MBCL-50. SAFETY AND EFFICACY OF CHEMOTHERAPY INTENSIFICATION WITH AUTOLOGOUS HEMATOPOIETIC STEM CELL RESCUE, WITHOUT RADIATION, FOR CHILDREN WITH CNS EMBRYONAL TUMORS. Issue 2 (22nd June 2018)
- Record Type:
- Journal Article
- Title:
- MBCL-50. SAFETY AND EFFICACY OF CHEMOTHERAPY INTENSIFICATION WITH AUTOLOGOUS HEMATOPOIETIC STEM CELL RESCUE, WITHOUT RADIATION, FOR CHILDREN WITH CNS EMBRYONAL TUMORS. Issue 2 (22nd June 2018)
- Main Title:
- MBCL-50. SAFETY AND EFFICACY OF CHEMOTHERAPY INTENSIFICATION WITH AUTOLOGOUS HEMATOPOIETIC STEM CELL RESCUE, WITHOUT RADIATION, FOR CHILDREN WITH CNS EMBRYONAL TUMORS
- Authors:
- Bavle, Abhishek
Gross, Naina
Gavula, Theresa
Confer, Michael
Peterson, Jo Elle
Fung, Kar-Ming
Rooms, Laura
Crawford, David
McNall-Knapp, Rene - Abstract:
- Abstract: INTRODUCTION: Survival for children with central nervous system (CNS) embryonal tumors has improved significantly with craniospinal irradiation, but at the cost of long-term adverse effects including second malignancies and significant neurocognitive deficits. One strategy to achieve cure, while avoiding radiation, is intensification of chemotherapy. We report our experience with this approach in 9 patients with embryonal tumors, whose parents declined radiation therapy. METHODS: Four patients with medulloblastoma (MB) (median age 2.6 years; 2 classic/M0, 1 anaplastic/M1, 1 desmoplastic-nodular/M0/SHH; 3 non-WNT, non-SHH; none MYCN amplified) and 5 patients with localized non-MB embryonal tumors (median age 3.7 years; 4 ETMR, 1 NOS) were treated per ACNS0334 (3 cycles of vincristine, cyclophosphamide, cisplatin, etoposide, then consolidation with 3 cycles of carboplatin, thiotepa with autologous hematopoietic stem cell rescue). RESULTS: Three of 4 patients with MB are alive a median of 3 years (1.5 - 4.5y) off-therapy; one patient is deceased secondary to congenital heart disease (germline NAA10 mutation) 1.4 years off-therapy. Of 5 non-MB patients, 3 are alive - 1 without radiation 3.4 years off-therapy; 2 after focal radiation for local progression. Median time to progression for 4 patients was 5 months. Grade 3 adverse events for all patients included mucositis, pancytopenia and fever/neutropenia (median 5 episodes), with no therapy-related deaths. CONCLUSIONS:Abstract: INTRODUCTION: Survival for children with central nervous system (CNS) embryonal tumors has improved significantly with craniospinal irradiation, but at the cost of long-term adverse effects including second malignancies and significant neurocognitive deficits. One strategy to achieve cure, while avoiding radiation, is intensification of chemotherapy. We report our experience with this approach in 9 patients with embryonal tumors, whose parents declined radiation therapy. METHODS: Four patients with medulloblastoma (MB) (median age 2.6 years; 2 classic/M0, 1 anaplastic/M1, 1 desmoplastic-nodular/M0/SHH; 3 non-WNT, non-SHH; none MYCN amplified) and 5 patients with localized non-MB embryonal tumors (median age 3.7 years; 4 ETMR, 1 NOS) were treated per ACNS0334 (3 cycles of vincristine, cyclophosphamide, cisplatin, etoposide, then consolidation with 3 cycles of carboplatin, thiotepa with autologous hematopoietic stem cell rescue). RESULTS: Three of 4 patients with MB are alive a median of 3 years (1.5 - 4.5y) off-therapy; one patient is deceased secondary to congenital heart disease (germline NAA10 mutation) 1.4 years off-therapy. Of 5 non-MB patients, 3 are alive - 1 without radiation 3.4 years off-therapy; 2 after focal radiation for local progression. Median time to progression for 4 patients was 5 months. Grade 3 adverse events for all patients included mucositis, pancytopenia and fever/neutropenia (median 5 episodes), with no therapy-related deaths. CONCLUSIONS: Intensified chemotherapy is a promising strategy to treat select MB patients without radiation, but appears less effective for non-MB embryonal tumors. Evaluation of the efficacy and safety of this approach for MB, with prospective trials informed by tumor biology, is warranted. … (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:
- i128
- Page End:
- i128
- 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/noy059.446 ↗
- 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
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12321.xml