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Response-adapted radiation therapy for newly diagnosed primary diffuse large B-cell lymphoma of the CNS treated with methotrexate-based systemic therapy
BACKGROUND: For patients with primary diffuse large B-cell lymphoma of the central nervous system (PCNSL), whole-brain radiation therapy (WBRT) to doses of ≥45 Gy are often given after a partial response (PR) to methotrexate-based induction chemotherapy. We conducted an exploratory analysis to deter...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6200878/ https://www.ncbi.nlm.nih.gov/pubmed/30370365 http://dx.doi.org/10.1016/j.adro.2018.07.001 |
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author | Sheu, Tommy Milgrom, Sarah A. Andraos, Therese Y. Gunther, Jillian R. Chi, Linda Nastoupil, Loretta Fowler, Nathan Oki, Yasuhiro Fanale, Michelle A. Fayad, Luis E. Hagemeister, Fredrick Neelapu, Sattva S. Medeiros, L. Jeffrey Hosing, Chitra Nieto, Yago Ahmed, Sairah Alousi, Amin M. Dabaja, Bouthaina Pinnix, Chelsea C. |
author_facet | Sheu, Tommy Milgrom, Sarah A. Andraos, Therese Y. Gunther, Jillian R. Chi, Linda Nastoupil, Loretta Fowler, Nathan Oki, Yasuhiro Fanale, Michelle A. Fayad, Luis E. Hagemeister, Fredrick Neelapu, Sattva S. Medeiros, L. Jeffrey Hosing, Chitra Nieto, Yago Ahmed, Sairah Alousi, Amin M. Dabaja, Bouthaina Pinnix, Chelsea C. |
author_sort | Sheu, Tommy |
collection | PubMed |
description | BACKGROUND: For patients with primary diffuse large B-cell lymphoma of the central nervous system (PCNSL), whole-brain radiation therapy (WBRT) to doses of ≥45 Gy are often given after a partial response (PR) to methotrexate-based induction chemotherapy. We conducted an exploratory analysis to determine whether lower-dose WBRT, given with a boost to sites of persistent disease, might be a reasonable alternative. METHODS AND MATERIALS: We retrospectively reviewed the records of 22 patients with PCNSL who received WBRT, with or without a boost, after methotrexate-based induction chemotherapy. Outcomes were compared among patients according to response to chemotherapy using the Kaplan-Meier method. RESULTS: Median follow-up was 52 months. All patients with a complete response (CR) (n = 5) received WBRT to 23.4 Gy. One CR patient died after an in-field relapse. Patients with partial response (PR) (n = 10) received a median whole-brain dose of 23.4 Gy with (n = 8) or without (n = 2) a boost; there were 2 relapses within the central nervous system (CNS). All PR patients were alive at the time of analysis. The overall survival (P = .127) and freedom from relapse within the CNS (P = .967) were not different for patients with CR versus PR. Baseline and follow-up neurocognitive evaluations were available for 4 PR patients, and there were no significant differences between pre- and post-treatment evaluations (P > .05 for language, memory, visual-spatial, attention, or motor functions). All patients who progressed or did not respond to chemotherapy and then received WBRT had died at a median time of 3.4 months. Patients who progressed or did not respond to chemotherapy had worse overall survival (P = .001) and freedom from CNS relapse (P = .005) compared with CR patients. CONCLUSIONS: Among patients with a PR to induction chemotherapy, reduced-dose WBRT with a boost to residual PCNSL may be a viable treatment approach that merits further investigation. |
format | Online Article Text |
id | pubmed-6200878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-62008782018-10-26 Response-adapted radiation therapy for newly diagnosed primary diffuse large B-cell lymphoma of the CNS treated with methotrexate-based systemic therapy Sheu, Tommy Milgrom, Sarah A. Andraos, Therese Y. Gunther, Jillian R. Chi, Linda Nastoupil, Loretta Fowler, Nathan Oki, Yasuhiro Fanale, Michelle A. Fayad, Luis E. Hagemeister, Fredrick Neelapu, Sattva S. Medeiros, L. Jeffrey Hosing, Chitra Nieto, Yago Ahmed, Sairah Alousi, Amin M. Dabaja, Bouthaina Pinnix, Chelsea C. Adv Radiat Oncol Lymphoma BACKGROUND: For patients with primary diffuse large B-cell lymphoma of the central nervous system (PCNSL), whole-brain radiation therapy (WBRT) to doses of ≥45 Gy are often given after a partial response (PR) to methotrexate-based induction chemotherapy. We conducted an exploratory analysis to determine whether lower-dose WBRT, given with a boost to sites of persistent disease, might be a reasonable alternative. METHODS AND MATERIALS: We retrospectively reviewed the records of 22 patients with PCNSL who received WBRT, with or without a boost, after methotrexate-based induction chemotherapy. Outcomes were compared among patients according to response to chemotherapy using the Kaplan-Meier method. RESULTS: Median follow-up was 52 months. All patients with a complete response (CR) (n = 5) received WBRT to 23.4 Gy. One CR patient died after an in-field relapse. Patients with partial response (PR) (n = 10) received a median whole-brain dose of 23.4 Gy with (n = 8) or without (n = 2) a boost; there were 2 relapses within the central nervous system (CNS). All PR patients were alive at the time of analysis. The overall survival (P = .127) and freedom from relapse within the CNS (P = .967) were not different for patients with CR versus PR. Baseline and follow-up neurocognitive evaluations were available for 4 PR patients, and there were no significant differences between pre- and post-treatment evaluations (P > .05 for language, memory, visual-spatial, attention, or motor functions). All patients who progressed or did not respond to chemotherapy and then received WBRT had died at a median time of 3.4 months. Patients who progressed or did not respond to chemotherapy had worse overall survival (P = .001) and freedom from CNS relapse (P = .005) compared with CR patients. CONCLUSIONS: Among patients with a PR to induction chemotherapy, reduced-dose WBRT with a boost to residual PCNSL may be a viable treatment approach that merits further investigation. Elsevier 2018-07-12 /pmc/articles/PMC6200878/ /pubmed/30370365 http://dx.doi.org/10.1016/j.adro.2018.07.001 Text en © 2018 The Authors on behalf of the American Society for Radiation Oncology http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Lymphoma Sheu, Tommy Milgrom, Sarah A. Andraos, Therese Y. Gunther, Jillian R. Chi, Linda Nastoupil, Loretta Fowler, Nathan Oki, Yasuhiro Fanale, Michelle A. Fayad, Luis E. Hagemeister, Fredrick Neelapu, Sattva S. Medeiros, L. Jeffrey Hosing, Chitra Nieto, Yago Ahmed, Sairah Alousi, Amin M. Dabaja, Bouthaina Pinnix, Chelsea C. Response-adapted radiation therapy for newly diagnosed primary diffuse large B-cell lymphoma of the CNS treated with methotrexate-based systemic therapy |
title | Response-adapted radiation therapy for newly diagnosed primary diffuse large B-cell lymphoma of the CNS treated with methotrexate-based systemic therapy |
title_full | Response-adapted radiation therapy for newly diagnosed primary diffuse large B-cell lymphoma of the CNS treated with methotrexate-based systemic therapy |
title_fullStr | Response-adapted radiation therapy for newly diagnosed primary diffuse large B-cell lymphoma of the CNS treated with methotrexate-based systemic therapy |
title_full_unstemmed | Response-adapted radiation therapy for newly diagnosed primary diffuse large B-cell lymphoma of the CNS treated with methotrexate-based systemic therapy |
title_short | Response-adapted radiation therapy for newly diagnosed primary diffuse large B-cell lymphoma of the CNS treated with methotrexate-based systemic therapy |
title_sort | response-adapted radiation therapy for newly diagnosed primary diffuse large b-cell lymphoma of the cns treated with methotrexate-based systemic therapy |
topic | Lymphoma |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6200878/ https://www.ncbi.nlm.nih.gov/pubmed/30370365 http://dx.doi.org/10.1016/j.adro.2018.07.001 |
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