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Tomsitz, Dirk ORCID logoORCID: https://orcid.org/0000-0003-0036-072X; Livingstone, Elisabeth; Loquai, Carmen; Kaatz, Martin; Leiter, Ulrike ORCID logoORCID: https://orcid.org/0000-0002-8019-1577; Schilling, Bastian ORCID logoORCID: https://orcid.org/0000-0001-8859-4103; Terheyden, Patrick; Hassel, Jessica; Sachse, Michael; Ulrich, Jens; Dippel, Edgar; Meiss, Frank; Pföhler, Claudia; Kreuter, Alexander; Herbst, Rudolf; Weichenthal, Michael; Zimmer, Lisa; Meier, Friedegund; Rauschenberg, Ricarda; Mohr, Peter; Brunnert, Fiona; von Wasielewski, Imke; Gutzmer, Ralf; Schadendorf, Dirk ORCID logoORCID: https://orcid.org/0000-0003-3524-7858; Berking, Carola ORCID logoORCID: https://orcid.org/0000-0003-0229-8931; Ugurel, Selma und Heinzerling, Lucie ORCID logoORCID: https://orcid.org/0000-0001-5718-3643 (22. März 2025): Early termination does not negatively impact the outcome of adjuvant immunotherapy in melanoma. In: Journal of the European Academy of Dermatology and Venereology, Bd. 39, Nr. 11: S. 1975-1986 [PDF, 1MB]

Abstract

Background: Adjuvant treatment with anti-PD1 antibodies has been shown to effectively reduce the risk of recurrence in patients with resected metastatic melanoma. Whether a full 12-month duration of treatment is needed to achieve full clinical benefit is not known. This study investigated the survival outcome depending on the duration of adjuvant anti-PD1 therapy.

Methods: From the prospective multicentre real-world skin cancer registry ADOREG data of 620 patients who finished adjuvant treatment with nivolumab or pembrolizumab for AJCCv8 stage III/IV resected melanoma was analyzed. Recurrence-free survival (RFS) and overall survival (OS) were compared between patients with regular treatment duration (52 ± 4 weeks; n = 229) and no disease recurrence during therapy (A1) and patients with a premature end of treatment (<48 weeks; n = 214, B). Patients with disease recurrence during adjuvant treatment were included in cohort A2.

Results: The median duration of follow-up was 26.0 months [interquartile range (IQR) 18.0–34.0] in group A1 [median treatment duration 51.3 weeks (IQR 50.0–52.1) and 19.0 months (IQR 13.0–29.0)] in group B [median treatment duration 22.2 weeks (IQR 10.0–34.8)]. Reasons for early discontinuation were treatment-related side effects in 45.3% (n = 97) and other reasons than toxicity in 54.7% (n = 117). The 2-year rate of RFS was 72.4% (95% CI, 68.5–76.3) for patients in group B and 51.5% (95% CI, 48.8–54.2) in patients with regular and intended regular treatment duration (A1 plus A2). When analysing the patients who did not relapse during adjuvant treatment (A1), there was a significantly higher RFS rate of 84.1% (95% CI, 81.5–86.7). When only assessing patients with a recurrence after more than 12 months after initiation of therapy, there was a trend towards better RFS in patients with regular treatment duration.

Conclusions: In patients with resected metastatic melanoma, shorter treatment duration with anti-PD1 antibodies is not associated with a worse outcome.

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