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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
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.
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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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