Metronomic vinorelbine combined with durvalumab plus tremelimumab dual immunotherapy in patients with metastatic prostate cancer

Author:

Coquan Elodie1,Hervieu Alice2,Cropet Claire3,Saada–Bouzina Esma4,Rouge Thibaut De La Motte5,Lavaud Pernelle6,Meriaux Emeline1,Borchiellini Delphine4,Crouzet Laurence5,Fuerea Alina6,Gravis Gwenaëlle7,Legrand François8,Dassé Emilie8,Gonçalves Anthony9

Affiliation:

1. Centre François Baclesse

2. Centre Georges-François Leclerc

3. Centre Léon Bérard

4. Centre Antoine Lacassagne

5. Centre Eugène Marquis

6. Gustave Roussy

7. Institut Paoli-Calmettes, Aix Marseille Univ, INSERM, CNRS

8. Unicancer

9. Aix-Marseille Univ, INSERM U1068, CNRS U7258, Institut Paoli-Calmettes

Abstract

Abstract

Immune checkpoint inhibitors (ICI) are a class of immunotherapy drugs that have shown significant success in treating various types of cancers. However, their effectiveness in treating prostate cancer (PC) has been more challenging due to an immunosuppressive tumor microenvironment. Low-dose metronomic chemotherapy have immunomodulatory properties that could enhance immunotherapy and is well-tolerated. MOVIE was a phase 1/2 multi-cohort study with a Bayesian design that evaluated the antitumor activity and safety of metronomic vinorelbine with durvalumab plus tremelimumab. Here, we report the results of the PC cohort during phase 2. Fifteen patients with locally advanced or metastatic PC, resistant to conventional therapies, presenting a measurable disease according to RECISTv1.1, and a performance status (PS)≤1, received metronomic oral vinorelbine 40mg three times a week, and durvalumab 1500mg plus tremelimumab 75mg intravenously at day 1 of 28-day cycles. Primary endpoint was the clinical benefit rate (CBR) evaluated using a Bayesian design. Secondary endpoints included safety, objective response rate (ORR), progression-free survival (PFS), and overall survival (OS). Mean estimated CBR according to a non-informative prior distribution was 12.5% (95% credible interval: 1.7-31.9). One patient achieved PR leading to an ORR of 7.7%, and 4 SD<24 weeks. Median PFS was 1.9 months (95% confidence interval [CI]: 1.7-3.8), and median OS 5.4 months (95%CI: 2.4-12.2). Most frequent treatment-related G≥3 AEs were anemia (13.3%) for vinorelbine, and colitis (20.0%) and diarrhea (13.3%) for ICI. One treatment-related G5 AE (sepsis) was observed. The study outcomes highlighted the complexities of treating advanced PC with ICI, even when combined with metronomic vinorelbine.

Publisher

Springer Science and Business Media LLC

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