BIOM-12. PROLONGED RESPONSE TO THIRD-LINE TREATMENT WITH COMBINATION CCNU/TMZ IN AN MGMT METHYLATED IDH-WILDTYPE GLIOBLASTOMA. (14th November 2022)
- Record Type:
- Journal Article
- Title:
- BIOM-12. PROLONGED RESPONSE TO THIRD-LINE TREATMENT WITH COMBINATION CCNU/TMZ IN AN MGMT METHYLATED IDH-WILDTYPE GLIOBLASTOMA. (14th November 2022)
- Main Title:
- BIOM-12. PROLONGED RESPONSE TO THIRD-LINE TREATMENT WITH COMBINATION CCNU/TMZ IN AN MGMT METHYLATED IDH-WILDTYPE GLIOBLASTOMA
- Authors:
- Pan, Peter
Haggiagi, Aya
Iwamoto, Fabio - Abstract:
- Abstract: INTRODUCTION: Multiply recurrent glioblastoma suffers from poor response rates to treatment, and limited durability. We describe a case of an impressive response to third-line CCNU/TMZ. BACKGROUND: Headaches brought a 76-year-old man to medical attention. MRI identified an enhancing right temporal mass -- path following resection demonstrated glioblastoma (IDH-wildtype, MGMT-methylated, TERT mutant; PTEN Y68H, CDKN2A/B loss, CCND3 amplification; VUS in POLE, ATM, GRIN2A, and ROS1). He received hypofractionated RT 40.05Gy/15-fractions plus 21-days concurrent TMZ 75 mg/m2, then 5-day-on / 23-day-off TMZ (150 mg/m2 cycles #1-3; 200 mg/m2 subsequent). MRI pre-cycle #6, nearly 6 months post-RT, showed increased enhancement/FLAIR consistent with local progression (POD).Second-Line: After screen-fail for clinical trial, initiated off-label regorafenib 160 mg/d, 21-days-on/7-days-off -- with partial response in enhancement at 3 weeks. With dose-reduction to 120 mg/d cycles #2-3 (for mounting fatigue), enhancement progressively worsened. Despite resuming higher 160 mg/d for cycle #4, enhancement progressed, consistent with POD.Third-Line: Given presence of MGMT promoter methylation (and extrapolating from CeTeG/NOA-09), combination CCNU 100 mg/m2 (day 1) and TMZ 100 mg/m2 (days 2-6; 8-week cycle) was started. There was improvement in enhancement/FLAIR, which continued to improve gradually through 6 cycles of CCNU/TMZ. Durability of response was surprising -- MRIsAbstract: INTRODUCTION: Multiply recurrent glioblastoma suffers from poor response rates to treatment, and limited durability. We describe a case of an impressive response to third-line CCNU/TMZ. BACKGROUND: Headaches brought a 76-year-old man to medical attention. MRI identified an enhancing right temporal mass -- path following resection demonstrated glioblastoma (IDH-wildtype, MGMT-methylated, TERT mutant; PTEN Y68H, CDKN2A/B loss, CCND3 amplification; VUS in POLE, ATM, GRIN2A, and ROS1). He received hypofractionated RT 40.05Gy/15-fractions plus 21-days concurrent TMZ 75 mg/m2, then 5-day-on / 23-day-off TMZ (150 mg/m2 cycles #1-3; 200 mg/m2 subsequent). MRI pre-cycle #6, nearly 6 months post-RT, showed increased enhancement/FLAIR consistent with local progression (POD).Second-Line: After screen-fail for clinical trial, initiated off-label regorafenib 160 mg/d, 21-days-on/7-days-off -- with partial response in enhancement at 3 weeks. With dose-reduction to 120 mg/d cycles #2-3 (for mounting fatigue), enhancement progressively worsened. Despite resuming higher 160 mg/d for cycle #4, enhancement progressed, consistent with POD.Third-Line: Given presence of MGMT promoter methylation (and extrapolating from CeTeG/NOA-09), combination CCNU 100 mg/m2 (day 1) and TMZ 100 mg/m2 (days 2-6; 8-week cycle) was started. There was improvement in enhancement/FLAIR, which continued to improve gradually through 6 cycles of CCNU/TMZ. Durability of response was surprising -- MRIs stable/improved at 15 months since starting CCNU/TMZ. DISCUSSION: This case illustrates impressive response to CCNU/TMZ in the third-line. Delayed RT treatment effect is less likely given time elapsed from RT at initial progression (after 5 cycles of adjuvant TMZ), convincing but short-lived improvement to regorafenib (that progressively worsened through 3 more regorafenib cycles), and robust response only with CCNU/TMZ. He was also never on steroids (except post-operatively) nor bevacizumab. This suggests that improvement was mediated by antitumor effect against progressing tumor, rather than delayed RT treatment effect. MGMT methylation may have played a role in this patient's response to dual alkylator therapy. … (more)
- Is Part Of:
- Neuro-oncology. Volume 24(2022)Supplement 7
- Journal:
- Neuro-oncology
- Issue:
- Volume 24(2022)Supplement 7
- Issue Display:
- Volume 24, Issue 7 (2022)
- Year:
- 2022
- Volume:
- 24
- Issue:
- 7
- Issue Sort Value:
- 2022-0024-0007-0000
- Page Start:
- vii6
- Page End:
- vii6
- Publication Date:
- 2022-11-14
- Subjects:
- Brain Neoplasms -- Periodicals
Brain -- Tumors -- Periodicals
Brain -- Cancer -- Periodicals
Nervous system -- Cancer -- Periodicals
616.99481 - Journal URLs:
- http://neuro-oncology.dukejournals.org/ ↗
http://neuro-oncology.oxfordjournals.org/ ↗
http://www.oxfordjournals.org/content?genre=journal&issn=1522-8517 ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/neuonc/noac209.022 ↗
- Languages:
- English
- ISSNs:
- 1522-8517
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.288000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24557.xml