Evidence map›Paper›PMID 32694243›Full record

ArticleOncology research and treatment2020

Patient Characteristics and Outcomes of Relapsed/Refractory Multiple Myeloma in Patients Treated with Proteasome Inhibitors in Germany.

H Tilman Steinmetz, Moushmi Singh, Andrea Lebioda, Sebastian Gonzalez-McQuire, Achim Rieth, Martina Schoehl, Wolfram Poenisch

Abstract read
In one paragraph

Article in Oncology research and treatment, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

7 authors.

H Tilman SteinmetzOncology Cologne, Center for Hematology and Oncology, Cologne, Germany, steinmetz@oncokoeln.de.
Moushmi SinghHealth Economics, Amgen Ltd., Uxbridge, United Kingdom.
Andrea LebiodaHealth Economics, Amgen GmbH, Munich, Germany.
Sebastian Gonzalez-McQuireHealth Economics, Amgen (Europe) GmbH, Rotkreuz, Switzerland.
Achim RiethMedical Development, Amgen GmbH, Munich, Germany.
Martina SchoehlMedical Development, Amgen GmbH, Munich, Germany.
Wolfram PoenischDepartment of Hematology and Cellular Therapy, Medical Clinic and Policlinic I, University of Leipzig, Leipzig, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionReal-world data reflects treatments and outcomes in clinical practice in contrast with controlled clinical trials. This study evaluates real-life multiple myeloma (MM) patients receiving proteasome inhibitor (PI)-based treatments in the second or third therapy line in 2017 in Germany.

methodsThis is a retrospective chart review on adult relapsed/refractory MM patients treated with ≥1 dose of a PI-based regimen in either the second or the third line of therapy. Participating physicians had ≥3 years of clinical experience in treating symptomatic MM patients and used PI according to the label.

resultsDistinct patient profiles for each PI-based regimen emerged. Younger, fitter, transplant-eligible patients received novel PI triplets such as carfilzomib in combination with lenalidomide and dexamethasone (KRd) or IRd. Patients receiving lenalidomide in first-line therapy mostly received lenalidomide-free regimens in second-line therapy. In high-risk patients, no clear treatment patterns could be ascertained. The complete response rates were highest with KRd (13.0%), followed by carfilzomib in combination with dexamethasone (Kd) (5.7%) and bortezomib (4.8%). The very good partial response rates were highest with IRd (76.9%), followed by KRd (53.7%), Kd (25.7%), and bortezomib (20.5%). None of the KRd- or IRd-treated patients responded below a partial response. DISCUSSION/

conclusionClear patient profiles for each PI type were observed. In second-line therapy, younger, fitter, transplant-eligible patients received novel-PI-based triplets, e.g., KRd or IRd. Patients treated with lenalidomide in first-line therapy mostly received lenalidomide-sparing regimens in second-line therapy. In high-risk patients no clear treatment patterns could be ascertained due to the limited sample size.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBoron CompoundsBortezomibDexamethasoneFemaleGermanyGlycineHumansLenalidomideMaleMiddle AgedMultiple MyelomaNeoplasm Recurrence, LocalBoron CompoundsBortezomibcarfilzomibDexamethasoneGlycineixazomibLenalidomideOligopeptidesProteasome InhibitorsChart reviewMultiple myelomaProteasome inhibitors

Identifiers

PMID32694243
PMCPMC7845445

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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.