| dc.contributor.author | Fawzy, Mohamed | en_US |
| dc.contributor.author | Hamoda, Asmaa | en_US |
| dc.contributor.author | Elhemaly, Ahmed | en_US |
| dc.contributor.author | Elkinaai, Naglaa | en_US |
| dc.contributor.author | Soliman, Sonya | en_US |
| dc.contributor.author | Reda, Hala | en_US |
| dc.contributor.author | Elmenawi, Salma | en_US |
| dc.contributor.author | Moussa, Emad | en_US |
| dc.date.accessioned | 1399-07-08T17:58:10Z | fa_IR |
| dc.date.accessioned | 2020-09-29T17:58:11Z | |
| dc.date.available | 1399-07-08T17:58:10Z | fa_IR |
| dc.date.available | 2020-09-29T17:58:11Z | |
| dc.date.issued | 2019-05-01 | en_US |
| dc.date.issued | 1398-02-11 | fa_IR |
| dc.date.submitted | 2018-10-28 | en_US |
| dc.date.submitted | 1397-08-06 | fa_IR |
| dc.identifier.citation | Fawzy, 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.2019.20.5.1519 | en_US |
| dc.identifier.issn | 1513-7368 | |
| dc.identifier.issn | 2476-762X | |
| dc.identifier.uri | https://dx.doi.org/10.31557/APJCP.2019.20.5.1519 | |
| dc.identifier.uri | http://journal.waocp.org/article_87381.html | |
| dc.identifier.uri | https://iranjournals.nlai.ir/handle/123456789/33279 | |
| dc.description.abstract | Introduction: 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.extent | 349 | |
| dc.format.mimetype | application/pdf | |
| dc.language | English | |
| dc.language.iso | en_US | |
| dc.publisher | West Asia Organization for Cancer Prevention (WAOCP) | en_US |
| dc.relation.ispartof | Asian Pacific Journal of Cancer Prevention | en_US |
| dc.relation.isversionof | https://dx.doi.org/10.31557/APJCP.2019.20.5.1519 | |
| dc.subject | neuroblastoma | en_US |
| dc.subject | refractory bone marrow | en_US |
| dc.subject | ICE | en_US |
| dc.subject | Topotecan/Cyclophosphamide | en_US |
| dc.subject | Solid tumors | en_US |
| dc.title | Does Salvage Chemotherapy Regimen Intensity Embark on Clearance of Bone Marrow Neuroblastoma? | en_US |
| dc.type | Text | en_US |
| dc.type | Research Articles | en_US |
| dc.contributor.department | Department of Pediatric Oncology, Children Cancer Hospital Egypt-57357 and National Cancer Institute (NCI), Cairo University, Cairo, Egypt. | en_US |
| dc.contributor.department | Department of Pediatric Oncology, Children Cancer Hospital Egypt-57357 and National Cancer Institute (NCI), Cairo University, Cairo, Egypt. | en_US |
| dc.contributor.department | Department of Pediatric Oncology, Children Cancer Hospital Egypt-57357 and National Cancer Institute (NCI), Cairo University, Cairo, Egypt. | en_US |
| dc.contributor.department | Department of Pathology, Children Cancer Hospital Egypt-57357 and National Cancer Institute (NCI), Cairo University, Cairo, Egypt. | en_US |
| dc.contributor.department | Department of Clinical Pathology, Children Cancer Hospital Egypt-57357 and National Cancer Institute (NCI), Cairo University, Cairo, Egypt. | en_US |
| dc.contributor.department | Department of Clinical Pathology, Children Cancer Hospital Egypt-57357 and National Cancer Institute (NCI), Cairo University, Cairo, Egypt. | en_US |
| dc.contributor.department | Clinical Research Unit,
Research Department, Children Cancer Hospital Egypt-57357 and National Cancer Institute (NCI), Cairo University, Cairo, Egypt. | en_US |
| dc.contributor.department | Department of Pediatric Oncology, Children Cancer Hospital Egypt-57357 and National Cancer Institute (NCI), Cairo University, Cairo, Egypt. | en_US |
| dc.citation.volume | 20 | |
| dc.citation.issue | 5 | |
| dc.citation.spage | 1519 | |
| dc.citation.epage | 1524 | |