Evidence map›Paper›PMID 31913498›Full record

SynthesisCancer2020

Venous thromboembolism risk with contemporary lenalidomide-based regimens despite thromboprophylaxis in multiple myeloma: A systematic review and meta-analysis.

Rajshekhar Chakraborty, Irbaz Bin Riaz, Saad Ullah Malik, Naimisha Marneni, Alex Mejia Garcia, Faiz Anwer, Alok A Khorana, S Vincent Rajkumar, Shaji Kumar, M Hassan Murad and 3 more

Registry-linked trialOpen access · greenAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05541978 (Thrombosis in Newly Diagnosed Multiple Myeloma Patients), which is not on this map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.2field-weighted citation impact, top 7% 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.

NCT05541978 completednot on this mapstarted 2022, after this paper: background citation

Thrombosis in Newly Diagnosed Multiple Myeloma Patients: a Clinical Audit of Intermediate Dose Low Molecular Weight Heparin

TypeobservationalSponsorCatalina CodreanuRan2022 to 2023Enrolled140ConditionsMultiple Myeloma, Venous Thromboembolism, Arterial ThromboembolismArmsMultiple myeloma
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Supportive care in myeloma-when treating the clone alone is not enough.Hematology. American Society of Hematology. Education Program · 2024
    Review
  8. Review
  9. Review
  10. Article
  11. Incidence of thromboembolism and associated factors in multiple myeloma patients treated with immunomodulatory drugs: a retrospective analysis in Belo Horizonte, Brazil.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2023
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Prevention of venous thromboembolism in hematologic neoplasms: an expert consensus from SEHH-SETH.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
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 at 4 institutions in 1 country.

Rajshekhar ChakrabortyTaussig Cancer Center, Cleveland Clinic, Cleveland, Ohio.ORCID 0000-0001-7336-3003
Irbaz Bin RiazDivision of Medical Oncology, Mayo Clinic, Rochester, Minnesota.
Saad Ullah MalikDepartment of Hematology and Oncology, University of Arizona, Tucson, Arizona.
Naimisha MarneniTaussig Cancer Center, Cleveland Clinic, Cleveland, Ohio.
Alex Mejia GarciaTaussig Cancer Center, Cleveland Clinic, Cleveland, Ohio.
Faiz AnwerTaussig Cancer Center, Cleveland Clinic, Cleveland, Ohio.
Alok A KhoranaTaussig Cancer Center, Cleveland Clinic, Cleveland, Ohio.
S Vincent RajkumarDivision of Hematology, Mayo Clinic, Rochester, Minnesota.
Shaji KumarDivision of Hematology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0001-5392-9284
M Hassan MuradCenter for the Science of Health Care Delivery, Mayo Clinic, Rochester, Minnesota.
Zhen WangCenter for the Science of Health Care Delivery, Mayo Clinic, Rochester, Minnesota.
Safi U KhanDepartment of Internal Medicine, West Virginia University, Morgantown, West Virginia.
Navneet S MajhailBlood and Marrow Transplant Program, Taussig Cancer Center, Cleveland Clinic, Cleveland, Ohio.ORCID 0000-0001-7082-891X
Cleveland Clinic · USMayo Clinic · USUniversity of Arizona · USWest Virginia University · US

Funding

West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Laura F. Gibson · 2012 to 2026
$81.0M
NIGMS NIH HHS U54 GM104942
6 · The paper itself

Abstract

backgroundThromboprophylaxis is routinely used with lenalidomide-based regimens in multiple myeloma because of a substantial risk of venous thromboembolism (VTE). However, little is known about the incidence of VTE with contemporary lenalidomide-based regimens. The objective of the current study was to estimate the incidence of VTE despite thromboprophylaxis with currently used lenalidomide-based regimens in patients with myeloma.

methodsThe Ovid MEDLINE, Embase, and Cochrane databases were queried from study inception to January 2019 for keywords to cover the following concepts: "lenalidomide," "venous thromboembolism," and "multiple myeloma." Phase 1, 2, and 3 clinical trials evaluating lenalidomide-based regimens with thromboprophylaxis were included. The pooled incidence rate of VTE was estimated using a random-effects model.

resultsThe search generated 1372 citations, with 51 clinical trials and 9069 patients included for analysis. The most common thromboprophylaxis agents were aspirin, low-molecular-weight heparin or warfarin, administered either per risk-stratification or at investigators' discretion. The pooled incidence of VTE in trials of patients who had newly diagnosed and relapsed/refractory myeloma was 6.2% (95% CI, 5.4%-7.1%) over median treatment durations ranging from 2 to 34 cycles, which translated into 1.2 VTE events per 100 patient-cycles (95% CI, 0.9-1.7 VTE events per 100 patient-cycles). Among contemporary regimens, the risk of VTE was low with combined lenalidomide and low-dose dexamethasone (0.2 [95% CI, 0.1-0.6] events/100 patient-cycles) and lenalidomide maintenance (0.0 [95% CI, 0.0-0.7] events per 100 patient-cycles). VTE risk was higher with combined lenalidomide and low-dose dexamethasone plus proteasome inhibitors (1.3 [95% CI, 0.7-2.3] events per 100 patient-cycles).

conclusionsDespite adequate thromboprophylaxis, lenalidomide-based regimens have a substantial risk of VTE in controlled clinical trial settings. Further studies are needed on new thromboprophylaxis strategies with regimens that have a high VTE risk.

Indexed as

Angiogenesis InhibitorsAnticoagulantsDexamethasoneHumansIncidenceLenalidomideMultiple MyelomaVenous ThromboembolismAngiogenesis InhibitorsAnticoagulantsDexamethasoneLenalidomidelenalidomidemultiple myelomasurvivorshipthromboprophylaxisvenous thromboembolism

Identifiers

PMID31913498
PMCPMC7453956
OpenAlexW2999553182

What OpenQuestion holds

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Registered trials

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.