Oncotarget

Research Papers:

This article has an addendum. Addendum in: Oncotarget. 2023; 14:753-753.

Effectiveness and toxicity of cetuximab with concurrent RT in locally advanced cutaneous squamous cell skin cancer: a case series

Mark Chang, Wolfram Samlowski _ and Raul Meoz

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Oncotarget. 2023; 14:709-718. https://doi.org/10.18632/oncotarget.28470

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Abstract

Mark Chang1, Wolfram Samlowski2,3,4 and Raul Meoz2,3

1 University Medical Center of Southern Nevada, Las Vegas, NV 89102, USA

2 Comprehensive Cancer Centers of Nevada, Las Vegas, NV 89148, USA

3 Department of Internal Medicine, University of Nevada, Las Vegas (UNLV), Las Vegas, NV 89102, USA

4 Department of Internal Medicine, University of Nevada, Reno, NV 89557, USA

Correspondence to:

Wolfram Samlowski, email: [email protected]

Keywords: keratinocyte carcinoma; squamous cell skin cancer; cetuximab; epidermal growth factor receptor; radiation therapy

Received: April 17, 2023     Accepted: June 19, 2023     Published: July 07, 2023

Copyright: © 2023 Chang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

ABSTRACT

Background: Treatment for locally advanced cutaneous squamous cell cancers (laCSCC) remains poorly defined. Most laCSCC tumors express high levels of epidermal growth factor receptors (EGFR). Cetuximab has activity in other EGFR expressing cancers and enhances the effectiveness of radiotherapy.

Methods: A retrospective review of institutional data identified eighteen patients with laCSCC treated with cetuximab induction and concurrent radiotherapy. The loading dose of cetuximab was 400 mg/m² IV. Subsequent weekly doses of 250 mg/m² IV were infused throughout the period of radiation. The treatment doses ranged from 4500–7000 cGy, with a dose fraction of 200-250 cGy.

Results: The objective response rate was 83.2% with 55.5% complete responses and 27.7% partial responses. Median progression-free survival was 21.6 months. Progression-free survival was 61% at 1 year and 40% at 2 years. With longer follow-up, some patients developed a local recurrence (16.7%), distant metastases (11.1%) or a second primary cancer (16.3%). Cetuximab was well tolerated, with 68.4% patients experienced only mild acneiform skin rash or fatigue (Grade 1 or 2). Radiotherapy produced expected side effects (skin erythema, moist desquamation, mucositis).

Discussion: Cetuximab plus radiotherapy represents an active and tolerable treatment option for laCSCC, including patients with contraindications for checkpoint inhibitor therapy.


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