Evidence map›Paper›PMID 37092520›Full record

ArticleHematology reports2023

Utilization of Genomic Tumor Profiling in Pediatric Liquid Tumors: A Clinical Series.

Ishna Sharma, Min Ji Son, Shoaleh Motamedi, Alice Hoeft, Christa Teller, Tyler Hamby, Anish Ray

Open access · goldAbstract 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. 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

7 authors at 2 institutions in 1 country.

Ishna SharmaTexas College of Osteopathic Medicine, The University of North Texas Health Science Center, Fort Worth, TX 76107, USA.ORCID 0000-0002-1396-1754
Min Ji SonTexas College of Osteopathic Medicine, The University of North Texas Health Science Center, Fort Worth, TX 76107, USA.
Shoaleh MotamediTexas College of Osteopathic Medicine, The University of North Texas Health Science Center, Fort Worth, TX 76107, USA.
Alice HoeftDepartment of Hematology/Oncology, Cook Children's Medical Center, Fort Worth, TX 76104, USA.
Christa TellerDepartment of Hematology/Oncology, Cook Children's Medical Center, Fort Worth, TX 76104, USA.
Tyler HambyDepartment of Research Operations, Cook Children's Medical Center, Fort Worth, TX 76104, USA.
Anish RayTexas College of Osteopathic Medicine, The University of North Texas Health Science Center, Fort Worth, TX 76107, USA.ORCID 0000-0002-6349-1869
University of North Texas · USCook Children's Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hematologic tumors are mostly treated with chemotherapies that have poor toxicity profiles. While molecular tumor profiling can expand therapeutic options, our understanding of potential targetable drivers comes from studies of adult liquid tumors, which does not necessarily translate to efficacious treatment in pediatric liquid tumors. There is also no consensus on when profiling should be performed and its use in guiding therapies. We describe a single institution's experience in integrating profiling for liquid tumors. Pediatric patients diagnosed with leukemia or lymphoma and who underwent tumor profiling were retrospectively reviewed. Ten (83.3%) patients had relapsed disease prior to tumor profiling. Eleven (91.7%) patients had targetable alterations identified on profiling, and three (25%) received targeted therapy based on these variants. Of the three patients that received targeted therapy, two (66.7%) were living, and one (33.3%) decreased. For a portion of our relapsing and/or treatment-refractory patients, genetic profiling was feasible and useful in tailoring therapy to obtain stable or remission states. Practitioners may hesitate to deviate from the 'standard of therapy', resulting in the underutilization of profiling results. Prospective studies should identify actionable genetic variants found more frequently in pediatric liquid tumors and explore the benefits of proactive tumor profiling prior to the first relapse.

Indexed as

actionable genetic variantsleukemialymphomamolecular profilingtargeted therapy

Identifiers

PMID37092520
PMCPMC10123750
OpenAlexW4366593758

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.