Evidence map›Paper›PMID 40719208›Full record

ArticleCancer medicine2025

Real-World Treatment Patterns and Outcomes in Patients With Relapsed/Refractory Multiple Myeloma and 1-3 Prior Lines of Therapy: Optum Database.

Binod Dhakal, Hermann Einsele, Jordan M Schecter, William Deraedt, Nikoletta Lendvai, Ana Slaughter, Carolina Lonardi, Sandhya Nair, Nirosha Elsem Varghese, Jianming He and 9 more

Abstract read
In one paragraph

Article in Cancer medicine, 2025. 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
–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

1 citing paper in PubMed.

  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

19 authors.

Binod DhakalMedical College of Wisconsin, Milwaukee, Wisconsin, USA.ORCID https://orcid.org/0000-0002-4377-9742
Hermann EinseleUniversitätsklinikum Würzburg, Medizinische Klinik und Poliklinik II, Würzburg, Germany.
Jordan M SchecterJohnson & Johnson, Raritan, New Jersey, USA.
William DeraedtJohnson & Johnson, Beerse, Belgium.
Nikoletta LendvaiJohnson & Johnson, Raritan, New Jersey, USA.
Ana SlaughterCilag GmbH International, Zug, Switzerland.
Carolina LonardiJohnson & Johnson, Buenos Aires, Argentina.
Sandhya NairJohnson & Johnson, Beerse, Belgium.
Nirosha Elsem VargheseJohnson & Johnson, Beerse, Belgium.
Jianming HeJohnson & Johnson, Raritan, New Jersey, USA.
Akshay KharatJohnson & Johnson, Horsham, Pennsylvania, USA.
Seina LeeJohnson & Johnson, Raritan, New Jersey, USA.
Patricia CostJohnson & Johnson, Raritan, New Jersey, USA.
Ravi PotluriPutnam Associates, New York, New York, USA.
Mythili KoneruLegend Biotech USA Inc., Somerset, New Jersey, USA.
Nitin PatelLegend Biotech USA Inc., Somerset, New Jersey, USA.
Erika FlorendoLegend Biotech USA Inc., Somerset, New Jersey, USA.
Paula Rodriguez-OteroClínica Universidad de Navarra, CIMA, CIBERONC, IDISNA, Pamplona, Spain.
Kwee YongUniversity College London Cancer Institute, London, UK.

Funding

Johnson & JohnsonLegend Biotech
6 · The paper itself

Abstract

backgroundEarly (often continuous) treatment of multiple myeloma (MM) with lenalidomide has become common practice, leading to an increase in lenalidomide-refractory disease.

methodsWe report real-world treatment patterns, health care resource utilization (HCRU), and outcomes for patients with lenalidomide-refractory MM using data from Optum US Claims and Optum electronic health record (EHR) databases with index date from January 2016 to March 2022 (Claims) or December 2021 (EHR). Eligible patients had received 1-3 prior lines of therapy (LOT), including a proteasome inhibitor.

resultsA total of 1383 and 1597 patients with lenalidomide-refractory disease were included from the Claims and EHR databases, respectively, with median ages of 72 and 68 years and mean Charlson Comorbidity Index scores of 4.0 and 3.1. The most common treatment combinations were daratumumab-pomalidomide-dexamethasone, daratumumab-bortezomib-dexamethasone, and pomalidomide-dexamethasone (~5% each). From LOT 2 to LOT 6, treatment attrition (patients who died or received no further treatment) was 95.2% to 95.9%. Median time to next treatment was 5.4 (Claims) and 5.9 months (EHR). Median OS was 35.2 (Claims) and 41.2 months (EHR). HCRU was consistent across LOT.

conclusionsPatients with lenalidomide-refractory MM who received 1-3 prior LOT had poor outcomes and moved quickly through available therapies, demonstrating an unmet need to improve outcomes in this difficult-to-treat patient population.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsMultiple MyelomaNeoplasm Recurrence, LocalAgedAged, 80 and overAntibodies, MonoclonalBortezomibDatabases, FactualDexamethasoneDrug Resistance, NeoplasmFemaleHumansLenalidomideMaleMiddle AgedThalidomideAntibodies, MonoclonalBortezomibdaratumumabDexamethasoneLenalidomidepomalidomideThalidomidehealth care resource utilizationmultiple myelomareal‐world outcomesrefractory

Identifiers

PMID40719208
PMCPMC12301936

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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.