Evidence map›Paper›PMID 34913555›Full record

ArticlePediatric blood & cancer2022

Phenotypic similarities within the morphologic spectrum of DICER1-associated sarcomas and pleuropulmonary blastoma: Histopathologic features guide diagnosis in the LMIC setting.

Paromita Roy, Anirban Das, Angad Singh, Joyshree Panda, Arpita Bhattacharya, Anisha Gehani, Mayur Parihar, Reghu K S, Rimpa Achari, Rita Alaggio and 4 more

Open access · greenAbstract read
In one paragraph

Article in Pediatric blood & cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

0 citing papers in PubMed, 7 citations in OpenAlex.

No citing paper in PubMed yet.

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

14 authors at 5 institutions in 3 countries.

Paromita RoyDepartment of Pathology, Tata Medical Center, Kolkata, West Bengal, India.ORCID 0000-0003-0379-5999
Anirban DasDepartment of Pediatric Oncology, Tata Medical Center, Kolkata, West Bengal, India.ORCID 0000-0001-7653-9529
Angad SinghDepartment of Pathology, Tata Medical Center, Kolkata, West Bengal, India.
Joyshree PandaDepartment of Pathology, Tata Medical Center, Kolkata, West Bengal, India.
Arpita BhattacharyaDepartment of Pediatric Oncology, Tata Medical Center, Kolkata, West Bengal, India.
Anisha GehaniDepartment of Radiology, Tata Medical Center, Kolkata, West Bengal, India.
Mayur PariharDepartment of Cytogenetics, Tata Medical Center, Kolkata, West Bengal, India.
Reghu K SDepartment of Pediatric Oncology, Tata Medical Center, Kolkata, West Bengal, India.
Rimpa AchariDepartment of Radiation Oncology, Tata Medical Center, Kolkata, West Bengal, India.
Rita AlaggioIRCCS Ospedale Pediatrico Bambino Gesu, Rome, Italy.
Amanda FieldResourcePath LLC, Sterling, Virginia, USA.
D Ashley HillResourcePath LLC, Sterling, Virginia, USA.
Louis P DehnerLauren V. Ackerman Laboratory of Surgical Pathology, Department of Pathology and Immunology, Washington University Medical Center, St. Louis, Missouri, USA.
Kris Ann P SchultzInternational Pleuropulmonary Blastoma/DICER1 Registry, Children's Hospitals and Clinics of Minnesota, Minneapolis, Minnesota, USA.
Tata Medical Center · INChildren’s Minnesota - St. Paul Hospital · USChildren's National · USUniversity of Padua · ITWashington University Medical Center · US

Funding

DICER1 and the Pleuropulmonary Blastoma Family Cancer SyndromeR01CA143167 · NCI · CHILDREN'S RESEARCH INSTITUTE · PI HILL, DANA ASHLEY · 2010 to 2020
$3.7M
Detecting DICER1: A global partnership to cure pediatric lung cancerR37CA244940 · NCI · CHILDREN'S HOSPITALS AND CLINICS · PI Kris Ann Pinekenstein Schultz · 2020 to 2026
$2.4M
NCI NIH HHS R01 CA143167NCI NIH HHS R37 CA244940
6 · The paper itself

Abstract

Extrapulmonary DICER1-associated sarcomas (DS) can harbor morphological features overlapping with pleuropulmonary blastoma. We report three children with intracranial and genital tract sarcomas, suspected to have DS based on a heterogeneous yet defining combination of spindle-cell sarcomatous and blastemal morphology, with rhabdomyomatous differentiation. Foci of immature cartilage at diagnosis (n = 2/3) and increased neuroepithelial differentiation at recurrence (n = 1) were noted. Morphological suspicion prompted somatic testing at reference centers, confirming likely biallelic, loss-of-function, and "hotspot" missense DICER1 variants in all three tumors. This can serve as a model for this diagnosis in resource-limited settings and has implications for germline testing, surveillance, and tumor management.

Indexed as

Pulmonary BlastomaSarcomaSoft Tissue NeoplasmsChildDEAD-box RNA HelicasesDeveloping CountriesGerm-Line MutationHumansRibonuclease IIIDEAD-box RNA HelicasesDICER1 protein, humanRibonuclease IIIDICER1-associated sarcomaDICER1 syndromerhabdomyosarcoma

Identifiers

PMID34913555
PMCPMC9248686
OpenAlexW4200365778

What OpenQuestion holds

Textmetadata
LicenceTDM
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.