Evidence map›Paper›PMID 41595265›Full record

ArticleCancers2026

Combination of Metronomic Chemotherapy and Rituximab in Frail and Elderly Patients with Relapsed/Refractory Follicular Lymphoma and Ineligible for Lenalidomide Treatment: A Retrospective Analysis.

Sabrina Pelliccia, Marta Banchi, Lucrezia De Marchi, Emanuele Cencini, Claudia Seimonte, Alberto Fabbri, Andrea Nunzi, Susanna Destefano, Guido Bocci, Maria Christina Cox

Abstract read
In one paragraph

Article in Cancers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Sabrina PellicciaHaematology Unit, Azienda Ospedaliera Universitaria Sant'Andrea, 00189 Rome, Italy.
Marta BanchiDepartment of Translational Research and New Technologies in Medicine and Surgery, School of Medicine, University of Pisa, 56126 Pisa, Italy.ORCID 0000-0003-0672-2066
Lucrezia De MarchiDepartment of Biomedicine and Prevention, University Tor Vergata, 00133 Rome, Italy.ORCID 0009-0009-3797-0741
Emanuele CenciniHaematology Unit, Azienda Ospedaliera Universitaria Senese, 53100 Siena, Italy.ORCID 0000-0002-0432-9706
Claudia SeimonteDepartment of Biomedicine and Prevention, University Tor Vergata, 00133 Rome, Italy.
Alberto FabbriHaematology Unit, Azienda Ospedaliera Universitaria Senese, 53100 Siena, Italy.ORCID 0000-0003-2603-9715
Andrea NunziDepartment of Biomedicine and Prevention, University Tor Vergata, 00133 Rome, Italy.ORCID 0009-0001-3514-7980
Susanna DestefanoClinical Pathology, University Tor Vergata, 00133 Rome, Italy.
Guido BocciDepartment of Translational Research and New Technologies in Medicine and Surgery, School of Medicine, University of Pisa, 56126 Pisa, Italy.ORCID 0000-0001-7120-9141
Maria Christina CoxHematology Unit, Fondazione Policlinico Tor Vergata, 00133 Rome, Italy.ORCID 0000-0002-8597-8459

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesRelapsed or refractory follicular lymphoma (rrFL) remains difficult to treat in elderly or frail patients who cannot tolerate standard-dose immuno-chemotherapy as well as novel therapies. Metronomic chemotherapy (mCHEMO) may offer sustained antitumor activity with reduced toxicity. This study assessed the clinical activity and safety of R-DEVEC or R-DEVEC-light in rrFL patients following lenalidomide discontinuation or ineligibility.

methodsData from the ReLLi Lymphoma Registry (2013-2025) were retrospectively analyzed. Eligible patients had rrFL after ≥1 prior therapy and initiated mCHEMO at least six months before data cutoff. Thirteen patients received DEVEC or the etoposide-free DEVEC-light regimen; all but one also received rituximab. Responders received maintenance vinorelbine, low-dose prednisone, and rituximab, followed by vinorelbine-only maintenance until progression or intolerance. Responses were assessed by CT after cycle two and PET/CT at completion of six induction cycles.

resultsmedian age was 77 years (range 58-92); most patients were frail and had advanced disease. At the end of induction, 84% achieved remission (46% CR, 38% PR), with three PR converting to CR during maintenance. After a median follow-up of 27 months, the PFS was 42% (95CI 15-69%) and the OS 73% (95CI 47-100%). A transformation occurred in one patient; the main toxicity was grade 3 neutropenia (31%). DEVEC-light showed improved tolerability versus full DEVEC, with manageable infections and rare discontinuations.

conclusionsMetronomic R-DEVEC-light is a feasible and effective disease-controlling strategy for frail, heavily pretreated rrFL patients who do not tolerate lenalidomide and are excluded from modern therapies. This schedule warrants further prospective evaluation and exploration in combination with targeted agents.

Indexed as

elderlyfollicular lymphomafraillenalidomide-ineligiblemetronomic chemotherapyrelapsed/refractoryrituximab

Identifiers

PMID41595265
PMCPMC12839310

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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.