Evidence map›Paper›PMID 30061664›Full record

Trial reportBlood cancer journal2018

Phase 1/2 trial of ixazomib, cyclophosphamide and dexamethasone in patients with previously untreated symptomatic multiple myeloma.

Shaji K Kumar, Francis K Buadi, Betsy LaPlant, Alese Halvorson, Nelson Leung, Prashant Kapoor, David Dingli, Morie A Gertz, Ronald S Go, P Leif Bergsagel and 15 more

Abstract readClinical Trial, Phase IClinical Trial, Phase II
In one paragraph

Trial report in Blood cancer journal, 2018. 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
–field-weighted citation impact
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.

  1. Pooled it
  2. Trial
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  5. Trial
  6. Article
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  10. Observational
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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.

Shaji K KumarDivision of Hematology, Mayo Clinic, Rochester, MN, USA. kumar.shaji@mayo.edu.ORCID http://orcid.org/0000-0001-5392-9284
Francis K BuadiDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Betsy LaPlantDepartment of Biostatistics, Mayo Clinic, Rochester, MN, USA.
Alese HalvorsonDepartment of Biostatistics, Mayo Clinic, Rochester, MN, USA.
Nelson LeungDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Prashant KapoorDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
David DingliDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Morie A GertzDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Ronald S GoDivision of Hematology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0002-8284-3495
P Leif BergsagelDivision of Hematology and Oncology, Mayo Clinic, Phoenix, AZ, USA.
Yi LinDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Angela DispenzieriDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Yi Lisa HwaDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Amie FonderDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Miriam HobbsDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Rafael FonsecaDivision of Hematology and Oncology, Mayo Clinic, Phoenix, AZ, USA.
Suzanne R HaymanDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
A Keith StewartDivision of Hematology and Oncology, Mayo Clinic, Phoenix, AZ, USA.
John A LustDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Joseph MikhaelDivision of Hematology and Oncology, Mayo Clinic, Phoenix, AZ, USA.
Wilson GonsalvesDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Craig ReederDivision of Hematology and Oncology, Mayo Clinic, Phoenix, AZ, USA.
Tomas SkacelTakeda Pharmaceutical Company Limited, Osaka, Japan.
S Vincent RajkumarDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Martha Q LacyDivision of Hematology, Mayo Clinic, Rochester, MN, USA.

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Rafael Fonseca · 2015 to 2026
$25.5M
NCI NIH HHS P30 CA015083NCI NIH HHS P50 CA186781
6 · The paper itself

Abstract

Ixazomib is the first oral proteasome inhibitor to enter the clinic. Given the efficacy of bortezomib in combination with cyclophosphamide and dexamethasone, we studied the combination of ixazomib, cyclophosphamide and dexamethasone (ICd) in newly diagnosed multiple myeloma (NDMM) and patients with measurable disease, irrespective of transplant eligibility, were enrolled. The phase 1 was to determine the maximum tolerated dose (MTD) of cyclophosphamide in the combination. Patients received ixazomib 4 mg (days 1, 8, 15), dexamethasone 40 mg (days 1, 8, 15, 22), and cyclophosphamide 300 or 400 mg/m

Indexed as

AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBoron CompoundsCombined Modality TherapyCyclophosphamideDexamethasoneFemaleGlycineHematopoietic Stem Cell TransplantationHumansMaleMiddle AgedMultiple MyelomaNeoplasm StagingBoron CompoundsCyclophosphamideDexamethasoneGlycineixazomib

Identifiers

PMID30061664
PMCPMC6066484

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.