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. 2017 Jun;13(14):1263-1279.
doi: 10.2217/fon-2017-0072. Epub 2017 Mar 28.

Systematic literature review of efficacy, safety and tolerability outcomes of chemotherapy regimens in patients with metastatic Merkel cell carcinoma

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Systematic literature review of efficacy, safety and tolerability outcomes of chemotherapy regimens in patients with metastatic Merkel cell carcinoma

Paul Nghiem et al. Future Oncol. 2017 Jun.

Abstract

Aim: Merkel cell carcinoma (MCC) is a rare neuroendocrine, cutaneous malignancy with poor prognosis once metastasized. The aim of this study was to conduct a systematic literature review to assess clinical outcomes associated with chemotherapy regimens in metastatic MCC.

Materials & methods: Embase®, MEDLINE®, MEDLINE®-In-Process and CENTRAL were searched for studies published in January 2016.

Results & conclusion: Overall, the literature on chemotherapy in patients with metastatic MCC is sparse, with most studies being case series/reports. Across all studies, response rates ranged from 20 to 61%, with higher response rates in first-line setting (53-61%) versus second-line setting (23-45%). Among responders, duration of response was short (≤8 months) in both first- and second-line settings. There is a need for novel agents that can induce durable responses in metastatic MCC.

Keywords: Merkel cell carcinoma; checkpoint inhibitors; chemotherapy; immunotherapy; metastasis; systematic literature review.

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Conflict of interest statement

Financial & competing interests disclosure

M Bharmal, L Mahnke and H Phatak are employees of Merck KGaA/EMD Serono. P Nghiem is a paid consultant for EMD Serono. JC Becker is a paid consultant for EMD Serono, Pfizer and BMS, and he has received research grants from EMD Serono and BMS. This study was sponsored by Merck KGaA, Darmstadt, Germany and EMD Serono, USA (a US subsidiary of Merck KGaA, Darmstadt, Germany) and is part of an alliance between Merck KGaA and Pfizer, Inc. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.

Medical writing support was provided by S Mardiguian, PAREXEL International, London, UK, and was funded by Merck KGaA, Darmstadt, Germany and Pfizer, Inc.

Figures

<b>Figure 1.</b>
Figure 1.. Preferred reporting items for systematic reviews and meta-analyses study flow diagram.
*The number of studies categorized into different types of metastases exceeds the total number of included studies (n = 35) as some studies reported outcomes for ≥1 type of metastases. MCC: Merkel cell carcinoma; PRISMA: Preferred reporting items for systematic reviews and meta-analyses; SGA: Subjective global assessment.

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