Evidence map›Paper›PMID 33305268›Full record

ArticleNeuro-oncology advances

HER2-targeted therapy prolongs survival in patients with HER2-positive breast cancer and intracranial metastatic disease: a systematic review and meta-analysis.

Anders W Erickson, Farinaz Ghodrati, Steven Habbous, Katarzyna J Jerzak, Arjun Sahgal, Manmeet S Ahluwalia, Sunit Das

Open access · goldAbstract read
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Article in Neuro-oncology advances. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

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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

7 authors at 6 institutions in 2 countries.

Anders W EricksonInstitute of Medical Science, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-6134-7812
Farinaz GhodratiInstitute of Medical Science, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-5853-5564
Steven HabbousOntario Health (Cancer Care Ontario), Toronto, Ontario, Canada.ORCID 0000-0002-9650-9105
Katarzyna J JerzakDivision of Medical Oncology, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.ORCID 0000-0002-3995-0308
Arjun SahgalDepartment of Radiation Oncology, Sunnybrook Hospital, Toronto, Ontario, Canada.ORCID 0000-0001-7991-8970
Manmeet S AhluwaliaBurkhardt Brain Tumor and Neuro-Oncology Center, Cleveland Clinic, Cleveland, Ohio, USA.ORCID 0000-0003-3794-9511
Sunit DasInstitute of Medical Science, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-2146-4168
University of Toronto · CACancer Care Ontario · CACleveland Clinic · USSt. Michael's Hospital · CASunnybrook Health Science Centre · CASunnybrook Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntracranial metastatic disease (IMD) is a serious and known complication of human epidermal growth factor receptor 2 (HER2)-positive breast cancer. The role of targeted therapy for patients with HER2-positive breast cancer and IMD remains unclear. In this study, we sought to evaluate the effect of HER2-targeted therapy on IMD from HER2-positive breast cancer.

methodsWe searched MEDLINE, EMBASE, CENTRAL, and gray literature sources for interventional and observational studies reporting survival, response, and safety outcomes for patients with IMD receiving HER2-targeted therapy. We pooled outcomes through meta-analysis and examined confounder effects through forest plot stratification and meta-regression. Evidence quality was evaluated using GRADE (PROSPERO CRD42020161209).

resultsA total of 97 studies (37 interventional and 60 observational) were included. HER2-targeted therapy was associated with prolonged overall survival (hazard ratio [HR] 0.47; 95% confidence interval [CI], 0.39-0.56) without significantly prolonged progression-free survival (HR 0.52; 95% CI, 0.27-1.02) versus non-targeted therapy; the intracranial objective response rate was 19% (95% CI, 12-27%), intracranial disease control rate 62% (95% CI, 55-69%), intracranial complete response rate 0% (95% CI, 0-0.01%), and grade 3+ adverse event rate 26% (95% CI, 11-45%). Risk of bias was high in 40% (39/97) of studies.

conclusionThese findings support a potential role for systemic HER2-targeted therapy in the treatment of patients with IMD from HER2-positive metastatic breast cancer.

Indexed as

brain metastasesbreast cancerHER2/neumolecular targeted therapy

Identifiers

PMID33305268
PMCPMC7720818
OpenAlexW3111168177

What OpenQuestion 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 OpenQuestion graph.