Evidence map›Paper›PMID 26524264›Full record

Trial reportBone marrow transplantation2016

Tandem high-dose chemotherapy with thiotepa and busulfan-melphalan and autologous stem cell transplantation in very high-risk neuroblastoma patients.

C Pasqualini, C Dufour, G Goma, M-A Raquin, V Lapierre, D Valteau-Couanet

Open access · bronzeAbstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Bone marrow transplantation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. The Impact ofChildren (Basel, Switzerland) · 2023
    Article
  6. Review
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  8. Article
  9. Review
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  12. KIR3DL1 Allelic Polymorphism and HLA-B Epitopes Modulate Response to Anti-GD2 Monoclonal Antibody in Patients With Neuroblastoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2016
    Article
  13. Article
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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

6 authors at 1 institution in 1 country.

C PasqualiniDepartment of Paediatric and Adolescent Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
C DufourDepartment of Paediatric and Adolescent Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
G GomaBiostatistics and Epidemiology Unit, Gustave Roussy Cancer Campus, Villejuif, France.
M-A RaquinDepartment of Paediatric and Adolescent Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
V LapierreCell Therapy Unit, Gustave Roussy Cancer Campus, Villejuif, France.
D Valteau-CouanetDepartment of Paediatric and Adolescent Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Institut Gustave Roussy · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-risk neuroblastoma is characterised by poor long-term survival, especially for very high-risk (VHR) patients (poor response of metastases after induction therapy). We report the results of an intensified high-dose chemotherapy (HDC) strategy to improve the prognosis of VHR patients. This strategy was based on tandem HDC with thiotepa and busulfan-melphalan (Bu-Mel) followed by autologous stem cell transplantation (ASCT). All data were prospectively recorded in the Gustave Roussy Paediatric ASCT database. From April 2004 to August 2011, 26 patients were eligible for tandem HDC. The median age at diagnosis was 4.4 years (1-15.9). All patients had metastatic disease. MYCN was amplified in 5/26 tumours. Despite the cumulative toxicity of alkylating agents, the toxicity of the intensified HDC strategy was manageable. Thiotepa-related toxicity was mainly digestive, whereas sinusoidal obstruction syndrome was the main toxicity observed after Bu-Mel. The 3-year event-free survival of this cohort was 37.3% (21.3-56.7). This strategy will be compared with combined (131)I-mIBG/Bu-Mel in the upcoming SIOPEN VHR Neuroblastoma Protocol.

Indexed as

NeuroblastomaStem Cell TransplantationAdolescentAntineoplastic Combined Chemotherapy ProtocolsAutograftsBusulfanChildChild, PreschoolDisease-Free SurvivalFemaleHumansInfantMaleMelphalanRetrospective StudiesSurvival RateBusulfanMelphalanThiotepa

Identifiers

PMID26524264
OpenAlexW2132163676

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.