Evidence map›Paper›PMID 37092519›Full record

ArticleHematology reports2023

Molecular Tumor Boards: The Next Step towards Precision Therapy in Cancer Care.

Angela Liu, Paige Vicenzi, Ishna Sharma, Kaci Orr, Christa Teller, Micha Koentz, Heidi Trinkman, Kelly Vallance, Anish Ray

Abstract read
In one paragraph

Article in Hematology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
–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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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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

9 authors.

Angela LiuTexas College of Osteopathic Medicine, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.ORCID 0000-0001-7902-538X
Paige VicenziDepartment of Pediatrics, Dell Children's Medical Center, Austin, TX 78723, USA.
Ishna SharmaTexas College of Osteopathic Medicine, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.ORCID 0000-0002-1396-1754
Kaci OrrTexas A&M Health Science Center School of Medicine, Bryan, TX 77807, USA.
Christa TellerDepartment of Pediatric Hematology/Oncology, Cook Children's Medical Center, Fort Worth, TX 76104, USA.
Micha KoentzDepartment of Pharmacy, Cook Children's Medical Center, Fort Worth, TX 76104, USA.
Heidi TrinkmanDepartment of Pharmacy, Cook Children's Medical Center, Fort Worth, TX 76104, USA.
Kelly VallanceDepartment of Pediatric Hematology/Oncology, Cook Children's Medical Center, Fort Worth, TX 76104, USA.
Anish RayDepartment of Pediatric Hematology/Oncology, Cook Children's Medical Center, Fort Worth, TX 76104, USA.ORCID 0000-0002-6349-1869

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The application of molecular tumor profiles in clinical decision making remains a challenge. To aid in the interpretation of complex biomarkers, molecular tumor boards (MTBs) have been established worldwide. In the present study, we show that a multidisciplinary approach is essential to the success of MTBs. Our MTB, consisting of pediatric oncologists, pathologists, and pharmacists, evaluated 115 cases diagnosed between March 2016 and September 2021. If targetable mutations were identified, pharmacists aided in the evaluation of treatment options based on drug accessibility. Treatable genetic alterations detected through molecular testing most frequently involved the cell cycle. For 85% of the cases evaluated, our MTB provided treatment recommendations based on the patient's history and results of molecular tumor testing. Only three patients, however, received MTB-recommended targeted therapy, and only one of these patients demonstrated an improved clinical outcome. For the remaining patients, MTB-recommended treatment often was not administered because molecular tumor profiling was not performed until late in the disease course. For the three patients who did receive MTB-recommended therapy, such treatment was not administered until months after diagnosis due to physician preference. Thus, the education of healthcare providers regarding the benefits of targeted therapy may increase acceptance of these novel agents and subsequently improve patient survival.

Indexed as

genetic profilingmolecular tumor boardpediatric oncologyprecision oncologytargeted therapy

Identifiers

PMID37092519
PMCPMC10123678

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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.