Evidence map›Paper›PMID 25976868›Full record

ArticleJournal of cancer research and clinical oncology2015

Stem cell mobilization and autologous stem cell transplantation after pretreatment with bendamustine, prednisone and bortezomib (BPV) in newly diagnosed multiple myeloma.

Wolfram Poenisch, Madlen Plötze, Bruno Holzvogt, Marc Andrea, Thomas Schliwa, Thomas Zehrfeld, Doreen Hammerschmidt, Maik Schwarz, Thomas Edelmann, Cornelia Becker and 15 more

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 11 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

25 authors at 8 institutions in 1 country.

Wolfram PoenischDepartment of Hematology, University of Leipzig, Johannisallee 32a, 04103, Leipzig, Germany. Wolfram.poenisch@medizin.uni-leipzig.de.
Madlen PlötzeDepartment of Hematology, University of Leipzig, Johannisallee 32a, 04103, Leipzig, Germany.
Bruno HolzvogtDepartment of Hematology, University of Leipzig, Johannisallee 32a, 04103, Leipzig, Germany.
Marc AndreaDepartment of Hematology, University of Leipzig, Johannisallee 32a, 04103, Leipzig, Germany.
Thomas SchliwaDepartment of Hematology, University of Leipzig, Johannisallee 32a, 04103, Leipzig, Germany.
Thomas ZehrfeldHospital Torgau, Christianistr. 1, 04860, Torgau, Germany.
Doreen HammerschmidtHELIOS Vogtland-Klinikum Plauen, Röntgenstraße 2, 08529, Plauen, Germany.
Maik SchwarzMedical Care Center Schöneck, Albertplatz 1, 08261, Schöneck, Germany.
Thomas EdelmannHematology Practise, Theodor-Heuss-Str. 2, 04435, Schkeuditz, Germany.
Cornelia BeckerHematology Practise, Biedermannstr. 84, 04277, Leipzig, Germany.
Franz Albert HoffmannHematology Practise, Biedermannstr. 84, 04277, Leipzig, Germany.
Andreas SchwarzerHematology Practise, Strümpellstr. 41, Dösen, 04289, Leipzig, Germany.
Ute KreibichHeinrich-Braun-Hospital, Karl-Keil-Str. 35, 08060, Zwickau, Germany.
Kerstin GutscheCarl-Thiem Klinikum Cottbus, Thiemstraße 111, 03048, Cottbus, Germany.
Kolja ReifenrathHospital Zittau, Görlitzer Straße 10, 02763, Zittau, Germany.
Heidrun SchwarzbachGeorgius-Agricola Hospital Zeitz, Lindenallee 1, 06712, Zeitz, Germany.
Simone HeynDepartment of Hematology, University of Leipzig, Johannisallee 32a, 04103, Leipzig, Germany.
Georg-Nikolaus FrankeDepartment of Hematology, University of Leipzig, Johannisallee 32a, 04103, Leipzig, Germany.
Madlen JentzschDepartment of Hematology, University of Leipzig, Johannisallee 32a, 04103, Leipzig, Germany.
Sabine LeibleinDepartment of Hematology, University of Leipzig, Johannisallee 32a, 04103, Leipzig, Germany.
Sebastian SchwindDepartment of Hematology, University of Leipzig, Johannisallee 32a, 04103, Leipzig, Germany.
Thoralf LangeDepartment of Hematology, University of Leipzig, Johannisallee 32a, 04103, Leipzig, Germany.
Vladan VucinicDepartment of Hematology, University of Leipzig, Johannisallee 32a, 04103, Leipzig, Germany.
Haifa-Katrin AlAliDepartment of Hematology, University of Leipzig, Johannisallee 32a, 04103, Leipzig, Germany.
Dietger NiederwieserDepartment of Hematology, University of Leipzig, Johannisallee 32a, 04103, Leipzig, Germany.
Leipzig University · DEAdelwitz Technologiezentrum (Germany) · DECarl-Thiem-Klinikum Cottbus · DEHelios Vogtland Klinikum Plauen · DEInternational University Institute · DEJohann Heinrich von Thünen-Institut · DEKlinikum St. Georg · DESociety for Chemical Engineering and Biotechnology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionReliable information on stem cell toxicity and mobilization of stem cells for autologous stem cell transplantation (SCT) after induction treatment with a combination of bendamustine, prednisone and bortezomib (BPV) is missing. MATERIALS AND

methodsA retrospective analysis of peripheral blood stem cell mobilization and autologous SCT was performed in 35 patients with MM who had received at least one cycle of a BPV-induction therapy consisting of bendamustine 60 mg/m(2) on days 1 and 2, bortezomib 1.3 mg/m(2) on days 1, 4, 8 and 11 and prednisone 100 mg on days 1, 2, 4, 8 and 11 between October 2008 and May 2014. The mobilization regimen consisted of cyclophosphamide 4 g/m(2) and G-CSF (2 × 5 μg/kg). Apheresis was started as soon as peripheral CD34(+) counts exceeded 20 × 10(6)/L with a harvest target of 8 × 10(6) CD34(+)/kg. The minimal accepted target was 2 × 10(6) CD34(+)/kg. The transplantation conditioning therapy consisted of melphalan 200 mg/m(2).

resultsA median number of two (range 1-5) BPV cycles were given. The majority of patients (n = 31, 89 %) responded with two sCR, five nCR, 11 VGPR and 13 PR after BPV induction. Three patients had MR, and one SD. Stem cell mobilization and harvest were successful in all patients. In 19 of 35 patients (54 %), a single apheresis was sufficient to reach the target. The median number of aphereses was one (range 1-4), and the median CD34(+) cell-count/kg was 13.5 (range 3.2-33.1)  × 106. All patients received an autologous SCT. Engraftment was successful in 34 of 35 patients. The median time to a leukocyte count >l × 10(9)/L was 11 days, and the time to untransfused platelet count of >50 × 10(9)/L was 13 days. Thirty-four patients (97 %) responded after the autologous SCT with 11 sCR, two CR, seven nCR, seven VGPR and seven PR. The progression-free survival at 18 months was 87 %, and overall survival was 92 %.

conclusionStem cell mobilization and autologous SCT are feasible in MM patients who have received BPV-induction therapy .

Indexed as

AdultAgedAntineoplastic Agents, AlkylatingAntineoplastic Agents, HormonalAntineoplastic Combined Chemotherapy ProtocolsBendamustine HydrochlorideBlood Component RemovalBortezomibDisease-Free SurvivalFemaleHematopoietic Stem Cell MobilizationHematopoietic Stem Cell TransplantationHumansMaleMiddle AgedMultiple MyelomaAntineoplastic Agents, AlkylatingAntineoplastic Agents, HormonalBendamustine HydrochlorideBortezomibPrednisoneAutologous stem cell transplantationBendamustineBortezomibNewly diagnosed multiple myelomaStem cell mobilization

Identifiers

PMID25976868
PMCPMC11823994
OpenAlexW228849395

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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.