Wenjie Cai1, Yayun Chen1, Kaixin Li1, Bingzhong Gao1, Runzhi Mao1 and Wanhua Chen2*
1Departments of Radiation Oncology, First Hospital of Quanzhou Affiliated to Fujian Medical University, Quanzhou, China
2Department of Clinical Laboratory, First Hospital of Quanzhou Affiliated to Fujian Medical University, China
*Corresponding author: Wanhua Chen, Department of Clinical Laboratory, First Hospital of Quanzhou Affiliated to Fujian Medical University, China
Submission: May 05, 2025;Published: June 02, 2025
ISSN: 2577-2007Volume9 Issue3
Introduction: Cutaneous Squamous Cell Carcinoma (cSCC) is a prevalent skin malignancy, with recurrent cases posing significant challenges, particularly in elderly patients. Immune checkpoint inhibitors, such as anti-PD-1 antibodies, have shown promise in advanced cSCC.
Objective: To report the efficacy and tolerability of Sintilimab, an anti-PD-1 monoclonal antibody, in an elderly patient with recurrent cSCC post-radiotherapy.
Research method: A case study was conducted on an 88-year-old female with recurrent stage III cSCC at Quanzhou First Hospital Affiliated to Fujian Medical University, Quanzhou, Fujian, China. She received Sintilimab (200mg intravenously every 21 days) for three cycles, with clinical outcomes assessed via physical examination and imaging.
Result: Sintilimab achieved significant tumor shrinkage and pain relief with excellent tolerability. No significant adverse effects were observed. The patient died of COVID-19, unrelated to her cancer treatment.
Keywords:Cutaneous squamous cell carcinoma; Sintilimab; Immunotherapy; Radiotherapy; Elderly; Recurrence
Cutaneous Squamous Cell Carcinoma (cSCC) is the second most common skin cancer, accounting for approximately 20% of non-melanoma skin cancers [1]. While early-stage cSCC is often curable with surgery or radiotherapy, recurrent or locally advanced cases are challenging, particularly in elderly patients with comorbidities [2]. Immune checkpoint inhibitors, such as anti-programmed death-1 (PD-1) antibodies, have revolutionized advanced cSCC management [3]. Sintilimab, a humanized anti-PD-1 antibody, is effective in various cancers but less studied in cSCC [4,5]. This case report describes the successful use of Sintilimab in an elderly patient with recurrent cSCC post-radiotherapy.
An 88-year-old female presented to Quanzhou First Hospital Affiliated to Fujian Medical University, Quanzhou, Fujian, China, in June 2021 with a six-month history of a right temporal ulcer. Biopsy (S202101006) confirmed cSCC, staged as T3N0M0 (stage III) per the American Joint Committee on Cancer (AJCC) 8th edition [1]. She underwent radical radiotherapy in June 2021 with the following parameters: gross tumor volume (GTV) was delineated by surface markers of the right temporal mass; clinical target volume 1 (CTV1) was GTV plus a 2.0cm margin; CTV2 was GTV plus a 1.0cm margin; planning target volume (PTV) was CTV1 plus a 0.3cm margin; and PTV2 was CTV2 plus a 0.3cm margin. The prescribed dose was 95% of PTV (first stage) at 200cGy/fraction, 4000cGy/20 fractions, followed by 95% of PTV2 (second stage) at 200cGy/fraction, 2000cGy/10 fractions. Radiotherapy significantly reduced the tumor size (Figure 1 & 2).
Figure 1:Right temporal cSCC lesion before immunotherapy. The lesion is an elliptical protrusion of about 8cmx8cm in size and 1cm in height. A concave ulcer with surface scabbing and yellow exudate is visible in the center of the lesion.
Figure 2:Right temporal cSCC lesion after immunotherapy. The lesion shows a marked reduction in size and elevation. The patient reports an improvement in pain.
In September 2022, the patient was readmitted due to progressive enlargement of the right temporal mass for five months. Physical examination revealed an 8cmx8cm elliptical protrusion, approximately 1cm in height, with a central concave ulcer, surface scabbing, and minimal yellow exudate. A head CT scan confirmed a right temporal scalp mass. Biopsy confirmed recurrent cSCC (T3N0M0, stage III). After discussion with the patient and her family, she opted for Sintilimab (200mg intravenously every 21 days) due to economic considerations. She received three cycles on September 7, September 28, and October 26, 2022.
Sintilimab was well-tolerated, with no significant abnormalities in electrocardiogram, myocardial enzyme spectrum, or pituitary, adrenal, thyroid, and pancreatic functions. The tumor shrank significantly, and pain improved. Unfortunately, the patient died of COVID-19 on January 5, 2023, unrelated to her cancer treatment.
Recurrent cSCC post-radiotherapy is difficult to manage, particularly in elderly patients who may not tolerate aggressive therapies [2]. Radiotherapy is effective for primary cSCC but has limited efficacy in recurrence [1]. Anti-PD-1 therapies, such as cemiplimab and pembrolizumab, have shown response rates of 40–50% in advanced cSCC [3,6]. Sintilimab, approved for various malignancies, offers a cost-effective alternative with a favorable safety profile [4,5]. In this case, Sintilimab induced tumor shrinkage and pain relief after three cycles, without notable toxicities, consistent with studies on anti-PD-1 safety in elderly patients [7].
The choice of Sintilimab was driven by its cost-effectiveness, a critical factor in resource-limited settings [8]. The absence of significant adverse effects supports its feasibility in elderly patients with comorbidities [9]. The patient’s death from COVID-19 highlights the vulnerability of elderly cancer patients to infections, emphasizing the need for comprehensive supportive care during immunotherapy [10]. Limitations include the short follow-up period and inability to assess long-term outcomes due to the patient’s death. The role of biomarkers, such as PD-L1 expression, in predicting Sintilimab response in cSCC requires further study [6]. Future research should explore optimal dosing and duration of Sintilimab for cSCC [5].
This case demonstrates Sintilimab’s efficacy and tolerability in an 88-year-old patient with recurrent cSCC post-radiotherapy, achieving tumor reduction and symptom improvement. Sintilimab is a promising, cost-effective option for elderly patients with advanced cSCC, particularly in resource-limited settings. Larger clinical trials are needed to validate these findings and optimize immunotherapy for recurrent cSCC.
Written informed consent was obtained from the patient for publication of this case report and accompanying images.
This treatment and case report were approved by the Ethics Committee of Quanzhou First Hospital Affiliated to Fujian Medical University.
The author has no conflicts of interest to declare.
This work was supported by the Natural Science Foundation of Fujian Province (2023J011787).
© 2025 Wanhua Chen. This is an open access article distributed under the terms of the Creative Commons Attribution License , which permits unrestricted use, distribution, and build upon your work non-commercially.