BONSAI-2 study: Nivolumab as therapeutic option after cabozantinib failure in metastatic collecting duct carcinoma patients

Sebastiano Buti, Francesca Trentini, Pierangela Sepe, Melanie Claps, Luca Isella, Elena Verzoni, Giuseppe Procopio, Sebastiano Buti, Francesca Trentini, Pierangela Sepe, Melanie Claps, Luca Isella, Elena Verzoni, Giuseppe Procopio

Abstract

Background: The BONSAI phase II trial recently demonstrated the activity of cabozantinib in metastatic collecting duct patients. The outcomes of patients in this setting treated with immunotherapy as second-line is unknown. The aim of the present report was to describe outcomes of patients enrolled in the BONSAI trial that received nivolumab as second-line treatment.

Material and methods: We describe the oncological outcomes in terms of overall response rate, progression-free survival, overall survival and safety. We excluded patients that did not receive any second-line treatment or were treated with agents other than nivolumab.

Results: We identified five patients of whom one was excluded due to lack of data. Three patients obtained clinical benefit (one partial response, two stable disease); the second-line progression-free survival (nivolumab) ranged from 2.8 to 19.9 months to and second-line overall survival ranged from 5.1 to 26.5 months. No new safety signals were observed.

Conclusions: Nivolumab may be considered as second-line therapy option after cabozantinib failure in selected metastatic collecting duct carcinoma patients.

Keywords: cabozantinib; collecting duct carcinoma; immunotherapy; nivolumab; second-line; sequence.

Conflict of interest statement

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Figures

Figure 1.
Figure 1.
Progression-free survival from first-line (cabozantinib) and from second-line (nivolumab). mo, months; PFS, Progression-free survival; Pt, patient.
Figure 2.
Figure 2.
Overall survival. mo, months; OS, overall survival; Pt, patient.

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Source: PubMed

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