Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster session 02

890P - Stereotactic body radiation therapy combined with chemotherapy and tislelizumab in metastatic nasopharyngeal carcinoma: A prospective, single-arm, phase II study

Date

14 Sep 2024

Session

Poster session 02

Topics

Tumour Immunology;  Immunotherapy;  Radiation Oncology

Tumour Site

Head and Neck Cancers

Presenters

Tongxin Liu

Citation

Annals of Oncology (2024) 35 (suppl_2): S613-S655. 10.1016/annonc/annonc1594

Authors

T. Liu, C. Tao, W. Qin, F. Jiang

Author affiliations

  • Department Of Radiation Oncology, Zhejiang Cancer Hospital, 310022 - Hangzhou/CN

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 890P

Background

There is an unmet need for more effective treatments in metastatic nasopharyngeal carcinoma (NPC) after chemo- and immune-therapy. The study aims to evaluate the outcomes of stereotactic body radiation therapy (SBRT) combined with chemotherapy and tislelizumab in treatment of metastatic NPC.

Methods

This is a single-centre, open-label, single-arm, phase II trial (NCT05652192). Patients(pts) should have at least one lesion eligible for SBRT (GTV 50Gy/5f). Then they received gemcitabine (1000 mg/m2, d1/8) or nab-paclitaxel (240 mg/m2, d1), cisplatin (80 mg/m2, d1), tislelizumab (200 mg, d1) every 3 weeks for four to six cycles. Tislelizumab was administrated on Day1 every 3 weeks until disease progression (PD), intolerable toxicity, up to 35 cycles (two years), death, or withdrawal of consent. The primary endpoint was progression-free survival (PFS). The secondary endpoint is objective response rate (ORR) per RECIST 1.1 and safety/tolerability per CTCAE v5.0 criteria.

Results

Between Oct 2022 and Jan 2024, 36 pts were enrolled (median age: 52 years old, range:29-72; male: 80.6%). At the data cutoff date on January 31, 2024, 47 metastatic leisions of 28 patients were eligible for the evaluation of tumor response. 97.9% of the lesions (46 of 47) had a response with complete response 91.5%(n=43) and partial response 6.4% (n=3). one patient was evaluated as stable disease. Grade 3-4 adverse reactions occurred in 11.1% patients (4 of 36 patients) and no fatal adverse events occurred.

Conclusions

This preliminary analysis indicated that metastatic NPC patients could get high response from metastases-directed SBRT in combination with tislelizumab. Ongoing analysis of predictive biomarker on efficacy and safety will be available in the future meeting.

Clinical trial identification

NCT05652192.

Editorial acknowledgement

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.