Copyright: ©Author(s) 2026.
World J Clin Cases. Jun 6, 2026; 14(16): 119831
Published online Jun 6, 2026. doi: 10.12998/wjcc.v14.i16.119831
Published online Jun 6, 2026. doi: 10.12998/wjcc.v14.i16.119831
Table 1 Electronic database search strategy
| Database | Search terms | Limits applied |
| PubMed | (“Patient Care Team”[Mesh] OR “Interdisciplinary Communication”[Mesh] OR “Delivery of Health Care, Integrated”[Mesh] OR “Clinical Decision-Making”[Mesh] OR multidisciplinary[tiab] OR “multidisciplinary team”[tiab] OR MDT[tiab] OR interdisciplinary[tiab] OR interprofessional[tiab] OR “team-based care”[tiab] OR “integrated care”[tiab] OR “collaborative care”[tiab] OR “tumor board”[tiab] OR “tumour board”[tiab] OR “molecular tumor board”[tiab] OR “case conference”[tiab] OR “expert panel”[tiab] OR “precision medicine board”[tiab] OR “genomic board”[tiab]) AND (“Rare Diseases”[Mesh] OR “Neoplasms”[Mesh] OR “Cardiovascular Diseases”[Mesh] OR “Nervous System Diseases”[Mesh] OR “Congenital Abnormalities”[Mesh] OR “Autoimmune Diseases”[Mesh] OR rare disease*[tiab] OR complex condition*[tiab] OR oncology[tiab] OR cancer*[tiab] OR cardiology[tiab] OR neurology[tiab] OR congenital[tiab] OR autoimmune[tiab]) AND (“Precision Medicine”[Mesh] OR “Artificial Intelligence”[Mesh] OR “Genomics”[Mesh] OR “High-Throughput Nucleotide Sequencing”[Mesh] OR “Decision Support Systems, Clinical”[Mesh] OR precision medicine[tiab] OR genomic*[tiab] OR AI[tiab] OR “artificial intelligence”[tiab] OR “machine learning”[tiab] OR “clinical decision support”[tiab]) | Humans; English; 2013-2025 |
| Cochrane Library | (Multidisciplinary OR interdisciplinary OR interprofessional OR “team-based care” OR “integrated care” OR “collaborative care” OR “tumor board” OR “tumour board” OR “case conference” OR “expert panel”) AND (rare OR complex OR oncology OR cancer OR cardiology OR neurology OR congenital OR autoimmune) | 2013-2025 |
Table 2 QUADAS-2 summary table
| Domain | Low risk | Unclear risk | High risk |
| Patient selection | 21-24 | 6-8 | 0 |
| MDT process/index test | 24-28 | 3-4 | 0 |
| Reference standard | 18-20 | 9-12 | 0 |
| Flow and timing | 20-24 | 7-8 | 0 |
Table 3 Characteristics and outcomes of included studies
| Domain | Summary | Representative references |
| Clinical area | Studies predominantly addressed oncology, with additional representation from cardiology, neurology, and autoimmune diseases. Rare cancers, congenital cardiovascular disease, complex neurological disorders, and atypical autoimmune syndromes were commonly reported | Oncology:[18,19,22,26-39,45,46]; cardiology/congenital heart disease:[21,40,41]; neurology:[42,47]; autoimmune/complex disease contexts:[43,48] |
| MDT composition | MDTs typically included physicians and surgeons, with regular involvement of radiologists and pathologists. Expanded MDTs incorporated molecular pathologists, geneticists, nurses, allied health professionals, and bioinformaticians in complex cases | [18,19,23,26-28,30,33-38,42,45,46] |
| MDT model | MDT formats included traditional tumor boards, molecular tumor boards, interdisciplinary case conferences, and virtual or network-based MDTs, particularly for rare or geographically dispersed cases | Traditional MDTs:[19,22,29,30,36,39,42]; molecular tumor boards:[18,23,26-28,31,34,38]; virtual/network MDTs:[23,36-37,44] |
| Innovation | Studies reported integration of genomics, precision medicine, high-throughput sequencing, and artificial intelligence-assisted clinical decision support within MDT workflows, particularly in oncology and rare disease care | Genomics/NGS:[18,26-28,31-35,38]; precision medicine:[18,26-28,44]; AI/ML decision support:[29,37] |
| Outcomes | MDT involvement was associated with improved diagnostic accuracy, treatment modification, and optimized care pathways. Evidence for survival and quality-of-life benefits was limited and heterogeneous, with outcomes often reported as intermediate or process-level measures | Diagnostic/treatment modification:[18,23,26-28,30,34,38]; care pathway optimization/process outcomes:[21,23,38,42,44]; limited survival/quality-of-life data:[19,22,30,39] |
| Dimensions | Findings |
| Clinical domains | Oncology (dominant), cardiology, autoimmune disease |
| MDT composition | Oncologists, surgeons, radiologists, pathologists, geneticists, cardiologists, nurses, bioinformaticians |
| MDT format | In-person MDTs, molecular tumor boards, virtual/tele-MDTs |
| Innovation integrated | NGS, molecular profiling, AI/ML decision tools, liquid biopsy, precision therapeutics |
| Primary MDT function | Diagnostic clarification, treatment selection, escalation/de-escalation decisions |
| Outcomes reported | Diagnostic reclassification, altered management, feasibility of innovation integration |
| Survival/quality-of-life data | Limited direct reporting; mostly surrogate and process outcomes |
| Study design heterogeneity | Case reports → cohorts → qualitative and consensus studies |
| Geographic distribution | Europe, North America, Latin America |
- Citation: Gavkare AM, Nanaware NL, Darade R, Dhotre SV, Mumbre SS, Nagoba BS. Systematic review of multidisciplinary team strategies and novel research in rare and complex clinical cases. World J Clin Cases 2026; 14(16): 119831
- URL: https://www.wjgnet.com/2307-8960/full/v14/i16/119831.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v14.i16.119831