Artificial Intelligence and Radiomics: Clinical Applications for Patients with Advanced Melanoma Treated with Immunotherapy

Author:

McGale Jeremy1,Hama Jakob2,Yeh Randy3,Vercellino Laetitia4,Sun Roger5ORCID,Lopci Egesta6ORCID,Ammari Samy78ORCID,Dercle Laurent1ORCID

Affiliation:

1. Department of Radiology, New York-Presbyterian Hospital, New York, NY 10032, USA

2. Queens Hospital Center, Icahn School of Medicine at Mt. Sinai, Queens, NY 10029, USA

3. Molecular Imaging and Therapy Service, Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA

4. Nuclear Medicine Department, INSERM UMR S942, Hôpital Saint-Louis, Assistance-Publique, Hôpitaux de Paris, Université Paris Cité, 75010 Paris, France

5. Department of Radiation Oncology, Gustave Roussy, 94800 Villejuif, France

6. Nuclear Medicine Unit, IRCCS—Humanitas Research Hospital, 20089 Rozzano, MI, Italy

7. Department of Medical Imaging, BIOMAPS, UMR1281 INSERM, CEA, CNRS, Gustave Roussy, Université Paris-Saclay, 94800 Villejuif, France

8. ELSAN Department of Radiology, Institut de Cancérologie Paris Nord, 95200 Sarcelles, France

Abstract

Immunotherapy has greatly improved the outcomes of patients with metastatic melanoma. However, it has also led to new patterns of response and progression, creating an unmet need for better biomarkers to identify patients likely to achieve a lasting clinical benefit or experience immune-related adverse events. In this study, we performed a focused literature survey covering the application of artificial intelligence (AI; in the form of radiomics, machine learning, and deep learning) to patients diagnosed with melanoma and treated with immunotherapy, reviewing 12 studies relevant to the topic published up to early 2022. The most commonly investigated imaging modality was CT imaging in isolation (n = 9, 75.0%), while patient cohorts were most frequently recruited retrospectively and from single institutions (n = 7, 58.3%). Most studies concerned the development of AI tools to assist in prognostication (n = 5, 41.7%) or the prediction of treatment response (n = 6, 50.0%). Validation methods were disparate, with two studies (16.7%) performing no validation and equal numbers using cross-validation (n = 3, 25%), a validation set (n = 3, 25%), or a test set (n = 3, 25%). Only one study used both validation and test sets (n = 1, 8.3%). Overall, promising results have been observed for the application of AI to immunotherapy-treated melanoma. Further improvement and eventual integration into clinical practice may be achieved through the implementation of rigorous validation using heterogeneous, prospective patient cohorts.

Publisher

MDPI AG

Subject

Clinical Biochemistry

Reference64 articles.

1. Shen, W., Sakamoto, N., and Yang, L. (2016). Melanoma-Specific Mortality and Competing Mortality in Patients with Non-Metastatic Malignant Melanoma: A Population-Based Analysis. BMC Cancer, 16.

2. (2023, March 27). Melanoma Research Alliance Melanoma Survival Rates. Available online: https://www.curemelanoma.org/about-melanoma/melanoma-staging/melanoma-survival-rates.

3. The Role of Tumor Microenvironment in Development and Progression of Malignant Melanomas—A Systematic Review;Gurzu;Rom. J. Morphol. Embryol.,2018

4. Improved Survival with Ipilimumab in Patients with Metastatic Melanoma;Hodi;N. Engl. J. Med.,2010

5. Pseudoprogression and Immune-Related Response in Solid Tumors;Chiou;J. Clin. Oncol.,2015

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