Evidence map›Paper›PMID 38946833›Full record

ArticleWorld journal of clinical oncology2024

Characteristics and distinct prognostic determinants of individuals with hepatosplenic T-cell lymphoma over the past two decades.

Ayrton Bangolo, Pierre Fwelo, Shraboni Dey, Tanni Sethi, Sowmya Sagireddy, Jawaria Chatta, Ashish Goel, Sneha Nagpaul, Eric Pin-Shiuan Chen, Chiranjeeve Saravanan and 17 more

Abstract read
In one paragraph

Article in World journal of clinical oncology, 2024. 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
–field-weighted citation impact
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.

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

27 authors.

Ayrton BangoloDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States. ayrtonbangolo0@gmail.com.
Pierre FweloDepartment of Epidemiology, Human Genetics, and Environmental Sciences, UTHealth School of Public Health, Houston, TX 77030, United States.
Shraboni DeyDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Tanni SethiDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Sowmya SagireddyDepartment of Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Jawaria ChattaDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Ashish GoelDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Sneha NagpaulDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Eric Pin-Shiuan ChenDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Chiranjeeve SaravananDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Sheeja GanganDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Joel ThomasDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Sarah PotiguaraDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Vignesh K NageshDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Daniel EliasDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Charlene MansourDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Prajakta H RatnaparkhiDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Priyanshu JainDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Midhun MathewDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Taylor PorterDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Shadiya SultanDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Shailaja AbbisettyDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Linh TranDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Megha ChawlaDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Abraham LoDepartment of Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Simcha WeissmanDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Christina ChoStem Cell Transplantation and Cellular Therapy, John Theurer Cancer Center, Hackensack, NJ 07601, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatosplenic T-cell lymphoma (HSTCL) is a rare and aggressive peripheral T-cell lymphoma with historically dismal outcomes, representing less than one percent of non-Hodgkin lymphomas. Given its rarity, the true incidence of HSTCL is unknown and most data have been extrapolated through case reports. To the best of our knowledge, the largest and most up to date study addressing the epidemiology and outcomes of patients with HSTCL in the United States covered a period from 1996 to 2014, with a sample size of 122 patients.

aimTo paint the most updated epidemiological picture of HSTCL.

methodsA total of 186 patients diagnosed with HSTCL, between 2000 and 2017, were ultimately enrolled in our study by retrieving data from the Surveillance, Epidemiology, and End Results database. We analyzed demographics, clinical characteristics, and overall mortality (OM) as well as cancer-specific mortality (CSM) of HSTCL. Variables with a

resultsMale gender was the most represented. HSTCL was most common in middle-aged patients (40-59) and less common in the elderly (80+). Non-Hispanic whites (60.75%) and non-Hispanic blacks (20.97%) were the most represented racial groups. Univariate Cox proportional hazard regression analysis of factors influencing all-cause mortality showed a higher OM among non-Hispanic black patients. CSM was also higher among non-Hispanic blacks and patients with distant metastasis. Multivariate Cox proportional hazard regression analysis of factors affecting CSM revealed higher mortality in patients aged 80 or older and non-Hispanic blacks.

conclusionOverall, the outlook for this rare malignancy is very grim. In this retrospective cohort study of the United States population, non-Hispanic blacks and the elderly had a higher CSM. This data highlights the need for larger prospective studies to investigate factors associated with worse prognosis in one ethnic group, such as treatment delays, which have been shown to increase mortality in this racial/ethnic group for other cancers.

Indexed as

AgeExtra nodal lymphomaMortalityRacial disparitySurvival

Identifiers

PMID38946833
PMCPMC11212601

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.