Camrelizumab combined with capecitabine as maintenance therapy for metastatic nasopharyngeal carcinoma: A phase II single-arm clinical trial.

X Xuecen Wang (Department of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China) Y Yangchan Li (Department of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China) Y Yun Huang M Mei Lin Q Qimiao Qiu (Department of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China) Q Qingsong Tan (Department of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China) Q Qiuyue Tang (Department of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China) Q Qianfeng Liang (Department of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China) C Chengtao Wang Y Yan Wang Y Yong Chen

Abstract

e18016 Background: Metastasis is the main cause of death in nasopharyngeal carcinoma (NPC). The current first-line treatment for metastatic NPC involves gemcitabine, cisplatin, and camrelizumab followed by camrelizumab maintenance. This phase II trial evaluates the efficacy and safety of camrelizumab combined with capecitabine as a novel maintenance therapy strategy after systemic treatment. Methods: This study enrolled 20 patients with metastatic nasopharyngeal carcinoma, comprising 11 with synchronous metastases and 9 with asynchronous (post-treatment) metastases. All patients received systemic therapy with camrelizumab (200mg d1) plus gemcitabine (1000 mg/m² d1 and 8) and cisplatin (80 mg/m² d1) intravenously every 3 weeks (4-6 cycles), followed by maintenance therapy with camrelizumab (200mg d1) plus capecitabine (1000 mg/m² bid d1–14). The primary endpoint was the 1-year progression-free survival (PFS) rate. Secondary endpoints included the 18-/24-month PFS rate, 12-/18-/24 month overall survival (OS) rate, and the incidence of adverse events. Results: As of December 31, 2025, 20 patients were enrolled, with a median age of 41 years (range: 26–62). Among them, 15 were male and 5 were female; 8 had a history of smoking; 18 tested positive for EB virus after metastasis; 6 patients underwent induction chemotherapy, and 9 underwent definitive radiotherapy prior to the development of metastasis. Two patients received 5 cycles of systemic therapy, while the remaining 18 completed 6 cycles. Additionally, liver metastasis was observed in 10 patients (50%), bone metastasis in 9 (45%), and lung metastasis in 6 (30%). All patients were alive, and the 12-month PFS rate (systemic therapy + maintenance therapy) was 81.48%. The median survival was not yet reached. The objective response rate (ORR) was 100%. Treatment-emergent adverse events (TEAEs) of any grade occurred in all 20 patients, with all patients experiencing at least one grade ≥3 event. The most common grade ≥3 TEAEs included anemia (55%), neutropenia (55%), thrombocytopenia (25%), elevated aspartate aminotransferase (5%), and diarrhea (5%). Once maintenance therapy is started, the adverse reactions are significantly alleviated. Conclusions: Camrelizumab combined with capecitabine as maintenance therapy effectively prolongs survival time in patients with metastatic nasopharyngeal carcinoma, demonstrating favorable efficacy and safety. Enrollment is ongoing, and further validation of specific data is awaited. Clinical trial information: ChiCTR2500111883.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (11)

X

Xuecen Wang

Department of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China

Y

Yangchan Li

Department of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China

Y

Yun Huang

M

Mei Lin

Q

Qimiao Qiu

Department of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China

Q

Qingsong Tan

Department of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China

Q

Qiuyue Tang

Department of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China

Q

Qianfeng Liang

Department of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China

C

Chengtao Wang

Y

Yan Wang

Y

Yong Chen