TY - JOUR
T1 - Real-world outcomes and prognostic factors in patients receiving nivolumab therapy for recurrent or metastatic head and neck carcinoma
AU - Hori, Ryusuke
AU - Shinohara, Shogo
AU - Kojima, Tsuyoshi
AU - Kagoshima, Hiroki
AU - Kitamura, Morimasa
AU - Tateya, Ichiro
AU - Tamaki, Hisanobu
AU - Kumabe, Yohei
AU - Asato, Ryo
AU - Harada, Hiroyuki
AU - Kitani, Yoshiharu
AU - Tsujimura, Takashi
AU - Honda, Keigo
AU - Ichimaru, Kazuyuki
AU - Omori, Koichi
N1 - Publisher Copyright:
© 2019 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2019/9
Y1 - 2019/9
N2 - Recently, a global phase III study demonstrated that nivolumab markedly improved patient outcomes in recurrent or metastatic head and neck carcinoma (RMHNC). However, the effcacy of nivolumab in patients who are ineligible for clinical trials is unknown. We investigated nivolumab eeecacy in real-world patients and prognostic factors associated with the response to nivolumab. This study was conducted at 11 institutes associated with Kyoto University and its Affliated Hospitals-Head and Neck Oncology Group. In total, 95 patients withRMHNCwho received nivolumab between May 2017 and May 2018 were retrospectively reviewed. Objective response rate (ORR), overall survival, and progression-free survival (PFS) were evaluated. Univariate and multivariate analyses were performed to identify prognostic factors. The ORRs in patients with squamous cell carcinoma (SCC) and non-SCC were 21.8% and 0%, respectively. In patients with SCC and non-SCC, the 1-year PFS rates were 28.7% and 8.9%, respectively. The hazard ratio (HR) for risk of PFS events (SCC versus non-SCC) was 2.28 (95% confidence interval: 1.21–4.1; log-rank p = 0.007). Univariate and multivariate analyses revealed radiotherapy history, platinum-refractory carcinoma, and treatment-related adverse events (TRAEs) as important prognostic factors associated with PFS in patients with SCC. In a real-world setting, non-SCC and platinum-refractory carcinoma were associated with a poorer prognosis, and a history of radiotherapy to the primary tumor, and the occurrence of TRAEs were associated with a better prognosis. These findings could be useful for clinicians and patients when selecting a treatment strategy.
AB - Recently, a global phase III study demonstrated that nivolumab markedly improved patient outcomes in recurrent or metastatic head and neck carcinoma (RMHNC). However, the effcacy of nivolumab in patients who are ineligible for clinical trials is unknown. We investigated nivolumab eeecacy in real-world patients and prognostic factors associated with the response to nivolumab. This study was conducted at 11 institutes associated with Kyoto University and its Affliated Hospitals-Head and Neck Oncology Group. In total, 95 patients withRMHNCwho received nivolumab between May 2017 and May 2018 were retrospectively reviewed. Objective response rate (ORR), overall survival, and progression-free survival (PFS) were evaluated. Univariate and multivariate analyses were performed to identify prognostic factors. The ORRs in patients with squamous cell carcinoma (SCC) and non-SCC were 21.8% and 0%, respectively. In patients with SCC and non-SCC, the 1-year PFS rates were 28.7% and 8.9%, respectively. The hazard ratio (HR) for risk of PFS events (SCC versus non-SCC) was 2.28 (95% confidence interval: 1.21–4.1; log-rank p = 0.007). Univariate and multivariate analyses revealed radiotherapy history, platinum-refractory carcinoma, and treatment-related adverse events (TRAEs) as important prognostic factors associated with PFS in patients with SCC. In a real-world setting, non-SCC and platinum-refractory carcinoma were associated with a poorer prognosis, and a history of radiotherapy to the primary tumor, and the occurrence of TRAEs were associated with a better prognosis. These findings could be useful for clinicians and patients when selecting a treatment strategy.
KW - Nivolumab
KW - Prognostic factor
KW - Recurrent or metastatic head and neck carcinoma
KW - Squamous cell carcinoma
KW - Treatment-related adverse events
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U2 - 10.3390/cancers11091317
DO - 10.3390/cancers11091317
M3 - Article
AN - SCOPUS:85073530387
SN - 2072-6694
VL - 11
JO - Cancers
JF - Cancers
IS - 9
M1 - 1317
ER -