Advances in Radiation Oncology (Oct 2018)

Response-adapted radiation therapy for newly diagnosed primary diffuse large B-cell lymphoma of the CNS treated with methotrexate-based systemic therapy

  • Tommy Sheu, MD,
  • Sarah A. Milgrom, MD,
  • Therese Y. Andraos, MD,
  • Jillian R. Gunther, MD, PhD,
  • Linda Chi, MD,
  • Loretta Nastoupil, MD,
  • Nathan Fowler, MD,
  • Yasuhiro Oki, MD,
  • Michelle A. Fanale, MD,
  • Luis E. Fayad, MD,
  • Fredrick Hagemeister, MD,
  • Sattva S. Neelapu, MD,
  • L. Jeffrey Medeiros, MD,
  • Chitra Hosing, MD,
  • Yago Nieto, MD, PhD,
  • Sairah Ahmed, MD,
  • Amin M. Alousi, MD,
  • Bouthaina Dabaja, MD,
  • Chelsea C. Pinnix, MD, PhD

Journal volume & issue
Vol. 3, no. 4
pp. 639 – 646

Abstract

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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.