Response-Adapted Surgical and Radiotherapy De-Escalation in Resectable Cutaneous Squamous Cell Cancer Using Pembrolizumab: The De-Squamate Study

R Rahul Ladwa (Princess Alexandra Hospital, Woolloongabba, QLD, Australia) J Jenny H. Lee (Chris O'Brien Lifehouse, Sydney, New South Wales, Australia) M Margaret McGrath (Princess Alexandra Hospital, Brisbane, Queensland, Australia) C Caroline Cooper (Princess Alexandra Hospital, Brisbane, Queensland, Australia) H Howard Liu J James Bowman R Ruta Gupta C Claire Cuscaden (Princess Alexandra Hospital, Brisbane, Queensland, Australia) M Michelle Nottage (Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia) J Jonathan R. Clark D Dieu Le (Princess Alexandra Hospital, Brisbane, Queensland, Australia) M Marketa Pauley (Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia) A Arutha Kulasinghe J Jazmina Gonzalez-Cruz (The University of Queensland, Brisbane, Queensland, Australia) S Sandro V. Porceddu (Department of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia) B Brett G.M. Hughes (The University of Queensland, Brisbane, Queensland, Australia) B Benedict Panizza (Princess Alexandra Hospital, Brisbane, Queensland, Australia)

Abstract

PURPOSE The high rates of pathologic complete response (pCR) after neoadjuvant immunotherapy have generated interest for a risk adaptive surgical and radiotherapy-free management approach to reduce morbidity in resectable cutaneous squamous cell carcinoma (cSCC). METHODS We conducted a phase II, multicenter study to evaluate pembrolizumab in patients with resectable stage II-IV (M0) cSCC. Patients received pembrolizumab, administered at a dose of 200 mg once every 3 weeks for four cycles, before undergoing a 18F-labeled fluorodeoxyglucose-positron emission tomography assessment. Patients who achieved a clinical complete response (cCR), defined as a complete metabolic response and negative mapping biopsies of the target site(s), avoided planned surgery and radiotherapy (total de-escalation). In the absence of a cCR, patients underwent surgery with the recommendation of omitting adjuvant radiotherapy (partial de-escalation) on the basis of a pCR. Patients proceeded to 13 additional cycles of maintenance pembrolizumab. The primary end point of a clinical or pathologic complete response (cpCR) was the combined rate of cCR and pCR. Key secondary end points included omission of surgery ± radiotherapy, event-free survival, and adverse events (AEs). RESULTS A total of 27 patients received pembrolizumab. A cpCR was observed in 17 patients (63% [95% CI, 42 to 80), composed of a pCR in four (15%) and a cCR in 13 (48%). Total and partial de-escalation was achieved in 48% and 15%, respectively. With a median follow-up of 18 months, no recurrence was seen in those patients with a cpCR. Treatment-related AEs of grade ≥3 were observed in two patients (7%). There were no treatment-related deaths. CONCLUSION Pembrolizumab led to a high rate of cpCR in resectable cSCC and demonstrated the potential to avoid surgery and radiotherapy.

Article Details

Volume / Issue Vol. 43, Issue 26
Published September 10, 2025
Pages 2888-2896
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (17)

R

Rahul Ladwa

Princess Alexandra Hospital, Woolloongabba, QLD, Australia

J

Jenny H. Lee

Chris O'Brien Lifehouse, Sydney, New South Wales, Australia

M

Margaret McGrath

Princess Alexandra Hospital, Brisbane, Queensland, Australia

C

Caroline Cooper

Princess Alexandra Hospital, Brisbane, Queensland, Australia

H

Howard Liu

J

James Bowman

R

Ruta Gupta

C

Claire Cuscaden

Princess Alexandra Hospital, Brisbane, Queensland, Australia

M

Michelle Nottage

Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia

J

Jonathan R. Clark

D

Dieu Le

Princess Alexandra Hospital, Brisbane, Queensland, Australia

M

Marketa Pauley

Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia

A

Arutha Kulasinghe

J

Jazmina Gonzalez-Cruz

The University of Queensland, Brisbane, Queensland, Australia

S

Sandro V. Porceddu

Department of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia

B

Brett G.M. Hughes

The University of Queensland, Brisbane, Queensland, Australia

B

Benedict Panizza

Princess Alexandra Hospital, Brisbane, Queensland, Australia