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Poster Discussion – Melanoma and other skin tumours

7194 - Phase II Study of Neoadjuvant Cemiplimab Prior to Surgery in Patients with Stage III/IV (M0) Cutaneous Squamous Cell Carcinoma of the Head and Neck (CSCC-HN)

Date

28 Sep 2019

Session

Poster Discussion – Melanoma and other skin tumours

Presenters

Neil Gross

Citation

Annals of Oncology (2019) 30 (suppl_5): v851-v934. 10.1093/annonc/mdz394

Authors

N. Gross1, R. Ferrarotto2, P. Nagarajan3, D. Bell3, A. El-Naggar3, J.M. Johnson4, Y. Yuan5, B.S. Glisson6, M. Wong7, D. Rosenthal8, B. Esmaeli9, M.R. Migden10, J. Wargo11, R.S. Weber1, J. Myers12

Author affiliations

  • 1 Head And Neck Surgery, The University of Texas M. D. Anderson Cancer Center, 77030 - Houston/US
  • 2 Md Anderson Cancer Center, The University of Texas, Houston/US
  • 3 Pathology, The University of Texas M. D. Anderson Cancer Center, 77030 - Houston/US
  • 4 Neuroradiology, The University of Texas M. D. Anderson Cancer Center, 77030 - Houston/US
  • 5 Biostatistics, The University of Texas M. D. Anderson Cancer Center, 77030 - Houston/US
  • 6 Thoracic/head And Neck Surgery, The University of Texas M. D. Anderson Cancer Center, 77030 - Houston/US
  • 7 Melanoma Medical Oncology Department, The University of Texas M. D. Anderson Cancer Center, 77030 - Houston/US
  • 8 Radiation Oncology, The University of Texas M. D. Anderson Cancer Center, 77030 - Houston/US
  • 9 Ophthalmic Plastic Surgery, The University of Texas M. D. Anderson Cancer Center, 77030 - Houston/US
  • 10 Dermatology And Head And Neck Surgery, The University of Texas M. D. Anderson Cancer Center, 77035 - Houston/US
  • 11 Surgical Oncology, The University of Texas MD Anderson Cancer Center, 77030-4095 - Houston/US
  • 12 Department Of Head And Neck Surgery, The University of Texas M. D. Anderson Cancer Center, 77030 - Houston/US
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Resources

Abstract 7194

Background

Cutaneous squamous cell carcinoma (CSCC) harbors a high tumor mutation burden (TMB) due to ultraviolet light-mediated DNA damage, and are highly immune-responsive. Cemiplimab, a monoclonal antibody directed against programmed death 1 (PD-1), is approved by the FDA and EMA as treatment for advanced CSCC patients who are not candidates for curative surgery. Here we explore the efficacy of neoadjuvant cemiplimab in CSCC- head and neck (HN) patients for whom surgery and radiation was planned.

Methods

Patients with stage III/IV (M0) (AJCC 8th Ed) CSCC-HN were treated with 2 doses of cemiplimab 350 mg intravenously every 3 weeks prior to surgery. The primary endpoint was overall response rate (ORR) per RECIST v1.1. Secondary endpoints included pathologic response rate, safety and tolerability, and analysis of candidate biomarkers from pre- and post-treatment blood and tumor specimens.

Results

Twenty patients (18M, 2F) enrolled with median age 69 years (range: 42-88) and stage III (n = 8) or IV (n = 12) disease. Seven (35%) patients experienced grade 1 or 2 adverse events (AEs); 6 (30%) grade 1 rash/pruritis, 1 (5%) grade 2 myalgia, and 1 (5%) grade 2 fatigue. There were no grade ≥ 3 AEs and no surgical delays. ORR by RECIST was 30% (6 partial response, 12 stable disease, 2 progressive disease). Pathologic complete response (pCR) was observed in 11 (55%) patients and major pathology response (MPR, ≤ 10% viable tumor) in an additional 3 (15%) patients. TMB and PD-L1 expression analyses in pre-treatment samples are in process. Eleven (55%) patients did not receive planned radiotherapy after surgery based on the pathologic responses. No recurrences have been observed with a median follow up of 3.8 months (range: 1.5-11.2).

Conclusions

Neoadjuvant cemiplimab was well-tolerated and induced a pCR or MPR in 70% of stage III/IV (M0) CSCC patients. A multicenter phase II study is planned to confirm these results and to describe the ability of neoadjuvant cemiplimab to allow less extensive treatment.

Clinical trial identification

NCT03565783.

Editorial acknowledgement

Legal entity responsible for the study

The University of Texas MD Anderson Cancer Center.

Funding

Regeneron.

Disclosure

N. Gross: Advisory / Consultancy, Research grant / Funding (self): Regeneron; Advisory / Consultancy: PDS Biotechnology; Advisory / Consultancy: Intuitive Surgical. B.S. Glisson: Research grant / Funding (institution): Pfizer; Research grant / Funding (self): ISA Pharmaceuticals. All other authors have declared no conflicts of interest.

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