Evidence map›Paper›PMID 31203575›Full record

Observational studyClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2020

A retrospective, multicenter study of the efficacy of lapatinib plus trastuzumab in HER2-positive metastatic breast cancer patients previously treated with trastuzumab, lapatinib, or both: the Trastyvere study.

J Gavilá, J De La Haba, B Bermejo, Á Rodríguez-Lescure, A Antón, E Ciruelos, J Brunet, E Muñoz-Couselo, M Santisteban, C A Rodríguez Sánchez and 11 more

Abstract readMulticenter StudyObservational Study
PubMed Publisher
In one paragraph

Observational study in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. Observational
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. 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

21 authors at 16 institutions in 1 country.

J GaviláMedical Oncology Department, Instituto Valenciano de Oncología, Valencia, Spain.
J De La HabaMedical Oncology Department, Hospital Reina Sofía, Córdoba, Spain.
B BermejoMedical Oncology Department, Hospital Clínico Valencia, Valencia, Spain.
Á Rodríguez-LescureMedical Oncology Department, Hospital General Elche, Elche, Spain.
A AntónMedical Oncology Department, Hospital Miguel Servet, Zaragoza, Spain.
E CiruelosMedical Oncology Department, Hospital 12 de Octubre, Madrid, Spain.
J BrunetMedical Oncology Department, Institut Català D'Oncologia, Girona, Spain.
E Muñoz-CouseloMedical Oncology Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
M SantistebanMedical Oncology Department, Clínica Universidad de Navarra, Pamplona, Spain.
C A Rodríguez SánchezMedical Oncology Department, Hospital Universitario de Salamanca - IBSAL, Salamanca, Spain.
A SantaballaMedical Oncology Department, Hospital Universitari i Politècnic La Fe, Valencia, Spain.
P Sánchez RoviraMedical Oncology Department, Complejo Hospitalario de Jaén, Jaén, Spain.
J Á García SáenzMedical Oncology Department, Hospital Clínico San Carlos, Madrid, Spain.
M Ruiz-BorregoMedical Oncology Department, Hospital Universitario Virgen del Rocío, Sevilla, Spain.
A L Guerrero-ZotanoMedical Oncology Department, Instituto Valenciano de Oncología, Valencia, Spain.
M HuertaMedical Oncology Department, Hospital Clínico Valencia, Valencia, Spain.
A Cotes-SanchísMedical Oncology Department, Hospital General Elche, Elche, Spain.
J Lao RomeraMedical Oncology Department, Hospital Miguel Servet, Zaragoza, Spain.
E AguirreMedical Oncology Department, Hospital de Día QuirónSalud, Zaragoza, Spain.
J CortésVall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
A Llombart-CussacMedica Scientia Innovation Research (MedSIR), Barcelona, Spain. antonio.llombart@medsir.org.
Fundación Instituto Valenciano de Oncología · ESHospital Clínico Universitario de Valencia · ESHospital General Universitario de Elche · ESHospital Universitario Miguel Servet · ESMedSIR (Spain) · ESClinica Universidad de Navarra · ESComplejo Hospitalario de Jaén · ESHospital Clínico San Carlos · ESHospital Quirónsalud Barcelona · ESHospital Universitari i Politècnic La Fe · ESHospital Universitario Reina Sofía · ESHospital Universitario Virgen del Rocío · ESInstitut Català d'Oncologia · ESInstituto de Investigación Biomédica de Salamanca · ESResearch Institute Hospital 12 de Octubre · ESVall d'Hebron Hospital Universitari · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo evaluate the efficacy and safety of lapatinib (L) and trastuzumab (T) combination in HER2-positive metastatic breast cancer (MBC) patients previously treated with T and/or L. MATERIALS AND

methodsWe conducted a retrospective, post-authorized, multicenter study including patients with HER2-positive MBC or locally advanced breast cancer (ABC) treated with the combination of L-T. Concomitant endocrine therapy, as well as brain metastasis and/or prior exposure to L, were allowed.

resultsOne hundred and fifteen patients from 14 institutions were included. The median age was 59.8 years. The median number of prior T regimens in the advanced setting was 3 and 73 patients had received a prior L regimen. The clinical benefit rate (CBR) was 34.8% (95% CI 26.1-43.5). Among other efficacy endpoints, the overall response rate was 21.7%, and median progression-free survival (PFS) and overall survival were 3.9 and 21.6 months, respectively. Heavily pretreated and ≥ 3 metastatic organ patients showed lower CBR and PFS than patients with a low number of previous regimens and < 3 metastatic organs. Moreover, CBR did not significantly change in L-pretreated compared with L-naïve patients (31.5% versus 40.5% for L-pretreated versus L-naïve). Grade 3/4 adverse events were reported in 19 patients (16.5%).

conclusionThe combination of L-T is an effective and well-tolerated regimen in heavily pretreated patients and remains active among patients progressing on prior L-based therapy. Our study suggests that the L-T regimen is a safe and active chemotherapy-free option for MBC patients previously treated with T and/or L.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesFemaleHumansLapatinibMiddle AgedNeoplasm MetastasisProtein Kinase InhibitorsRetrospective StudiesSpainTrastuzumabTreatment OutcomeERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesLapatinibProtein Kinase InhibitorsTrastuzumabDual HER2 blockadeHuman epidermal growth factor receptor 2 positiveLapatinibMetastatic breast cancerTrastuzumabTyrosine kinase inhibitor

Identifiers

PMID31203575
OpenAlexW2952905991

What OpenQuestion holds

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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.