TY - JOUR
T1 - Adjuvant re-irradiation vs. no early re-irradiation of resected recurrent glioblastoma
T2 - pooled comparative cohort analysis from two tertiary centers
AU - Straube, Christoph
AU - Combs, Stephanie E.
AU - Bernhardt, Denise
AU - Gempt, Jens
AU - Meyer, Bernhard
AU - Zimmer, Claus
AU - Schmidt-Graf, Friederike
AU - Vajkoczy, Peter
AU - Grün, Arne
AU - Ehret, Felix
AU - Zips, Daniel
AU - Kaul, David
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/5
Y1 - 2024/5
N2 - Background: The optimal management strategy for recurrent glioblastoma (rGBM) remains uncertain, and the impact of re-irradiation (Re-RT) on overall survival (OS) is still a matter of debate. This study included patients who achieved gross total resection (GTR) after a second surgery after recurrence, following the GlioCave criteria. Methods: Inclusion criteria include being 18 years or older, having histologically confirmed locally recurrent IDHwt or IDH unknown GBM, achieving MRI-proven GTR after the second surgery, having a Karnofsky performance status of at least 60% after the second surgery, having a minimum interval of 6 months between the first radiotherapy and the second surgery, and a maximum of 8 weeks from second surgery to the start of Re-RT. Results: A total of 44 patients have met the inclusion criteria. The median OS after the second surgery was 14 months. All patients underwent standard treatment after initial diagnosis, including maximum safe resection, adjuvant radiochemotherapy and adjuvant chemotherapy. Re-RT did not significantly impact OS. However, MGMT promoter methylation status and a longer interval (> 12 months) between treatments were associated with better OS. Multivariate analysis revealed the MGMT status as the only significant predictor of OS. Conclusion: Factors such as MGMT promoter methylation status and treatment interval play crucial roles in determining patient outcomes after second surgery. Personalized treatment strategies should consider these factors to optimize the management of rGBM. Prospective research is needed to define the value of re-RT after second surgery and to inform decision making in this situation.
AB - Background: The optimal management strategy for recurrent glioblastoma (rGBM) remains uncertain, and the impact of re-irradiation (Re-RT) on overall survival (OS) is still a matter of debate. This study included patients who achieved gross total resection (GTR) after a second surgery after recurrence, following the GlioCave criteria. Methods: Inclusion criteria include being 18 years or older, having histologically confirmed locally recurrent IDHwt or IDH unknown GBM, achieving MRI-proven GTR after the second surgery, having a Karnofsky performance status of at least 60% after the second surgery, having a minimum interval of 6 months between the first radiotherapy and the second surgery, and a maximum of 8 weeks from second surgery to the start of Re-RT. Results: A total of 44 patients have met the inclusion criteria. The median OS after the second surgery was 14 months. All patients underwent standard treatment after initial diagnosis, including maximum safe resection, adjuvant radiochemotherapy and adjuvant chemotherapy. Re-RT did not significantly impact OS. However, MGMT promoter methylation status and a longer interval (> 12 months) between treatments were associated with better OS. Multivariate analysis revealed the MGMT status as the only significant predictor of OS. Conclusion: Factors such as MGMT promoter methylation status and treatment interval play crucial roles in determining patient outcomes after second surgery. Personalized treatment strategies should consider these factors to optimize the management of rGBM. Prospective research is needed to define the value of re-RT after second surgery and to inform decision making in this situation.
KW - 2nd surgery
KW - Adjuvant radiotherapy
KW - Cohort study
KW - GTR
KW - Glioblastoma
KW - Gross total resection
KW - Re-irradiation
KW - Re-irradiation
KW - Recurrence
UR - http://www.scopus.com/inward/record.url?scp=85188318813&partnerID=8YFLogxK
U2 - 10.1007/s11060-024-04633-2
DO - 10.1007/s11060-024-04633-2
M3 - Article
AN - SCOPUS:85188318813
SN - 0167-594X
VL - 168
SP - 49
EP - 56
JO - Journal of Neuro-Oncology
JF - Journal of Neuro-Oncology
IS - 1
ER -