Evidence map›Paper›PMID 28622306›Full record

ArticleBlood cancer journal2017

Changes in uninvolved immunoglobulins during induction therapy for newly diagnosed multiple myeloma.

P Ravi, S Kumar, W Gonsalves, F Buadi, M Q Lacy, R S Go, A Dispenzieri, P Kapoor, J A Lust, D Dingli and 7 more

Abstract read
In one paragraph

Article in Blood cancer journal, 2017. 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
–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

5 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. 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

17 authors.

P RaviDepartment of Internal Medicine, Mayo Clinic, Rochester, MN, USA.
S KumarDivision of Hematology, Mayo Clinic, Rochester, MN, USA.ORCID 0000-0001-5392-9284
W GonsalvesDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
F BuadiDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
M Q LacyDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
R S GoDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
A DispenzieriDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
P KapoorDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
J A LustDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
D DingliDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Y LinDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
S J RussellDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
N LeungDivision of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, USA.ORCID 0000-0002-5651-1411
M A GertzDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
R A KyleDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
P L BergsagelDivision of Hematology and Oncology, Mayo Clinic Arizona, Scottsdale, AZ, USA.
S V RajkumarDivision of Hematology, Mayo Clinic, Rochester, MN, USA.

Funding

Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Rafael Fonseca · 2015 to 2026
$25.5M
Prevalence and Progression of Monoclonal GammopathiesR01CA107476 · NCI · MAYO CLINIC ROCHESTER · PI KUMAR, SHAJI KUNNATHU, RAJKUMAR, S VINCENT · 2004 to 2018
$4.6M
Onset and biomarkers for progression of monoclonal gammopathiesR01CA168762 · NCI · MAYO CLINIC ROCHESTER · PI KUMAR, SHAJI KUNNATHU, RAJKUMAR, S VINCENT · 2012 to 2024
$3.2M
NCI NIH HHS P50 CA186781NCI NIH HHS R01 CA107476NCI NIH HHS R01 CA168762
6 · The paper itself

Abstract

Little is known about the impact of multiple myeloma (MM) treatment on uninvolved immunoglobulins (Ig). We identified 448 patients who received high-dose dexamethasone (HD-DEX), lenalidomide and dexamethasone (RD), bortezomib and dexamethasone (VD), bortezomib, cyclophosphamide and dexamethasone (VCD) or bortezomib, lenalidomide and dexamethasone (VRD) for newly diagnosed MM at our institution between 2000 and 2013, and who had available data on absolute lymphocyte count (ALC) and quantitative uninvolved Ig at baseline and at the end of four cycles of therapy. Changes in ALC and uninvolved Ig were significantly different across treatments, with VCD and HD-DEX producing reductions in uninvolved Ig, and RD, VD and VRD leading to increases in uninvolved Ig. In addition, treatment with RD, VD and VRD was independently associated with higher odds of achieving a ⩾25% increase in or normalization of the primary uninvolved Ig on multivariate analysis. Although achievement of a humoral response in the primary uninvolved Ig was associated with a higher odds of achieving VGPR or better after four cycles of therapy, it was not associated with improved overall survival. These data highlight the different mechanisms of action of MM drugs and point toward a possible role for the use of VCD in treating antibody-mediated autoimmune disease.

Indexed as

AdultAgedAged, 80 and overCohort StudiesDisease-Free SurvivalFemaleHumansMaleMiddle AgedMultiple MyelomaRemission InductionTreatment Outcome

Identifiers

PMID28622306
PMCPMC5584483

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.