Evidence map›Paper›PMID 35448196›Full record

ReviewCurrent oncology (Toronto, Ont.)2022

Novel Therapies for the Treatment of HER2-Positive Advanced Breast Cancer: A Canadian Perspective.

Cristiano Ferrario, Anna Christofides, Anil Abraham Joy, Kara Laing, Karen Gelmon, Christine Brezden-Masley

Open access · goldAbstract readReview
In one paragraph

Review in Current oncology (Toronto, Ont.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Personalized treatment approach for HER2-positive metastatic breast cancer.Medical oncology (Northwood, London, England) · 2024
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Third-line treatment patterns in HER2-positive metastatic breast cancer: a retrospective analysis of real-world data in Canada.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2023
    Article
  9. 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 at 6 institutions in 1 country.

Cristiano FerrarioDepartment of Oncology, McGill University, Montreal, QC H3A OG4, Canada.
Anna ChristofidesIMPACT Medicom Inc., Toronto, ON M6S 3K2, Canada.ORCID 0000-0001-6421-8728
Anil Abraham JoyDepartment of Oncology, University of Alberta, Edmonton, AB T6G 2R3, Canada.
Kara LaingFaculty of Medicine, Cancer Care Program, Memorial University, St. John's, NL A1B 3V6, Canada.
Karen GelmonDepartment of Medical Oncology, University of British Columbia, Vancouver, BC V6T 1Z4, Canada.
Christine Brezden-MasleyDepartment of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada.
Fluidigm (Canada) · CAJewish General Hospital · CAMemorial University of Newfoundland · CAMount Sinai Hospital · CAUniversity of Alberta · CAUniversity of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The advent of anti-HER2 targeted therapies has dramatically improved the outcome of HER2-positive breast cancer; however, resistance to treatment in the metastatic setting remains a challenge, highlighting the need for novel therapies. The arrival of new treatment options and clinical trials examining the efficacy of novel agents may improve outcomes in the metastatic setting, including in patients with brain metastases. In the first-line setting, we can potentially cure a selected number of patients treated with pertuzumab + trastuzumab + taxane. In the second-line setting, clinical trials show that trastuzumab deruxtecan (T-DXd) is a highly effective option, resulting in a shift from trastuzumab emtansine (T-DM1) as the previous standard of care. Moreover, we now have data for patients with brain metastases to show that tucatinib + trastuzumab + capecitabine can improve survival in this higher-risk group and be an effective regimen for all patients in the third-line setting. Finally, we have a number of effective anti-HER2 therapies that can be used in subsequent lines of therapy to improve patient outcomes. This review paper discusses the current treatment options and presents a practical treatment sequencing algorithm in the context of the Canadian landscape.

Indexed as

Brain NeoplasmsBreast NeoplasmsAdo-Trastuzumab EmtansineAntineoplastic Combined Chemotherapy ProtocolsCanadaErb-b2 Receptor Tyrosine KinasesFemaleHumansTrastuzumabAdo-Trastuzumab EmtansineErb-b2 Receptor Tyrosine KinasesTrastuzumabbreast cancerHER2human epidermal growth factor receptor 2oncology

Identifiers

PMID35448196
PMCPMC9026432
OpenAlexW4224091336

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.