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Avelumab for advanced Merkel cell carcinoma in the Netherlands: A real-world cohort

Levy, S., Aarts, M. J. B., Eskens, F. A. L. M., Keymeulen, K. B. M. I., Been, L. B., Grunhagen, D., Van Akkooi, A., Jalving, M. & Tesselaar, M. E. T., 18-Sep-2020, In : Journal for immunotherapy of cancer. 8, 2, 7 p., e001076.

Research output: Contribution to journalArticleAcademicpeer-review

  • Sonja Levy
  • Maureen J.B. Aarts
  • Ferry A.L.M. Eskens
  • Kristien B.M.I. Keymeulen
  • Lukas B. Been
  • Dirk Grunhagen
  • Alexander Van Akkooi
  • Mathilde Jalving
  • Margot E.T. Tesselaar

Background Merkel cell carcinoma (MCC) is associated with high recurrence rates and poor survival when metastatic disease is present. The immune checkpoint inhibitor avelumab has shown high response rates (RRs) and durable responses in patients with advanced MCC (aMCC) in clinical trials. To date, only results from clinical trials, patients treated in an expanded access program and very small numbers of patients have been reported. In this study, detailed real-world efficacy and toxicity data of avelumab in patients with aMCC are reported. Methods Patients with aMCC treated in four dedicated referral centers in the Netherlands were analyzed from February 2017 until December 2019. Patients were included if they had received at least one administration of avelumab, regardless of previous lines of therapy. Patient data were collected retrospectively from patient records. Primary endpoints were response rate (RR) and duration of response (DOR). Secondary endpoints were progression-free survival (PFS), overall survival (OS), and toxicity. Results Fifty-four patients received avelumab. Eight (15%) patients had locally advanced disease (laMCC). In 40 (74%) patients, avelumab was first-line treatment, these included all patients with laMCC. The median follow-up was 8.9 (range 0.5-35.9) months. RR was 57% (n=31) with 24% (n=13) of patients achieving a complete response. The median DOR was 8.4 (range 1.3-22.1) months and 23 (43%) patients had an ongoing response at the end of the study. The median PFS was 8.6 (95% CI 1.6-15.5) months, and the median OS was 25.8 (95% CI 9.1-42.4) months. Six (11%) patients experienced grade 3 toxicity. No grade 4-5 toxicity was seen. Conclusions In this real-world cohort, clinical efficacy and toxicity outcomes in clinical practice were in line with results from clinical trials and showed relatively high RRs and durable responses in patients with aMCC.

Original languageEnglish
Article numbere001076
Number of pages7
JournalJournal for immunotherapy of cancer
Volume8
Issue number2
Publication statusPublished - 18-Sep-2020

    Keywords

  • immunotherapy, programmed cell death 1 receptor, skin neoplasms

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