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Cocktail and Poster Display session

100P - Impact of IDH mutation and adjuvant chemo(radio)therapy on survival outcome in grade II/III astrocytoma

Date

26 Feb 2024

Session

Cocktail and Poster Display session

Topics

Pathology/Molecular Biology

Tumour Site

Presenters

Mohammad Hamad

Citation

Annals of Oncology (2024) 9 (suppl_1): 1-9. 10.1016/esmoop/esmoop102310

Authors

M.M. Hamad1, A. Ellaithy2

Author affiliations

  • 1 Faculty Of Medicine, IAU - The University of Jordan, 11942 - Amman/JO
  • 2 Faculty Of Medicine, Suez Canal University Hospital, 41522 - Ismailia/EG

Resources

This content is available to ESMO members and event participants.

Abstract 100P

Background

Astrocytoma is a primary brain tumour arising from specific glial cells called astrocytes. Isocitrate dehydrogenase (IDH) mutations represent an early oncogenic event in glioma evolution. The 2-hydroxyglutarate builds up and is produced in grade II/III astrocytoma. Adjuvant chemo(radio)therapy is the standard treatment. Optimal treatment strategies are controversial due to the risk-benefit ratio. This study aims to assess the effect of IDH mutation on survival outcomes with different treatment modalities for a better understanding of the disease.

Methods

Data were obtained from the SEER program for patients with diffuse and anaplastic astrocytoma diagnosed from 2018-2020. Patients were divided into wild-type (wIDH) and mutant-type (mIDH) groups and subclassified based on the received adjuvant therapy (chemotherapy, radiotherapy, chemoradiotherapy). All patients had surgery (tumour destruction, local excision, partial, radial, and total gross resection). SPSS 27 was used for statistical analysis, the Kaplan-Meier curve, and the long-rank test for survival analysis.

Results

Out of 811 patients, 486 (59.9%) had mIDH, and 325 (40.1%)had wIDH. The 2-year relative survival for mIDH was 95%, and 51% for the wIDH, P<0.001. The highest 2-year relative survival among the mIDH group was for patients who received adjuvant chemotherapy (100%), compared to adjuvant chemoradiotherapy (95.3%) and adjuvant radiotherapy (81.2%), P=0.051. The 2-year survival for wIDH who received adjuvant chemotherapy, combined adjuvant chemoradiotherapy and adjuvant radiotherapy were 66%, 51% and 42%, respectively; P=0.022.

Conclusions

The mIDH had better 2-year relative survival compared to wIDH across all treatment modalities. Adjuvant chemotherapy had more than 20% survival benefit compared to radiotherapy in mIDH and wIDH. These results suggest adjuvant chemotherapy as the modality of choice for mIDH to improve the survival outcome and avoid radiotherapy's unfavourable side effects.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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