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Successful Sequential Multimodal Therapy for Lingual Rhabdomyosarcoma in a Young Adult: Case Report
Jonathan Villanueva Dominguez1, Josué Vázquez Arizmendi1, Vianey Guadalupe Saldaña Herrera2
1State Cancer Institute "Dr. Arturo Beltrán Ortega", Acapulco, Guerrero, Mexico.
Case Reports in Oncological Medicine
|July 22, 2026
Summary
Adult lingual rhabdomyosarcoma (RMS) is rare. This case study shows sequential therapy, including immunotherapy and antiangiogenic agents, achieved durable control and preserved function in a young adult.
Area of Science:
- Oncology
- Head and Neck Surgery
- Medical Genetics
Background:
- Lingual rhabdomyosarcoma (RMS) is an exceptionally rare cancer in adults, lacking established treatment protocols.
- Adult RMS presents unique challenges due to its rarity and the absence of standardized therapeutic guidelines.
Purpose of the Study:
- To report a case of adult lingual RMS managed with a sequential, multimodal treatment approach.
- To evaluate the efficacy and safety of integrating immunotherapy and antiangiogenic therapy in advanced lingual RMS.
Main Methods:
- A 19-year-old male with lingual RMS received sequential chemotherapy regimens (doxorubicin/ifosfamide, cisplatin/5-fluorouracil, vincristine/actinomycin D/cyclophosphamide with pembrolizumab).
- Subsequent treatment involved cetuximab and bevacizumab, followed by intensity-modulated radiotherapy (IMRT).
Main Results:
- Initial chemotherapy regimens led to disease progression.
- Third-line therapy (VAC + pembrolizumab) provided transient stabilization but was limited by toxicity.
- Cetuximab + bevacizumab induced a significant partial response with good tolerance.
- IMRT consolidation resulted in durable locoregional control without systemic disease.
- Swallowing and phonation functions were preserved.
Conclusions:
- Individualized, stepwise management is crucial for adult lingual RMS.
- Combining immunotherapy and antiangiogenic therapy may offer significant tumor control and functional preservation in select adult RMS cases.
- This approach highlights a potential strategy for managing rare adult malignancies.