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Adjuvant treatment with anti-PD-1 in acral melanoma: A nationwide study.
Bloem, Manja; van Not, Olivier J; Aarts, Maureen J B; van den Berkmortel, Franchette W P J; Blank, Christian U; Blokx, Willeke A M; Boers-Sonderen, Marye J; Bonenkamp, Johannes J; de Groot, Jan-Willem B; Haanen, John B; Hospers, Geke A P; Kapiteijn, Ellen W; de Meza, Melissa M; Piersma, Djura; van Rijn, Rozemarijn S; Stevense-den Boer, Marion A M; van der Veldt, Astrid A M; Vreugdenhil, Gerard; van den Eertwegh, Alfons J M; Suijkerbuijk, Karijn P M; Wouters, Michel W J M.
Afiliação
  • Bloem M; Scientific Bureau, Dutch Institute for Clinical Auditing, Leiden, The Netherlands.
  • van Not OJ; Department of Biomedical Data Sciences, Leiden University Medical Centre, Leiden, The Netherlands.
  • Aarts MJB; Department of Surgical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • van den Berkmortel FWPJ; Scientific Bureau, Dutch Institute for Clinical Auditing, Leiden, The Netherlands.
  • Blank CU; Department of Medical Oncology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
  • Blokx WAM; Department of Medical Oncology, GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Boers-Sonderen MJ; Department of Medical Oncology, Zuyderland Medical Centre Sittard, Sittard-Geleen, The Netherlands.
  • Bonenkamp JJ; Department of Medical Oncology and Immunology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • de Groot JB; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Haanen JB; Department of Medical Oncology, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Hospers GAP; Department of Surgery, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Kapiteijn EW; Isala Oncology Center, Zwolle, The Netherlands.
  • de Meza MM; Department of Medical Oncology and Immunology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Piersma D; Department of Medical Oncology, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
  • van Rijn RS; Department of Medical Oncology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Stevense-den Boer MAM; Scientific Bureau, Dutch Institute for Clinical Auditing, Leiden, The Netherlands.
  • van der Veldt AAM; Department of Biomedical Data Sciences, Leiden University Medical Centre, Leiden, The Netherlands.
  • Vreugdenhil G; Department of Surgical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • van den Eertwegh AJM; Department of Internal Medicine, Medisch Spectrum Twente, Enschede, The Netherlands.
  • Suijkerbuijk KPM; Department of Internal Medicine, Medical Centre Leeuwarden, Leeuwarden, The Netherlands.
  • Wouters MWJM; Department of Internal Medicine, Amphia Hospital, Breda, The Netherlands.
Int J Cancer ; 155(8): 1455-1465, 2024 Oct 15.
Article em En | MEDLINE | ID: mdl-38922879
ABSTRACT
Previous studies demonstrated limited efficacy of immune checkpoint inhibitors in unresectable acral melanoma (AM); it remains unclear how this translates to the adjuvant setting. This study investigates clinical outcomes of acral compared to cutaneous melanoma (CM) patients treated with adjuvant anti-PD-1 after complete resection. All stages III-IV AM and CM patients receiving adjuvant anti-PD-1 after complete resection between 2018 and 2022 were included from the prospective nationwide Dutch Melanoma Treatment Registry. We analyzed recurrence-free survival (RFS), distant metastasis-free survival (DMFS), and overall survival (OS). A multivariable Cox regression analysis of RFS was performed to adjust for potential confounders. We included 1958 (86 AM and 1872 CM) patients. At baseline, AM patients more frequently had KIT mutations, higher disease stages, and Eastern Cooperative Oncology Group Performance Status, and fewer BRAF and NRAS mutations. Median RFS was 14.8 months (95% confidence interval [CI] 11.5-29.3) in AM and 37.4 months (95% CI 34.6 to not reached) in CM (p = .002). After correcting for potential confounders, AM remained associated with a higher risk of recurrence (HRadj 1.53; 95% CI 1.07-2.17; p = .019). Two-year DMFS tended to be worse for AM than for CM 64.5% versus 79.7% (p = .050). Two-year OS was significantly lower in AM (71.5% vs. 84.3%; p = .027). The results of this study suggest a poorer outcome of adjuvant-treated AM compared to CM. Studies assessing the added value of adjuvant treatment in AM are needed. Future research should investigate alternative treatment strategies to improve outcomes of high-risk AM.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Inibidores de Checkpoint Imunológico / Melanoma Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Int J Cancer Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Inibidores de Checkpoint Imunológico / Melanoma Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Int J Cancer Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Holanda