78% of patients with advanced melanoma who elected to discontinue anti-PD-1 therapy remained progression-free 18 months after treatment cessation

October 6, 2019

Abstract

Background: Programmed cell death protein 1 (PD-1) blocking monoclonal antibodies improve the overall survival of patients with advanced melanoma but the optimal duration of treatment has not been established.

Patients and Methods: This academic real-world cohort study investigated the outcome of 185 advanced melanoma patients who electively discontinued anti-PD-1 therapy with pembrolizumab (N = 167) or nivolumab (N = 18) in the absence of disease progression (PD) or treatment limiting toxicity (TLT) at 14 medical centres across Europe and Australia.

Results: Median time on treatment was 12 months (range 0.7–43). The best objective tumour response at the time of treatment discontinuation was complete response (CR) in 117 (63%) patients, partial response (PR) in 44 (24%) patients and stable disease (SD) in 16 (9%) patients; 8 (4%) patients had no evaluable disease (NE). After a median follow-up of 18 months (range 0.7–48) after treatment discontinuation, 78% of patients remained free of progression. Median time to progression was 12 months (range 2–23). PD was less frequent in patients with CR (14%) compared with patients with PR (32%) and SD (50%). Six out of 19 (32%) patients who were retreated with an anti-PD-1 at the time of PD obtained a new antitumour response.

Conclusions: In this real-world cohort of advanced melanoma patients discontinuing anti-PD-1 therapy in the absence of TLT or PD, the duration of anti-PD-1 therapy was shorter when compared with clinical trials. In patients obtaining a CR, and being treated for >6 months, the risk of relapse after treatment discontinuation was low. Patients achieving a PR or SD as best tumour response were at higher risk for progression after discontinuing therapy, and defining optimal treatment duration in such patients deserves further study. Retreatment with an anti-PD-1 at the time of progression may lead to renewed antitumour activity in some patients.

Clinical trial registration: NCT02673970 (https://clinicaltrials.gov/ct2/show/NCT02673970?cond=melanoma&cntry=BE&city=Jette&rank=3)

Source:

Y J L Jansen, E A Rozeman, R Mason, S M Goldinger, M H Geukes Foppen, L Hoejberg, H Schmidt, J V van Thienen, J B A G Haanen, L Tiainen, I M Svane, S Mäkelä, T Seremet, A Arance, R Dummer, L Bastholt, M Nyakas, O Straume, A M Menzies, G V Long, V Atkinson, C U Blank, B Neyns, Discontinuation of anti-PD-1 antibody therapy in the absence of disease progression or treatment limiting toxicity: clinical outcomes in advanced melanoma, Annals of Oncology, Volume 30, Issue 7, July 2019, Pages 1154–1161, https://doi.org/10.1093/annonc/mdz110

https://academic.oup.com/annon...



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