Evidence map›Paper›PMID 35247612›Full record

ArticleTransplantation and cellular therapy2022

Patterns and Predictors of Functional Decline after Allogeneic Hematopoietic Cell Transplantation in Older Adults.

Li-Wen Huang, Ying Sheng, Charalambos Andreadis, Aaron C Logan, Gabriel N Mannis, Catherine C Smith, Karin M L Gaensler, Thomas G Martin, Lloyd E Damon, Chiung-Yu Huang and 1 more

Open access · greenAbstract read
In one paragraph

Article in Transplantation and cellular therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. How old is too old? Frailty and geriatric assessments of older patients undergoing allogeneic HCT.Hematology. American Society of Hematology. Education Program · 2023
    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

11 authors at 3 institutions in 1 country.

Li-Wen HuangHelen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, California; Division of Hematology/Oncology, Department of Medicine, San Francisco VA Medical Center, San Francisco, California.
Ying ShengDepartment of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, California.
Charalambos AndreadisHelen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, California.
Aaron C LoganHelen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, California.
Gabriel N MannisDivision of Hematology, Department of Medicine, Stanford University, Stanford, California.
Catherine C SmithHelen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, California.
Karin M L GaenslerHelen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, California.
Thomas G MartinHelen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, California.
Lloyd E DamonHelen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, California.
Chiung-Yu HuangDepartment of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, California.
Rebecca L OlinHelen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, California. Electronic address: rebecca.olin@ucsf.edu.
University of California, San Francisco · USSan Francisco VA Medical Center · USStanford University · US

Funding

VARC CoreP30AG044281 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Louise C. Walter · 2013 to 2026
$19.9M
RESEARCH TRAINING IN GERIATRIC MEDICINET32AG000212 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Alexander Keliimoeanu Smith · 1991 to 2026
$7.7M
Cognitive trajectories and risk factors for cognitive decline in older adults with hematologic malignanciesR03AG067935 · NIA · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI HUANG, LI-WEN · 2021 to 2022
$307k
NIA NIH HHS P30 AG044281NIA NIH HHS R03 AG067935NIA NIH HHS T32 AG000212
6 · The paper itself

Abstract

As allogeneic hematopoietic cell transplantation (alloHCT) is increasingly offered to older adults, geriatric assessment (GA) has been identified as a useful tool for predicting outcomes, particularly functional status. However, very few studies have examined the longitudinal change in GA measures in the post-alloHCT period. The objectives of this study were to describe the longitudinal change in GA and quality of life (QoL) measures after alloHCT and to identify predictors of greater functional decline post-transplantation. In this single-center prospective cohort study, patients age ≥50 years scheduled for alloHCT completed a cancer-specific GA and the Functional Assessment of Cancer Therapy-Bone Marrow Transplant (FACT-BMT) survey at baseline prior to alloHCT and then at 3, 6, and 12 months post-transplantation. Changes in GA and QoL measures at each post-transplantation time point (3, 6, and 12 months) compared to baseline were analyzed using paired t-tests. Exploration of potential predictors of greater post-transplantation functional decline, as measured by instrumental activities of daily living (IADL) and the Medical Outcomes Study Physical Health scale (MOS-PH), were examined using linear regression and the chi-square 2-sample test of proportions. Mean functional status generally exhibited a pattern of decline at 3 to 6 months post-alloHCT, with recovery to near baseline by 12 months. Mean mental health and emotional QoL were lowest at baseline and improved at all post-transplantation time points. Differences in baseline clinical characteristics were not associated with any differences in functional trajectories. Differences in baseline GA measures-patient-rated Karnofsky Performance Status, IADL, MOS-PH, Timed-Up-and-Go, Blessed Orientation-Memory-Concentration test, and Mental Health Inventory 5-also did not predict greater functional decline at 3 months. Patients whose IADL was improved or maintained at 3 months generally maintained their functional status at 6 and 12 months. Similarly, most patients who had an IADL decline at 3 months still had a functional decline at 6 months, although a proportion did have functional recovery by 12 months. Compared with patients who had improved/maintained IADL at 3 months, those with a decline in IADL at 3 months were significantly more likely to have persistent functional decline at 6 months (P < .0001) and 12 months (P = .02). In older alloHCT recipients, mean functional status declines short term after alloHCT with the possibility of recovery by 6 to 12 months, whereas mean mental and emotional health improve post-alloHCT. Functional decline at 3 months post-alloHCT is associated with persistent functional decline at 12 months.

Indexed as

Hematopoietic Stem Cell TransplantationNeoplasmsActivities of Daily LivingAgedHumansMiddle AgedProspective StudiesQuality of LifeAllogeneic transplantFunctional statusGeriatric assessmentOlder adults

Identifiers

PMID35247612
PMCPMC9198006
OpenAlexW4214943500

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.