Evidence map›Paper›PMID 25144888›Full record

ReviewGenetics in medicine : official journal of the American College of Medical Genetics2015

Adverse events in cancer patients with sickle cell trait or disease: case reports.

Helen Swede, Biree Andemariam, David I Gregorio, Beth A Jones, Dejana Braithwaite, Thomas E Rohan, Richard G Stevens

Open access · bronzeAbstract readCase ReportsReview
PubMed Publisher
In one paragraph

Review in Genetics in medicine : official journal of the American College of Medical Genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 4 institutions in 1 country.

Helen SwedeDepartment of Community Medicine, University of Connecticut School of Medicine, Farmington, Connecticut, USA.
Biree AndemariamLea's Foundation Center for Hematologic Disorders, Division of Hematology/Oncology, Connecticut School of Medicine, Farmington, Connecticut, USA.
David I GregorioDepartment of Community Medicine, University of Connecticut School of Medicine, Farmington, Connecticut, USA.
Beth A JonesDepartment of Chronic Disease Epidemiology, Yale School of Public Health, New Haven, Connecticut, USA.
Dejana BraithwaiteDepartment of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, California, USA.
Thomas E RohanDepartment of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, New York, USA.
Richard G StevensDepartment of Community Medicine, University of Connecticut School of Medicine, Farmington, Connecticut, USA.
University of Connecticut · USAlbert Einstein College of Medicine · USUniversity of California, San Francisco · USYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeGiven the relatively high prevalence of sickle cell trait and disease among African Americans and established racial disparities in cancer outcomes, we reviewed the literature regarding adverse events in cancer patients with these hematologic genotypes. Erythrocyte sickling can result from extreme hypoxia and other physiologic stressors, as might occur during cancer therapy. Further, tumoral hypoxia, a poor prognostic and predictive factor, could lead to a cycle of local sickling and increased hypoxia.

methodsA search of PubMed produced 150 publications, most of which were excluded because of incidental relevance. Eleven case reports of patients diagnosed from 1993 to 2013 were reviewed.

resultsTwo reports of patients with sickle cell trait describe an abundance of sickled erythrocytes within tumors, and a third report describes sickling-related events requiring multiday hospitalization. Eight reports of patients with sickle cell disease delineated multiorgan failure, vaso-occlusive crises, and rapid renal deterioration. Hypothesized triggers are delayed clearance of anticancer agents attributable to baseline kidney damage, activation of vasoadherent neutrophils from treatment to counter chemotherapy-induced neutropenia, hypoxia from general anesthesia, and intratumoral hypoxia.

conclusionClinical implications include pretreatment genotyping for prophylaxis, dose adjustment, and enhanced patient monitoring. With the current lack of high-quality evidence, however, the scope of poor outcomes remains unknown.

Indexed as

AdolescentAnemia, Sickle CellAntineoplastic AgentsAntisickling AgentsChildFemaleHumansMaleMiddle AgedNeoplasmsSickle Cell TraitAntineoplastic AgentsAntisickling Agents

Identifiers

PMID25144888
OpenAlexW2085317357

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.