نمایش مختصر رکورد

dc.contributor.authorFawzy, Mohameden_US
dc.contributor.authorHamoda, Asmaaen_US
dc.contributor.authorElhemaly, Ahmeden_US
dc.contributor.authorElkinaai, Naglaaen_US
dc.contributor.authorSoliman, Sonyaen_US
dc.contributor.authorReda, Halaen_US
dc.contributor.authorElmenawi, Salmaen_US
dc.contributor.authorMoussa, Emaden_US
dc.date.accessioned1399-07-08T17:58:10Zfa_IR
dc.date.accessioned2020-09-29T17:58:11Z
dc.date.available1399-07-08T17:58:10Zfa_IR
dc.date.available2020-09-29T17:58:11Z
dc.date.issued2019-05-01en_US
dc.date.issued1398-02-11fa_IR
dc.date.submitted2018-10-28en_US
dc.date.submitted1397-08-06fa_IR
dc.identifier.citationFawzy, Mohamed, Hamoda, Asmaa, Elhemaly, Ahmed, Elkinaai, Naglaa, Soliman, Sonya, Reda, Hala, Elmenawi, Salma, Moussa, Emad. (2019). Does Salvage Chemotherapy Regimen Intensity Embark on Clearance of Bone Marrow Neuroblastoma?. Asian Pacific Journal of Cancer Prevention, 20(5), 1519-1524. doi: 10.31557/APJCP.2019.20.5.1519en_US
dc.identifier.issn1513-7368
dc.identifier.issn2476-762X
dc.identifier.urihttps://dx.doi.org/10.31557/APJCP.2019.20.5.1519
dc.identifier.urihttp://journal.waocp.org/article_87381.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/33279
dc.description.abstractIntroduction: Neuroblastoma (NBL) is the most common extracranial solid tumor in children. It accounts for 15%<br />of the deaths from cancer in the pediatric age group. Approximately half of the newly diagnosed children are at “high<br />risk" (HR) of treatment failure. This study aim was to evaluate the impact of salvage chemotherapy ICE (ifosfamide,<br />carboplatin, and etoposide) versus TC (topotecan/cyclophosphamide) when administered to NBL HR patients having<br />residual bone marrow disease after primary tumor control on the first line treatment regimen. Materials and Methods:<br />The present retrospective study included two groups of eligible stage 4 NBL patients with persistent bone marrow<br />disease. Group (1), 29 patients, received ICE whereas less intensive TC was administered to Group (2), 32 patients.<br />Data analysis included epidemiological variables, pathology subtype, MYCN gene status, primary tumor response<br />and their correlation with bone marrow disease clearance on each regimen. Results: A higher tendency of complete<br />bone marrow clearance was reported in patients who received ICE compared to TC; 41.4% versus 25.0%, respectively.<br />However, the difference was not statistically significant (p= 0.174). Conclusion: TC regimen appears to be a good<br />alternative to ICE as salvage treatment in an attempt to clear NBL bone marrow residual, with the privilege of being<br />less toxic and can be given on outpatient basis. Further randomized trials of larger study sample size with survival<br />impact analysis are warranted.en_US
dc.format.extent349
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherWest Asia Organization for Cancer Prevention (WAOCP)en_US
dc.relation.ispartofAsian Pacific Journal of Cancer Preventionen_US
dc.relation.isversionofhttps://dx.doi.org/10.31557/APJCP.2019.20.5.1519
dc.subjectneuroblastomaen_US
dc.subjectrefractory bone marrowen_US
dc.subjectICEen_US
dc.subjectTopotecan/Cyclophosphamideen_US
dc.subjectSolid tumorsen_US
dc.titleDoes Salvage Chemotherapy Regimen Intensity Embark on Clearance of Bone Marrow Neuroblastoma?en_US
dc.typeTexten_US
dc.typeResearch Articlesen_US
dc.contributor.departmentDepartment of Pediatric Oncology, Children Cancer Hospital Egypt-57357 and National Cancer Institute (NCI), Cairo University, Cairo, Egypt.en_US
dc.contributor.departmentDepartment of Pediatric Oncology, Children Cancer Hospital Egypt-57357 and National Cancer Institute (NCI), Cairo University, Cairo, Egypt.en_US
dc.contributor.departmentDepartment of Pediatric Oncology, Children Cancer Hospital Egypt-57357 and National Cancer Institute (NCI), Cairo University, Cairo, Egypt.en_US
dc.contributor.departmentDepartment of Pathology, Children Cancer Hospital Egypt-57357 and National Cancer Institute (NCI), Cairo University, Cairo, Egypt.en_US
dc.contributor.departmentDepartment of Clinical Pathology, Children Cancer Hospital Egypt-57357 and National Cancer Institute (NCI), Cairo University, Cairo, Egypt.en_US
dc.contributor.departmentDepartment of Clinical Pathology, Children Cancer Hospital Egypt-57357 and National Cancer Institute (NCI), Cairo University, Cairo, Egypt.en_US
dc.contributor.departmentClinical Research Unit, Research Department, Children Cancer Hospital Egypt-57357 and National Cancer Institute (NCI), Cairo University, Cairo, Egypt.en_US
dc.contributor.departmentDepartment of Pediatric Oncology, Children Cancer Hospital Egypt-57357 and National Cancer Institute (NCI), Cairo University, Cairo, Egypt.en_US
dc.citation.volume20
dc.citation.issue5
dc.citation.spage1519
dc.citation.epage1524


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