TY - JOUR
T1 - Effectiveness of nivolumab affected by prior cetuximab use and neck dissection in Japanese patients with recurrent or metastatic head and neck cancer
T2 - results from a retrospective observational study in a real-world setting
AU - Kariya, Shin
AU - Shimizu, Yasushi
AU - Hanai, Nobuhiro
AU - Yasumatsu, Ryuji
AU - Yokota, Tomoya
AU - Fujii, Takashi
AU - Tsukahara, Kiyoaki
AU - Yoshida, Masafumi
AU - Hanyu, Kenji
AU - Ueda, Tsutomu
AU - Hirakawa, Hitoshi
AU - Takahashi, Shunji
AU - Ono, Takeharu
AU - Sano, Daisuke
AU - Yamauchi, Moriyasu
AU - Watanabe, Akihito
AU - Omori, Koichi
AU - Yamazaki, Tomoko
AU - Monden, Nobuya
AU - Kudo, Naomi
AU - Arai, Makoto
AU - Yonekura, Shuji
AU - Asakage, Takahiro
AU - Fujiwara, Akinori
AU - Yamada, Takayuki
AU - Homma, Akihiro
N1 - Funding Information:
Medical writing support was provided by Dr. Jidnyasa Mulekar, PhD, of Cactus Life Sciences (part of Cactus Communications, Mumbai, India) and was funded by Bristol-Myers Squibb and Ono Pharmaceutical Co., Ltd.
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/6
Y1 - 2021/6
N2 - Background: To examine the effect of prior use of cetuximab and neck dissection on the effectiveness of nivolumab, we conducted a large-scale subgroup analysis in Japanese patients with recurrent/metastatic head and neck cancer. Methods: Data on the effectiveness of nivolumab were extracted from patient medical records. All patients were analyzed for effectiveness by prior cetuximab use. In the analyses for prior neck dissection, only patients with locally advanced disease were included. Results: Of 256 patients analyzed, 155 had received prior cetuximab. Nineteen of 50 patients with local recurrence underwent neck dissection. The objective response rate was 14.7 vs 17.2% (p = 0.6116), median progression-free survival was 2.0 vs 3.1 months (p = 0.0261), and median overall survival was 8.4 vs 12 months (p = 0.0548) with vs without prior cetuximab use, respectively. The objective response rate was 23.1 vs 25.9% (p = 0.8455), median progression-free survival was 1.8 vs 3.0 months (p = 0.6650), and median overall survival was 9.1 vs 9.9 months (p = 0.5289) with vs without neck dissection, respectively. Conclusions: These findings support the use of nivolumab for patients with recurrent/metastatic head and neck cancer regardless of prior cetuximab use or neck dissection history. Trial registration number: UMIN-CTR (UMIN000032600), Clinicaltrials.gov (NCT03569436)
AB - Background: To examine the effect of prior use of cetuximab and neck dissection on the effectiveness of nivolumab, we conducted a large-scale subgroup analysis in Japanese patients with recurrent/metastatic head and neck cancer. Methods: Data on the effectiveness of nivolumab were extracted from patient medical records. All patients were analyzed for effectiveness by prior cetuximab use. In the analyses for prior neck dissection, only patients with locally advanced disease were included. Results: Of 256 patients analyzed, 155 had received prior cetuximab. Nineteen of 50 patients with local recurrence underwent neck dissection. The objective response rate was 14.7 vs 17.2% (p = 0.6116), median progression-free survival was 2.0 vs 3.1 months (p = 0.0261), and median overall survival was 8.4 vs 12 months (p = 0.0548) with vs without prior cetuximab use, respectively. The objective response rate was 23.1 vs 25.9% (p = 0.8455), median progression-free survival was 1.8 vs 3.0 months (p = 0.6650), and median overall survival was 9.1 vs 9.9 months (p = 0.5289) with vs without neck dissection, respectively. Conclusions: These findings support the use of nivolumab for patients with recurrent/metastatic head and neck cancer regardless of prior cetuximab use or neck dissection history. Trial registration number: UMIN-CTR (UMIN000032600), Clinicaltrials.gov (NCT03569436)
KW - Cetuximab
KW - Immune microenvironment
KW - Neck dissection
KW - Nivolumab
KW - Recurrent or metastatic head and neck cancer
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U2 - 10.1007/s10147-021-01900-4
DO - 10.1007/s10147-021-01900-4
M3 - Article
C2 - 33830342
AN - SCOPUS:85104078417
SN - 1341-9625
VL - 26
SP - 1049
EP - 1056
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 6
ER -