1. Context
2. Methods
2.1. Study Design
2.2. Search Strategy
2.3. Study Selection
2.4. Data Extraction
2.5. Quality Assessment
3. Results
3.1. Search Results
3.2. Quality Assessment Result
3.3. Treatment Response Prediction
| Authors (Year) | AI Application | Patient Characteristics | Study Methodology | Sample Size | AI Algorithms Used | Key Findings |
|---|---|---|---|---|---|---|
| Wei et al. (2023) (22) | Peripheral blood immune cell markers | Cancer patients who received ICI therapy | Dynamic monitoring of peripheral blood immune cell markers | 160 | Lasso, ASR, and Cox models | Development of AI-based non-invasive, specific, and sensitive monitoring model |
| Chen et al. (2022) (23) | Pretreatment radiomics features | Non-small cell lung cancer patients who received definitive concurrent chemoradiotherapy | Identification of pre-treatment computed tomography-based radiomics features | 298 | Integrated feature selection and model training approach | Identification of 9 features for long-term predicting patient’s survival after treatment |
| Ali et al. (2016) (24) | Digital pathology slides | Breast cancer patients who received neoadjuvant chemotherapy | Evaluation of computational metrics from tissue pathology | 768 | Univariate and multivariate logistic regression | I dentification of lymphocyte density as an independent predictor |
| George et al. (2022) (25) | MRI radiometric | Glioblastoma patients who received immunotherapy | Progression-free survival and overall survival of patients with MRI-based machine learning | 113 | Random survival forest algorithm | Development of MRI radiometric-based AI model to predict patient survival |
| Pfob et al. (2022) (26) | Vacuum-assisted biopsy | Breast cancer patients who received NST | Detection of residual cancers using patient, imaging, tumor, and vacuum-assisted biopsy variables | 318 | Extreme Gradient Boosting Tree algorithm | Development of an intelligent vacuum-assisted biopsy model to identify NST responders |
| González-Garcia, I. et al. (2020) (27) | Tumor size data and patients’ demographic and clinical data | Head and neck cancer patients who received immunotherapy | Prediction of overall response and survival | 482 | Nonlinear mixed-effects modeling and a machine learning classification algorithm | Development of computational frame work to predict overall response and survival |
| Terranova et al. (2021) (28) | Patients’ characteristics and laboratory biomarkers | Gastric cancer or gastroesophageal junction cancer who received chemotherapy | Prediction of long-term overall survival | 805 | Random forests, SIDEScreen, and variable-importance assessments | Identification factors associated with overall survival including age, gamma-glutamyl transferase concentration, absence of peritoneal carcinomatosis; neutrophil-lymphocyte ratio, lactate dehydrogenase, or C-reactive protein |
| Wilbaux et al. (2022) (29) | Patients’ characteristics | Hepatocellular carcinoma patients who received Roblitinib | Prediction of tumor growth inhibition profile | 127 | Random forest, neural net, and support vector machine | Development of a machine learning model for the prediction of pharmacokinetic based on patient’s baseline characteristics |
| Wang et al. (2020) (30) | Cytokine data | Cancer patients who received nivolumb monnotherapy | Prediction of overall survival | 468 | Random forest (Boruta) algorithm | Prediction of overall survival using 16 immunomodulatory cytokines signature |
| Shipp et al. (2002) (31) | Expression levels of 6817 genes in tumor biopsy | Diffuse large B-cell lymphoma patients who received CHOP-based chemotherapy | Prediction of clinical outcomes by supervised learning method | 77 | Weighted-voting algorithm and cross-validation testing | Classification of two patient categories with significantly different 5-year overall survival rate |
| Deng et al. (2022) (32) | Clinicopathological characteristics and radiomics features of the tumor lesion | Hepatocellular carcinoma patients who underwent radical hepatectomy | Prediction of overall survival | 150 | LASSO algorithm | Prediction of patients’ overall survival with alpha-fetoprotein, neutrophil-to-lymphocyte ratio, and radiomics signature |
Abbreviations: AI, artificial intelligence; ASR, all-subsets regression; CHOP, cyclophosphamide, adriamycin, vincristine, and prednisone; ICI, immune checkpoint inhibitor; LASSO, least absolute shrinkage and selection operator; MRI, magnetic resonance imaging; NST, neoadjuvant systemic treatment.
3.4. Treatment Adverse Events Prediction
| Authors (Year) | AI Application | Patient Characteristics | Study Methodology | Sample Size | AI Algorithms Used | Key Findings |
|---|---|---|---|---|---|---|
| Zheng et al. (2022) (37) | 46 clinical and drug-related variables | Esophageal cancer patients who received chemotherapy | Predicting chemotherapy-related adverse events | 1446 | Random forest | Prediction of myelosuppression incidence to provide preventative measurements |
| Mei et al. (2022) (34) | Vomiting, psychological state, quality of life, and cancer biomarkers | Lung cancer patients who received chemotherapy | Development of comfort care to reduce chemotherapy-related adverse events | 118 | Diffusion-weighted imaging under the weighted nuclear norm minimization noise reduction algorithm | AI-based comfort care can significantly ameliorate vomiting response after chemotherapy |
| Ou et al. (2022) (38) | Pre-treatment peripheral blood test | Cervical cancer patients who underwent radical hysterectomy | Development of predictive algorithm for surgical-related adverse events | 1260 | Gradient Boosting Machine, Support Vector Machine with Gaussian kernel, Random Forest, Conditional Random Forest, Naive Bayes, and Elastic Net | Prediction of pathologic risk factors in cervical cancer patients prior to surgical intervention |
| Dercle et al. (2022) (39) | CT images | Melanoma patients who received immunotherapy | Prediction of overall survival and estimation of treatment benefits | 575 | Random forest | Identification of a signature from CT image features to estimate overall survival for 6 months and predict the potential immunotherapy risk factors |
| Bedon et al. (2021) (33) | Clinical, blood biochemistry, and genotype data | Metastatic colorectal cancer patients who received chemotherapy | Pre-treatment prediction of chemotherapy toxicity | 45 | Random forest | Identification of hemoglobin, serum glutamic oxaloacetic transaminase, and albumin as predictive factors related to chemotherapy toxicity |
Abbreviation: CT, computed tomography.
3.5. Precision Medicine
| Authors (Year) | AI Application | Patient Characteristics | Study Methodology | Sample Size | AI Algorithms Used | Key Findings |
|---|---|---|---|---|---|---|
| Xu et al. (2023) (43) | Pre-treatment symptoms | Older adults with advanced cancer who will receive a new treatment | Unsupervised machine learning to cluster patients’ symptom severity | 706 | K-means with Euclidean distance algorithm | Clustering patients with different symptom severity for administration of distinct treatment regimens |
| Sove et al. (2022) (44) | Laboratory biomarkers | Hepatocellular carcinoma patients who will receive nivolumab and ipilimumab | Conducting virtual clinical trial | 5000 | Markov Chain Monte Carlo optimization algorithm | Patient selection conducted based on the underlying pathophysiology |
| Sasak et al. (2021) (45) | Patient characteristics, and cytogenetic and molecular response | Chronic myeloid leukemia patients who will receive tyrosine kinase inhibitors | Optimization treatment approach | 504 | Ensemble learning with XGBoost package and hyperparameter optimization | Improvement of decision tree method for optimal treatment suggestion |
| Nicolae et al. (2020) (46) | Dosimetry recommendation | Prostate cancer patients who will receive I-125 low-dose-rate monotherapy | Evaluation of AI-based treatment recommendation and conventional manual recommendation | 41 | Adaptation of prostate implant planning algorithm | AI produced timely and efficient recommendation that was a non-inferior postoperative dosimetry to that of expert |
| Kaidar-Person et al. (2023) (47) | Clinical data report forms | Breast cancer patients who will receive a new treatment | Evaluation of AI-based treatment recommendation and standard conventional recommendation | 515 | Multinomial regression models | Pre-treatment AI evaluation can result in higher satisfaction, well-being, and better psychosocial status |
| Li et al. (2023) (48) | Patient and tumor characteristics, and treatment details | Hepatocellular carcinoma patients who will receive a new treatment | Presentation of surgery and chemotherapy treatment options | 1136 | Cox proportional hazards mode, neural network multitask logistic regression, DeepSurv, and random survival forest | Substantial improvement of chemotherapy recommendation therapies |
| Liu et al. (2022) (49) | The European Organization for Research and Treatment of Cancer quality of life questionnaire | Thyroid cancer patients who underwent thyroidectomy | Prediction of quality-of-life following thyroidectomy | 286 | Random forest | Optimization of health care by accurately predicting quality of life for 3 months |
| Al‑Hilli et al. (2023) (50) | Survey evaluating their knowledge of breast cancer and evaluating their satisfaction with their decision | Patients with breast cancer who will undergo genetic testing | Evaluating Chatbot counseling with in-person testing | 37 | Not Available | Comparable satisfaction and comprehension in patients undergoing pre-test genetic counseling with Chat bot to in-person testing |
3.6. Emerging Framework
Emerging framework for the use of artificial intelligence (AI) in cancer treatment – the figure illustrates the components of the emerging framework for the use of AI in cancer treatment, including data collection, AI algorithms, and treatment optimization, deep response, and challenges and limitations.


