Evidence map›Paper›PMID 31174615›Full record

ArticleJournal for immunotherapy of cancer2019

Opportunities and challenges of active immunotherapy in dogs with B-cell lymphoma: a 5-year experience in two veterinary oncology centers.

Laura Marconato, Luca Aresu, Damiano Stefanello, Stefano Comazzi, Valeria Martini, Roberta Ferrari, Fulvio Riondato, Nicole Rouquet, Patrick Frayssinet, Silvia Sabattini

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Journal for immunotherapy of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.3field-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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  4. Predictive value ofThe veterinary quarterly · 2024
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  11. Frontiers in veterinary science · 2022
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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 at 5 institutions in 2 countries.

Laura MarconatoCentro Oncologico Veterinario, Sasso Marconi, via San Lorenzo ¼, 40037 Sasso Marconi, Bologna, Italy. lauramarconato@yahoo.it.ORCID 0000-0002-7843-615X
Luca AresuDepartment of Veterinary Science, University of Turin, Grugliasco, Turin, Italy.
Damiano StefanelloDepartment of Veterinary Medicine, University of Milan, Milan, Italy.
Stefano ComazziDepartment of Veterinary Medicine, University of Milan, Milan, Italy.
Valeria MartiniDepartment of Veterinary Medicine, University of Milan, Milan, Italy.
Roberta FerrariDepartment of Veterinary Medicine, University of Milan, Milan, Italy.
Fulvio RiondatoDepartment of Veterinary Science, University of Turin, Grugliasco, Turin, Italy.
Nicole RouquetUrodelia, St Lys, Toulouse, France.
Patrick FrayssinetUrodelia, St Lys, Toulouse, France.
Silvia SabattiniDepartment of Veterinary Medical Sciences, University of Bologna, Bologna, Italy.
University of Milan · ITArtelia (France) · FRUniversity of Turin · ITUniversity of Bologna · ITVeterinary Oncological Center · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPet dogs spontaneously develop lymphoma. An anthracycline-based multidrug chemotherapy regimen represents the treatment cornerstone; however, cure is rarely achieved. We have been treating dogs with B-cell lymphoma with an autologous vaccine (APAVAC®) and CHOP-based chemotherapy since 2011.

methodsTo better characterize the safety and efficacy of APAVAC®, and to find the best candidates for immunotherapy, we designed a retrospective study on all dogs treated with chemo-immunotherapy to date and compared them with those dogs treated with chemotherapy only. All dogs were completely staged and re-staged at the end of treatment. The primary endpoint was the effectiveness of chemo-immunotherapy, measured as time to progression (TTP), lymphoma-specific survival (LSS), and 1-, 2-, and 3-year survival rates. The secondary objective was safety.

resultsThree hundred dogs were included: 148 (49.3%) received chemotherapy and 152 (50.7%) chemo-immunotherapy. Overall, the latter survived significantly longer (median LSS, 401 vs 220; P <  0.001). Among dogs with diffuse large B-cell lymphoma, the 1-, 2- and 3-year survival rates were 20, 13 and 8% for chemotherapy, and 51, 19 and 10% for chemo-immunotherapy. The benefit of chemo-immunotherapy was particularly relevant in dogs with concurrent high serum LDH, stage V, substage a disease and not previously treated with steroids (median LSS, 480 vs 85 days; P <  0.001). Among dogs with nodal marginal zone lymphoma, those having at least 3 of the aforementioned characteristics significantly benefited from chemo-immunotherapy (median LSS, 680 vs 160 days, P <  0.001). The 1-, 2- and 3-year survival rates were 30, 16 and 10% for chemotherapy, and 55, 28 and 10% for chemo-immunotherapy. Among dogs with follicular lymphoma, lack of immunotherapy administration was the only variable significantly associated with increased risk of tumor-related death. Chemo-immunotherapy was remarkably well tolerated, with no local or systemic adverse events.

conclusionsOverall, the addition of immunotherapy to a traditional CHOP protocol is associated with improved outcome in dogs with B-cell lymphoma, regardless of histotype and evaluated prognostic factors. Moreover, the identikit of the best candidate for immune-therapy was delineated for the most common histotypes. The study also confirms the excellent tolerability of the vaccine.

Indexed as

AnimalsChildChild, PreschoolDogsFemaleHumansImmunotherapy, ActiveLymphoma, Large B-Cell, DiffuseMalePrognosisTime FactorsAutologous vaccineCancer immunotherapyDLBCLDogFollicular lymphomaLymphomaMZLPrognosisSpontaneous cancer

Identifiers

PMID31174615
PMCPMC6554898
OpenAlexW2953347040

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.