ATRT-28. RETROSPECTIVE ANALYSIS OF ATYPICAL TERATOID RHABDOID TUMOR IN THE ERA OF MULTIMODAL TREATMENT IN JAPAN. Issue 2 (22nd June 2018)
- Record Type:
- Journal Article
- Title:
- ATRT-28. RETROSPECTIVE ANALYSIS OF ATYPICAL TERATOID RHABDOID TUMOR IN THE ERA OF MULTIMODAL TREATMENT IN JAPAN. Issue 2 (22nd June 2018)
- Main Title:
- ATRT-28. RETROSPECTIVE ANALYSIS OF ATYPICAL TERATOID RHABDOID TUMOR IN THE ERA OF MULTIMODAL TREATMENT IN JAPAN
- Authors:
- Yamasaki, Kai
Watanabe, Yuko
Isobe, Kiyotaka
Koga, Yuhki
Kiyotani, Chikako
Terashima, Keita
Arakawa, Yoshiki
Hasegawa, Daiichiro
Kosaka, Yoshiyuki
Goto, Hiroaki
Koh, Katsuyoshi
Hara, Junichi - Abstract:
- Abstract: BACKGROUND: Recent progress of multimodal therapy including intrathecal and/or intraventricular chemotherapy improved the prognosis of atypical teratoid rhabdoid tumor (ATRT). To know historical control data for a new trial, we retrospectively collected clinical information of locally diagnosed ATRT in eight major pediatric cancer centers in Japan. RESULT: From 2005 to 2016, 38 ATRT cases with INI-1 immunostaining negative were enrolled in this analysis. Median age was 1.3 years (2m to 11.8yr) and male to female ratio was 2:1. More than half of patients were positive for metastases (M1: 6, M2: 7, M3: 7, M4: 2). Four patients died of cerebral herniation or intratumoral hemorrhage before the initiation of chemotherapy. Postoperative chemotherapy was performed in all remaining patients. Intrathecal methotrexate was added in 30/34 (88.2%) cases. Most patients received high-dose chemotherapy (n=8), radiotherapy (n=9) or both (n=13). By a median follow up of 40.9 month, the 3-year progression free survival (PFS) and overall survival (OS) in treated patients were 39.1 ± 8.7% and 58.5 ± 9.1%, respectively. 3yr-PFS was 56.0 ± 11.8% for M0-1 and 21.4 ± 11.0% for M2-3 cases (p=0.0427) and 76.2 ± 14.8% for GTR and 25.8 ± 9.2% for non GTR (p=0.0361). Neither HDC nor radiotherapy was prognostic, however, all three patients treated with chemotherapy alone relapsed (n=3). Notably, three patients with late relapse survived long periods after relapse (40m, 46m, 80m). CONCLUSION: AAbstract: BACKGROUND: Recent progress of multimodal therapy including intrathecal and/or intraventricular chemotherapy improved the prognosis of atypical teratoid rhabdoid tumor (ATRT). To know historical control data for a new trial, we retrospectively collected clinical information of locally diagnosed ATRT in eight major pediatric cancer centers in Japan. RESULT: From 2005 to 2016, 38 ATRT cases with INI-1 immunostaining negative were enrolled in this analysis. Median age was 1.3 years (2m to 11.8yr) and male to female ratio was 2:1. More than half of patients were positive for metastases (M1: 6, M2: 7, M3: 7, M4: 2). Four patients died of cerebral herniation or intratumoral hemorrhage before the initiation of chemotherapy. Postoperative chemotherapy was performed in all remaining patients. Intrathecal methotrexate was added in 30/34 (88.2%) cases. Most patients received high-dose chemotherapy (n=8), radiotherapy (n=9) or both (n=13). By a median follow up of 40.9 month, the 3-year progression free survival (PFS) and overall survival (OS) in treated patients were 39.1 ± 8.7% and 58.5 ± 9.1%, respectively. 3yr-PFS was 56.0 ± 11.8% for M0-1 and 21.4 ± 11.0% for M2-3 cases (p=0.0427) and 76.2 ± 14.8% for GTR and 25.8 ± 9.2% for non GTR (p=0.0361). Neither HDC nor radiotherapy was prognostic, however, all three patients treated with chemotherapy alone relapsed (n=3). Notably, three patients with late relapse survived long periods after relapse (40m, 46m, 80m). CONCLUSION: A comparable result as previous reports was shown in Japan. We are currently planning a new clinical trial for ATRT. … (more)
- Is Part Of:
- Neuro-oncology. Volume 20:Issue 2(2018)supplement 2
- Journal:
- Neuro-oncology
- Issue:
- Volume 20:Issue 2(2018)supplement 2
- Issue Display:
- Volume 20, Issue 2 (2018)
- Year:
- 2018
- Volume:
- 20
- Issue:
- 2
- Issue Sort Value:
- 2018-0020-0002-0000
- Page Start:
- i33
- Page End:
- i34
- Publication Date:
- 2018-06-22
- Subjects:
- Brain Neoplasms -- Periodicals
Brain -- Tumors -- Periodicals
Brain -- Cancer -- Periodicals
Nervous system -- Cancer -- Periodicals
616.99481 - Journal URLs:
- http://neuro-oncology.dukejournals.org/ ↗
http://neuro-oncology.oxfordjournals.org/ ↗
http://www.oxfordjournals.org/content?genre=journal&issn=1522-8517 ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/neuonc/noy059.026 ↗
- Languages:
- English
- ISSNs:
- 1522-8517
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.288000
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