Evidence map›Paper›PMID 31788054›Full record

ArticleOncology letters2019

High efficacy and safety of VTD as an induction protocol in patients with newly diagnosed multiple myeloma eligible for high dose therapy and autologous stem cell transplantation: A report of the Polish Myeloma Study Group.

Iwona Hus, Joanna Mańko, Dariusz Jawniak, Artur Jurczyszyn, Grzegorz Charliński, Katarzyna Poniewierska-Jasak, Lidia Usnarska-Zubkiewicz, Mateusz Sawicki, Agnieszka Druzd-Sitek, Alina Świderska and 16 more

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 25% 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, 9 citations in OpenAlex.

  1. Review
  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

26 authors at 11 institutions in 1 country.

Iwona HusDepartment of Clinical Transplantology, Medical University of Lublin, 20-081 Lublin, Poland.
Joanna MańkoDepartment of Hematooncology and Bone Marrow Transplantation, Medical University of Lublin, 20-081 Lublin, Poland.
Dariusz JawniakDepartment of Hematooncology and Bone Marrow Transplantation, Medical University of Lublin, 20-081 Lublin, Poland.
Artur JurczyszynDepartment of Hematology, Collegium Medicum, Jagiellonian University, 30-051 Cracow, Poland.
Grzegorz CharlińskiDepartment of Hematology, Specialist Muncipial Hospital, 87-100 Torun, Poland.
Katarzyna Poniewierska-JasakDepartment of Hematology, Holycross Cancer Center, 25-734 Kielce, Poland.
Lidia Usnarska-ZubkiewiczDepartment of Hematology, Blood Neoplasms and Bone Marrow Transplantation, Wroclaw Medical University, 50-367 Wroclaw, Poland.
Mateusz SawickiDepartment of Hematology, Blood Neoplasms and Bone Marrow Transplantation, Wroclaw Medical University, 50-367 Wroclaw, Poland.
Agnieszka Druzd-SitekDepartment of Lymphoid Malignancies, Institute of Oncology, 02-781 Warsaw, Poland.
Alina ŚwiderskaDepartment of Hematology, University Hospital in Zielona Góra, 65-046 Zielona Góra, Poland.
Anna KopińskaDepartment of Hematology and Bone Marrow Transplantation, Medical University of Silesia, 40-032 Katowice, Poland.
Norbert GrząśkoDepartment of Hematology, St. John of Dukla Lublin Region Cancer Center, 20-090 Lublin, Poland.
Małgorzata RaźnyDepartment of Hematology, Ludwik Rydygier Memorial Specialized Hospital, 31-826 Cracow, Poland.
Aleksandra WędłowskaDepartment of Hematology and Transplantology, Medical University of Gdansk, 80-211 Gdansk, Poland.
Aleksander PerzyńskiDepartment of Hematology, Institute of Hematology and Transfusion Medicine, 00-791 Warsaw, Poland.
Aleksandra GałązkaDepartment of Hematology, Institute of Hematology and Transfusion Medicine, 00-791 Warsaw, Poland.
Dominik DytfeldDepartment of Hematology and Bone Marrow Transplantation, Poznan University of Medical Sciences, 60-569 Poznan, Poland.
Tadeusz KubickiDepartment of Hematology and Bone Marrow Transplantation, Poznan University of Medical Sciences, 60-569 Poznan, Poland.
Marek RodzajDepartment of Hematology, Ludwik Rydygier Memorial Specialized Hospital, 31-826 Cracow, Poland.
Anna Waszczuk-GajdaDepartment of Hematology, Oncology and Internal Medicine, Medical University of Warsaw, 02-097 Warsaw, Poland.
Joanna Drozd-SokołowskaDepartment of Hematology, Oncology and Internal Medicine, Medical University of Warsaw, 02-097 Warsaw, Poland.
Bartłomiej PogłódekDepartment of Oncologic Hematology, Specialist Hospital, 36-200 Brzozów, Poland.
Anna PasternakDepartment of Hematology, Independent Public Health Care of Ministry of The Interior and Administration, 10-228 Olsztyn, Poland.
Monika Długosz-DaneckaDepartment of Hematology, Collegium Medicum, Jagiellonian University, 30-051 Cracow, Poland.
Agnieszka SzymczykDepartment of Clinical Transplantology, Medical University of Lublin, 20-081 Lublin, Poland.
Anna DmoszyńskaDepartment of Clinical Transplantology, Medical University of Lublin, 20-081 Lublin, Poland.
Medical University of Lublin · PLInstytut Hematologii i Transfuzjologi · PLJagiellonian University · PLMedical University of Warsaw · PLPoznan University of Medical Sciences · PLWroclaw Medical University · PLGdańsk Medical University · PLHoly Cross University · PLLublin Oncology Center · PLMedical University of Silesia · PLUniversity of Zielona Góra · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present retrospective analysis evaluated the efficacy and safety of the VTD (bortezomib, thalidomide, dexamethasone) regimen in 205 newly-diagnosed patients with multiple myeloma (MM) eligible for high dose therapy and autologous stem cell transplantation (HDT/ASCT) in routine clinical practice. With a median of 6 cycles (range, 1-8), at least partial response was achieved in 94.6% and at least very good partial response (VGPR) was achieved in 67.8% of patients. Peripheral neuropathy (PN) grade 2-4 was observed in 28.7% of patients. In 72% of patients undergoing stem cell mobilization one apheresis allowed the number of stem cells sufficient for transplantation to be obtained. Following HDT/ASCT the sCR rate increased from 4.9 to 14.4% and CR from 27.8 to 35.6%. The results demonstrated that VTD as an induction regimen was highly efficient in transplant eligible patients with MM with increased at least VGPR rate following prolonged treatment (≥6 cycles). Therapy exhibited no negative impact on stem cell collection, neutrophils and platelets engraftment following ASCT. Therapy was generally well tolerated and PN was the most common reason of dose reduction or treatment discontinuation.

Indexed as

first-line therapymultiple myelomatransplant-eligible patientsVTD

Identifiers

PMID31788054
PMCPMC6865789
OpenAlexW2976688542

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.