Evidence map›Paper›PMID 30319330›Full record

ReviewBreast care (Basel, Switzerland)2018

Late Administration of Trastuzumab Emtansine Might Lead to Loss of Chance for Better Outcome in Patients with HER2-Positive Metastatic Breast Cancer.

Luis Manso, Alfonso Sanchez-Muñoz, Isabel Calvo, Yann Izarzugaza, Jessica Plata, Cesar Rodriguez

Abstract readReview
In one paragraph

Review in Breast care (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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. Observational
  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

6 authors.

Luis MansoMedical Oncology Department, 12 de Octubre University Hospital, Madrid, Spain.
Alfonso Sanchez-MuñozClinical and Translational Cancer Research, Biomedical Research Institute of Málaga (IBIMA), Regional and Virgen de la Victoria University Hospital, Málaga, Spain.
Isabel CalvoMedical Oncology Department, HM Sanchinarro University Hospital, Madrid, Spain.
Yann IzarzugazaMedical Oncology Department, Fundación Jiménez Díaz University Hospital, Madrid, Spain.
Jessica PlataMedical Oncology Department, Jaen University Hospital Complex, Jaén, Spain.
Cesar RodriguezMedical Oncology Department, Salamanca Clinic University Hospital, Salamanca, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The optimal sequence of anti-human epidermal growth factor receptor 2 (HER2) therapies in metastatic breast cancer (MBC) is still undetermined. Physicians must therefore make decisions based on clinical trials and their own experience for the best treatment sequence in these patients. The objective of this review is to summarize the efficacy and safety data for trastuzumab emtansine (T-DM1) in patients with MBC. Additionally, the concept of 'loss of chance for a better outcome' is investigated. It applies to patients who are not receiving the best possible treatment for their disease. Physicians should strive to offer the best possible care, although getting optimal results in each individual patient is not guaranteed. Lastly, the number of patients with MBC lost per treatment line is evaluated. We conclude that both concepts reinforce the importance of giving the most active treatments as soon as possible in the course of disease to secure the longest possible survival for HER2-positive MBC patients.

Indexed as

Antineoplastic agentsHER2-positiveLoss of chanceMetastatic breast cancerOncologistsTrastuzumab emtansine

Identifiers

PMID30319330
PMCPMC6170918

What OpenQuestion holds

Textmetadata
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.