Addition of Immunotherapy to Standard of Care First-Line Regimen Delays Disease Progression in Advanced Nasopharyngeal Carcinoma

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For immediate release
June 3, 2021


Rachel Cagan

ASCO Perspective
“Treatment advances for late-stage nasopharyngeal carcinoma have lagged behind those of other cancers. Findings from the JUPITER-02 study offer new hope for patients with advanced disease, changing how we care for them,” said ASCO Chief Medical Officer and Executive Vice President Julie R. Gralow, MD, FACP, FASCO.

ALEXANDRIA, Va. — The addition of the immunotherapy agent toripalimab to standard first-line chemotherapy significantly delayed disease progression for patients with recurrent or metastatic nasopharyngeal carcinoma (NPC), according to new research. The phase III international study, to be presented at the 2021 American Society of Clinical Oncology (ASCO) Annual Meeting, may represent a paradigm shift in the care of these patients, for whom there are currently few treatment options.

Study at a Glance


Efficacy and safety of toripalimab in combination with gemcitabine-cisplatin chemotherapy as first-line treatment for recurrent or metastatic NPC.


289 patients with recurrent or metastatic NPC with no prior chemotherapy


  • The time to disease progression (progression-free survival, PFS) was significantly longer for patients who received chemotherapy and toripalimab, compared with chemotherapy and placebo, with a median of 11.7 versus 8.0 months respectively.
  • At 1 year, 49% of patients who received toripalimab had not experienced disease progression, compared with 28% of those who received placebo.
  • Adverse and serious adverse events were comparable for the two treatments.


JUPITER-02 is one of the first studies in NPC to positively integrate a PD-1-blocking immunotherapy with upfront chemotherapy. Pending approval, the combination stands to become the new standard of care.

Key Findings
NPC, a type of head and neck cancer that starts in the nasopharynx, represents a significant global health problem. The cancer is particularly prevalent in East and Southeast Asia, which accounted for more than 70% of the approximate 129,000 new diagnoses worldwide in 2018.1,2 Platinum-based therapy is currently standard first-line treatment for recurrent or metastatic NPC. However, the duration of response is, on average, less than six months.3

The JUPITER-02 trial demonstrated that the addition of the immunotherapy toripalimab to standard first-line chemotherapy lengthened the time to disease progression compared with placebo, with a median of 11.7 months versus. 8.0 months, respectively. At 1 year, 49% of patients who received toripalimab had not experienced disease progression, compared to 28% of those who received placebo.

Serious adverse events (AEs) grade 3 or greater were similar for both groups — 89.0% for toripalimab versus 89.5% for placebo, with discontinuation of treatment in 7.5% of immunotherapy patients, compared to 4.9% that took placebo. Fatal AEs were similar between the two arms, 2.7% and 2.8%, respectively.

Immune-related AEs were more common with toripalimab, 39.7%, compared with placebo,18.9%. Immune-related AEs grade 3 or greater were also more common with toripalimab (7.5%) than with placebo (0.7%). 

Toripalimab is an immune therapy known as a checkpoint inhibitor that works by blocking programmed cell death protein 1 (PD-1) found on the surface of immune cells, allowing the immune system to continue working properly.

“Nasopharyngeal carcinoma is challenging as it is typically diagnosed in an advanced stage when current therapy options are extremely limited. The extended response in patients that received with toripalimab marks a significant advance for treatment of this disease,” said Rui-hua Xu, MD, PhD, of the department of medical oncology at Sun Yat-sen University Cancer Center in Guangzhou, China.

About the Study
In this phase III trial, 289 patients with recurrent or metastatic NPC, who had not received previous chemotherapy, were randomized 1:1 to receive toripalimab (146 patients) or placebo (143). Patients in both groups also received gemcitabine/cisplatin chemotherapy. The study’s primary endpoint was PFS in all study patients. Secondary end points included overall response rate, duration of response, and overall survival (OS).

Next Steps
Patients will continue to be followed for OS and other secondary end points.

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For your readers:

View the disclosures for the 2021 Cancer Communications Committee:  

View the disclosures for Dr. Gralow 

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1. Bray F, Ferlay J, Soerjomataram I, et al: Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 68:394-424, 2018.

2. Chen YP, Chan ATC, Le QT, et al: Nasopharyngeal carcinoma. Lancet 394:64-80, 2019.

3. Zhang L, Huang Y, Hong S, et al: Gemcitabine plus cisplatin versus fluorouracil plus cisplatin in recurrent or metastatic nasopharyngeal carcinoma: a multicentre, randomised, open-label, phase 3 trial. Lancet 388:1883-1892, 2016.

Dr. Xu's Embargoed Presscast Presentation

About ASCO: 

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