% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Tomsitz:300103,
author = {D. Tomsitz and E. Livingstone$^*$ and C. Loquai and M.
Kaatz and U. Leiter and B. Schilling and P. Terheyden and J.
Hassel and M. Sachse and J. Ulrich and E. Dippel and F.
Meiss and C. Pföhler and A. Kreuter and R. Herbst and M.
Weichenthal and L. Zimmer$^*$ and F. Meier and R.
Rauschenberg and P. Mohr and F. Brunnert and I. von
Wasielewski and R. Gutzmer and D. Schadendorf$^*$ and C.
Berking and S. Ugurel$^*$ and L. Heinzerling},
title = {{E}arly termination does not negatively impact the outcome
of adjuvant immunotherapy in melanoma.},
journal = {Journal of the European Academy of Dermatology and
Venereology},
volume = {nn},
issn = {0926-9959},
address = {Oxford [u.a.]},
publisher = {Wiley-Blackwell},
reportid = {DKFZ-2025-00603},
pages = {nn},
year = {2025},
note = {epub},
abstract = {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.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.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.In patients with resected
metastatic melanoma, shorter treatment duration with
anti-PD1 antibodies is not associated with a worse outcome.},
cin = {ED01},
ddc = {610},
cid = {I:(DE-He78)ED01-20160331},
pnm = {899 - ohne Topic (POF4-899)},
pid = {G:(DE-HGF)POF4-899},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:40119686},
doi = {10.1111/jdv.20650},
url = {https://inrepo02.dkfz.de/record/300103},
}