Published August 2015 | Version v1
Journal article

Single-fraction radiation therapy in patients with metastatic Merkel cell carcinoma

  • 1. Department of Medicine/Dermatology, University of Washington, Seattle, Washington (United States)
  • 2. Department of Radiation Oncology, University of Washington, Seattle, Washington (United States)
  • 3. Fred Hutchinson Cancer Research Center, Seattle, Washington (United States)
  • 4. Department of Medicine/Oncology, University of Washington, Seattle, Washington (United States)
  • 5. Seattle Cancer Care Alliance, Seattle, Washington (United States)

Description

Merkel cell carcinoma (MCC) is an aggressive, polyomavirus-associated cancer with limited therapeutic options for metastatic disease. Cytotoxic chemotherapy is associated with high response rates, but responses are seldom durable and toxicity is considerable. Here, we report our experience with palliative single-fraction radiotherapy (SFRT) in patients with metastatic MCC. We conducted retrospective analyses of safety and efficacy outcomes in patients that received SFRT (8 Gy) to MCC metastases between 2010 and 2013. Twenty-six patients were treated with SFRT to 93 MCC tumors located in diverse sites that included skin, lymph nodes, and visceral organs. Objective responses were observed in 94% of the measurable irradiated tumors (86/92). Complete responses were observed in 45% of tumors (including bulky tumors up to 16 cm). "In field" lesion control was durable with no progression in 77% (69/89) of treated tumors during median follow-up of 277 days among 16 living patients. Clinically significant toxicity was seen in only two patients who had transient side effects. An exploratory analysis suggested a higher rate of in-field progression in patients with an immunosuppressive comorbidity or prior recent chemotherapy versus those without (30% and 9%, respectively; P = 0.03). Use of SFRT in palliating MCC patients was associated with an excellent in field control rate and durable responses at treated sites, and with minimal toxicity. SFRT may represent a convenient and appealing alternative to systemic chemotherapy for palliation, for which most patients with oligometastatic MCC are eligible. SFRT may also synergize with emerging systemic immune stimulants by lowering tumor burden and enhancing presentation of viral/tumor antigens

Availability note (English)

Available from http://dx.doi.org/10.1002/cam4.458; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4559027

Additional details

Publishing Information

Journal Title
Cancer Medicine
Journal Volume
4
Journal Issue
8
Journal Page Range
p. 1161-1170
ISSN
2045-7634

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
46124086
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
CHEMOTHERAPY; EPITHELIOMAS; LYMPH NODES; PATIENTS; SIDE EFFECTS; SKIN; TOXICITY
Descriptors DEC
BODY; CARCINOMAS; DISEASES; LYMPHATIC SYSTEM; MEDICINE; NEOPLASMS; ORGANS; THERAPY

Optional Information

Copyright
Copyright (c) 2015 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.
Notes
PMCID: PMC4559027; PMID: 25908228; OAI: oai:pubmedcentral.nih.gov:4559027