{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,10]],"date-time":"2026-09-10T04:31:52Z","timestamp":1789014712202,"version":"build-2803163510"},"reference-count":18,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2018,12,21]],"date-time":"2018-12-21T00:00:00Z","timestamp":1545350400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Br J Haematol"],"published-print":{"date-parts":[[2019,2]]},"abstract":"<jats:title>Summary<\/jats:title><jats:p>Bendamustine (B) with rituximab (R) is a standard frontline treatment for medically fit follicular lymphoma (<jats:styled-content style=\"fixed-case\">FL<\/jats:styled-content>) patients. The safety and efficacy of maintenance rituximab (<jats:styled-content style=\"fixed-case\">MR<\/jats:styled-content>) after <jats:styled-content style=\"fixed-case\">BR<\/jats:styled-content> induction has not been formally compared to observation for <jats:styled-content style=\"fixed-case\">FL<\/jats:styled-content>, resulting in disparate practice patterns. Prospective trials have shown benefit of <jats:styled-content style=\"fixed-case\">MR<\/jats:styled-content> after R\u2010<jats:styled-content style=\"fixed-case\">CHOP<\/jats:styled-content> (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone) or R\u2010<jats:styled-content style=\"fixed-case\">CVP<\/jats:styled-content> (rituximab, cyclophosphamide, vincristine, prednisone), yet recent data from the <jats:styled-content style=\"fixed-case\">GALLIUM<\/jats:styled-content> study comparing outcomes of patients treated with chemotherapy with R or obinutuzumab (G) showed higher than anticipated fatal adverse events with <jats:styled-content style=\"fixed-case\">BR<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">BG<\/jats:styled-content>. In order to assess the efficacy and tolerability of <jats:styled-content style=\"fixed-case\">MR<\/jats:styled-content> after <jats:styled-content style=\"fixed-case\">BR<\/jats:styled-content>, we retrospectively collected data on 640 newly diagnosed patients treated with <jats:styled-content style=\"fixed-case\">FL<\/jats:styled-content>. We found that patients who achieved partial remission (<jats:styled-content style=\"fixed-case\">PR<\/jats:styled-content>) after \u22654 cycles of <jats:styled-content style=\"fixed-case\">BR<\/jats:styled-content> had improved duration of response (<jats:styled-content style=\"fixed-case\">DOR<\/jats:styled-content>) with <jats:styled-content style=\"fixed-case\">MR<\/jats:styled-content> vs. no maintenance, whereas those in complete remission did not. These findings were confirmed in a validation cohort. In the entire study population, the known fatal adverse event rate after <jats:styled-content style=\"fixed-case\">BR<\/jats:styled-content> was 2\u00b75% and did not significantly differ in those receiving <jats:styled-content style=\"fixed-case\">MR <\/jats:styled-content><jats:italic>versus<\/jats:italic> no maintenance. [Correction added on 14 January 2019, after online publication: The preceding sentence has been corrected in this current version.] Within the limitations inherent to retrospective analysis, these data suggest that <jats:styled-content style=\"fixed-case\">FL<\/jats:styled-content> patients with a <jats:styled-content style=\"fixed-case\">PR<\/jats:styled-content> to <jats:styled-content style=\"fixed-case\">BR<\/jats:styled-content> experience prolongation of remission with <jats:styled-content style=\"fixed-case\">MR<\/jats:styled-content> with an acceptable safety profile.<\/jats:p>","DOI":"10.1111\/bjh.15720","type":"journal-article","created":{"date-parts":[[2018,12,21]],"date-time":"2018-12-21T15:09:48Z","timestamp":1545404988000},"page":"524-535","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":48,"title":["Maintenance rituximab or observation after frontline treatment with bendamustine\u2010rituximab for follicular lymphoma"],"prefix":"10.1111","volume":"184","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8781-3327","authenticated-orcid":false,"given":"Brian T.","family":"Hill","sequence":"first","affiliation":[{"name":"Cleveland Clinic Cleveland OH USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Loretta","family":"Nastoupil","sequence":"additional","affiliation":[{"name":"The University of Texas MD Anderson Cancer Center Houston TX USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Allison M.","family":"Winter","sequence":"additional","affiliation":[{"name":"Cleveland Clinic Cleveland OH USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6295-5433","authenticated-orcid":false,"given":"Melody R.","family":"Becnel","sequence":"additional","affiliation":[{"name":"The University of Texas MD Anderson Cancer Center Houston TX 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