Clinical Experience With RIST-Based Multimodality Therapy in Relapsed Ewing Sarcoma: A Descriptive Single-center Case Series.

J Pediatr Hematol OncolSep 28, 2026 (epub)

Mahdi Asleh, Yotam Eshel, Miriam Ben Harosh et al.

✦ AI-curated · Sources linked

Case in brief

This single-center case series described three patients with relapsed Ewing sarcoma treated with RIST (rapamycin, irinotecan, dasatinib, and temozolomide). The patient with measurable disease had an early partial response but progressed at 9 months. Two patients received RIST after local therapy while they had no evidence of disease; they maintained disease control for 41 and 44 months. Toxicities were manageable, primarily hematologic, and did not lead to treatment discontinuation.

What made this case unusual

RIST was used both for measurable relapsed disease and as post-local-therapy consolidation in patients with no evidence of disease, with prolonged disease control reported in the latter two cases.

Diagnostic / clinical pearl

Interpret outcomes in this small descriptive series by treatment context: the measurable-disease response was followed by progression, whereas prolonged disease control was reported with post-local-therapy consolidation.

Why it matters

The authors report that prolonged outpatient RIST administration was feasible; its role as multimodality consolidation requires prospective evaluation.

Source

Published in J Pediatr Hematol Oncol. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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