Evidence map›Paper›PMID 39110988›Full record

ArticleBlood advances2024

Real-world treatment patterns and outcomes in relapsed/refractory multiple myeloma (1-3 prior lines): Flatiron database.

Binod Dhakal, Hermann Einsele, Jordan M Schecter, William Deraedt, Nikoletta Lendvai, Ana Slaughter, Carolina Lonardi, Sandhya Nair, Jianming He, Akshay Kharat and 3 more

Abstract read
In one paragraph

Article in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 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

13 authors.

Binod DhakalDivision of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, WI.ORCID 0000-0002-4377-9742
Hermann EinseleDepartment of Internal Medicine II, Medizinische Klinik und Poliklinik II, Universitätsklinikum Würzburg, Würzburg, Germany.
Jordan M SchecterJanssen Research & Development, Raritan, NJ.
William DeraedtJanssen Pharmaceutica NV, Beerse, Belgium.ORCID 0000-0003-1414-2387
Nikoletta LendvaiJanssen Research & Development, Raritan, NJ.
Ana SlaughterCilag GmbH International, Zug, Switzerland.
Carolina LonardiJanssen, Buenos Aires, Argentina.
Sandhya NairJanssen Pharmaceutica NV, Beerse, Belgium.
Jianming HeJanssen Global Services, LLC, Raritan, NJ.ORCID 0000-0002-5015-3713
Akshay KharatJanssen Scientific Affairs, LLC, Horsham, PA.
Patricia CostJanssen Global Services, LLC, Raritan, NJ.
Satish ValluriJanssen Global Services, LLC, Raritan, NJ.
Kwee YongDepartment of Haematology, Cancer Institute, University College London Cancer Institute, London, United Kingdom.ORCID 0000-0002-6487-276X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractIn the context of multiple myeloma (MM), early use of the immunomodulatory drug lenalidomide has led to an increased population of patients with lenalidomide-refractory MM in early-line settings, but their outcomes are not well characterized. Herein, we report treatment patterns, survival outcomes, prognostic variables, and attrition rates for patients with proteasome inhibitor-exposed, lenalidomide-refractory MM, treated with 1 to 3 prior lines of therapy (LOT). From 12 767 patients with MM in the Flatiron Health database between January 2016 and April 2022, 1455 met the inclusion criteria. The most common subsequent treatments were triplet combinations (41.6% of patients); daratumumab/pomalidomide/dexamethasone was the most common treatment regimen (13.2%). Median real-world progression-free survival (RW-PFS) and overall survival (OS) were 6.5 months and 44.4 months, respectively. RW-PFS was similar in patients with 1, 2, or 3 prior LOT. International Staging System stage III, Eastern Cooperative Oncology Group performance status of 1, hemoglobin <12 g/dL, high-risk cytogenetics, and refractoriness to anti-CD38 antibody at baseline were associated with worse RW-PFS and OS. Outcomes remained similar for patients who received National Comprehensive Cancer Network-preferred treatments and those who received treatments after 2020. In 561 patients with 1 prior LOT at inclusion, the cumulative attrition rate from LOT 2 to 5 was 85%, which included 25% patients who died and 60% with no further treatment. Patients with lenalidomide-refractory MM who have received 1 to 3 prior LOT have poor outcomes and progress rapidly through available therapies, highlighting the need for more effective treatments early in the disease course, before patients are lost to attrition.

Indexed as

Multiple MyelomaAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsDatabases, FactualDexamethasoneDrug Resistance, NeoplasmFemaleHumansLenalidomideMaleMiddle AgedPrognosisThalidomideTreatment OutcomeDexamethasoneLenalidomideThalidomide

Identifiers

PMID39110988
PMCPMC11459902

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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.