Evidence map›Paper›PMID 24156028›Full record

ArticleCancer medicine2013

Management and outcome of 239 adolescent and adult rhabdomyosarcoma patients.

Sarah N Dumont, Dejka M Araujo, Mark F Munsell, Jason A Salganick, Amaury G Dumont, Kevin A Raymond, Claude Linassier, Shreyaskumar Patel, Robert S Benjamin, Jonathan C Trent

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Pleomorphic rhabdomyosarcoma in adults: a case report.Journal of medical case reports · 2025
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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

10 authors at 4 institutions in 2 countries.

Sarah N DumontHematology Oncology Department Sylvester Comprehensive Cancer Center, University of Miami Miami, Florida ; Department of Sarcoma Medical Oncology MD Anderson Cancer Center, University of Texas Houston, Texas.
Dejka M Araujo
Mark F Munsell
Jason A Salganick
Amaury G Dumont
Kevin A Raymond
Claude Linassier
Shreyaskumar Patel
Robert S Benjamin
Jonathan C Trent
The University of Texas Health Science Center at Houston · USThe University of Texas MD Anderson Cancer Center · USSylvester Comprehensive Cancer Center · USUniversité de Tours · FR

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Mechanism/activity/resistance/Gleevec/GI stromal tumors (K23M)K23CA109060 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI TRENT, JONATHAN C · 2004 to 2008
$680k
NCI NIH HHS 1K23CA109060-05NCI NIH HHS CA016672NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Adult rhabdomyosarcoma (RMS) is a rare tumor that has inferior outcome compared to younger patient population. The present work aims to study the age-related differences in management of adolescents and adults with RMS. Under an institutional review board-approved protocol, we retrospectively analyzed 239 patients, 10 years of age and greater, diagnosed with RMS at MD Anderson Cancer Center from 1957 through 2003. Of the 239 patients, 163 patients were nonmetastatic with a median overall survival (OS) of 3.8 years (95% CI 2.8-7.6). In the multivariate analysis, age >50 was significantly associated with shorter OS and recurrence-free survival (RFS) for primary patients. Metastases were present in 76 patients, the median OS was 1.4 years. Approximately 13% of metastatic patients <50 years old had a long-term survival exceeding 15 years. Multimodality therapy, including surgery, radiotherapy, and chemotherapy was significantly associated with longer OS in primary and metastatic patients. Use of bi- and triple modality treatment decreased in metastatic patients over 50 years of age compared to younger patients. RMS in adolescents and adults has a poor outcome compared with younger individuals. Increased use of multidisciplinary therapy may improve older patient clinical outcome.

Indexed as

AdolescentAdultAgedAge FactorsCombined Modality TherapyFemaleHumansMaleMiddle AgedNeoplasm MetastasisNeoplasm StagingRetrospective StudiesRhabdomyosarcomaRisk FactorsTreatment OutcomeYoung AdultAdolescentadultagemultimodality treatmentrhabdomyosarcoma

Identifiers

PMID24156028
PMCPMC3799290
OpenAlexW1963743043

What OpenQuestion holds

Textmetadata
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.