AI Article Synopsis

  • Adult Diffuse midline glioma (DMG) is a rare brain tumor in adults, treated primarily with radiotherapy and chemotherapy, but the effectiveness of these treatments has been under-evaluated.
  • A study of 49 patients revealed that while concurrent chemotherapy didn’t improve overall survival (OS), adjuvant temozolomide treatment significantly extended OS from 9.0 to 21.2 months.
  • The results suggest that following initial treatment with radiotherapy, adjuvant chemotherapy can enhance survival outcomes, and for patients who experience disease progression, second-line systemic treatment could offer further survival benefits.

Article Abstract

Purpose: Adult Diffuse midline glioma (DMG) is a very rare disease. DMGs are currently treated with radiotherapy and chemotherapy even if only a few retrospective studies assessed the impact on overall survival (OS) of these approaches.

Methods: We carried out an Italian multicentric retrospective study of adult patients with H3K27-altered DMG to assess the effective role of systemic therapy in the treatment landscape of this rare tumor type.

Results: We evaluated 49 patients from 6 Institutions. The median age was 37.3 years (range 20.1-68.3). Most patients received biopsy as primary approach (n = 30, 61.2%) and radiation therapy after surgery (n = 39, 79.6%). 25 (51.0%) of patients received concurrent chemotherapy and 26 (53.1%) patients received adjuvant temozolomide. In univariate analysis, concurrent chemotherapy did not result in OS improvement while adjuvant temozolomide was associated with longer OS (21.2 vs. 9.0 months, HR 0.14, 0.05-0.41, p < 0.001). Multivariate analysis confirmed the role of adjuvant chemotherapy (HR 0.1, 95%CI: 0.03-0.34, p = 0.003). In patients who progressed after radiation and/or chemotherapy the administration of a second-line systemic treatment had a significantly favorable impact on survival (8.0 vs. 3.2 months, HR 0.2, 95%CI 0.1-0.65, p = 0.004).

Conclusion: In our series, adjuvant treatment after radiotherapy can be useful in improving OS of patients with H3K27-altered DMG. When feasible another systemic treatment after treatment progression could be proposed.

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Source
http://dx.doi.org/10.1007/s11060-024-04589-3DOI Listing

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