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.

Highlights

  • IntroductionAn anthracycline-based multidrug chemotherapy regimen represents the treatment cornerstone; cure is rarely achieved

  • Anthracycline-based multidrug chemotherapy represents the cornerstone for the treatment of canine B-cell lymphoma across all disease stages; the majority of dogs eventually relapses and develops chemo-resistance, and cure is rarely achieved [2]

  • Median lymphoma-specific survival (LSS) was 220 days for dogs receiving chemotherapy and 401 days for those receiving chemoimmunotherapy (P < 0.001)

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Summary

Introduction

An anthracycline-based multidrug chemotherapy regimen represents the treatment cornerstone; cure is rarely achieved. We have been treating dogs with B-cell lymphoma with an autologous vaccine (APAVAC®) and CHOP-based chemotherapy since 2011. Pet dogs most often spontaneously develop B-cell lymphoma [1], for which survival without treatment is measured in weeks or months. Anthracycline-based multidrug chemotherapy represents the cornerstone for the treatment of canine B-cell lymphoma across all disease stages; the majority of dogs eventually relapses and develops chemo-resistance, and cure is rarely achieved [2]. Immunotherapy represents a powerful way to treat cancer, and the last decade has witnessed unprecedented advancements in the understanding of both the molecular drivers of lymphomagenesis and mechanisms by which lymphoma circumvents anti-tumor immunity [3, 4]. Within the first few years of its introduction to the European market, the investigational use of APAVAC® was extended to indolent B-cell lymphomas with suggestive signals of potential usefulness [8]

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