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Natural Killer Cells in Paediatric Soft Tissue Sarcomas: A Systematic Review
Raya Dean1,2, Lara V Graham1,2, Christina Putnam2
1School of Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Pediatric Blood & Cancer
|July 25, 2026
Summary
Natural killer (NK) cells show promise in treating paediatric soft tissue sarcomas (pSTS). Preclinical data suggest NK cell therapies, including CAR-NK cells, are effective against pSTS, particularly rhabdomyosarcoma (RMS).
Area of Science:
- Oncology
- Immunology
- Cell Biology
Background:
- Paediatric soft tissue sarcomas (pSTS) are rare, heterogeneous cancers originating from mesenchymal tissues.
- The role of natural killer (NK) cells in pSTS pathogenesis and treatment is not well-defined, with limited evidence from small studies.
Purpose of the Study:
- To systematically review existing preclinical and clinical evidence on NK cell involvement in pSTS.
- To evaluate the therapeutic potential of NK cells and NK cell-based therapies for pSTS.
Main Methods:
- Conducted a systematic literature review following PRISMA guidelines.
- Searched major databases including MEDLINE, EMBASE, and Web of Science.
- Included preclinical studies and early-phase clinical trials.
Main Results:
- Preclinical studies show pSTS subtypes, including rhabdomyosarcoma (RMS) and non-RMS soft tissue sarcomas (NRSTS), are sensitive to NK cell-mediated killing.
- Cytokine activation and sensitizing agents enhance NK cell cytotoxicity against pSTS cells in vitro.
- Chimeric antigen receptor NK (CAR-NK) cells exhibit potent anti-tumor activity against RMS in vitro and in vivo.
Conclusions:
- NK cells display significant preclinical efficacy in pSTS, with a strong focus on RMS.
- Ongoing clinical trials are investigating adoptive NK cell transfer for pSTS patients.
- Further research is needed in both RMS and NRSTS to translate these findings into clinical benefits.