Evidence map›Paper›PMID 38409530›Full record

Trial reportLeukemia2024

Long-term outcomes by bone marrow B-cell depletion from the R2W trial of bortezomib with cyclophosphamide and rituximab in Waldenstrőm macroglobulinaemia.

Ruth de Tute, Nicholas Counsell, Laura Clifton-Hadley, Shirley D'Sa, Guy Pratt, Gavin Campbell, Lauren Campbell, Ross Sadler, William Townsend, Bilyana Popova and 4 more

Open access · greenAbstract readRandomized Controlled TrialClinical Trial, Phase II
In one paragraph

Trial report in Leukemia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

14 authors at 7 institutions in 1 country.

Ruth de Tute *St James's University Hospital, Leeds, UK.
Nicholas Counsell *CR UK and UCL Cancer Trials Centre, London, UK.ORCID 0000-0002-0688-9192
Laura Clifton-HadleyCR UK and UCL Cancer Trials Centre, London, UK.
Shirley D'SaUniversity College London Hospital, London, UK.
Guy PrattUniversity Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Gavin CampbellColchester General Hospital, Colchester, UK.
Lauren CampbellOxford University Hospitals NHS Foundation Trust, Oxford, UK.
Ross SadlerOxford University Hospitals NHS Foundation Trust, Oxford, UK.
William TownsendUniversity College London Hospital, London, UK.
Bilyana PopovaCR UK and UCL Cancer Trials Centre, London, UK.
Paul SmithCR UK and UCL Cancer Trials Centre, London, UK.
Oliver SchofieldCR UK and UCL Cancer Trials Centre, London, UK.
Roger OwenSt James's University Hospital, Leeds, UK.
Rebecca AuerBarts Health NHS Trust, London, UK. Rebecca.auer@nhs.net.ORCID 0000-0001-7169-7659
University College London · GBOxford University Hospitals NHS Trust · GBSt James's University Hospital · GBUniversity College Hospital · GBBarts Health NHS Trust · GBColchester Hospital · GBUniversity Hospitals Birmingham NHS Foundation Trust · GB

Funding

Cancer Research UK 14139Cancer Research UK (CRUK) C26303/A14139
6 · The paper itself

Abstract

There remains a lack of consensus as to the most appropriate primary therapy in Waldenstrőm macroglobulinemia (WM). We evaluated a novel bortezomib-based combination and developed a sensitive WM-specific flow cytometry assay (limit of detection 0.004% of leucocytes) to assess bone marrow (BM) response. Sixty treatment-naïve WM patients were enroled into this phase II trial and randomised (2:1) to receive cyclophosphamide and rituximab with either bortezomib (BRC) or fludarabine (FCR). The primary objective was to assess the overall response rate (ORR) in eligible patients receiving BRC (N = 41). An ORR of 97.6% (95%CI:87.1-99.9) was observed; 27 (65.9%) patients remain alive without progression after 62.6 months median follow-up, with 2-, 3- and 5-year progression-free survival (PFS) rates of 92.7% (95%CI:79.0-97.6), 80.5% (95%CI:64.8-89.7) and 65.5% (95%CI:48.8-77.9). Persistent WM B-cells were demonstrable in 19/38 patients at the end of treatment (median 0.24%, range 0.02-11.2%). PFS was markedly longer in patients with BM B-cell depletion (<0.004%) compared to those who had persistent BM B-cells detectable at end of treatment (HR = 0.06, 95%CI:0.01-0.47, p < 0.001), and remained independently associated after adjusting for baseline risk stratification or investigator-assessed response. BRC is a tolerable, highly efficacious regimen for treatment-naïve WM patients. BM B-cell depletion is independently associated with patient outcomes.

Indexed as

Waldenstrom MacroglobulinemiaAntineoplastic Combined Chemotherapy ProtocolsBone MarrowBortezomibCyclophosphamideHumansRituximabBortezomibCyclophosphamideRituximab

Identifiers

PMID38409530
PMCPMC7617639
OpenAlexW4392168088

What OpenQuestion holds

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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.