carmustine has been researched along with Craniopharyngioma 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.
Craniopharyngioma: A benign pituitary-region neoplasm that originates from Rathke's pouch. The two major histologic and clinical subtypes are adamantinous (or classical) craniopharyngioma and papillary craniopharyngioma. The adamantinous form presents in children and adolescents as an expanding cystic lesion in the pituitary region. The cystic cavity is filled with a black viscous substance and histologically the tumor is composed of adamantinomatous epithelium and areas of calcification and necrosis. Papillary craniopharyngiomas occur in adults, and histologically feature a squamous epithelium with papillations. (From Joynt, Clinical Neurology, 1998, Ch14, p50)
Excerpt | Relevance | Reference |
---|---|---|
"Ten patients, nine with pituitary adenomas and one with a craniopharyngioma, underwent implantation of from two to eight Gliadel wafers." | 2.71 | Gliadel for pituitary adenomas and craniopharyngiomas. ( Laws, ER; Maartens, N; Morris, AM, 2003) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (50.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Laws, ER | 1 |
Morris, AM | 1 |
Maartens, N | 1 |
Bremer, AM | 1 |
Nguyen, TQ | 1 |
Balsys, R | 1 |
Gildenberg, PL | 1 |
Bloom, HJ | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Phase I Trial of AZD8055, An Oral MTOR Kinase Inhibitor, for Adults With Recurrent Gliomas[NCT01316809] | Phase 1 | 22 participants (Actual) | Interventional | 2011-03-04 | Completed | ||
(11C)N-Desmethyl-Loperamide as a Marker of P-Glycoprotein Function in Patients With Gliomas[NCT01281982] | 2 participants (Actual) | Observational | 2011-01-13 | Terminated | |||
Phase I Trial of AZD7451, A Topomysin-Receptor Kinase (TRK) Inhibitor, For Adults With Recurrent Glioblastoma Multiforme (GBM)[NCT01468324] | Phase 1 | 14 participants (Actual) | Interventional | 2011-10-05 | Completed | ||
A Phase I/II Study of the Safety and Feasibility of Administering T Cells Expressing Anti-EGFRvIII Chimeric Antigen Receptor to Patients With Malignant Gliomas Expressing EGFRvIII[NCT01454596] | Phase 1/Phase 2 | 18 participants (Actual) | Interventional | 2012-05-16 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
CAR and vector presence were quantitated in peripheral blood mononuclear cell (PBMC) samples using established polymerase chain reaction (PCR) techniques (NCT01454596)
Timeframe: 1 month post transplant
Intervention | K/µL (Median) |
---|---|
Group A (Steroids) - Cohort 1: 1x10(7) | 23 |
Group A (Steroids) - Cohort 2: 3x10(7) | 70 |
Group A (Steroids) - Cohort 3: 1x10(8) | 36 |
Group B (No Steroids) - Cohort 1: 1x10(7) | 67 |
Group B (No Steroids) - Cohort 2: 3x10(7) | 7 |
Group B (No Steroids) - Cohort 3: 1x10(8) | 43 |
Group B (No Steroids) - Cohort 4: 3x10(8) | 28 |
Group B (No Steroids) - Cohort 5: 1x10(9) | 25 |
Combined Steroids/no Steroids) - Cohort 6: 3x10(9) | 12 |
Combined Steroids/no Steroids) - Cohort 7: 1x10(10) | 67.5 |
Combined Steroids/no Steroids) - Cohort 8: 3-6x10(10) | NA |
Combined Steroids/no Steroids) - Cohort 9: 3x10(10) | 8 |
Here is the count of participants with serious and non-serious adverse events assessed by the Common Terminology Criteria in Adverse Events (CTCAE v4.0). A non-serious adverse event is any untoward medical occurrence. A serious adverse event is an adverse event or suspected adverse reaction that results in death, a life threatening adverse drug experience, hospitalization, disruption of the ability to conduct normal life functions, congenital anomaly/birth defect or important medical events that jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the previous outcomes mentioned. (NCT01454596)
Timeframe: 51 dys Grp A, Cohort 1; Cohort 2:68 dys; Cohort 3:40 dys; Grp B, Cohort 1:67 dys; Cohort 2:48 dys; Cohort 3:55 dys; Cohort 4: 46 dys; Cohort 5:147 dys; C. Ster/No Ster Grp, Cohort 6:12 mos, 26 dys; Cohort 7:11 mos, 18 dys; Cohort 8:7 dys; Cohort 9:70 dys.
Intervention | Participants (Count of Participants) |
---|---|
Group A (Steroids) - Cohort 1: 1x10(7) | 1 |
Group A (Steroids) - Cohort 2: 3x10(7) | 1 |
Group A (Steroids) - Cohort 3: 1x10(8) | 1 |
Group B (No Steroids) - Cohort 1: 1x10(7) | 1 |
Group B (No Steroids) - Cohort 2: 3x10(7) | 1 |
Group B (No Steroids) - Cohort 3: 1x10(8) | 1 |
Group B (No Steroids) - Cohort 4: 3x10(8) | 1 |
Group B (No Steroids) - Cohort 5: 1x10(9) | 3 |
Combined Steroids/no Steroids) - Cohort 6: 3x10(9) | 3 |
Combined Steroids/no Steroids) - Cohort 7: 1x10(10) | 3 |
Combined Steroids/no Steroids) - Cohort 8: 3-6x10(10) | 1 |
Combined Steroids/no Steroids) - Cohort 9: 3x10(10) | 1 |
Objective response was assessed by comparison with baseline dynamic contrast enhanced magnetic resonance imaging with perfusion using Neuro-oncology Working Group proposed guidelines. Complete Response is disappearance of all measurable and non-measurable disease for at least 4 weeks. Partial Response is >/= 50% decrease in lesions for at least 4 weeks. Stable Disease does not meet the criteria for complete response, partial response or progression and requires stable lesions compared with baseline. Progression is >/= 25% increase in lesions. (NCT01454596)
Timeframe: 4 weeks after cell infusion and monthly as feasible up to 12 months
Intervention | Participants (Count of Participants) |
---|---|
Group A (Steroids) - Cohort 1: 1x10(7) | 0 |
Group A (Steroids) - Cohort 2: 3x10(7) | 0 |
Group A (Steroids) - Cohort 3: 1x10(8) | 0 |
Group B (No Steroids) - Cohort 1: 1x10(7) | 0 |
Group B (No Steroids) - Cohort 2: 3x10(7) | 0 |
Group B (No Steroids) - Cohort 3: 1x10(8) | 0 |
Group B (No Steroids) - Cohort 4: 3x10(8) | 0 |
Group B (No Steroids) - Cohort 5: 1x10(9) | 0 |
Combined Steroids/no Steroids) - Cohort 6: 3x10(9) | 0 |
Combined Steroids/no Steroids) - Cohort 7: 1x10(10) | 0 |
Combined Steroids/no Steroids) - Cohort 8: 3-6x10(10) | 0 |
Combined Steroids/no Steroids) - Cohort 9: 3x10(10) | 0 |
Aggregate of all adverse events ≥Grade 3 that are possibly, probably, and definitely related to treatment. Adverse events were assessed by the Common Terminology Criteria in Adverse Events (CTCAE v4.0). Per CTCAE, Grade 3 adverse events are severe, Grade 4 is life threatening, and Grade 5 is death. (NCT01454596)
Timeframe: From 4 weeks after cell infusion up to 77 days
Intervention | adverse events (Number) |
---|---|
Group A (Steroids) - Cohort 1: 1x10(7) | 0 |
Group A (Steroids) - Cohort 2: 3x10(7) | 0 |
Group A (Steroids) - Cohort 3: 1x10(8) | 0 |
Group B (No Steroids) - Cohort 1: 1x10(7) | 0 |
Group B (No Steroids) - Cohort 2: 3x10(7) | 0 |
Group B (No Steroids) - Cohort 3: 1x10(8) | 0 |
Group B (No Steroids) - Cohort 4: 3x10(8) | 0 |
Group B (No Steroids) - Cohort 5: 1x10(9) | 0 |
Combined Steroids/no Steroids) - Cohort 6: 3x10(9) | 0 |
Combined Steroids/no Steroids) - Cohort 7: 1x10(10) | 0 |
Combined Steroids/no Steroids) - Cohort 8: 3-6x10(10) | 1 |
Combined Steroids/no Steroids) - Cohort 9: 3x10(10) | 1 |
Progression was assessed by the Response Assessment in Neuro-Oncology (RANO) criteria and is defined as the circumstance when the magnetic resonance imaging (MRI) scan is ranked -2 (definitely worse) or -3 (development of a new lesion). (NCT01454596)
Timeframe: Time from the date of registration to the date of first observation of progressive disease up to 6 months after end of treatment
Intervention | months (Median) |
---|---|
Group A (Steroids) - Cohort 1: 1x10(7) | 1.1 |
Group A (Steroids) - Cohort 2: 3x10(7) | 1.1 |
Group A (Steroids) - Cohort 3: 1x10(8) | 1.3 |
Group B (No Steroids) - Cohort 1: 1x10(7) | 1.9 |
Group B (No Steroids) - Cohort 2: 3x10(7) | 2.0 |
Group B (No Steroids) - Cohort 3: 1x10(8) | 1.5 |
Group B (No Steroids) - Cohort 4: 3x10(8) | 1.2 |
Group B (No Steroids) - Cohort 5: 1x10(9) | 1.1 |
Combined Steroids/no Steroids) - Cohort 6: 3x10(9) | 2.7 |
Combined Steroids/no Steroids) - Cohort 7: 1x10(10) | 1.1 |
Combined Steroids/no Steroids) - Cohort 8: 3-6x10(10) | 0 |
Combined Steroids/no Steroids) - Cohort 9: 3x10(10) | 2.0 |
1 review available for carmustine and Craniopharyngioma
Article | Year |
---|---|
Combined modality therapy for intracranial tumors.
Topics: Antigens, Neoplasm; Antineoplastic Agents; Astrocytoma; Brain Neoplasms; Carmustine; Child; Cranioph | 1975 |
Combined modality therapy for intracranial tumors.
Topics: Antigens, Neoplasm; Antineoplastic Agents; Astrocytoma; Brain Neoplasms; Carmustine; Child; Cranioph | 1975 |
Combined modality therapy for intracranial tumors.
Topics: Antigens, Neoplasm; Antineoplastic Agents; Astrocytoma; Brain Neoplasms; Carmustine; Child; Cranioph | 1975 |
Combined modality therapy for intracranial tumors.
Topics: Antigens, Neoplasm; Antineoplastic Agents; Astrocytoma; Brain Neoplasms; Carmustine; Child; Cranioph | 1975 |
Combined modality therapy for intracranial tumors.
Topics: Antigens, Neoplasm; Antineoplastic Agents; Astrocytoma; Brain Neoplasms; Carmustine; Child; Cranioph | 1975 |
Combined modality therapy for intracranial tumors.
Topics: Antigens, Neoplasm; Antineoplastic Agents; Astrocytoma; Brain Neoplasms; Carmustine; Child; Cranioph | 1975 |
Combined modality therapy for intracranial tumors.
Topics: Antigens, Neoplasm; Antineoplastic Agents; Astrocytoma; Brain Neoplasms; Carmustine; Child; Cranioph | 1975 |
Combined modality therapy for intracranial tumors.
Topics: Antigens, Neoplasm; Antineoplastic Agents; Astrocytoma; Brain Neoplasms; Carmustine; Child; Cranioph | 1975 |
Combined modality therapy for intracranial tumors.
Topics: Antigens, Neoplasm; Antineoplastic Agents; Astrocytoma; Brain Neoplasms; Carmustine; Child; Cranioph | 1975 |
Combined modality therapy for intracranial tumors.
Topics: Antigens, Neoplasm; Antineoplastic Agents; Astrocytoma; Brain Neoplasms; Carmustine; Child; Cranioph | 1975 |
Combined modality therapy for intracranial tumors.
Topics: Antigens, Neoplasm; Antineoplastic Agents; Astrocytoma; Brain Neoplasms; Carmustine; Child; Cranioph | 1975 |
Combined modality therapy for intracranial tumors.
Topics: Antigens, Neoplasm; Antineoplastic Agents; Astrocytoma; Brain Neoplasms; Carmustine; Child; Cranioph | 1975 |
Combined modality therapy for intracranial tumors.
Topics: Antigens, Neoplasm; Antineoplastic Agents; Astrocytoma; Brain Neoplasms; Carmustine; Child; Cranioph | 1975 |
Combined modality therapy for intracranial tumors.
Topics: Antigens, Neoplasm; Antineoplastic Agents; Astrocytoma; Brain Neoplasms; Carmustine; Child; Cranioph | 1975 |
Combined modality therapy for intracranial tumors.
Topics: Antigens, Neoplasm; Antineoplastic Agents; Astrocytoma; Brain Neoplasms; Carmustine; Child; Cranioph | 1975 |
Combined modality therapy for intracranial tumors.
Topics: Antigens, Neoplasm; Antineoplastic Agents; Astrocytoma; Brain Neoplasms; Carmustine; Child; Cranioph | 1975 |
1 trial available for carmustine and Craniopharyngioma
Article | Year |
---|---|
Gliadel for pituitary adenomas and craniopharyngiomas.
Topics: Adenoma; Adult; Aged; Antineoplastic Agents, Alkylating; Carmustine; Craniopharyngioma; Drug Carrier | 2003 |
2 other studies available for carmustine and Craniopharyngioma
Article | Year |
---|---|
Therapeutic benefits of combination chemotherapy with vincristine, BCNU, and procarbazine on recurrent cystic craniopharyngioma. A case report.
Topics: Adult; Antineoplastic Combined Chemotherapy Protocols; Brain Neoplasms; Carmustine; Craniopharyngiom | 1984 |
Multimodality program involving stereotactic surgery in brain tumor management.
Topics: Adult; Antineoplastic Agents, Alkylating; Biopsy; Brachytherapy; Brain Neoplasms; Carmustine; Chemot | 2000 |