Evidence map›Paper›PMID 28436974›Full record

ArticleBone marrow transplantation2017

High-dose thiotepa-based chemotherapy with autologous stem cell support in elderly patients with primary central nervous system lymphoma: a European retrospective study.

E Schorb, C P Fox, K Fritsch, L Isbell, A Neubauer, A Tzalavras, R Witherall, S Choquet, O Kuittinen, D De-Silva and 12 more

Open access · bronzeAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

31 citing papers in PubMed, 69 citations in OpenAlex.

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  10. Radiotherapy for newly diagnosed primary central nervous system lymphoma: role and perspective.Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology · 2023
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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

22 authors at 10 institutions in 4 countries.

E SchorbDepartment of Haematology, Oncology and Stem Cell Transplantation, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
C P FoxDepartment of Clinical Haematology, Nottingham University Hospitals NHS Trust, Nottingham, UK.
K FritschDepartment of Haematology, Oncology and Stem Cell Transplantation, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
L IsbellDepartment of Haematology, Oncology and Stem Cell Transplantation, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
A NeubauerStuttgart Cancer Centre, Klinikum Stuttgart, Stuttgart, Germany.
A TzalavrasStuttgart Cancer Centre, Klinikum Stuttgart, Stuttgart, Germany.
R WitherallDepartment of Clinical Haematology, Nottingham University Hospitals NHS Trust, Nottingham, UK.
S ChoquetDepartment of Haematology, APHP, Sorbonne Universités, Hospital Pitié-Salpêtrière, Paris, France.
O KuittinenDepartment of Oncology, Oulu University Hospital, Oulu, Finland.
D De-SilvaDepartment of Haematology, University College Hospital, London, UK.
K CwynarskiDepartment of Haematology, University College Hospital, London, UK.
C HouillierDepartment of Neurology, APHP, Sorbonne Universités, UPMC Hospital Pitié-Salpêtrière, LOC network, Paris, France.
K Hoang-XuanDepartment of Neurology, APHP, Sorbonne Universités, UPMC Hospital Pitié-Salpêtrière, LOC network, Paris, France.
V TouitouDepartment of Ophthalmolgy, APHP, Sorbonne Universités, UPMC Hospital Pitié-Salpêtrière, LOC network, Paris, France.
N CassouxDepartment of Ophthalmology, Curie Institute-Rene Huguenin Hospital, LOC network, Saint-Cloud, France.
J-P MarolleauDepartment of Haematology, University Hospital, Amiens, LOC network, Amiens, France.
J TamburiniDepartment of Haematology, Cochin University Hospital, LOC network, Paris, France.
R HouotDepartment of Haematology, University Hospital, LOC network, Rennes, France.
V DelwailDepartment of Haematology, University Hospital, LCO network, Poitiers, France.
G IllerhausStuttgart Cancer Centre, Klinikum Stuttgart, Stuttgart, Germany.
C SoussainDepartment of Haematology, Curie Institute-Rene Huguenin Hospital, LOC network, Saint-Cloud, France.
B KasendaStuttgart Cancer Centre, Klinikum Stuttgart, Stuttgart, Germany.
Klinikum Stuttgart · DEAssistance Publique – Hôpitaux de Paris · FRUniversity of Freiburg · DEHôpital René Huguenin · FRNottingham University Hospitals NHS Trust · GBCentre Hospitalier Universitaire Amiens-Picardie · FROulu University Hospital · FISorbonne Université · FRUniversity College Hospital · GBUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this retrospective multicentre study, we investigated the outcomes of elderly primary central nervous system lymphoma (PCNSL) patients (⩾65 years) who underwent high-dose chemotherapy followed by autologous stem cell transplantation (HDT-ASCT) at 11 centres between 2003 and 2016. End points included remission, progression-free survival (PFS), overall survival (OS) and treatment-related mortality. We identified 52 patients (median age 68.5 years, median Karnofsky Performance Status before HDT-ASCT 80%) who all underwent thiotepa-based HDT-ASCT. Fifteen patients (28.8%) received HDT-ASCT as first-line treatment and 37 (71.2%) received it as second or subsequent line. Remission status before HDT-ASCT was: CR 34.6%, PR 51.9%, stable disease 3.8% and progressive disease 9.6%. Following completion of HDT-ASCT, 36 patients (69.2%) achieved CR (21.2% first-line setting and 48.1% second or subsequent line setting) and 9 (17.3%) PR (5.8% first-line setting and 11.5% second or subsequent line setting). With a median follow-up of 22 months after HDT-ASCT, median PFS and OS were reached after 51.1 and 122.3 months, respectively. The 2-year PFS and OS rates were 62.0% and 70.8%, respectively. We observed two HDT-ASCT-associated deaths (3.8%). In selected elderly PCNSL patients, HDT-ASCT, using thiotepa-based conditioning regimes, is feasible and effective. Further prospective and comparative studies are warranted to further evaluate the role of HDT-ASCT in elderly PCNSL patients.

Indexed as

AgedAged, 80 and overAntineoplastic Agents, AlkylatingCentral Nervous System NeoplasmsCombined Modality TherapyDisease-Free SurvivalEuropeHematopoietic Stem Cell TransplantationHumansRemission InductionRetrospective StudiesSurvival AnalysisThiotepaTransplantation, AutologousTransplantation ConditioningAntineoplastic Agents, AlkylatingThiotepa

Identifiers

PMID28436974
OpenAlexW2608394083

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.