lomustine has been researched along with Pinealoma in 4 studies
Pinealoma: Neoplasms which originate from pineal parenchymal cells that tend to enlarge the gland and be locally invasive. The two major forms are pineocytoma and the more malignant pineoblastoma. Pineocytomas have moderate cellularity and tend to form rosette patterns. Pineoblastomas are highly cellular tumors containing small, poorly differentiated cells. These tumors occasionally seed the neuroaxis or cause obstructive HYDROCEPHALUS or Parinaud's syndrome. GERMINOMA; CARCINOMA, EMBRYONAL; GLIOMA; and other neoplasms may arise in the pineal region with germinoma being the most common pineal region tumor. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2064; Adams et al., Principles of Neurology, 6th ed, p670)
Excerpt | Relevance | Reference |
---|---|---|
"The outcome of a child with a primitive neuroectodermal tumors arising supratentorially (SPNET) is not well characterized and may differ from the outcome of a patient with a histologically similar cerebellar tumor (medulloblastoma [MB])." | 1.31 | Outcome for children with supratentorial primitive neuroectodermal tumors treated with surgery, radiation, and chemotherapy. ( Janss, AJ; Packer, RJ; Phillips, PC; Reddy, AT; Weiss, HL, 2000) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (25.00) | 18.7374 |
1990's | 2 (50.00) | 18.2507 |
2000's | 1 (25.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cohen, BH | 1 |
Zeltzer, PM | 2 |
Boyett, JM | 2 |
Geyer, JR | 2 |
Allen, JC | 2 |
Finlay, JL | 1 |
McGuire-Cullen, P | 1 |
Milstein, JM | 1 |
Rorke, LB | 2 |
Stanley, P | 2 |
Jakacki, RI | 1 |
Albright, AL | 1 |
Stevens, KR | 1 |
Wisoff, J | 1 |
Reddy, AT | 1 |
Janss, AJ | 1 |
Phillips, PC | 1 |
Weiss, HL | 1 |
Packer, RJ | 1 |
Carcavilla, LI | 1 |
Gómez Perún, J | 1 |
Alberdi, J | 1 |
Eiras, J | 1 |
Arana, T | 1 |
Pisón, J | 1 |
2 trials available for lomustine and Pinealoma
Article | Year |
---|---|
Prognostic factors and treatment results for supratentorial primitive neuroectodermal tumors in children using radiation and chemotherapy: a Childrens Cancer Group randomized trial.
Topics: Antineoplastic Combined Chemotherapy Protocols; Brain Neoplasms; Child; Child, Preschool; Combined M | 1995 |
Survival and prognostic factors following radiation and/or chemotherapy for primitive neuroectodermal tumors of the pineal region in infants and children: a report of the Childrens Cancer Group.
Topics: Adolescent; Adult; Antineoplastic Combined Chemotherapy Protocols; Brain Neoplasms; Child; Child, Pr | 1995 |
2 other studies available for lomustine and Pinealoma
Article | Year |
---|---|
Outcome for children with supratentorial primitive neuroectodermal tumors treated with surgery, radiation, and chemotherapy.
Topics: Adolescent; Antineoplastic Agents; Antineoplastic Agents, Alkylating; Antineoplastic Agents, Phytoge | 2000 |
[Abdominal metastasis of a pineal germinoma in a child with a ventriculo-peritoneal shunt].
Topics: Abdominal Neoplasms; Brain Neoplasms; Cerebrospinal Fluid Shunts; Child; Humans; Liver Neoplasms; Lo | 1987 |