Evidence map›Paper›PMID 30327374›Full record

ArticleBlood advances2018

The mutational landscape of accelerated- and blast-phase myeloproliferative neoplasms impacts patient outcomes.

Caroline J McNamara, Tony Panzarella, James A Kennedy, Andrea Arruda, Jaime O Claudio, Georgina Daher-Reyes, Jenny Ho, Nancy Siddiq, Rebecca Devlin, Hubert Tsui and 14 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

48 citing papers in PubMed, 72 citations in OpenAlex.

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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

24 authors at 2 institutions in 1 country.

Caroline J McNamaraDepartment of Medical Oncology and Hematology and.
Tony PanzarellaDepartment of Biostatistics, Princess Margaret Cancer Centre, Toronto, ON, Canada.
James A KennedyDepartment of Medical Oncology and Hematology and.
Andrea ArrudaDepartment of Medical Oncology and Hematology and.
Jaime O ClaudioDepartment of Medical Oncology and Hematology and.
Georgina Daher-ReyesDepartment of Medical Oncology and Hematology and.
Jenny HoDepartment of Medical Oncology and Hematology and.
Nancy SiddiqDepartment of Medical Oncology and Hematology and.
Rebecca DevlinDepartment of Medical Oncology and Hematology and.
Hubert TsuiDepartment of Laboratory Hematology, Toronto General Hospital, Toronto, ON, Canada.
Jie SuDepartment of Biostatistics, Princess Margaret Cancer Centre, Toronto, ON, Canada.
Tracy StockleyAdvanced Molecular Diagnostics Laboratory, Princess Margaret Cancer Centre, Toronto, ON, Canada.
Mahadeo SukhaiAdvanced Molecular Diagnostics Laboratory, Princess Margaret Cancer Centre, Toronto, ON, Canada.
Nisha KanwarAdvanced Molecular Diagnostics Laboratory, Princess Margaret Cancer Centre, Toronto, ON, Canada.
Steven ChanDepartment of Medical Oncology and Hematology and.
Dawn MazeDepartment of Medical Oncology and Hematology and.
Aaron SchimmerDepartment of Medical Oncology and Hematology and.
Andre SchuhDepartment of Medical Oncology and Hematology and.
Hassan SibaiDepartment of Medical Oncology and Hematology and.
Auro ViswabandyaDepartment of Medical Oncology and Hematology and.
Karen YeeDepartment of Medical Oncology and Hematology and.
Mark D MindenDepartment of Medical Oncology and Hematology and.
Suzanne Kamel-ReidAdvanced Molecular Diagnostics Laboratory, Princess Margaret Cancer Centre, Toronto, ON, Canada.
Vikas GuptaDepartment of Medical Oncology and Hematology and.
Princess Margaret Cancer Centre · CAToronto General Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a paucity of data regarding the impact of mutations on outcomes in accelerated-phase (AP) and blast-phase (BP) myeloproliferative neoplasms (MPNs). Moreover, it is unknown whether mutational status affects survival, as seen in chronic-phase MPNs. Therefore, we performed a retrospective analysis of all patients treated at our institution with AP/BP MPNs (N = 122; AP = 14; BP = 108) to comprehensively describe the mutational profile and correlate with clinical outcomes. Targeted sequencing with a 54-gene panel was performed. Forty-four patients were treated with intensive therapy, 27 with nonintensive therapy, and 51 with best supportive care (BSC). The most common mutation was

Indexed as

Blast CrisisFemaleHumansMaleMyeloproliferative DisordersTreatment Outcome

Identifiers

PMID30327374
PMCPMC6199664
OpenAlexW2896678815

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.