Page last updated: 2024-10-24

carmustine and Cognition Disorders

carmustine has been researched along with Cognition Disorders in 4 studies

Carmustine: A cell-cycle phase nonspecific alkylating antineoplastic agent. It is used in the treatment of brain tumors and various other malignant neoplasms. (From Martindale, The Extra Pharmacopoeia, 30th ed, p462) This substance may reasonably be anticipated to be a carcinogen according to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985). (From Merck Index, 11th ed)
carmustine : A member of the class of N-nitrosoureas that is 1,3-bis(2-chloroethyl)urea in which one of the nitrogens is substituted by a nitroso group.

Cognition Disorders: Disorders characterized by disturbances in mental processes related to learning, thinking, reasoning, and judgment.

Research Excerpts

ExcerptRelevanceReference
"Patients with brain metastases had improvements in their cognitive trajectory, especially memory and executive function, after treatment with resection plus CW."2.78Preservation of neurocognitive function and local control of 1 to 3 brain metastases treated with surgery and carmustine wafers. ( Booth-Jones, M; Brem, S; Ewend, MG; Jain, S; Meyers, CA; Palmer, G, 2013)

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (75.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Brem, S1
Meyers, CA1
Palmer, G1
Booth-Jones, M1
Jain, S1
Ewend, MG1
Corn, BW1
Wang, M1
Fox, S1
Michalski, J1
Purdy, J1
Simpson, J1
Kresl, J1
Curran, WJ1
Diaz, A1
Mehta, M1
Movsas, B1
Harder, H1
Holtel, H1
Bromberg, JE1
Poortmans, P1
Haaxma-Reiche, H1
Kluin-Nelemans, HC1
Menten, J1
van den Bent, MJ1
Alvarnas, JC1
Negrin, RS1
Horning, SJ1
Hu, WW1
Long, GD1
Schriber, JR1
Stockerl-Goldstein, K1
Tierney, K1
Wong, R1
Blume, KG1
Chao, NJ1

Clinical Trials (4)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Phase 2, Multicenter, Exploratory Study, Evaluating the Treatment Effect of Surgery Plus GLIADELĀ® Wafer in Patients With Metastatic Brain Cancer[NCT00525590]Phase 269 participants (Actual)Interventional2007-12-12Completed
Prospective and Retrospective Memory Perception Assessment in Central/Non-central Nervous System Cancers[NCT03975959]420 participants (Anticipated)Interventional2019-05-10Recruiting
Phase I/II Radiation Dose Escalation Study Applying Conformal Radiation Therapy in Supratentorial Glioblastoma Multiforme[NCT00003417]Phase 1/Phase 240 participants (Anticipated)Interventional1998-09-30Completed
Evaluating the MBVP Chemotherapy Schedule Followed by Consolidating Radiotherapy in Non-AIDS Related Primary Central Nervous System Lymphoma (NAPCL)[NCT00003061]Phase 250 participants (Anticipated)Interventional1997-07-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Percentage of Participants With Neurologic Death

Neurologic Death was defined as death due to progression of neurologic disease. (NCT00525590)
Timeframe: Up to Month 12 (from baseline until evidence of neurological deterioration, had a local recurrence, withdrawn, died, lost to follow-up, or the study was closed)

Interventionpercentage of participants (Number)
GLIADEL1.9

Rate of Deterioration in Neurocognitive Functioning (NF) at Month 12

NF was assessed as the performance of 3 neurocognitive domains:memory(MD),executive function(EFD), fine motor coordination(FMCD). For each domain, z-scores were derived from participant's scores in individual neurocognitive tests using an age-adjusted and education-adjusted normative distribution of scores from an unimpaired population.Individual z-scores from related tests were averaged to determine overall z-score.If a z-score average decreased from baseline by greater than or equal to(>=)3 standard deviations(SD)in tests' normative age-adjusted distribution on 2 consecutive visits or decreased by >=3 SD on last follow-up visit, participant were considered to have significant deterioration in their NF at time of the first decrease in z-score.Deterioration in NF:demonstrated deterioration for at least two of the three neurocognitive domains based on these changes from screening.Rate of deterioration in NF was measured as estimated percentage of participants using Kaplan-Meier method. (NCT00525590)
Timeframe: Month 12

Interventionpercentage of participants (Number)
GLIADEL2.8

Time to Neurocognitive Deterioration

The time to neurocognitive deterioration was defined as the number of days between the date of study treatment and the date of neurocognitive deterioration based on NF assessment. This was assessed using Kaplan Meier method. (NCT00525590)
Timeframe: Up to Month 12 (from baseline until evidence of neurological deterioration, had a local recurrence, withdrawn, died, lost to follow-up, or the study was closed)

Interventionmonths (Number)
GLIADELNA

Correlation of Tumor Recurrence (Local, Distant or Overall) With NF Domain Scores

The correlation between recurrence (local, distant or overall) & NF was assessed by presenting change in NF domain scores (memory domain [MD], executive function domain [EFD], fine motor coordination domain [FMCD]) after tumor recurrence (Visits X, X+1, X+2, and X+3) compared to before tumor recurrence (Visit X-1). Here 'Visit X' refers to visit at which participants had tumor recurrence, Visit X-1 refers to visit immediately before the recurrence and X+1, X+2, X+3 refers to subsequent first, second & third visit after the recurrence.NF domain z-scores were derived from participant's scores in individual neurocognitive tests using an age-adjusted &education-adjusted normative distribution of scores from an unimpaired population. Individual z-scores from related tests were averaged to determine overall z-score for each of NF domains. (NCT00525590)
Timeframe: Up to Month 12 (from baseline until evidence of neurological deterioration, had a local recurrence, withdrawn, died, lost to follow-up, or the study was closed)

Interventionz-score (Mean)
Local Recurrence: MD at Visit (X-1)Local Recurrence: MD Change at Visit (X-1)Local Recurrence: MD Change at Visit (X+1)Local Recurrence: MD Change at Visit (X+2)Local Recurrence: MD Change at Visit (X+3)Local Recurrence: EFD at Visit (X-1)Local Recurrence: EFD Change at Visit (X-1)Local Recurrence: EFD Change at Visit (X+1)Local Recurrence: EFD Change at Visit (X+2)Local Recurrence: EFD Change at Visit (X+3)Local Recurrence: FMCD at Visit (X-1)Local Recurrence: FMCD Change at Visit (X-1)Local Recurrence: FMCD Change at Visit (X+1)Local Recurrence: FMCD Change at Visit (X+2)Local Recurrence: FMCD Change at Visit (X+3)Distant Recurrence: MD at Visit (X-1)Distant Recurrence: MD Change at Visit (X-1)Distant Recurrence: MD Change at Visit (X+1)Distant Recurrence: MD Change at Visit (X+2)Distant Recurrence: MD Change at Visit (X+3)Distant Recurrence: EFD at Visit (X-1)Distant Recurrence: EFD Change at Visit (X-1)Distant Recurrence: EFD Change at Visit (X+1)Distant Recurrence: EFD Change at Visit (X+2)Distant Recurrence: EFD Change at Visit (X+3)Distant Recurrence: FMCD at Visit (X-1)Distant Recurrence: FMCD Change at Visit (X-1)Distant Recurrence: FMCD Change at Visit (X+1)Distant Recurrence: FMCD Change at Visit (X+2)Distant Recurrence: FMCD Change at Visit (X+3)Overall Recurrence: MD at Visit (X-1)Overall Recurrence: MD Change at Visit (X-1)Overall Recurrence: MD Change at Visit (X+1)Overall Recurrence: MD Change at Visit (X+2)Overall Recurrence: MD Change at Visit (X+3)Overall Recurrence: EFD at Visit (X-1)Overall Recurrence: EFD Change at Visit (X-1)Overall Recurrence: EFD Change at Visit (X+1)Overall Recurrence: EFD Change at Visit (X+2)Overall Recurrence: EFD Change at Visit (X+3)Overall Recurrence: FMCD at Visit (X-1)Overall Recurrence: FMCD Change at Visit (X-1)Overall Recurrence: FMCD Change at Visit (X+1)Overall Recurrence: FMCD Change at Visit (X+2)Overall Recurrence: FMCD Change at Visit (X+3)
GLIADEL-0.9-1.10.70.1-0.8-0.4-0.50.2-0.0-1.1-1.50.40.5-0.40.3-1.00.2-0.2-0.2-0.7-0.2-0.2-0.5-0.8-0.8-1.2-0.1-0.4-1.1-0.1-0.9-0.1-0.1-0.2-0.7-0.1-0.3-0.5-0.6-0.8-1.20.0-0.3-0.9-0.1

Number of Participants With Neurocognitive Domains Preserved at Month 12

Preservation of NF was defined as a decrease of less than or equal to (<=) 1 SD, any increase, or no change (0 SD) in z-score for each domain (memory domain, executive function domain, and fine motor coordination domain). (NCT00525590)
Timeframe: Month 12

InterventionParticipants (Count of Participants)
Domains preserved=3Domains preserved=2Domains preserved=1Domains preserved=0
GLIADEL9500

Number of Participants With Neurocognitive Domains Preserved at Month 2

Preservation of NF was defined as a decrease of <=1 SD, any increase, or no change (0 SD) in z-score for each domain (memory domain, executive function domain, and fine motor coordination domain). (NCT00525590)
Timeframe: Month 2

InterventionParticipants (Count of Participants)
Domains preserved=3Domains preserved=2Domains preserved=1Domains preserved=0
GLIADEL261243

Number of Participants With Neurocognitive Domains Preserved at Month 4

Preservation of NF was defined as a decrease of <=1 SD, any increase, or no change (0 SD) in z-score for each domain (memory domain, executive function domain, and fine motor coordination domain). (NCT00525590)
Timeframe: Month 4

InterventionParticipants (Count of Participants)
Domains preserved=3Domains preserved=2Domains preserved=1Domains preserved=0
GLIADEL24921

Number of Participants With Neurocognitive Domains Preserved at Month 6

Preservation of NF was defined as a decrease of <=1 SD, any increase, or no change (0 SD) in z-score for each domain (memory domain, executive function domain, and fine motor coordination domain). (NCT00525590)
Timeframe: Month 6

InterventionParticipants (Count of Participants)
Domains preserved=3Domains preserved=2Domains preserved=1Domains preserved=0
GLIADEL17520

Number of Participants With Neurocognitive Domains Preserved at Month 9

Preservation of NF was defined as a decrease of <=1 SD, any increase, or no change (0 SD) in z-score for each domain (memory domain, executive function domain, and fine motor coordination domain). (NCT00525590)
Timeframe: Month 9

InterventionParticipants (Count of Participants)
Domains preserved=3Domains preserved=2Domains preserved=1Domains preserved=0
GLIADEL14600

Percentage of Participants With Brain Tumor Recurrence (Local Recurrence, Distant Recurrence and Overall Recurrence)

(NCT00525590)
Timeframe: Up to Month 12 (from baseline until evidence of neurological deterioration, had a local recurrence, withdrawn, died, lost to follow-up, or the study was closed)

Interventionpercentage of participants (Number)
Local RecurrenceDistant RecurrenceOverall Recurrence
GLIADEL28.048.062.0

Percentage of Participants With Neurocognitive Decline in NF by Severity (Memory Domain, Executive Function Domain, and Fine Motor Coordination Domain)

Neurocognitive decline was defined as any decrease in NF scores less than (<) 0 SD from baseline. Here, in category titles EFD represents Executive Function Domain and FMCD represents Fine Motor Coordination Domain. (NCT00525590)
Timeframe: Months 2, 4, 6, 9 and 12

Interventionpercentage of participants (Number)
Month 2: Memory Domain, decline <0 to -1 SDMonth 2: Memory Domain, decline <-1 to -2 SDMonth 2: Memory Domain, decline <-2 to -3 SDMonth 2: Memory Domain, decline <-3 to -4 SDMonth 2: Memory Domain, decline <-4 to -5 SDMonth 2: Memory Domain, decline <-5 SDMonth 2: EFD, decline <0 to -1 SDMonth 2: EFD, decline <-1 to -2 SDMonth 2: EFD, decline <-2 to -3 SDMonth 2: EFD, decline <-3 to -4 SDMonth 2: EFD, decline <-4 to -5 SDMonth 2: EFD, decline <-5 SDMonth 2: FMCD, decline <0 to -1 SDMonth 2: FMCD, decline <-1 to -2 SDMonth 2: FMCD, decline <-2 to -3 SDMonth 2: FMCD, decline <-3 to -4 SDMonth 2: FMCD, decline <-4 to -5 SDMonth 2: FMCD, decline <-5 SDMonth 4: Memory Domain, decline <0 to -1 SDMonth 4: Memory Domain, decline <-1 to -2 SDMonth 4: Memory Domain, decline <-2 to -3 SDMonth 4: Memory Domain, decline <-3 to -4 SDMonth 4: Memory Domain, decline <-4 to -5 SDMonth 4: Memory Domain, decline <-5 SDMonth 4: EFD, decline <0 to -1 SDMonth 4: EFD, decline <-1 to -2 SDMonth 4: EFD, decline <-2 to -3 SDMonth 4: EFD, decline <-3 to -4 SDMonth 4: EFD, decline <-4 to -5 SDMonth 4: EFD, decline <-5 SDMonth 4: FMCD, decline <0 to -1 SDMonth 4: FMCD, decline <-1 to -2 SDMonth 4: FMCD, decline <-2 to -3 SDMonth 4: FMCD, decline <-3 to -4 SDMonth 4: FMCD, decline <-4 to -5 SDMonth 4: FMCD, decline <-5 SDMonth 6: Memory Domain, decline <0 to -1 SDMonth 6: Memory Domain, decline <-1 to -2 SDMonth 6: Memory Domain, decline <-2 to -3 SDMonth 6: Memory Domain, decline <-3 to -4 SDMonth 6: Memory Domain, decline <-4 to -5 SDMonth 6: Memory Domain, decline <-5 SDMonth 6: EFD, decline <0 to -1 SDMonth 6: EFD, decline <-1 to -2 SDMonth 6: EFD, decline <-2 to -3 SDMonth 6: EFD, decline <-3 to -4 SDMonth 6: EFD, decline <-4 to -5 SDMonth 6: EFD, decline <-5 SDMonth 6: FMCD, decline <0 to -1 SDMonth 6: FMCD, decline <-1 to -2 SDMonth 6: FMCD, decline <-2 to -3 SDMonth 6: FMCD, decline <-3 to -4 SDMonth 6: FMCD, decline <-4 to -5 SDMonth 6: FMCD, decline <-5 SDMonth 9: Memory Domain, decline <0 to -1 SDMonth 9: Memory Domain, decline <-1 to -2 SDMonth 9: Memory Domain, decline <-2 to -3 SDMonth 9: Memory Domain, decline <-3 to -4 SDMonth 9: Memory Domain, decline <-4 to -5 SDMonth 9: Memory Domain, decline <-5 SDMonth 9: EFD, decline <0 to -1 SDMonth 9: EFD, decline <-1 to -2 SDMonth 9: EFD, decline <-2 to -3 SDMonth 9: EFD, decline <-3 to -4 SDMonth 9: EFD, decline <-4 to -5 SDMonth 9: EFD, decline <-5 SDMonth 9: FMCD, decline <0 to -1 SDMonth 9: FMCD, decline <-1 to -2 SDMonth 9: FMCD, decline <-2 to -3 SDMonth 9: FMCD, decline <-3 to -4 SDMonth 9: FMCD, decline <-4 to -5 SDMonth 9: FMCD, decline <-5 SDMonth 12: Memory Domain, decline <0 to -1 SDMonth 12: Memory Domain, decline <-1 to -2 SDMonth 12: Memory Domain, decline <-2 to -3 SDMonth 12: Memory Domain, decline <-3 to -4 SDMonth 12: Memory Domain, decline <-4 to -5 SDMonth 12: Memory Domain, decline <-5 SDMonth 12: EFD, decline <0 to -1 SDMonth 12: EFD, decline <-1 to -2 SDMonth 12: EFD, decline <-2 to -3 SDMonth 12: EFD, decline <-3 to -4 SDMonth 12: EFD, decline <-4 to -5 SDMonth 12: EFD, decline <-5 SDMonth 12: FMCD, decline <0 to -1 SDMonth 12: FMCD, decline <-1 to -2 SDMonth 12: FMCD, decline <-2 to -3 SDMonth 12: FMCD, decline <-3 to -4 SDMonth 12: FMCD, decline <-4 to -5 SDMonth 12: FMCD, decline <-5 SD
GLIADEL27.315.94.500037.88.1000023.87.12.42.40019.48.3002.82.829.00000017.111.402.90012.504.200018.24.5000012.520.8000025.05.0000036.85.3000020.010.05.000014.37.1000033.3000007.114.30000

Time to Recurrence (Local, Distant and Overall)

(NCT00525590)
Timeframe: Up to Month 12 (from baseline until evidence of neurological deterioration, had a local recurrence, withdrawn, died, lost to follow-up, or the study was closed)

Interventionmonths (Median)
Time to Local RecurrenceTime to Distant RecurrenceTime to Overall Recurrence
GLIADELNA8.56.1

Trials

2 trials available for carmustine and Cognition Disorders

ArticleYear
Preservation of neurocognitive function and local control of 1 to 3 brain metastases treated with surgery and carmustine wafers.
    Cancer, 2013, Nov-01, Volume: 119, Issue:21

    Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents, Alkylating; Brain Neoplasms; Carmustine; Cogn

2013
Preservation of neurocognitive function and local control of 1 to 3 brain metastases treated with surgery and carmustine wafers.
    Cancer, 2013, Nov-01, Volume: 119, Issue:21

    Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents, Alkylating; Brain Neoplasms; Carmustine; Cogn

2013
Preservation of neurocognitive function and local control of 1 to 3 brain metastases treated with surgery and carmustine wafers.
    Cancer, 2013, Nov-01, Volume: 119, Issue:21

    Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents, Alkylating; Brain Neoplasms; Carmustine; Cogn

2013
Preservation of neurocognitive function and local control of 1 to 3 brain metastases treated with surgery and carmustine wafers.
    Cancer, 2013, Nov-01, Volume: 119, Issue:21

    Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents, Alkylating; Brain Neoplasms; Carmustine; Cogn

2013
Health related quality of life and cognitive status in patients with glioblastoma multiforme receiving escalating doses of conformal three dimensional radiation on RTOG 98-03.
    Journal of neuro-oncology, 2009, Volume: 95, Issue:2

    Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents, Alkylating; Brain Neoplasms; Carmustine; Cogn

2009

Other Studies

2 other studies available for carmustine and Cognition Disorders

ArticleYear
Cognitive status and quality of life after treatment for primary CNS lymphoma.
    Neurology, 2004, Feb-24, Volume: 62, Issue:4

    Topics: Adult; Antineoplastic Combined Chemotherapy Protocols; Atrophy; Brain; Carmustine; Case-Control Stud

2004
High-dose therapy with hematopoietic cell transplantation for patients with central nervous system involvement by non-Hodgkin's lymphoma.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2000, Volume: 6, Issue:3A

    Topics: Actuarial Analysis; Adult; Antineoplastic Combined Chemotherapy Protocols; Bone Marrow Purging; Carm

2000