Abstract
Simple SummarySquamous cell carcinoma is the second most common type of skin cancer, with incidence rates rising each year. Micrographic urgery is the treatment of choice for large, aggressive, or recurrent lesions. To ensure complete removal, excised tissue is frozen or embedded in paraffin, cut by a microtome, and stained for examination by an expert Mohs surgeon or a dermatopathologist. Thus, resection of tumor is performed in multiple steps, resulting in delayed wound closure, patient discomfort, longer hospital stay, and in turn, higher healthcare costs. In the last few years, ex vivo confocal laser scanning microscopy (CLSM) has shown promising results in intraoperative almost-real-time detection of skin cancers. This technology is not yet widespread in part due to necessity of training for laboratory technicians, surgeon and dermatopathologists. To increase efficiency and objectivity in the image interpretation process, we have built a machine learning model to detect squamous cell carcinoma lesions in excised tissues.Image classification with convolutional neural networks (CNN) offers an unprecedented opportunity to medical imaging. Regulatory agencies in the USA and Europe have already cleared numerous deep learning/machine learning based medical devices and algorithms. While the field of radiology is on the forefront of artificial intelligence (AI) revolution, conventional pathology, which commonly relies on examination of tissue samples on a glass slide, is falling behind in leveraging this technology. On the other hand, ex vivo confocal laser scanning microscopy (ex vivo CLSM), owing to its digital workflow features, has a high potential to benefit from integrating AI tools into the assessment and decision-making process. Aim of this work was to explore a preliminary application of CNN in digitally stained ex vivo CLSM images of cutaneous squamous cell carcinoma (cSCC) for automated detection of tumor tissue. Thirty-four freshly excised tissue samples were prospectively collected and examined immediately after resection. After the histologically confirmed ex vivo CLSM diagnosis, the tumor tissue was annotated for segmentation by experts, in order to train the MobileNet CNN. The model was then trained and evaluated using cross validation. The overall sensitivity and specificity of the deep neural network for detecting cSCC and tumor free areas on ex vivo CLSM slides compared to expert evaluation were 0.76 and 0.91, respectively. The area under the ROC curve was equal to 0.90 and the area under the precision-recall curve was 0.85. The results demonstrate a high potential of deep learning models to detect cSCC regions on digitally stained ex vivo CLSM slides and to distinguish them from tumor-free skin.
Highlights
Cutaneous squamous cell carcinoma is a subtype of keratinocyte cancer (KC), that usually presents as a solitary, firm papule, or plaque with a hyperkeratotic surface, on chronically sun exposed areas
To test the performance of a machine learning algorithm in detection of Cutaneous squamous cell carcinoma (cSCC) in images acquired by ex vivo CLSM, we collected fresh tissue scans of 22 invasive cSCCs from 17 patients (5 females and 12 males, mean age 78.6)
The overall sensitivity and specificity of the deep neural network in detecting cSCC and tumor free skin in the ex vivo CLSM images compared to the expert examination were 0.76 and 0.91, respectively, using a classification threshold of 0.3 along with aforementioned post processing steps
Summary
Cutaneous squamous cell carcinoma (cSCC) is a subtype of keratinocyte cancer (KC), that usually presents as a solitary, firm papule, or plaque with a hyperkeratotic surface, on chronically sun exposed areas. Clinical diagnosis of cSCC may be challenging, due to overlapping clinical features with other skin neoplasms such as keratoacanthoma, basal cell carcinoma (BCC), Bowen’s carcinoma or Merkel cell carcinoma [3]. In comparison to paraffin sections, frozen sections are less time-consuming and are often preferred in situations where timely decisions are needed (e.g., Mohs surgery) This rapid diagnostic process comes at the expense of partial loss in tissue cellular architecture caused by freezing artifacts, difficulty in cut resulting in tissue folds, and poor staining quality, just to name a few [5,6]. Individual factors, such as pathologist’s level of experience and expertise may result in an inter-and intraobserver variability as well as variations in efficiency [7,8,9]
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