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Tomsitz, Dirk; Zimmermann, Petra; Kunz, Wolfgang G. ORCID logoORCID: https://orcid.org/0000-0002-5021-1952; Neumann, Jens; Siegmund, Birte J.; Weiss, Bernhard G. ORCID logoORCID: https://orcid.org/0000-0002-8368-0149; Kauke, Teresa ORCID logoORCID: https://orcid.org/0000-0001-6569-9703; Sienel, Wulf; French, Lars E. ORCID logoORCID: https://orcid.org/0000-0002-4629-1486; Klauschen, Frederick ORCID logoORCID: https://orcid.org/0000-0002-9131-2389 und Heinzerling, Lucie ORCID logoORCID: https://orcid.org/0000-0001-5718-3643 (2025): Neoadjuvant treatment with immune checkpoint inhibitors in patients with melanoma: A real‐life retrospective study. In: JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Bd. 23, Nr. 5: S. 600-608

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Abstract

Background: Neoadjuvant treatment with ipilimumab and nivolumab has shown efficacy in melanoma patients with nodal metastases in clinical trials. Real world data on neoadjuvant therapies is lacking.

Patients and Methods: This study investigates the effectiveness of neoadjuvant therapy in a real-world setting and included all melanoma patients who received combined anti-CTLA4/PD1 immunotherapy prior to resection. Pathologic and radiologic responses as well as treatment-related adverse events were assessed, and recurrence-free survival (RFS) was compared between patients with major pathologic response (mPR) and patients without mPR.

Results: In total, 24 patients were analyzed, including patients with distant metastases and patients with prior adjuvant treatment. Median follow-up was 21.5 months. Upon histologic assessment, mPR was achieved in 50% (12/24) of the patients, including two patients with lung metastases and three patients who progressed after prior adjuvant anti-PD1 therapy. Radiologic response after neoadjuvant treatment correlated with mPR. No patient with mPR relapsed during follow-up (median RFS not reached) compared to six out of 12 patients without mPR (median RFS = 13 months, p = 0.005).

Conclusions: Neoadjuvant treatment with ipilimumab and nivolumab is effective in real-world patients with different melanoma subtypes, different stages of disease and even advanced primary tumor.

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