Evidence map›Paper›PMID 32817059›Full record

ArticleESMO open2020

Clinical outcomes of patients with breast cancer relapsing after (neo)adjuvant trastuzumab and receiving trastuzumab rechallenge or lapatinib-based therapy: a multicentre retrospective cohort study.

Eva Blondeaux, Arlindo R Ferreira, Francesca Poggio, Fabio Puglisi, Claudia Bighin, Federico Sottotetti, Filippo Montemurro, Elena Poletto, Antonella Lai, Valentina Sini and 7 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in ESMO open, 2020. 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
0.3field-weighted citation impact, top 39% 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, 8 citations in OpenAlex.

  1. Article
  2. Observational
  3. Article
  4. Review
  5. 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 9 institutions in 2 countries.

Eva BlondeauxU.O.S.D. Breast Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Arlindo R FerreiraBreast Unit, Champalimaud Clinical Center, Champalimaud Foundation, Lisbon, Portugal.
Francesca PoggioU.O.S.D. Breast Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.ORCID 0000-0002-4518-2827
Fabio PuglisiDepartment of Medical Oncology, IRCCS Centro di Riferimento Oncologico, Aviano, Italy.ORCID 0000-0003-0573-4938
Claudia BighinU.O.S.D. Breast Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Federico SottotettiUnità Dipartimentale di Oncologia Medica, Fondazione Salvatore Maugeri IRCCS, Pavia, Italy.
Filippo MontemurroDay Hospital Oncologico Multidisciplinare, Istituto di Candiolo FPO-IRCCS, Candiolo, Italy.
Elena PolettoDepartment of Oncology, University of Udine, Udine, Italy.
Antonella LaiOncologia Medica, Azienda Ospedaliera Universitaria di Sassari, Sassari, Italy.
Valentina SiniU.O. Centro Oncologico S. Spirito-Nuovo Regina Margherita, ASL Roma 1, Rome, Italy.
Gabriele MinutiDepartment of Oncology and Hematology, AUSL Romagna, Ravenna, Italy.
Silvia MuraU.O.C. Medical Oncology, Ospedale Civile Santissima Annunziata, Sassari, Italy.
Andrea FontanaPolo Oncologico, Azienda Ospedaliero Universitaria Pisana, Pisa, Italy.
Piero FregattiDepartment of Surgical Oncology, U.O. Chirurgia Senologica, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Barbara CardinaliU.O.S.D. Breast Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Matteo LambertiniDepartment of Medical Oncology, U.O. Clinica di Oncologia Medica, IRCCS Ospedale Policlinico San Martino, Genova, Italy.ORCID 0000-0003-1797-5296
Lucia Del MastroU.O.S.D. Breast Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy lucia.delmastro@hsanmartino.it.ORCID 0000-0002-9546-5841
Ospedale Policlinico San Martino · ITUniversity of Udine · ITAzienda Ospedaliera Universitaria Pisana · ITAzienda Ospedaliero Universitaria di Sassari · ITAzienda Unità Sanitaria Locale Della Romagna · ITCandiolo Cancer Institute · ITChampalimaud Foundation · PTFondazione Salvatore Maugeri · ITOspedale SS. Annunziata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn the prepertuzumab era, we evaluated the clinical outcomes of patients with human epidermal growth factor receptor 2 (HER2)-positive metastatic breast cancer who underwent first-line trastuzumab-based or lapatinib-based therapy according to prior exposure to (neo)adjuvant trastuzumab. MATERIALS AND

methodsIn this multicentre retrospective cohort study conducted in 14 Italian centres of the Gruppo Italiano Mammella, consecutive patients undergoing first-line trastuzumab or lapatinib-based therapy were included. Analyses were performed according to the type of first-line therapy for metastatic disease (trastuzumab or lapatinib). Dichotomous clinical outcomes were analysed using logistic regression and time-to-event outcomes using Cox proportional hazard models controlling for relevant demographic, clinicopathological and therapy characteristics.

resultsOut of 450 patients included in the study, 416 (92%) received trastuzumab and 34 (7.5%) lapatinib. As compared with the trastuzumab cohort, more patients in the lapatinib cohort had a trastuzumab-free interval <1 month (37% vs 13.9%; p=0.017) and brain metastasis as first site of relapse (38.2% vs 9.4%; p<0.001). Among the 128 patients who relapsed after prior (neo)adjuvant trastuzumab, 101 (78.9%) received first-line trastuzumab and 27 (21.1%) first-line lapatinib. The following outcomes were observed with first-line lapatinib or trastuzumab, respectively: overall response rate 45.5% vs 61.3% (p=0.184), clinical benefit rate 68.2% vs 72.5% (p=0.691), median progression-free survival (PFS) 11.4 vs 12.0 months (p=0.814) and median overall survival (OS) 34.7 vs 48.2 months (p=0.722). In patients with brain metastasis as first site of relapse, median PFS was 12.2 vs 9.9 months (p=0.093) and median OS 33.7 vs 28.5 months (p=0.280), respectively.

conclusionsIn patients with HER2-positive breast cancer relapsing after prior (neo)adjuvant trastuzumab, first-line treatment with trastuzumab or lapatinib was not associated with a significant difference in the clinical outcomes. A non-significant trend favouring the use of lapatinib was observed in patients with brain metastasis as the first site of relapse.

Indexed as

Breast NeoplasmsAdultAntineoplastic Combined Chemotherapy ProtocolsChemotherapy, AdjuvantDisease-Free SurvivalErb-b2 Receptor Tyrosine KinasesFemaleHumansItalyLapatinibMiddle AgedNeoplasm Recurrence, LocalQuinazolinesRetrospective StudiesTrastuzumabTreatment OutcomeErb-b2 Receptor Tyrosine KinasesLapatinibQuinazolinesTrastuzumabfirst-line therapyHER2-positivelapatinibmetastatic breast cancertrastuzumab

Identifiers

PMID32817059
PMCPMC7437709
OpenAlexW3070707351

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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.