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Poster Display session

415P - Preliminary safety and efficacy results from phase II study pulsed radiotherapy with tislelizumab in patients with recurrent head & neck cancer

Date

07 Dec 2024

Session

Poster Display session

Presenters

Ximei Zhang

Citation

Annals of Oncology (2024) 35 (suppl_4): S1554-S1574. 10.1016/annonc/annonc1692

Authors

X. Zhang1, Y. Chai1, S. Jiang1, G. Liang1, P. Wang2, Z. Yuan3

Author affiliations

  • 1 Radiotherapy, TMUCIH - Tianjin Medical University Cancer Institute and Hospital, 300060 - Tianjin/CN
  • 2 Radiotherapy, Tianjin Medical University Cancer Institute and Hospital, Tianjin/CN
  • 3 Radiotherapy, Tianjin Cancer Hospital Airport Hospital, 300308 - Tianjin/CN

Resources

This content is available to ESMO members and event participants.

Abstract 415P

Background

Although immunotherapy has been the standard treatment for recurrent head and neck cancer, patients have limited benefit from this treatment. It is better to combine with radiotherapy, especially pulsed low dose rate radiotherapy (PLDR), since researches have confirmed that PLDR is the best way to treat recurrent tumors as well as to magnify immune response.

Methods

Clinical locoregional recurrent HNSCC patients were enrolled in the study. All the tumors were unresectable either for wrapping around the vessels or old ages. Patients received pulsed radiation therapy concurrent with 3 cycles of tislelizumab (200mg Q3W) followed by an additional 32 cycles of tislelizumab maintenance therapy. The primary endpoint was the objective response rate (ORR).

Results

Between Sep 2022 and Dec 2023, 12 patients (6 oral cavity, 3 hypopharynx and 3 larynx) were enrolled. The median age was 62 (53-80) years, 75.0% smoking history, 75.0% alcohol history and 83.3% male. The median long diameter of the primary lesion was 7.4 cm (2.6-12 cm). All patients completed radiotherapy with the CR rate was 58.3% (7/12), and the PR rate of 41.7% (5/12). At a median follow-up of 13.7 months, the median PFS or OS was not reached and 1-year PFS rate was 50.9 %. The most common adverse events were mucositis (100%) and G3-4 mucositis was found in 1 patient (8.3%). All patients with adverse events in this study were managed well.

Conclusions

The efficacy and safety of PLDR with tislelizumab is superior to standard of care (immunochemotherapy) and deserves further exploration.

Clinical trial identification

NCT05595590.

Editorial acknowledgement

Legal entity responsible for the study

Tianjin Medical University Cancer Institute & Hospital.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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