Evidence map›Paper›PMID 25310307›Full record

ArticleBone marrow transplantation2015

Adoptive therapy with donor lymphocyte infusion after allogenic hematopoietic SCT in pediatric patients.

J Gozdzik, K Rewucka, A Krasowska-Kwiecien, A Pieczonka, R Debski, A Zaucha-Prazmo, K Drabko, J Krukowska-Jaros, M Wozniak, J Kowalczyk and 5 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

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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

15 authors.

J Gozdzik1] Department of Clinical Immunology and Transplantation, Polish-American Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland [2] Department of Transplantation, Children's University Hospital in Krakow, Krakow, Poland.
K RewuckaDepartment and Clinic of Bone Marrow Transplantation, Pediatrics Oncology and Hematology, Medical University in Wroclaw, Wroclaw, Poland.
A Krasowska-Kwiecien1] Department of Clinical Immunology and Transplantation, Polish-American Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland [2] Department of Transplantation, Children's University Hospital in Krakow, Krakow, Poland.
A PieczonkaDepartment and Clinic of Pediatrics Oncology, Hematology and Transplantation, Medical University in Poznan, Poznan, Poland.
R DebskiDepartment of Pediatrics, Hematology and Oncology, Nicolaus Copernicus University, Medical College in Bydgoszcz, Bydgoszcz, Poland.
A Zaucha-PrazmoDepartment of Pediatric Hematology, Oncology and Transplantology, Medical University in Lublin, Lublin, Poland.
K DrabkoDepartment of Pediatric Hematology, Oncology and Transplantology, Medical University in Lublin, Lublin, Poland.
J Krukowska-JarosDepartment and Clinic of Bone Marrow Transplantation, Pediatrics Oncology and Hematology, Medical University in Wroclaw, Wroclaw, Poland.
M WozniakDepartment of Transplantation, Children's University Hospital in Krakow, Krakow, Poland.
J KowalczykDepartment of Pediatric Hematology, Oncology and Transplantology, Medical University in Lublin, Lublin, Poland.
M WysockiDepartment of Pediatrics, Hematology and Oncology, Nicolaus Copernicus University, Medical College in Bydgoszcz, Bydgoszcz, Poland.
E GorczynskaDepartment and Clinic of Bone Marrow Transplantation, Pediatrics Oncology and Hematology, Medical University in Wroclaw, Wroclaw, Poland.
K KalwakDepartment and Clinic of Bone Marrow Transplantation, Pediatrics Oncology and Hematology, Medical University in Wroclaw, Wroclaw, Poland.
A ChybickaDepartment and Clinic of Bone Marrow Transplantation, Pediatrics Oncology and Hematology, Medical University in Wroclaw, Wroclaw, Poland.
J WachowiakDepartment and Clinic of Pediatrics Oncology, Hematology and Transplantation, Medical University in Poznan, Poznan, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to analyse the experience of Polish Pediatric Group for Hematopoietic Stem Cell Transplantation in respect to donor lymphocyte infusion procedure. The study included 51 pediatric patients with malignant (45) and non-malignant (6) diseases treated with DLI in the period 1993-2012. The indications for DLI were as follows: (1) increasing recipient chimerism after non-ablative hematopoietic SCT (18 patients); (2) immunomodulation after a reduced intensity conditioning regimen (2 patients); (3) increase in minimal residual disease detection (3 patients); and (4) relapse (28 patients). DLI was carried out at a median of 6 (0.5-79) months after SCT. DLI was administered as either a single-dose (in 19 cases) or in escalating-dose regimens (in 32 cases). The median total dose of CD3-positive T cells was 28.0 (0.1-730.0) × 10(6)/kg body weight. The time for assessment of DLI efficacy ranged from 0 to 70 (median 3) months. At evaluation, 18 patients experienced CR, 3 achieved PR, 19 showed relapse and 11 rejected the graft. DLI was found to be effective in 39% of cases. Complications of the procedure occurred in 18 patients; of these, 2 died. To sum up DLI shows efficacy in a significant percentage of children. Mortality related to the therapy adverse effects is low. However, this method requires standardization.

Indexed as

Hematopoietic Stem Cell TransplantationLiving DonorsLymphocyte TransfusionAllograftsChildChild, PreschoolDisease-Free SurvivalFemaleHematologic NeoplasmsHumansInfantInfant, NewbornMaleRetrospective StudiesSurvival Rate

Identifiers

PMID25310307

What OpenQuestion holds

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Registered trials

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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.