Evidence map›Paper›PMID 33097652›Full record

ArticleESMO open2020

Haematopoietic stem cell transplantation in adult soft-tissue sarcoma: an analysis from the European Society for Blood and Marrow Transplantation.

Christoph E Heilig, Manuela Badoglio, Myriam Labopin, Stefan Fröhling, Simona Secondino, Jürgen Heinz, Emmanuelle Nicolas-Virelizier, Didier Blaise, Clément Korenbaum, Armando Santoro and 10 more

Open access · goldAbstract read
In one paragraph

Article in ESMO open, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.1field-weighted citation impact, top 45% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Guideline
  2. Article
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

20 authors at 16 institutions in 6 countries.

Christoph E HeiligDepartment of Translational Medical Oncology (TMO), National Center for Tumor Diseases (NCT) and German Cancer Research Center (DKFZ), Heidelberg, Germany; German Cancer Consortium (DKTK), Heidelberg, Baden-Württemberg, Germany; Department of Medicine V, University Hospital Heidelberg, Heidelberg, Baden-Württemberg, Germany. Electronic address: christoph.heilig@nct-heidelberg.de.
Manuela BadoglioEBMT Paris study office, Department of Haematology, Hospital Saint-Antoine, Paris, Île-de-France, France.
Myriam LabopinSaint Antoine Hospital, Université Pierre et Marie Curie, Paris, Île-de-France, France.
Stefan FröhlingDepartment of Translational Medical Oncology (TMO), National Center for Tumor Diseases (NCT) and German Cancer Research Center (DKFZ), Heidelberg, Germany; German Cancer Consortium (DKTK), Heidelberg, Baden-Württemberg, Germany.
Simona SecondinoMedical Oncology, I.R.C.C.S. San Matteo University Hospital Foundation, Pavia, Italy.
Jürgen HeinzMedicine I, University Medical Center Freiburg, Freiburg, Baden-Württemberg, Germany.
Emmanuelle Nicolas-VirelizierHematology Department, Centre Léon Bérard, Lyon, Rhône-Alpes, France.
Didier BlaiseInstitut Paoli Calmettes, Departement D'Hematologie, Centre de Recherche en Cancerologie de Marseille, Marseille, Provence-Alpes-Côte d'Azu, France.
Clément KorenbaumMedical Oncology and Cellular Therapy, Hospital Tenon Medical Oncology, Paris, Île-de-France, France.
Armando SantoroDepartment of Oncology-Haematology, Humanitas Cancer Center, IRCCS, Milan, Italy.
Mareike VerbeekInternal Medicine III, Technical University of Munich, Munchen, Bayern, Germany.
William KrügerHaematology/Oncology, University Medicine Greifswald, Greifswald, Mecklenburg-Vorpommern, Germany.
Salvatore SienaNiguarda Cancer Center, Grande Ospedale Metropolitano Niguarda, Milan, Italy; Oncology and Hemato-Oncology, Università degli Studi di Milano, Milano, Italy.
Jakob R PasswegDivision of Hematology, University Hospital Basel, Basel, BS, Switzerland.
Massimo Di NicolaUnit of Immunotherapy and Innovative Therapeutics, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.
Jose RifónHematology Service and Cell Therapy Area, Clínica Universidad de Navarra, Pamplona, Navarra, Spain.
Peter DregerDepartment of Medicine V, University Hospital Heidelberg, Heidelberg, Baden-Württemberg, Germany.
Ulrike KoehlInstitute of Clinical Immunology, Fraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Sachsen, Germany; Institute of Cellular Therapeutics, Hannover Medical School, Hannover, Niedersachsen, Germany.
Christian ChabannonCentre de Thérapie Cellulaire, Département de Biologie du Cancer, Institut Paoli-Calmettes, Inserm CBT-1409, Marseille, Provence-Alpes-Côte d'Azu, France.
Paolo PedrazzoliInternal Medicine and Medical Therapy, Università degli Studi di Pavia, Pavia, Lombardia, Italy.
Sorbonne Université · FRGerman Cancer Research Center · DEUniversity of Pavia · ITCentre de Recherche en Cancérologie de Marseille · FRCentre Léon Bérard · FRClinica Universidad de Navarra · ESHeidelberg University · DEHumanitas University · ITInserm · FRIstituti di Ricovero e Cura a Carattere Scientifico · ITMedizinische Hochschule Hannover · DEUniversität Bayern · DEUniversitätsmedizin Greifswald · DEUniversity Hospital of Basel · CHUniversity Medical Center Freiburg · DEUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe role of high-dose chemotherapy with autologous stem cell transplantation (ASCT) in the treatment of soft-tissue sarcoma (STS) remains an unsettled issue. Prospective clinical trials failed to prove a benefit of the procedure but were limited by small and heterogeneous patient cohorts. Thus, it is unknown if ASCT may be a valuable treatment option in specific patient subgroups.

methodsThe purpose of this study was to investigate the value of ASCT according to histological subtype in STS patients who were registered in the European Society for Blood and Marrow Transplantation database between 1996 and 2016.

resultsMedian progression-free (PFS) and overall survival (OS) in the entire cohort of 338 patients were 8.3 and 19.8 months, respectively, and PFS and OS at 5 years were 13% and 25%, respectively. Analysis of outcomes in different subgroups showed that younger age, better remission status before transplantation and melphalan-based preparative regimen were predictive of benefit from ASCT, whereas histology and grading had no statistically significant impact.

conclusionsOutcomes after ASCT compared favorably to those of recent trials on conventional chemotherapies and targeted therapies in STS, including histology-tailored approaches. ASCT, thus, should be reinvestigated in clinical trials focusing on defined patient subgroups.

Indexed as

Hematopoietic Stem Cell TransplantationSarcomaAdultAntineoplastic Combined Chemotherapy ProtocolsBone MarrowHumansProspective StudiesTransplantation, Autologoushigh-dose chemotherapysoft-tissue sarcomastem cell transplantation

Identifiers

PMID33097652
PMCPMC7590345
OpenAlexW3094048200

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.