Evidence map›Paper›PMID 35787784›Full record

Trial reporteLife2022

Genomic landscape of lymphatic malformations: a case series and response to the PI3Kα inhibitor alpelisib in an

Montaser F Shaheen, Julie Y Tse, Ethan S Sokol, Margaret Masterson, Pranshu Bansal, Ian Rabinowitz, Christy A Tarleton, Andrey S Dobroff, Tracey L Smith, Thèrése J Bocklage and 9 more

Registry-linked trialOpen access · goldAbstract readClinical Trial
In one paragraph

Trial report in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03941782 (INST UNM 1601), which is not on this map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.8field-weighted citation impact, top 9% 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.

NCT03941782 no longer availablenot on this map

INST UNM 1601: Compassionate Use of BYL 719 Alpelisib

Typeexpanded_accessSponsorNew Mexico Cancer Research AllianceConditionsLymphangiomaArmsAlpelisib
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Targeted Therapies for Slow-Flow Vascular Malformations.The Australasian journal of dermatology · 2025
    Review
  5. Review
  6. Molecular landscape and classification of vascular anomalies.Hematology. American Society of Hematology. Education Program · 2024
    Review
  7. Review
  8. Updates in Genetic Testing for Head and Neck Vascular Anomalies.Oral and maxillofacial surgery clinics of North America · 2024
    Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. 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

19 authors at 6 institutions in 2 countries.

Montaser F Shaheen *University of Arizona Cancer Center, Tucson, United States.
Julie Y Tse *Foundation Medicine, Inc, Cambridge, United States.
Ethan S SokolFoundation Medicine, Inc, Cambridge, United States.
Margaret MastersonRutgers Cancer Institute of New Jersey, New Brunswick, United States.
Pranshu BansalUniversity of New Mexico Comprehensive Cancer Center, Albuquerque, United States.
Ian RabinowitzUniversity of New Mexico Comprehensive Cancer Center, Albuquerque, United States.
Christy A TarletonUniversity of New Mexico Comprehensive Cancer Center, Albuquerque, United States.
Andrey S DobroffUniversity of New Mexico Comprehensive Cancer Center, Albuquerque, United States.ORCID 0000-0003-2162-9951
Tracey L SmithRutgers Cancer Institute of New Jersey, Newark, United States.
Thèrése J BocklageUniversity of New Mexico Comprehensive Cancer Center, Albuquerque, United States.
Brian K MannakeeUniversity of Arizona Cancer Center, Tucson, United States.
Ryan N GutenkunstUniversity of Arizona Cancer Center, Tucson, United States.ORCID 0000-0002-8659-0579
Joyce BischoffVascular Biology Program, Boston Children's Hospital, Boston, United States.ORCID 0000-0002-6367-1974
Scott A NessUniversity of New Mexico Comprehensive Cancer Center, Albuquerque, United States.
Gregory M RiedlingerRutgers Cancer Institute of New Jersey, New Brunswick, United States.
Roman GroisbergRutgers Cancer Institute of New Jersey, New Brunswick, United States.
Renata PasqualiniRutgers Cancer Institute of New Jersey, Newark, United States.
Shridar GanesanRutgers Cancer Institute of New Jersey, New Brunswick, United States.
Wadih ArapRutgers Cancer Institute of New Jersey, Newark, United States.ORCID 0000-0002-8686-4584
Rutgers, The State University of New Jersey · USUniversity of New Mexico · USUniversity of Arizona · USEmergency Medicine Foundation · USBoston Children's Hospital · USUniversity of Kentucky · US

Funding

VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Dan Theodorescu · 1985 to 2026
$110.2M
TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Tracie Saunders · 1997 to 2026
$94.5M
WOMEN'S CANCERS RESEARCH PROGRAMP30CA118100 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Yolanda Sanchez · 2005 to 2026
$57.1M
NCI NIH HHS P30 CA023074NCI NIH HHS P30 CA072720NCI NIH HHS P30 CA118100
6 · The paper itself

Abstract

Background: Lymphatic malformations (LMs) often pose treatment challenges due to a large size or a critical location that could lead to disfigurement, and there are no standardized treatment approaches for either refractory or unresectable cases. Methods: We examined the genomic landscape of a patient cohort of LMs ( Results: These LMs had low mutational burden with hotspot Conclusions: Our findings establish that LM patients with conventional or kaposiform histology have distinct, yet targetable, driver mutations. Funding: R.P. and W.A. are supported by awards from the Levy-Longenbaugh Fund. S.G. is supported by awards from the Hugs for Brady Foundation. This work has been funded in part by the NCI Cancer Center Support Grants (CCSG; P30) to the University of Arizona Cancer Center (CA023074), the University of New Mexico Comprehensive Cancer Center (CA118100), and the Rutgers Cancer Institute of New Jersey (CA072720). B.K.M. was supported by National Science Foundation via Graduate Research Fellowship DGE-1143953. Clinical trial number: NCT03941782.

Indexed as

Antineoplastic AgentsClass I Phosphatidylinositol 3-KinasesGTP PhosphohydrolasesLymphangiomaLymphatic AbnormalitiesMembrane ProteinsThiazolesClass Ia Phosphatidylinositol 3-KinaseEndothelial CellsGenomicsHigh-Throughput Nucleotide SequencingHumansImmunohistochemistryMutationSequence Analysis, DNAAlpelisibAntineoplastic AgentsClass Ia Phosphatidylinositol 3-KinaseClass I Phosphatidylinositol 3-KinasesGTP PhosphohydrolasesMembrane ProteinsNRAS protein, humanPIK3CA protein, humanThiazolesgenomicshumanlymphatic malformationsmedicineNGSPI3Kα

Identifiers

PMID35787784
PMCPMC9255965
OpenAlexW4283820964

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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 Socratic graph.