TY - JOUR
T1 - Efficacy and safety of molecularly targeted agents and immune checkpoint inhibitors for unresectable or recurrent/metastatic oral cancer in Japan
AU - Otsuru, Mitsunobu
AU - Yamakawa, Nobuhiro
AU - Kirita, Tadaaki
AU - Yamada, Shin ichi
AU - Kurita, Hiroshi
AU - Kugimoto, Takuma
AU - Harada, Hiroyuki
AU - Hasegawa, Takumi
AU - Akashi, Masaya
AU - Takeshita, Akinori
AU - Uzawa, Narikazu
AU - Umeda, Masahiro
AU - Yanamoto, Souichi
AU - Yamada, Tomohiro
N1 - Publisher Copyright:
© 2024 Association for Dental Sciences of the Republic of China
PY - 2024/7
Y1 - 2024/7
N2 - Background/purpose: For unresectable recurrent/metastatic head and neck cancer, pembrolizumab alone or pembrolizumab combined with cisplatin and 5-fluorouracil is the first-line therapy, depending on the PD-L1 combined positive score (CPS). However, this is based on clinical studies of head and neck cancer, and few similar studies have been conducted on oral cancer alone. This study aimed to investigate the current status of pharmacotherapy for unresectable, recurrent, or metastatic oral cancer. Materials and methods: Patients with unresectable or recurrent/metastatic oral cancer who received cetuximab, nivolumab, or pembrolizumab as first-line treatment were reviewed. Overall survival (OS), progression-free survival (PFS), PFS 2 (PFS2), overall response rate (ORR), disease control rate (DCR), and immune-related adverse events were obtained from medical records. Results: A total of 155 patients were enrolled from six hospitals. The ORR in the nivolumab, pembrolizumab, and cetuximab groups was 17.2 %, 4.2 %, and 21.6 %, respectively, and the DCR was 37.9 %, 41.7 %, and 58.8 %, respectively. Median OS in nivolumab, pembrolizumab, and cetuximab groups was 10.3, 9.5, and 11.1 months, respectively. No significant differences were observed in survival among the three groups. The small number of cases and the retrospective nature of the study precluded the determination of the more effective first-line treatment among the three drugs. Conclusion: The current statuses of nivolumab, pembrolizumab, and cetuximab in unresectable recurrent metastatic oral cancer was reported.
AB - Background/purpose: For unresectable recurrent/metastatic head and neck cancer, pembrolizumab alone or pembrolizumab combined with cisplatin and 5-fluorouracil is the first-line therapy, depending on the PD-L1 combined positive score (CPS). However, this is based on clinical studies of head and neck cancer, and few similar studies have been conducted on oral cancer alone. This study aimed to investigate the current status of pharmacotherapy for unresectable, recurrent, or metastatic oral cancer. Materials and methods: Patients with unresectable or recurrent/metastatic oral cancer who received cetuximab, nivolumab, or pembrolizumab as first-line treatment were reviewed. Overall survival (OS), progression-free survival (PFS), PFS 2 (PFS2), overall response rate (ORR), disease control rate (DCR), and immune-related adverse events were obtained from medical records. Results: A total of 155 patients were enrolled from six hospitals. The ORR in the nivolumab, pembrolizumab, and cetuximab groups was 17.2 %, 4.2 %, and 21.6 %, respectively, and the DCR was 37.9 %, 41.7 %, and 58.8 %, respectively. Median OS in nivolumab, pembrolizumab, and cetuximab groups was 10.3, 9.5, and 11.1 months, respectively. No significant differences were observed in survival among the three groups. The small number of cases and the retrospective nature of the study precluded the determination of the more effective first-line treatment among the three drugs. Conclusion: The current statuses of nivolumab, pembrolizumab, and cetuximab in unresectable recurrent metastatic oral cancer was reported.
KW - Immune checkpoint inhibitors (ICIs)
KW - Japan
KW - Oral cancer
KW - PFS 2 (PFS2)
KW - Progression-free survival (PFS)
UR - http://www.scopus.com/inward/record.url?scp=85180311277&partnerID=8YFLogxK
U2 - 10.1016/j.jds.2023.11.024
DO - 10.1016/j.jds.2023.11.024
M3 - 学術論文
C2 - 39035308
AN - SCOPUS:85180311277
SN - 1991-7902
VL - 19
SP - 1628
EP - 1637
JO - Journal of Dental Sciences
JF - Journal of Dental Sciences
IS - 3
ER -