Evidence map›Paper›PMID 35595226›Full record

ArticleTransplantation and cellular therapy2022

Geriatric Assessment Reveals Actionable Impairments in Hematopoietic Stem Cell Transplantation Candidates Age 18 to 80 Years.

Meagan V Lew, Yi Ren, Yen P Lowder, Sharareh Siamakpour-Reihani, Sendhilnathan Ramalingam, Kristi M Romero, Jillian C Thompson, Lauren M Bohannon, Jackie McIntyre, Helen Tang and 40 more

2 registry-linked trialsOpen 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. It is linked to 2 registered trials, which are not on this map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.1field-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.

NCT06802406 narecruitingnot on this mapstarted 2025, after this paper: background citation

Nutrition OUtReach In Systems of Healthcare

TypeinterventionalSponsorUniversity of Kansas Medical CenterRan2025 to 2029Enrolled210ConditionsALLOGENEIC HEMATOPOIETIC STEM CELL TRANSPLANTATION, Autologous Haemopoietic Stem Cell Transplant, CAR-T Cell Therapy, Food InsecurityArmsFood Bags
NCT07516314 nanot yet recruitingnot on this mapstarted 2026, after this paper: background citation

ACT to Reduce Morbidity and Mortality in Hematopoietic Stem Cell Transplant (HCT) Patients (ACTivate)

TypeinterventionalSponsorAnthony Sung, MDRan2026 to 2031Enrolled476ConditionsStem Cell Transplant PatientsArmsACTivate sessions
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Observational
  4. Article
  5. Frailty phenotype in adults with sickle cell disease.The journals of gerontology. Series A, Biological sciences and medical sciences · 2026
    Article
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  8. Review
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  12. Article
  13. Review
  14. How old is too old? Frailty and geriatric assessments of older patients undergoing allogeneic HCT.Hematology. American Society of Hematology. Education Program · 2023
    Article
  15. 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

50 authors at 5 institutions in 3 countries.

Meagan V LewDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Yi RenDuke Cancer Institute Biostatistics Shared Resources, Durham, North Carolina.
Yen P LowderDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Sharareh Siamakpour-ReihaniDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Sendhilnathan RamalingamDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Kristi M RomeroDuke University School of Medicine, Durham, North Carolina.
Jillian C ThompsonDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Lauren M BohannonDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Jackie McIntyreDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Helen TangDuke University School of Medicine, Durham, North Carolina.
Jolien Van OpstalDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina; Faculty of Medicine, KU Leuven, Leuven, Belgium.
Ernaya JohnsonDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Harvey Jay CohenClaude D. Pepper Older Americans Independence Center, Center for the Study of Aging and Human Development, Duke University Medical Center, Durham, North Carolina.
David B BartlettClaude D. Pepper Older Americans Independence Center, Center for the Study of Aging and Human Development, Duke University Medical Center, Durham, North Carolina; School of Biosciences and Medicine, University of Surrey, Surrey, United Kingdom.
Amy M PastvaClaude D. Pepper Older Americans Independence Center, Center for the Study of Aging and Human Development, Duke University Medical Center, Durham, North Carolina; Department of Orthopedic Surgery, Division of Physical Therapy, Duke University Medical Center, Durham, North Carolina.
Miriam MoreyClaude D. Pepper Older Americans Independence Center, Center for the Study of Aging and Human Development, Duke University Medical Center, Durham, North Carolina; Geriatric Research, Education and Clinical Center, Durham VA Healthcare System, Durham, North Carolina.
Katherine S HallClaude D. Pepper Older Americans Independence Center, Center for the Study of Aging and Human Development, Duke University Medical Center, Durham, North Carolina; Geriatric Research, Education and Clinical Center, Durham VA Healthcare System, Durham, North Carolina.
Patrick SmithPsychiatry and Behavioral Sciences, Duke University Medical Center, Durham, North Carolina.
Katherine B PetersDepartments of Neurology and Neurosurgery, The Preston Robert Tisch Brain Tumor Center, Duke University Medical Center, Durham, North Carolina.
Tamara J SomersPsychiatry and Behavioral Sciences, Duke University Medical Center, Durham, North Carolina.
Sarah KelleherPsychiatry and Behavioral Sciences, Duke University Medical Center, Durham, North Carolina.
Sophia K SmithSchool of Nursing, Duke University Medical Center, Durham, North Carolina.
Paul E WischmeyerDepartment of Anesthesiology, Duke University Medical Center, Durham, North Carolina.
Pao-Hwa LinDuke Molecular Physiology Institute, Duke University School of Medicine, Durham, North Carolina.
William A WoodDivision of Hematology, Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Glynnis ThorpeDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Kerry MinorDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Kristi WigginsDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Therese HennigDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Tanya HelmsDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Renee WelchDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Brittany MatthewsDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
JoAnn LiuDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Jill BurlesonDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Thomas AberantDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Ashley K EngemannDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Bethany HenshallDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Maurisa DarbyDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Christina ProchDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Michelle DellascioDuke Health Department of Physical Therapy and Occupational Therapy, Durham, North Carolina.
Alyssa PittmanDuke Health Department of Physical Therapy and Occupational Therapy, Durham, North Carolina.
Jacob SuminguitUniversity of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Taewoong ChoiDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Cristina GasparettoDivision of Hematologic Malignancies and Cellular Therapy, Department of Medicine, Duke University Medical Center, Durham, North Carolina.
Gwynn D LongDivision of Hematologic Malignancies and Cellular Therapy, Department of Medicine, Duke University Medical Center, Durham, North Carolina.
Richard D LopezDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Stefanie SarantopoulosDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Mitchell E HorwitzDivision of Hematologic Malignancies and Cellular Therapy, Department of Medicine, Duke University Medical Center, Durham, North Carolina.
Nelson J ChaoDivision of Hematologic Malignancies and Cellular Therapy, Department of Medicine, Duke University Medical Center, Durham, North Carolina.
Anthony D SungDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina; Claude D. Pepper Older Americans Independence Center, Center for the Study of Aging and Human Development, Duke University Medical Center, Durham, North Carolina. Electronic address: anthony.sung@duke.edu.
Duke Medical Center · USDuke University · USDuke Regional Hospital · USUniversity of North Carolina at Chapel Hill · USDuke Cancer Institute

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI DONNA NIEDZWIECKI · 1985 to 2026
$174.8M
Resource Core 3 - Metabolomics CoreP30AG028716 · NIA · DUKE UNIVERSITY · PI Virginia B Kraus · 2006 to 2026
$24.6M
Evaluating Effects of Age-related Microbiota Modulations in Hematopoietic Stem Cell Transplant PatientsR21AG066388 · NIA · DUKE UNIVERSITY · PI CHAO, NELSON J., SUNG, ANTHONY · 2019 to 2020
$443k
NCI NIH HHS P30 CA014236NIA NIH HHS P30 AG028716NIA NIH HHS R21 AG066388
6 · The paper itself

Abstract

Allogeneic hematopoietic stem cell transplantation (HCT) is a potentially curative treatment for both malignant and nonmalignant hematologic diseases; however, reported rates of treatment-related mortality approach 30%. Outcomes are worse in patients who begin HCT with functional impairments. To detect such impairments, a geriatric assessment (GA) is recommended in adults age ≥65 years. Younger HCT candidates also may be impaired because of chemotherapy regimens pre-HCT. Therefore, we hypothesized that GA can be beneficial for adult patients of all ages and subsequently created a clinical pretransplantation optimization program to assess all HCT candidates using a modified GA. One-hundred fifty-seven patients were evaluated in 4 functional domains- physical, cognitive, nutritional, and psychological-at 2 time points prior to HCT-new patient evaluation (NPE) and sign-off (SO)-between October 2017 and January 2020. At NPE, 80.9% of the patients had at least 1 domain with a functional impairment, and physical (P = .006), cognitive (P = .04), and psychological (P = .04) impairments were associated with an increased likelihood of not proceeding to HCT. In addition, patients age 18 to 39 years were more likely than older patients to have a physical function impairment (P = .001). Between NPE and SO, 51.9% of the patients had resolution of 1 or more impairments, and nutritional impairment at SO was predictive of worse overall survival (P = .01). Our study shows that GA can identify functional impairments in patients of all ages. Early identification of impairments could facilitate referrals to supportive care and resolution of impairments prior to HCT, suggesting that GA could be recommended for HCT candidates of all ages.

Indexed as

Hematopoietic Stem Cell TransplantationTransplantation ConditioningAdolescentAdultAgedAged, 80 and overGeriatric AssessmentHumansMiddle AgedRisk AssessmentTransplantation, HomologousYoung AdultAllogeneic hematopoietic stem cell transplantationFunctional domainsGeriatric assessmentTransplantation outcomeTreatment-related mortality

Identifiers

PMID35595226
PMCPMC10042624
OpenAlexW4280650301

What OpenQuestion holds

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Registered trials

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.