Evidence map›Paper›PMID 32871820›Full record

ArticleIn vivo (Athens, Greece)

Safety and Effectiveness of Ixazomib Dose-escalating Strategy in Ixazomib-Lenalidomide-Dexamethasone Treatment for Relapsed/Refractory Multiple Myeloma.

Yasukata Ohashi, Megumi Yatabe, Daisuke Niijima, Kentaro Tani, Chiaki Ogawa, Yutaka Yachi, Toshiya Kagoo, Saigen Boku, Hironori Ueno, Takahiro Yano and 2 more

Open access · diamondAbstract read
In one paragraph

Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 51% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

12 authors at 3 institutions in 1 country.

Yasukata OhashiDepartment of Pharmacy, National Hospital Organization Tokyo Medical Center, Tokyo, Japan yasu970554126@gmail.com.
Megumi YatabeDepartment of Pharmacy, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
Daisuke NiijimaDepartment of Pharmacy, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
Kentaro TaniDepartment of Pharmacy, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
Chiaki OgawaDepartment of Pharmacy, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
Yutaka YachiDepartment of Pharmacy, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
Toshiya KagooDivision of Hematology, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
Saigen BokuDivision of Hematology, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
Hironori UenoDivision of Hematology, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
Takahiro YanoDivision of Hematology, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
Koji HigaiLaboratory of Medical Biochemistry, Faculty of Pharmaceutical Sciences Toho University, Chiba, Japan.
Akihiro YokoyamaDivision of Hematology, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
National Hospital Organization · JPTokyo Medical Center · JPToho University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimGastrointestinal toxicity is common in patients receiving common therapy of ixazomib with lenalidomide and low-dose dexamethasone (IRd) for relapsed/refractory multiple myeloma. Here, we investigated the safety and effectiveness of ixazomib dosing schedules. PATIENTS AND

methodsWe retrospectively evaluated 17 consecutive patients treated with IRd (10 patients on ixazomib dose-escalation strategy (2.3 mg starting dose); seven patients on standard dose).

resultsThe incidence of grade 3 or more haematological and grade 2 or more non-haematological adverse events was lower in the dose-escalation group than in the standard-dose group, and only that of diarrhoea was significantly lower. The median time to treatment interruption was significantly longer in the dose-escalation group than in the standard-dose group. There was no significant difference in the overall response rate (20% vs. 43%) and disease control rate (70% vs. 86%).

conclusionA dose-escalation strategy to optimise ixazomib dosing may reduce treatment interruption due to adverse events without compromising its antitumor activity.

Indexed as

Boron CompoundsDexamethasoneLenalidomideMultiple MyelomaAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsGlycineHumansNeoplasm Recurrence, LocalRetrospective StudiesThalidomideAntineoplastic AgentsBoron CompoundsDexamethasoneGlycineixazomibLenalidomideThalidomidedose-escalationeffectivenessIxazomiblenalidomiderelapsed/refractory multiple myelomasafety

Identifiers

PMID32871820
PMCPMC7652488
OpenAlexW3082802670

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.