentiniDepartment of Medical Oncology, University Hospital of Modena, Modena, Italy.
Luca MoscettiDepartment of Medical Oncology, University Hospital of Modena, Modena, Italy.
Giuliana D'AuriaDepartment of Medical Oncology, Medical Oncology Unit, Sandro Pertini Hospital, Rome, Italy.
Teresa GamucciDepartment of Medical Oncology, Medical Oncology Unit, Sandro Pertini Hospital, Rome, Italy.
Marco MazzottaDepartment of Medical Oncology, Medical Oncology Unit, Sandro Pertini Hospital, Rome, Italy.
Laura PizzutiUOSD Sperimentazioni di fase IV, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Patrizia ViciUOSD Sperimentazioni di fase IV, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Elisabetta CretellaDepartment of Medical Oncology, Medical Oncology Unit, Ospedale Di Bolzano, Azienda Sanitaria Alto Adige, Bolzano, Italy.
Paola ScavinaDepartment of Medical Oncology, Medical Oncology Unit, San Giovanni Addolorata Hospital, Rome, Italy.
Annalisa La CesaDepartment of Medical Oncology, Campus Bio-Medico University, Rome, Italy.
Mara PersanoDepartment of Medical Oncology, University Hospital and University of Cagliari, Cagliari, Italy.
Francesco AtzoriDepartment of Medical Oncology, University Hospital and University of Cagliari, Cagliari, Italy.
Enzo Maria RuggeriDepartment of Oncology and Hematology, Medical Oncology and Breast Unit, Central Hospital of Belcolle, Viterbo, Italy.
Ospedale di Belcolle · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITOspedale Sandro Pertini · ITSapienza University of Rome · ITAgostino Gemelli University Polyclinic · ITOspedale di Santo Spirito · ITUniversity of Cagliari · ITUniversity of Modena and Reggio Emilia · ITAzienda Ospedaliera San Giovanni Addolorata · ITOspedale di Bolzano · ITUniversità Campus Bio-Medico · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Clinical trials have shown a significant increase in pathologic complete response (pCR) with the addition of pertuzumab to neoadjuvant chemotherapy for patients with early-stage HER-2 positive breast cancer. To date, limited studies have examined comparative outcomes of neoadjuvant pertuzumab in real-world setting. The Neopearl study aimed to assess comparative real-life efficacy and safety of neoadjuvant pertuzumab for these patients. Methods: We conducted a nationwide retrospective analysis involving 17 oncology facilities with a certified multidisciplinary breast cancer treatment committee. We identified patients with HER-2 positive stage II-III breast cancer treated with neoadjuvant chemotherapy based on trastuzumab and taxanes with or without pertuzumab. All patients underwent breast surgery and received a comprehensive cardiologic evaluation at baseline and after neoadjuvant treatment. Patients who received the combination of pertuzumab, trastuzumab, and chemotherapy constituted case cohort (PTCT), whereas those treated with trastuzumab and chemotherapy accounted for control cohort (TCT). The pCR rate and 5-year event free survival (EFS) were the primary outcomes. Secondary end-points were rates of conversion from planned modified radical mastectomy (MRM) to breast conservation surgery (BCS) and cardiotoxicities. Results: From March 2014 to April 2021, we included 271 patients, 134 (49%) and 137 (51%) in TCT and PTCT cohort, respectively. Positive axillary lymph nodes and stage III were more frequent in PTCT cohort. The pCR rate was significantly increased in patients who received pertuzumab (49% vs 62%; OR 1.74, 95%CI 1.04-2.89) and with HER-2 enriched subtypes (16% vs 85%; OR 2.94, 95%CI 1.60-5.41). After a median follow-up of 5 years, the 5-year EFS was significantly prolonged only in patients treated with pertuzumab (81% vs 93%; HR 2.22, 95%CI 1.03-4.79). The same analysis performed on propensity score matched population showed concordant results. On univariate analysis, only patients with positive lymph nodes were found to benefit from pertuzumab for both pCR and 5-year EFS. The rates of conversion from MRM to BCS and cardiologic toxicities did not differ between the cohorts. Conclusion: Our findings support previous data on improved outcomes with the addition of pertuzumab to trastuzumab-based neoadjuvant chemotherapy. This benefit seems to be more significant in patients with clinically positive lymph nodes.

Indexed as

breast cancerHER-2 positiveneoadjuvant chemotherapypertuzumabreal-world datatrastuzumab

Identifiers

PMID37441419
PMCPMC10335743
OpenAlexW4382451260

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.