Evidence map›Paper›PMID 24331192›Full record

ReviewSeminars in oncology2013

Cognitive effects of cancer and its treatments at the intersection of aging: what do we know; what do we need to know?

Jeanne S Mandelblatt, Arti Hurria, Brenna C McDonald, Andrew J Saykin, Robert A Stern, John W VanMeter, Meghan McGuckin, Tiffani Traina, Neelima Denduluri, Scott Turner and 4 more

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in oncology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed, 7 pooled it
8.1field-weighted citation impact, top 2% 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

94 citing papers in PubMed, 7 syntheses or guidelines pooled it, 135 citations in OpenAlex.

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  11. Subjective cognition and mood in persistent chemotherapy-related cognitive impairment.Journal of cancer survivorship : research and practice · 2022
    Trial
  12. Nicotinic treatment of post-chemotherapy subjective cognitive impairment: a pilot study.Journal of cancer survivorship : research and practice · 2019
    Trial
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34 more citing papers are in PubMed but not listed here.

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

14 authors at 7 institutions in 1 country.

Jeanne S MandelblattDepartments of Oncology and Population Sciences, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC. Electronic address: mandelbj@georgetown.edu.
Arti HurriaDepartment of Medical Oncology and Therapeutics Research, City of Hope Comprehensive Cancer Center, Duarte, CA.
Brenna C McDonaldCenter for Neuroimaging, Department of Radiology and Imaging Sciences and the Melvin and Bren Simon Cancer Center, Indiana University School of Medicine, Indianapolis, IN.
Andrew J SaykinCenter for Neuroimaging, Department of Radiology and Imaging Sciences and the Melvin and Bren Simon Cancer Center, Indiana University School of Medicine, Indianapolis, IN.
Robert A SternDepartments of Neurology and Neurosurgery and Director, Clinical Core, BU Alzheimer's Disease Center, Boston University School of Medicine, Boston, MA.
John W VanMeterDepartment of Neurology, Georgetown University Medical Center, Georgetown University, Washington, DC.
Meghan McGuckinDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC.
Tiffani TrainaDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Neelima DenduluriDepartment of Medicine, Georgetown University; Virginia Cancer Specialists, US Oncology, Arlington, VA.
Scott TurnerDepartment of Neurology, Georgetown University Medical Center, Georgetown University, Washington, DC.
Darlene HowardDepartment of Psychology, Georgetown University, Washington, DC.
Paul B JacobsenDivision of Population Science, Moffitt Cancer Center, Tampa, FL.
Tim AhlesDepartment of Psychiatry and Behavioral Sciences, Memorial Sloan-Kettering Cancer Center, New York, NY; Department of Psychiatry, Weill Cornell Medical College, New York, NY.
Thinking and Living With Cancer Study
Georgetown University · USIndiana University School of MedicineMemorial Sloan Kettering Cancer Center · USBoston University · USCity of Hope · USGeorgetown University Medical Center · USMoffitt Cancer Center · US

Funding

National Centralized Repository for Alzheimer's Disease and Related Dementias (NCRAD)U24AG021886 · NIA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI TATIANA M. FOROUD · 2002 to 2026
$119.8M
Tissue Culture Shared ResourceP30CA051008 · NCI · GEORGETOWN UNIVERSITY · PI STEPHEN W BYERS · 1990 to 2026
$71.5M
Tumor Microenvironment and Metastasis ProgramP30CA082709 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI Jun Wan · 1999 to 2026
$59.3M
Research Education ComponentP30AG010133 · NIA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI GHETTI, BERNARDINO FRANCESCO · 1991 to 2020
$37.3M
Neuropathology CoreP30AG013846 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI KOWALL, NEIL W. · 1996 to 2020
$29.1M
Training and Career Development CoreU54CA132378 · NCI · CITY COLLEGE OF NEW YORK · PI Tim Alan Ahles, ADRIANA ESPINOSA · 2008 to 2026
$28.9M
Training and Career Development and Education CoreU54CA137788 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Daniel Alan Heller · 2008 to 2026
$28.1M
INDIANA CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTE (UL1): BPCAUL1RR025761 · NCRR · INDIANA UNIVERSITY INDIANAPOLIS · PI SHEKHAR, ANANTHA · 2008 to 2011
$21.0M
OLDER BREAST CANCER PATIENTS: RISK FOR COGNITIVE DECLINER01CA129769 · NCI · GEORGETOWN UNIVERSITY · PI AHLES, TIM ALAN, MANDELBLATT, JEANNE · 2009 to 2020
$7.3M
Memory Circuitry in MCI and Early Alzheimer’s Disease Prodrome: Molecular DriversR01AG019771 · NIA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI SAYKIN, ANDREW J · 2001 to 2021
$6.9M
Training in Research for Behavioral Oncology and Cancer Control ProgramR25CA117865 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI CHAMPION, VICTORIA LEE · 2006 to 2015
$4.1M
EXTRAMURAL RESEARCH FACILITIES IMPROVEMENT: NEUROLOGICAL DISORDERS:ALZ, PDC06RR020128 · NCRR · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI FIFE, ROSE S · 2004 to 2004
$3.7M
NCI NIH HHS K05 CA096940NCI NIH HHS K05CA096940NCI NIH HHS P30 CA051008NCI NIH HHS P30 CA082709NCI NIH HHS P30CA51008NCI NIH HHS R01 CA087845NCI NIH HHS R01 CA101318NCI NIH HHS R01CA101318NCI NIH HHS R01 CA127617NCI NIH HHS R01CA127617NCI NIH HHS R01 CA129769NCI NIH HHS R01CA129769NCI NIH HHS R25 CA117865NCI NIH HHS R25CA117865NCI NIH HHS U10 CA084131NCI NIH HHS U10CA84131NCI NIH HHS U54 CA132378NCI NIH HHS U54 CA137788NCRR NIH HHS C06 RR020128NCRR NIH HHS C06RR020128NCRR NIH HHS S10 RR027710NCRR NIH HHS S10RR027710NCRR NIH HHS U54RR025761NCRR NIH HHS UL1 RR025761NIA NIH HHS F30 AG039959NIA NIH HHS F30AG039959NIA NIH HHS P30 AG010133NIA NIH HHS P30AG010133NIA NIH HHS P30 AG013846NIA NIH HHS P30-AG13846NIA NIH HHS R01 AG019771NIA NIH HHS R01AG019771NIA NIH HHS U24 AG021886NIA NIH HHS U24AG021886PHS HHS U54132378
6 · The paper itself

Abstract

There is a fairly consistent, albeit non-universal body of research documenting cognitive declines after cancer and its treatments. While few of these studies have included subjects aged 65 years and older, it is logical to expect that older patients are at risk of cognitive decline. Here, we use breast cancer as an exemplar disease for inquiry into the intersection of aging and cognitive effects of cancer and its therapies. There are a striking number of common underlying potential biological risks and pathways for the development of cancer, cancer-related cognitive declines, and aging processes, including the development of a frail phenotype. Candidate shared pathways include changes in hormonal milieu, inflammation, oxidative stress, DNA damage and compromised DNA repair, genetic susceptibility, decreased brain blood flow or disruption of the blood-brain barrier, direct neurotoxicity, decreased telomere length, and cell senescence. There also are similar structure and functional changes seen in brain imaging studies of cancer patients and those seen with "normal" aging and Alzheimer's disease. Disentangling the role of these overlapping processes is difficult since they require aged animal models and large samples of older human subjects. From what we do know, frailty and its low cognitive reserve seem to be a clinically useful marker of risk for cognitive decline after cancer and its treatments. This and other results from this review suggest the value of geriatric assessments to identify older patients at the highest risk of cognitive decline. Further research is needed to understand the interactions between aging, genetic predisposition, lifestyle factors, and frailty phenotypes to best identify the subgroups of older patients at greatest risk for decline and to develop behavioral and pharmacological interventions targeting this group. We recommend that basic science and population trials be developed specifically for older hosts with intermediate endpoints of relevance to this group, including cognitive function and trajectories of frailty. Clinicians and their older patients can advance the field by active encouragement of and participation in research designed to improve the care and outcomes of the growing population of older cancer patients.

Indexed as

CognitionCognitive ReserveAgedAgingAntineoplastic AgentsBreast NeoplasmsCognition DisordersFemaleFrail ElderlyGeriatric AssessmentHumansAntineoplastic Agents

Identifiers

PMID24331192
PMCPMC3880205
OpenAlexW2010156191

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.