Evidence map›Paper›PMID 30176169›Full record

ArticleJournal of the European Academy of Dermatology and Venereology : JEADV2019

Survival, disease progression and prognostic factors in elderly patients with mycosis fungoides and Sézary syndrome: a retrospective analysis of 174 patients.

E Lebowitz, S Geller, E Flores, M Pulitzer, S Horwitz, A Moskowitz, M Kheterpal, P L Myskowski

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the European Academy of Dermatology and Venereology : JEADV, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
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

8 authors at 2 institutions in 1 country.

E LebowitzWeill Cornell Medical College, New York, NY, USA.
S GellerWeill Cornell Medical College, New York, NY, USA.ORCID http://orcid.org/0000-0003-1206-1057
E FloresDermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
M PulitzerWeill Cornell Medical College, New York, NY, USA.
S HorwitzWeill Cornell Medical College, New York, NY, USA.
A MoskowitzWeill Cornell Medical College, New York, NY, USA.
M KheterpalWeill Cornell Medical College, New York, NY, USA.
P L MyskowskiWeill Cornell Medical College, New York, NY, USA.
Memorial Sloan Kettering Cancer Center · USCornell University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
ADC TherapeuticsCelgeneInfinity PharmaceuticalsKyowa Hakko KirinMillennium Pharmaceuticals IncNCI NIH HHS P30 CA008748NIH/NCI Cancer Center Support P30 CA008748Seattle Genetics IncSpectrum Pharmaceuticals
6 · The paper itself

Abstract

backgroundAdvanced age at diagnosis is considered a poor prognostic factor in mycosis fungoides (MF) and Sézary syndrome (SS).

objectiveTo evaluate the outcomes and prognostic factors in patients diagnosed at an advanced age (≥65 years) with MF/SS.

methodsSurvival, progression rates and various clinical and histopathological variables were studied in a group of 174 elderly patients diagnosed with MF/SS between 1992 and 2015 at a single referral cancer center in the United States. Kaplan-Meier estimates were used to determine survival and progression and Cox proportional hazards regression univariate and multivariate models were used to identify prognostic factors.

resultsOf 174 elderly patients, 76.4% were diagnosed with early-stage (clinical stages IA-IIA) and 23.6% with late-stage MF/SS (IIB-IV). Advanced age was associated with poor overall survival, but not with disease-specific survival (DSS) or progression-free survival (PFS). Gender, increasing clinical stage, T and B classifications, elevated lactate dehydrogenase (LDH) levels and development of large cell transformation (LCT) were significant predictors of poor survival or disease progression. Patients with early-stage MF and <10% total skin involvement (T1 classification) or patch-only disease (T1a/T2a) showed better PFS with no observed disease-specific mortality. Folliculotropic MF was associated with poor DSS in patients with early-stage disease.

conclusionsOlder age at diagnosis of MF/SS does not predict worse disease-specific outcomes. Elderly patients with early-stage disease, specifically involving less than 10% of the skin surface with patches but without plaques or folliculotropism, have an excellent prognosis. However, the development of LCT is a strong prognostic indicator of poor survival in elderly patients with MF/SS.

Indexed as

AgedAged, 80 and overAge FactorsDisease ProgressionFemaleHumansKaplan-Meier EstimateL-Lactate DehydrogenaseMaleMycosis FungoidesNeoplasm StagingPrognosisProgression-Free SurvivalProportional Hazards ModelsRetrospective StudiesSex FactorsL-Lactate Dehydrogenase

Identifiers

PMID30176169
PMCPMC6338490
OpenAlexW2891046501

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.