Diagnostic performance of eNose technology in detecting colorectal cancer recurrence: A prospective evaluation

TL;DR

This study evaluated eNose technology for detecting colorectal cancer recurrence after surgery but found it to be inaccurate, suggesting the need for larger studies.

Contribution

The study prospectively evaluated eNose technology's diagnostic performance for detecting CRC recurrence, revealing limitations in accuracy and reproducibility.

Findings

eNose showed promising training set results with an AUC of 0.90 but low accuracy (0.56).

Test set performance was poor with an AUC of 0.51 and low sensitivity and accuracy.

eNose technology is not currently reliable for detecting CRC recurrence.

Abstract

After curative treatment for colorectal cancer (CRC), there is a 15% risk of recurrence. Early detection of an asymptomatic recurrence may lead to curative treatment options. To date, follow-up strategies do not have optimal sensitivity and specificity. In this prospective study, we aimed to assess the diagnostic performance of eNose technology to detect recurrent CRC following curative surgery.

A prospective evaluation study was performed to investigate whether eNose can discriminate patients with recurrent CRC following curative resection from patients without recurrent CRC based on VOC patterns during follow-up. The primary outcome measure is the diagnostic accuracy of eNose for detecting recurrence in CRC patients. With machine learning, a model was developed, and several performance metrics were used to evaluate the diagnostic performance of the eNose model.

A total of 406 patients who underwent curative resection for CRC between 2018−2023, were included in the study. VOC analysis was used to detect recurrent CRC during follow-up. Although the eNose model demonstrated promising results in the train set with an AUC of 0.90 (95% CI:0.84–0.96), the corresponding accuracy of 0.56 was low. Moreover, with a corresponding sensitivity of 0.52, accuracy of 0.51, and AUC of 0.51 (95% CI:0.38–0.64), the performances in the test set, declined.

eNose technology is not able to accurately detect recurrent CRC after curative resection of the primary tumour. Larger studies are needed before clinical implementation can be realized, while the lack of reproducibility must be addressed.

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