TY - JOUR
T1 - Systemic treatment of patients with advanced cutaneous squamous cell carcinoma
T2 - response rates and outcomes of the regimes used
AU - Ogata, Dai
AU - Namikawa, Kenjiro
AU - Otsuka, Masaki
AU - Asai, Jun
AU - Kato, Hisoshi
AU - Yasuda, Masahito
AU - Maekawa, Takeo
AU - Fujimura, Taku
AU - Kato, Junji
AU - Takenouchi, Tatsuya
AU - Nagase, Kotaro
AU - Kawaguchi, Masakazu
AU - Kaji, Tatsuya
AU - Kuwatsuka, Yutaka
AU - Shibayama, Yoshitsugu
AU - Takai, Toshihiro
AU - Okumura, Mao
AU - Kambayashi, Yumi
AU - Yoshikawa, Syusuke
AU - Yamazaki, Naoya
AU - Tsuchida, Tetsuya
N1 - Funding Information:
This work was partly supported by the National Cancer Center Research and Development Fund (29-A-3).
Funding Information:
This work was partly supported by the National Cancer Center Research and Development Fund (29-A-3).
Publisher Copyright:
© 2019 Elsevier Ltd
PY - 2020/3
Y1 - 2020/3
N2 - Background: Cutaneous squamous cell carcinoma (cSCC) is the second most common type of skin cancer. Few patients with cSCC experience metastases, but the prognosis of advanced cSCC (acSCC) is dismal. Evidence regarding systemic therapy for acSCC is limited. Therefore, we aimed to determine the most effective systemic treatment for acSCC. Patients and methods: This retrospective study involved 16 Japanese institutions. We documented patient and tumour characteristics and disease course of patients with acSCC who received systemic therapy between 1st January 2006 and 31st December 2015. We compared the overall survival (OS) and progression-free survival (PFS) for (1) platinum versus non-platinum groups, (2) radiation plus chemotherapy first-line therapy (RCT) versus non-RCT groups and (3) platinum-based RCT versus non–platinum-based RCT groups. Results: Although the use of platinum-based systemic therapy was not associated with statistically significant improvements in PFS and OS, there were significant differences between the RCT and non-RCT groups (PFS: p < 0.001, OS: p = 0.003). In the subgroup analysis, RCT significantly prolonged PFS and OS in the nodal SCC (nSCC) group. For the RCT and non-RCT groups, the median OS was 110 and 14 months, respectively, and the 5-year OS rate was 54% and 21%, respectively. Conclusion: RCT could improve OS in patients with nSCC. However, further multicenter prospective studies are needed to establish evidence for superiority of RCT.
AB - Background: Cutaneous squamous cell carcinoma (cSCC) is the second most common type of skin cancer. Few patients with cSCC experience metastases, but the prognosis of advanced cSCC (acSCC) is dismal. Evidence regarding systemic therapy for acSCC is limited. Therefore, we aimed to determine the most effective systemic treatment for acSCC. Patients and methods: This retrospective study involved 16 Japanese institutions. We documented patient and tumour characteristics and disease course of patients with acSCC who received systemic therapy between 1st January 2006 and 31st December 2015. We compared the overall survival (OS) and progression-free survival (PFS) for (1) platinum versus non-platinum groups, (2) radiation plus chemotherapy first-line therapy (RCT) versus non-RCT groups and (3) platinum-based RCT versus non–platinum-based RCT groups. Results: Although the use of platinum-based systemic therapy was not associated with statistically significant improvements in PFS and OS, there were significant differences between the RCT and non-RCT groups (PFS: p < 0.001, OS: p = 0.003). In the subgroup analysis, RCT significantly prolonged PFS and OS in the nodal SCC (nSCC) group. For the RCT and non-RCT groups, the median OS was 110 and 14 months, respectively, and the 5-year OS rate was 54% and 21%, respectively. Conclusion: RCT could improve OS in patients with nSCC. However, further multicenter prospective studies are needed to establish evidence for superiority of RCT.
KW - Cemiplimab
KW - Chemotherapy
KW - Cisplatin
KW - Cutaneous squamous cell carcinoma
KW - EGFR inhibitor
KW - Metastasis
KW - Radiotherapy
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U2 - 10.1016/j.ejca.2019.12.018
DO - 10.1016/j.ejca.2019.12.018
M3 - Article
C2 - 32004792
AN - SCOPUS:85078493032
SN - 0959-8049
VL - 127
SP - 108
EP - 117
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -