Evidence map›Paper›PMID 36398133›Full record

ArticleHemaSphere2022

Real-world Outcomes of Relapsed/Refractory Diffuse Large B-cell Lymphoma Treated With Polatuzumab Vedotin-based Therapy.

Lisa Argnani, Alessandro Broccoli, Cinzia Pellegrini, Alberto Fabbri, Benedetta Puccini, Riccardo Bruna, Maria Chiara Tisi, Francesco Masia, Leonardo Flenghi, Maria Elena Nizzoli and 14 more

Open access · goldAbstract read
In one paragraph

Article in HemaSphere, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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.

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

10 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Observational
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. 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

24 authors at 19 institutions in 1 country.

Lisa ArgnaniIRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.
Alessandro BroccoliIRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.
Cinzia PellegriniIRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.
Alberto FabbriUOC Ematologia, Azienda Ospedaliero-Universitaria Senese, Siena, Italy.
Benedetta PucciniAzienda Ospedaliera Universitaria Careggi, Firenze, Italy.
Riccardo BrunaDivision of Hematology, Department of Translational Medicine University of Eastern Piedmont and AOU Maggiore della Carità di Novara, Italy.
Maria Chiara TisiCell Therapy and Hematology, San Bortolo Hospital, Vicenza, Italy.
Francesco MasiaDepartment of Medicine and Surgery, University of Perugia, Italy.
Leonardo FlenghiEmatologia, Azienda Ospedaliera di Perugia, Italy.
Maria Elena NizzoliEmatologia, AUSL/IRCSS Reggio Emilia, Italy.
Maurizio MussoOncoematologia e TMO, Dip. Oncologico La Maddalena, Palermo, Italy.
Marilena SalernoUOC Ematologia ARNAS Garibaldi, Catania, Italy.
Potito Rosario ScalzulliIRCCS "Casa Sollievo della Sofferenza" Hospital, SC Ematologia e Trapianto di Cellule Staminali, San Giovanni Rotondo, Italy.
Daniela Dessi'Unità operativa di Ematologia e CTMO ospedale Businco Arnas AOB, Cagliari, Italy.
Isacco FerrariniDepartment of Medicine, Section of Hematology, University of Verona, Italy.
Elsa PenneseUOSD Centro Diagnosi e Terapia dei Linfomi, Dipartimento Oncologico-Ematologico, Presidio Ospedaliero Santo Spirito, Pescara, Italy.
Elisa LucchiniSC Ematologia, Azienda Sanitaria Universitaria Giuliano Isontina, Trieste, Italy.
Francesca Gaia RossiDivision of Hematology, Fondazione IRCCS Ospedale Maggiore Policlinico, Università degli Studi di Milano, Italy.
Carla MinoiaHematology Unit-IRCCS Istituto Tumori "Giovanni Paolo II" Bari, Italy.
Filippo GherlinzoniAzienda ULSS 2 Marca Trevigiana Ospedale Ca' Foncello, Treviso, Italy.
Pellegrino MustoDipartimento dell'Emergenza e dei Trapianti di Organi (DETO) Scuola di Medicina, Università degli Studi "Aldo Moro", Bari, Italy.
Caterina PattiDivision of Onco-Hematology, Azienda Villa Sofia-Cervello, Palermo, Italy.
Vittorio StefoniIRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.
Pier Luigi ZinzaniIRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.
Istituto di Ematologia di Bologna · ITAzienda Ospedaliera di Perugia · ITAzienda Ospedaliera Universitaria Senese · ITAzienda Ospedaliero-Universitaria Careggi · ITAzienda Sanitaria Unità Locale di Reggio Emilia · ITAzienda Sanitaria Universitaria Integrata di Trieste · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITIstituto Tumori Bari · ITLa Maddalena · ITOspedale Garibaldi · ITOspedale San Bortolo · ITOspedale Vincenzo Cervello · ITPresidio Ospedaliero · ITUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITUniversity of Bari Aldo Moro · ITUniversity of Bologna · ITUniversity of Milan · ITUniversity of Perugia · ITUniversity of Verona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

After FDA and EMA approval of the regimen containing polatuzumab vedotin plus rituximab and bendamustine (PolaBR), eligible relapsed/refractory diffuse large B-cell lymphoma (DLBCL) patients in Italy were granted early access through a Named Patient Program. A multicentric observational retrospective study was conducted focusing on the effectiveness and safety of PolaBR in everyday clinical practice. Fifty-five patients were enrolled. There were 26 females (47.3%), 32 patients were primary refractory and 45 (81.8%) resulted refractory to their last therapy. The decision to add or not bendamustine was at physician's discretion. Thirty-six patients underwent PolaBR, and 19 PolaR. The 2 groups did not differ in most of baseline characteristics. The final overall response rate was 32.7% (18.2% complete response rate), with a best response rate of 49.1%. Median disease-free survival was reached at 12 months, median progression-free survival at 4.9 months and median overall survival at 9 months, respectively. Overall, 88 adverse events (AEs) were registered during treatment in 31 patients, 22 of grade ≥3. Eight cases of neuropathy occurred, all of grades 1-2 and all related to polatuzumab. The two groups of treatment did not differ for effectiveness endpoints but presented statistically significant difference in AEs occurrence, especially in hematological AEs, in AEs of grade equal or greater than 3 and in incidence of neuropathy. Our data add useful information on the effectiveness of Pola(B)R in the setting of heavily pretreated DLBCL and may also suggest a better tolerability in absence of bendamustine without compromise of efficacy.

Identifiers

PMID36398133
PMCPMC9663137
OpenAlexW4308792141

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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 Socratic graph.