Evidence map›Paper›PMID 32897884›Full record

ArticleThe Journal of clinical investigation2020

Germ cell tumors and associated hematologic malignancies evolve from a common shared precursor.

Justin Taylor, Mark Ta Donoghue, Caleb Ho, Kseniya Petrova-Drus, Hikmat A Al-Ahmadie, Samuel A Funt, Yanming Zhang, Umut Aypar, Pavitra Rao, Shweta S Chavan and 17 more

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in The Journal of clinical investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 51 citations in OpenAlex.

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  14. Overcoming Barriers to Tumor Genomic Profiling through Direct-to-Patient Outreach.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors at 4 institutions in 2 countries.

Justin TaylorHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Mark Ta DonoghueMarie-Josée and Henry R. Kravis Center for Molecular Oncology.
Caleb HoDepartment of Pathology.
Kseniya Petrova-DrusDepartment of Pathology.
Hikmat A Al-AhmadieDepartment of Pathology.
Samuel A FuntGenitourinary Oncology Service, Department of Medicine.
Yanming ZhangDepartment of Pathology.
Umut AyparDepartment of Pathology.
Pavitra RaoMarie-Josée and Henry R. Kravis Center for Molecular Oncology.
Shweta S ChavanMarie-Josée and Henry R. Kravis Center for Molecular Oncology.
Michael HaddadinHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Roni TamariBone Marrow Transplant Service, Department of Medicine.
Sergio GiraltBone Marrow Transplant Service, Department of Medicine.
Martin S TallmanLeukemia Service, Department of Medicine.
Raajit K RampalLeukemia Service, Department of Medicine.
Priscilla BaezHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Rajya KappagantulaHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Satyajit KosuriBone Marrow Transplant Service, Department of Medicine.
Ahmet DoganDepartment of Pathology.
Satish K TickooDepartment of Pathology.
Victor E ReuterDepartment of Pathology.
George J BoslGenitourinary Oncology Service, Department of Medicine.
Christine A Iacobuzio-DonahueHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
David B SolitHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Barry S TaylorHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Darren R FeldmanGenitourinary Oncology Service, Department of Medicine.
Omar Abdel-WahabHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Memorial Sloan Kettering Cancer Center · USBone Marrow Foundation · USMolecular Oncology (United States) · USSpanish Oncology Genitourinary Group · ES

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Elisa de Stanchina · 1985 to 2026
$347.4M
Defining the Biological and Mechanistic Implications of XPO1 Mutations in Hematologic MalignanciesK08CA230319 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI TAYLOR, JUSTIN · 2018 to 2023
$1.2M
NCI NIH HHS K08 CA230319NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Germ cell tumors (GCTs) are the most common cancer in men between the ages of 15 and 40. Although most patients are cured, those with disease arising in the mediastinum have distinctly poor outcomes. One in every 17 patients with primary mediastinal nonseminomatous GCTs develop an incurable hematologic malignancy and prior data intriguingly suggest a clonal relationship exists between hematologic malignancies and GCTs in these cases. To date, however, the precise clonal relationship between GCTs and the diverse additional somatic malignancies arising in such individuals have not been determined. Here, we traced the clonal evolution and characterized the genetic features of each neoplasm from a cohort of 15 patients with GCTs and associated hematologic malignancies. We discovered that GCTs and hematologic malignancies developing in such individuals evolved from a common shared precursor, nearly all of which harbored allelically imbalanced p53 and/or RAS pathway mutations. Hematologic malignancies arising in this setting genetically resembled mediastinal GCTs rather than de novo myeloid neoplasms. Our findings argue that this scenario represents a unique clinical syndrome, distinct from de novo GCTs or hematologic malignancies, initiated by an ancestral precursor that gives rise to the parallel evolution of GCTs and blood cancers in these patients.

Indexed as

Hematologic NeoplasmsMutationNeoplasms, Germ Cell and EmbryonalNeoplasms, Second PrimaryTumor Suppressor Protein p53AdolescentAdultFemaleHumansMiddle AgedSignal TransductionTP53 protein, humanTumor Suppressor Protein p53CancerGeneticsHematologyLeukemias

Identifiers

PMID32897884
PMCPMC7685753
OpenAlexW3084208051

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.