Cancers (Oct 2019)

The Management of Oligoprogression in the Landscape of New Therapies for Metastatic Melanoma

  • Michele Guida,
  • Nicola Bartolomeo,
  • Ivana De Risi,
  • Livia Fucci,
  • Andrea Armenio,
  • Ruggero Filannino,
  • Eustachio Ruggieri,
  • Francesco Macina,
  • Michele Traversa,
  • Annalisa Nardone,
  • Francesco Figliuolo,
  • Federica De Luca,
  • Fabio Mele,
  • Stefania Tommasi,
  • Sabino Strippoli

DOI
https://doi.org/10.3390/cancers11101559
Journal volume & issue
Vol. 11, no. 10
p. 1559

Abstract

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Background: A limited degree of progression after a response to treatment is labelled as oligoprogression and is a hot topic of metastatic melanoma (MM) management. Rogue progressive metastases could benefit from local treatment, which could allow the continuation of ongoing systemic therapy, also known as treatment beyond progression (TBP). Methods: We retrospectively reviewed 214 selected MM patients who were treated with v-Raf murine sarcoma viral oncogene homolog B (BRAF)/mitogen-activated-extracellular signal-regulated kinase (MEK) or programmed cell death protein 1 (PD-1) inhibitors and received a local treatment continuing TBP. We performed univariate and multivariable analyses to assess the association between therapy outcomes and a series of clinical and biological features. Results: We identified 27 (10%) oligoprogressed patients treated locally with surgery (14), radiosurgery (11), and electrochemotherapy (2). TBP included PD-1 inhibitors (13) and BRAF/MEK inhibitors (14). The median progression-free survival post oligoprogression (PFSPO) was 14 months (5–19 95% confidence interval (C.I.)). In the univariate analysis, a significantly longer PFSPO was associated with complete response (CR), Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0, neutrophils/lymphocytes ratio (N/L) <2, and progression-free survival (PFS) at oligoprogression >11 months. Nevertheless, in the multivariable analysis, only CR and N/L <2 were found to be associated with longer PFSPO. Conclusions: In selected patients, local treatments contribute to controlling oligoprogression for a long time, allowing the continuation of systemic treatment and prolongation of overall survival (OS). Increasing biological and clinical knowledge is improving the accuracy in identifying patients to apply for local ablative therapies.

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