Evidence map›Paper›PMID 25822227›Full record

ArticleBone marrow transplantation2015

Hematopoietic stem cell transplantation in relapsed ALK+ anaplastic large cell lymphoma in children and adolescents: a study on behalf of the SFCE and SFGM-TC.

M Strullu, C Thomas, M-C Le Deley, A Chevance, J Kanold, Y Bertrand, C Jubert, J-H Dalle, C Paillard, A Baruchel and 3 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 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

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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

13 authors at 9 institutions in 1 country.

M StrulluDepartment of Pediatric Oncology and Hematology, Hôpital Mère-Enfant, Nantes, France.
C ThomasDepartment of Pediatric Oncology and Hematology, Hôpital Mère-Enfant, Nantes, France.
M-C Le Deley1] Biostatistics and Epidemiology Unit, Gustave Roussy, Villejuif, France [2] Paris Sud University, Le Kremlin-Bicêtre, France.
A ChevanceBiostatistics and Epidemiology Unit, Gustave Roussy, Villejuif, France.
J KanoldDepartment of Pediatric Oncology and Hematology, Hôpital Estaing, Clermont-Ferrand, France.
Y BertrandDepartment of Pediatric Hematology, IHOP, Lyon, France.
C JubertDepartment of Pediatric Oncology and Hematology, Hôpital Pellegrin, Bordeaux, France.
J-H DalleDepartment of Pediatric Hematology, Hôpital Robert Debré, Paris, France.
C PaillardDepartment of Pediatric Oncology and Hematology, Hôpital Hautepierre, Strasbourg, France.
A BaruchelDepartment of Pediatric Hematology, Hôpital Robert Debré, Paris, France.
L LamantDepartment of Pathology, Hôpital Purpan, Toulouse, France.
G MichelDepartment of Pediatric Hematology, Hôpital La Timone, Marseille, France.
L BrugièresDepartment of Children and Adolescent Oncology, Gustave Roussy, Villejuif, France.
Institut Gustave Roussy · FRHôpital Mère-Enfant · FRHôpital Robert-Debré · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRHôpital de la Timone · FRHôpital d'Hautepierre · FRHôpital Pellegrin · FRHôpital Purpan · FRInstitut d’Hématologie et d’Oncologie Pédiatrique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allogeneic hematopoietic stem cell transplantation (allo-SCT) is a treatment option for relapsed anaplastic large cell lymphoma (ALCL) in children, but reports on its efficacy in this disease are still limited. We analyzed data concerning 34 patients under 18 years of age prospectively registered in the French SFGM-TC database, who had undergone an allo-SCT for the treatment of ALK+ ALCL between 1993 and 2011. At transplant, 28 patients (82.4%) were in CR, whereas 6 exhibited detectable disease. Conditioning regimens were mostly myelo-ablative (n=31). With a median follow-up of 6 years, 5-year overall and event-free survival rates were 70% (SE=8%) and 58% (SE=9%), respectively. The 5-year cumulative incidence of relapse and treatment-related mortality was 18% (SE=7%) and 24% (SE=8%), respectively. Six patients had relapsed (median time, 141 days (35-235)). A durable CR had been obtained in 4/6 patients after injection of donor lymphocytes (n=1) or vinblastine-corticosteroid therapy (n=3). Ten patients had died, eight due to transplant toxicity and two due to progressive disease. Allo-SCT is an efficient treatment for pediatric patients with high-risk relapsed ALK+ ALCL. However, the overall morbidity of allo-SCT raises questions about its place, given the efficacy of targeted agents currently under development in this disease.

Indexed as

Hematopoietic Stem Cell TransplantationReceptor Protein-Tyrosine KinasesTransplantation ConditioningAdolescentAllograftsAnaplastic Lymphoma KinaseChildChild, PreschoolDisease-Free SurvivalFemaleFollow-Up StudiesHumansInfantLymphoma, Large-Cell, AnaplasticMaleRecurrenceALK protein, humanAnaplastic Lymphoma KinaseReceptor Protein-Tyrosine Kinases

Identifiers

PMID25822227
OpenAlexW2037748996

What OpenQuestion holds

Textmetadata
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.