Evidence map›Paper›PMID 30247203›Full record

ArticleMelanoma research2019

Patterns of treatment and BRAF testing with immune checkpoint inhibitors and targeted therapy in patients with metastatic melanoma presumed to be BRAF positive.

Sameer Ghate, Raluca Ionescu-Ittu, Rebecca Burne, Briana Ndife, François Laliberté, Antonio Nakasato, Mei Sheng Duh

Abstract read
In one paragraph

Article in Melanoma research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Observational
  2. Treatment patterns of melanoma byMelanoma management · 2019
    Article
  3. Review
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.

Sameer GhateNovartis Pharmaceuticals Corporation, East Hanover, New Jersey.
Raluca Ionescu-IttuGroupe d'analyse, Ltée, Montréal, Québec, Canada.
Rebecca BurneGroupe d'analyse, Ltée, Montréal, Québec, Canada.
Briana NdifeNovartis Pharmaceuticals Corporation, East Hanover, New Jersey.
François LalibertéGroupe d'analyse, Ltée, Montréal, Québec, Canada.
Antonio NakasatoNovartis Pharmaceuticals Corporation, East Hanover, New Jersey.
Mei Sheng DuhAnalysis Group Inc., Boston, Massachusetts, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with BRAF V600 (BRAF) mutated metastatic melanoma are eligible for therapy with both immune checkpoint inhibitors and targeted therapies, making treatment choice a complex decision. The present study aimed to describe patterns of treatment with immunotherapy and targeted therapy and BRAF testing in patients with metastatic melanoma presumed to have BRAF mutations (BRAF+) in the years following the approval of the newer generation of immune checkpoint inhibitors and targeted therapies (2014-2016). Two large US commercial claims databases [Truven Health Analytics MarketScan and IQVIA Real-World Data Adjudicated Claims - USA (IQVIA RWD Adjudicated Claims - USA)] were used. Patients were presumed BRAF+ if they received at least 2 lines of therapy of which at least 1 included targeted therapy. Sequence of lines of therapy and regimens used in first (1L), second (2L), and third (3L), as well as timing of BRAF testing by sequence of therapy were described. In the Truven sample (n=162), targeted therapy was used by 66% in 1L and by 54% in 2L, and 62% had a BRAF test; in the IQVIA RWD Adjudicated Claims - USA sample (n=247), targeted therapy was used by 62% in 1L and by 50% in 2L, and 68% had a BRAF test. Among those with a claim for a BRAF test prior to 1L, over two-thirds were initiated on targeted therapy. These findings suggest that the rate of BRAF testing remained low in the years following the approval of BRAF-targeted regimens for metastatic disease. Given the recently approved adjuvant treatment options for stage III melanoma, improving the rates of BRAF testing becomes increasingly important.

Indexed as

MutationAgedAntineoplastic Agents, ImmunologicalFemaleFollow-Up StudiesHumansImmunotherapyLymphatic MetastasisMaleMelanomaMiddle AgedMolecular Targeted TherapyPrognosisProto-Oncogene Proteins B-rafRetrospective StudiesSkin NeoplasmsAntineoplastic Agents, ImmunologicalBRAF protein, humanProto-Oncogene Proteins B-raf

Identifiers

PMID30247203
PMCPMC6494034

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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.