Evidence map›Paper›PMID 18940674›Full record

ArticleBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2008

Pretreatment C-reactive protein is a predictor for outcomes after reduced-intensity allogeneic hematopoietic cell transplantation.

Andrew S Artz, Amittha Wickrema, Shira Dinner, Lucy A Godley, Masha Kocherginsky, Olatoyosi Odenike, Elizabeth S Rich, Wendy Stock, Jodie Ulaszek, Richard A Larson and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 2 pooled it
2.5field-weighted citation impact, top 11% 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

45 citing papers in PubMed, 2 syntheses or guidelines pooled it, 86 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pharmacodynamic Monitoring Predicts Outcomes of CCR5 Blockade as Graft-versus-Host Disease Prophylaxis.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2018
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  18. Validation of the Hematopoietic Cell Transplantation-Specific Comorbidity Index in Nonmyeloablative Allogeneic Stem Cell Transplantation.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2017
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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 2 institutions in 1 country.

Andrew S ArtzSection of Hematology/Oncology, Department of Medicine, University of Chicago, The University of Chicago Cancer Research Center, Chicago, Illinois 60637, USA. aartz@medicine.bsd.uchicago.edu
Amittha Wickrema
Shira Dinner
Lucy A Godley
Masha Kocherginsky
Olatoyosi Odenike
Elizabeth S Rich
Wendy Stock
Jodie Ulaszek
Richard A Larson
Koen van Besien
Cancer Research Center · USUniversity of Chicago · US

Funding

Immunologic and pharmacologic studies in allotransplantK24CA116471 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI VAN BESIEN, KOEN WALTER · 2007 to 2011
$882k
Busulfan conditioning: optimization, kinetics, genomicsR21CA115097 · NCI · UNIVERSITY OF CHICAGO · PI VAN BESIEN, KOEN WALTER · 2006 to 2007
$551k
NCI NIH HHS CA116471-01NCI NIH HHS K24 CA116471NCI NIH HHS R21 CA115097
6 · The paper itself

Abstract

We tested the independent prognostic impact of 2 commonly used biomarkers, C-reactive protein (CRP) and interleukin (IL)-6, on the outcomes of allogeneic hematopoietic cell transplantation (HCT). Consecutive patients who underwent a uniform reduced-intensity conditioning (RIC) regimen of fludarabine (Flu), melphalan (Mel), and alemtuzumab were evaluated retrospectively. Cryopreserved serum samples drawn before the RIC were available to measure CRP levels in 81 patients and IL-6 levels in 79 patients. Patients with CRP levels above the median of 18.5 mg/L had significantly more grade 3-4 hepatic toxicity (P=.01), longer HCT hospital stay (P=.005), more acute graft-versus-host disease (aGVHD) (P=.003), greater nonrelapse mortality (NRM) (P=.01), and inferior overall survival (OS; P=.02). Higher baseline CRP showed no significant correlation with grade 3-4 infectious toxicity (P=.09). In contrast to CRP, pre-HCT IL-6 levels above the median of 78.3 pg/mL did not confer a statistically significant increased risk of toxicity or mortality. An elevated HCT comorbidity index (HCT-CI) did not predict for any measure of HCT morbidity. After adjustment for disease status, comorbidity, performance status, and age, elevated CRP concentration remained predictive of NRM. These data require confirmation in non-T cell-depleted conditioning regimens. If validated, they suggest that preconditioning CRP holds promise for enhancing estimates of transplantation tolerance.

Indexed as

Hematopoietic Stem Cell TransplantationTransplantation ConditioningAcute DiseaseAdultAgedAge FactorsBiomarkers, TumorC-Reactive ProteinDisease-Free SurvivalFemaleGraft vs Host DiseaseHematologic NeoplasmsHumansInterleukin-6Length of StayLiver DiseasesBiomarkers, TumorC-Reactive ProteinIL6 protein, humanInterleukin-6Myeloablative Agonists

Identifiers

PMID18940674
PMCPMC2668514
OpenAlexW2170284288

What OpenQuestion holds

Textmetadata
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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.