Evidence map›Paper›PMID 36813626›Full record

ArticleClinical lymphoma, myeloma & leukemia2023

Sex Disparities in Myelodysplastic Syndromes: Genotype, Phenotype, and Outcomes.

Sara M Tinsley-Vance, Najla Al Ali, Somedeb Ball, Luis E Aguirre, Akriti G Jain, Mohammad Omar Hussaini, Onyee Chan, Andrew Kuykendall, Kendra Sweet, Jeffrey Lancet and 3 more

Open access · greenAbstract read
In one paragraph

Article in Clinical lymphoma, myeloma & leukemia, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 7 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

13 authors at 1 institution in 1 country.

Sara M Tinsley-VanceDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL. Electronic address: sara.tinsley@moffitt.org.
Najla Al AliDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Somedeb BallDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Luis E AguirreDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Akriti G JainDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Mohammad Omar HussainiDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Onyee ChanDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Andrew KuykendallDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Kendra SweetDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Jeffrey LancetDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Eric PadronDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
David A SallmanDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Rami S KomrokjiDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Moffitt Cancer Center · US

Funding

Development of a Quality of Life Decision-Making Model for Older Patients with Acute Myeloid LeukemiaK23NR018488 · NINR · H. LEE MOFFITT CANCER CTR & RES INST · PI TINSLEY, SARA · 2020 to 2022
$474k
NINR NIH HHS K23 NR018488
6 · The paper itself

Abstract

Introduction/Background The impact of biological sex on the clinical phenotype, genotype, and outcomes among patients with MDS is not well characterized. Materials and Methods We retrospectively reviewed the clinical and genomic data from male and female patients included in our institutional MDS database at Moffitt Cancer Center. Results Among 4580 patients with MDS, 2922 (66%) were men and 1658 (34%) were women. Women were younger (mean age 66.5 vs. 69 years for men, P < .001) at diagnosis. There were more Hispanic/black women than men (9% vs. 5%, P =<.001). Women had lower hemoglobin and higher platelet counts than men. More women had del 5q/monosomy 5 abnormalities compared to men (P =<.001). Therapy related MDS were more common in women than men (25% vs.17%, P=<.001). On assessment of molecular profile, SRSF2, U2AF1, ASXL1, and RUNX1 mutations were more frequent in men. The median overall survival (mOS) was 37.5 months (mo) for females compared to 35 monthsfor males, (P = .002). The mOS was significantly prolonged for women in lower-risk MDS, but not in higher-risk MDS. Women were more likely to respond to immunosuppression with ATG/CSA than men (38% vs. 19%, P= 0.04).Conclusion Ongoing research is needed for understanding the impact of sex on phenotype, genotype, and outcomes in patients diagnosed with MDS.

Indexed as

Myelodysplastic SyndromesFemaleGenotypeHumansMaleMutationPhenotypePrognosisRetrospective StudiesSplicing Factor U2AFSplicing Factor U2AFsex differences, genomic data, splicing machinery mutationssomatic mutations

Identifiers

PMID36813626
PMCPMC10121764
OpenAlexW4316654327

What OpenQuestion holds

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Registered trials

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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.