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. 2022 Mar 31;22(1):349.
doi: 10.1186/s12885-022-09469-5.

Irinotecan plus temozolomide in relapsed Ewing sarcoma: an integrated analysis of retrospective studies

Affiliations

Irinotecan plus temozolomide in relapsed Ewing sarcoma: an integrated analysis of retrospective studies

Bi-Cheng Wang et al. BMC Cancer. .

Abstract

Background: The prognosis of patients with relapsed Ewing sarcoma is poor. In this study, we aimed to pooled-analyze the efficacy and safety of the combination of irinotecan and temozolomide in treating patients with relapsed Ewing sarcoma.

Methods: PubMed, Cochrane CENTRAL, Web of Science, and EMBASE were systematically searched on September 27, 2021. The primary outcomes were rates of objective response and disease control, and the secondary outcomes were toxicities.

Results: Six retrospective studies with 184 patients were enrolled in the analysis. The median age ranged from 14 to 21. The integrated rates were 44% (95% confidence interval [CI] 31-58) for objective response and 66% (55-77) for disease control. Grade 3-4 neutropenia, thrombocytopenia, and diarrhea occurred in 8% (3-16), 7% (3-11), and 8% (5-10) of chemotherapeutic cycles, respectively. 18% (7-32) and 6% (2-11) of patients suffered grade 3-4 neutropenia and thrombocytopenia after irinotecan plus temozolomide treatment.

Conclusion: Irinotecan plus temozolomide combination chemotherapy showed antitumor activity and an acceptable safety profile in patients with relapsed Ewing sarcoma. More future prospective studies are needed to confirm the retrospective results.

Keywords: Chemotherapy; Ewing sarcoma; Integrated analysis; Irinotecan; Temozolomide.

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Conflict of interest statement

No conflict of interest.

Figures

Fig. 1
Fig. 1
Flowchart of selecting the eligible studies
Fig. 2
Fig. 2
Pooled objective response rate (A) and disease control rate (B) in the analysis
Fig. 3
Fig. 3
Pooled incidences of neutropenia, thrombocytopenia, and diarrhea in the cycle (A) and patient (B) levels
Fig. 4
Fig. 4
Sensitivity analysis and the risk of publication bias in the study. A and C Objective response rate; (B and D) Disease control rate

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