Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2015 Sep;56(5):849-55.
doi: 10.1093/jrr/rrv038. Epub 2015 Jul 9.

Initial experience of radiotherapy plus cetuximab for Japanese head and neck cancer patients

Affiliations

Initial experience of radiotherapy plus cetuximab for Japanese head and neck cancer patients

Marie Kurokawa et al. J Radiat Res. 2015 Sep.

Abstract

In Japan, cetuximab with concurrent bioradiotherapy (BRT) for squamous cell carcinoma of head and neck (SCCHN) was approved in December 2012. We herein report our initial experience of BRT, with special emphasis on acute toxicities of this combination therapy. Thirty-one non-metastatic SCCHN patients who underwent BRT using cetuximab between July 2013 and June 2014 were retrospectively evaluated. All patients received cetuximab with a loading dose of 400 mg/m(2) one week before the start of radiotherapy, followed by 250 mg/m(2) per week during radiotherapy. The median cycle of cetuximab was seven cycles and the median dose of radiotherapy was 70 Gy. Twenty-five patients (80.6%) accomplished planned radiotherapy and six cycles or more cetuximab administration. Six patients (19.4%) discontinued cetuximab. Grade 3 dermatitis, mucositis and infusion reaction occurred in 19.4%, 48.3% and 3.2%, respectively. One patient experienced Grade 3 gastrointestinal bleeding caused by diverticular hemorrhage during BRT. Grade 3 drug-induced pneumonitis occurred in two patients. The response rate was 74%, including 55% with a complete response. BRT using cetuximab for Japanese patients with SCCHN was feasible as an alternative for cisplatin-based concurrent chemoradiation, although longer follow-up is necessary to evaluate late toxicities.

Keywords: acute toxicity; cetuximab; head and neck cancer; initial experience; radiotherapy.

PubMed Disclaimer

Figures

Fig. 1.
Fig. 1.
(A) Hypopharyngeal tumor with pool of saliva and normal mucosa before the start of bioradiotherapy. (B) Decrease in the tumor bulk and development of Grade 3 mucositis during bioradiotherapy. (C) Confluent mucositis one month after the end of bioradiotherapy.
Fig. 2.
Fig. 2.
(A) Grade 3 dermatitis with contact bleeding occurred at one week after bioradiotherapy. (B) Resolution of dermatitis at 4 weeks after bioradiotherapy.
Fig. 3.
Fig. 3.
Drug-induced lung injury (DLI) developed at 2 weeks after the end of bioradiotherapy in patient with oropharynx cancer. He also had diverticular hemorrhage at the second week of bioradiotherapy. (A) Bilateral interstitial infiltration and consolidation can be seen on chest X-ray image. (B) Chest computed tomography scan shows widespread ground-glass opacity with peribroncho-vascular thickness that was predominant bilaterally in upper lung.

Similar articles

Cited by

References

    1. Katanoda K, Matsuda T, Matsuda A, et al. An updated report of the trends in cancer incidence and mortality in Japan. Jpn J Clin Oncol 2013;43:492–507. - PubMed
    1. Matsuda T, Marugame T, Kamo K-I, et al. Cancer incidence and incidence rates in Japan in 2006: based on data from 15 population-based cancer registries in the monitoring of cancer incidence in Japan (MCIJ) project. Jpn J Clin Oncol 2012;42:139–47. - PubMed
    1. Pignon J-P, le Maître A, Maillard E, et al. Meta-analysis of chemotherapy in head and neck cancer (MACH-NC): an update on 93 randomised trials and 17,346 patients. Radiother Oncol 2009;92:4–14. - PubMed
    1. Pignon J, Bourhis J, Domenge C, et al. Chemotherapy added to locoregional treatment for head and neck squamous-cell carcinoma: three meta-analyses of updated individual data. Lancet 2000;355:949–55. - PubMed
    1. Ciardiello F, Tortora G. EGFR antagonists in cancer treatment. N Engl J Med 2008;358:1160–74. - PubMed