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Peer-reviewedCC BY 4.0Frontiers in Oncology

Spatially fractionated (GRID) radiotherapy in a patient with metastatic pleomorphic rhabdomyosarcoma: a case report

Abstract

Adult pleomorphic rhabdomyosarcoma is an exceedingly rare, aggressive, high-grade soft tissue sarcoma with a poor prognosis. Treatment for metastatic pleomorphic rhabdomyosarcoma typically involves a combination of chemotherapy, radiation, and surgical resection, though optimal treatment strategies remain undefined. We present here a case of a 52-year-old otherwise healthy male who was diagnosed with metastatic pleomorphic rhabdomyosarcoma with a rapidly progressive, bulky, and symptomatic left upper back tumor. He was treated with multi-line systemic chemotherapy, spatially fractionated (GRID) radiotherapy to his primary back tumor, stereotactic body radiotherapy (SBRT) to his metastatic lung nodule, and long-term maintenance pazopanib, achieving a durable partial response followed by sustained disease control exceeding four years. Adult pleomorphic rhabdomyosarcoma remains a difficult cancer to treat, and more research is needed to better understand its disease course and optimal treatment regimens. This case highlights the potential role of GRID radiotherapy as a component of treatment for bulky, unresectable tumors and underscores the need for further investigation of this modality in aggressive soft tissue sarcomas.

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BibTeX
@article{zhang2026spatially,
  title = {{Spatially fractionated (GRID) radiotherapy in a patient with metastatic pleomorphic rhabdomyosarcoma: a case report}},
  author = {Jessica Zhang and Fahad Faruqi and Yuri Velichko and Borislav Alexiev and Lacey Durham and Pedro Hermida de Viveiros and Seth M. Pollack and Vinai Gondi},
  journal = {Frontiers in Oncology},
  year = {2026},
  month = nov,
  doi = {10.3389/fonc.2026.1931079},
  url = {https://www.frontiersin.org/articles/10.3389/fonc.2026.1931079},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Spatially fractionated (GRID) radiotherapy in a patient with metastatic pleomorphic rhabdomyosarcoma: a case report
AU  - Jessica Zhang
AU  - Fahad Faruqi
AU  - Yuri Velichko
AU  - Borislav Alexiev
AU  - Lacey Durham
AU  - Pedro Hermida de Viveiros
AU  - Seth M. Pollack
AU  - Vinai Gondi
PY  - 2026
DA  - 2026/11/05
JO  - Frontiers in Oncology
DO  - 10.3389/fonc.2026.1931079
UR  - https://www.frontiersin.org/articles/10.3389/fonc.2026.1931079
AB  - Adult pleomorphic rhabdomyosarcoma is an exceedingly rare, aggressive, high-grade soft tissue sarcoma with a poor prognosis. Treatment for metastatic pleomorphic rhabdomyosarcoma typically involves a combination of chemotherapy, radiation, and surgical resection, though optimal treatment strategies remain undefined. We present here a case of a 52-year-old otherwise healthy male who was diagnosed with metastatic pleomorphic rhabdomyosarcoma with a rapidly progressive, bulky, and symptomatic left upper back tumor. He was treated with multi-line systemic chemotherapy, spatially fractionated (GRID) radiotherapy to his primary back tumor, stereotactic body radiotherapy (SBRT) to his metastatic lung nodule, and long-term maintenance pazopanib, achieving a durable partial response followed by sustained disease control exceeding four years. Adult pleomorphic rhabdomyosarcoma remains a difficult cancer to treat, and more research is needed to better understand its disease course and optimal treatment regimens. This case highlights the potential role of GRID radiotherapy as a component of treatment for bulky, unresectable tumors and underscores the need for further investigation of this modality in aggressive soft tissue sarcomas.
SN  - 2234-943X
ER  -