Evidence map›Paper›PMID 32912820›Full record

ArticleClinical lymphoma, myeloma & leukemia2020

Feasibility of Long-term Proteasome Inhibition in Multiple Myeloma by in-class Transition From Bortezomib to Ixazomib.

Sudhir Manda, Habte A Yimer, Stephen J Noga, Saulius Girnius, Christopher A Yasenchak, Veena Charu, Roger Lyons, Jack Aiello, Kimberly Bogard, Renda H Ferrari and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical lymphoma, myeloma & leukemia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
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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

19 authors at 12 institutions in 2 countries.

Sudhir MandaArizona Oncology/US Oncology Research, Tucson, AZ.
Habte A YimerTexas Oncology/US Oncology Research, Tyler, TX.
Stephen J NogaMillennium Pharmaceuticals, Inc, Cambridge, MA, a wholly owned subsidiary of Takeda Pharmaceutical Company Limited, Tokyo, Japan.
Saulius GirniusTrihealth Cancer Institute, Cincinnati, OH.
Christopher A YasenchakWillamette Valley Cancer Institute and Research Center/US Oncology Research, Eugene, OR.
Veena CharuPacific Cancer Medical Center, Anaheim, CA.
Roger LyonsTexas Oncology/US Oncology Research, San Antonio, TX.
Jack AielloPatient Empowerment Network, San Jose, CA.
Kimberly BogardMillennium Pharmaceuticals, Inc, Cambridge, MA, a wholly owned subsidiary of Takeda Pharmaceutical Company Limited, Tokyo, Japan.
Renda H FerrariMillennium Pharmaceuticals, Inc, Cambridge, MA, a wholly owned subsidiary of Takeda Pharmaceutical Company Limited, Tokyo, Japan.
Dasha CherepanovMillennium Pharmaceuticals, Inc, Cambridge, MA, a wholly owned subsidiary of Takeda Pharmaceutical Company Limited, Tokyo, Japan.
Brittany DemersMillennium Pharmaceuticals, Inc, Cambridge, MA, a wholly owned subsidiary of Takeda Pharmaceutical Company Limited, Tokyo, Japan.
Vickie LuMillennium Pharmaceuticals, Inc, Cambridge, MA, a wholly owned subsidiary of Takeda Pharmaceutical Company Limited, Tokyo, Japan.
Presley WhiddenMillennium Pharmaceuticals, Inc, Cambridge, MA, a wholly owned subsidiary of Takeda Pharmaceutical Company Limited, Tokyo, Japan.
Suman KambhampatiKansas City Veterans Affairs Medical Center, Kansas City, MO.
Ruemu E BirhirayHematology Oncology of Indiana/American Oncology Network, Indianapolis, IN.
Haresh S JhangianiCompassionate Cancer Care Medical Group, Fountain Valley, CA.
Ralph BocciaCenter for Cancer and Blood Disorders, Bethesda, MD.
Robert M RifkinRocky Mountain Cancer Centers/US Oncology Research, Denver, CO. Electronic address: robert.rifkin@usoncology.com.
Millennium Engineering and Integration (United States) · USTexas Oncology · USArizona Oncology · USCalifornia Pacific Medical Center · USCenter for Cancer and Blood Disorders · USCompassionate Cancer Care · USEmpowerment Program · USRocky Mountain Cancer Centers · USThe US Oncology Network · USTriHealth · USVeterans Health Administration · USWillamette Valley Cancer Institute and Research Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe ongoing US MM-6 study is investigating in-class transition (iCT) from parenteral bortezomib-based induction to all-oral IRd (ixazomib-lenalidomide-dexamethasone) with the aim of increasing proteasome inhibitor (PI)-based treatment adherence and duration while maintaining patients' health-related quality of life (HRQoL) and improving outcomes. PATIENTS AND

methodsUS community sites are enrolling non-transplant-eligible patients with newly diagnosed multiple myeloma (MM) with no evidence of progressive disease after 3 cycles of bortezomib-based therapy to receive IRd (up to 39 cycles or until progression or toxicity). The patients use mobile or wearable digital devices to collect actigraphy (activity and sleep) data and electronically complete HRQoL, treatment satisfaction and medication adherence questionnaires. The primary endpoint is progression-free survival. The key secondary endpoints include response rates and therapy duration.

resultsAt the data cutoff, 84 patients had been treated (median age 73 years; 44% aged ≥ 75 years; 49% men; 15% Black or African American; and 10% Hispanic or Latino). Of the 84 patients, 62% were continuing therapy. The mean duration of total PI therapy was 10.1 months and for the IRd regimen was 7.3 months. With an 8-month median follow-up, the 12-month progression-free survival rate was 86% (95% confidence interval, 73%-93%) from both the start of bortezomib-based treatment and the start of IRd. The overall response rate was 62% (complete response, 4%; very good partial response, 25%; partial response, 33%) after bortezomib-based induction and 70% (complete response, 26%; very good partial response, 29%; partial response, 15%) after iCT. The IRd safety profile was consistent with previous clinical trial data, and HRQoL and treatment satisfaction were maintained.

conclusionThe patients included in the US MM-6 study are representative of the real-world US MM population. The use of iCT might permit prolonged PI-based therapy with promising efficacy, without impacting patients' HRQoL or treatment satisfaction.

Indexed as

AgedAntineoplastic Combined Chemotherapy ProtocolsBoron CompoundsBortezomibFemaleGlycineHumansMaleMultiple MyelomaProgression-Free SurvivalProteasome InhibitorsSurvival AnalysisTreatment OutcomeBoron CompoundsBortezomibGlycineixazomibProteasome InhibitorsDuration of treatmentMedication adherenceOral therapyPatient-reported outcomesReal-world community

Identifiers

PMID32912820
PMCPMC7336931
OpenAlexW3038822856

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.