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Intravenous (IV) Saline: Additional treatment with intravenous (IV) saline may be indicated.","id":"EG000","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":0,"seriousNumAtRisk":6,"title":"Non-Randomized to 70 mg/m2 Bendamustine-Rituximab"},{"deathsNumAffected":0,"deathsNumAtRisk":6,"description":"Treatment Assignment Code 5 (TAC 5) Rituximab + Bendamustine at 90 mg/m\\^2 for initial tolerability study (closed) Rituximab 375 mg/m\\^2 on day 1, 15 for 6 x 28-day cycles Bendamustine: 6 participants to bendamustine 90 mg/m\\^2/day, days 1 and 2 each cycle Acetaminophen: Treatment of infusion-related symptoms with acetaminophen is recommended.\n\nDiphenhydramine: Treatment of infusion-related symptoms with diphenhydramine is recommended.\n\nEpinephrine: Epinephrine should be available for immediate use in the event of a hypersensitivity reaction to Rituximab.\n\nAntihistamines: Antihistamines should be available for immediate use in the event of a hypersensitivity reaction to Rituximab.\n\nCorticosteroids: Corticosteroids should be available for immediate use in the event of a hypersensitivity reaction to Rituximab.\n\nBronchodilators: Additional treatment with bronchodilators may be indicated. Intravenous (IV) Saline: Additional treatment with intravenous (IV) saline may be indicated","id":"EG001","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":0,"seriousNumAtRisk":6,"title":"Non-randomized to 90 mg/m^2 Bendamustine-Rituximab"},{"deathsNumAffected":3,"deathsNumAtRisk":28,"description":"Treatment Assignment Code 5 (TAC 5) Rituximab + Bendamustine at 90 mg/m\\^2 Rituximab: 28 participants Rituximab 375 mg/m\\^2 on day 1, 15 for 6 x 28-day cycles Bendamustine:28 participants to bendamustine 90 mg/m\\^2/day, days 1 and 2 each cycle, days 1 and 2 each cycle Acetaminophen: Treatment of infusion-related symptoms with acetaminophen is recommended.\n\nDiphenhydramine: Treatment of infusion-related symptoms with diphenhydramine is recommended.\n\nEpinephrine: Epinephrine should be available for immediate use in the event of a hypersensitivity reaction to Rituximab.\n\nAntihistamines: Antihistamines should be available for immediate use in the event of a hypersensitivity reaction to Rituximab.\n\nCorticosteroids: Corticosteroids should be available for immediate use in the event of a hypersensitivity reaction to Rituximab.\n\nBronchodilators: Additional treatment with bronchodilators may be indicated. Intravenous (IV) Saline: Additional treatment with intravenous (IV) saline may be indicated.","id":"EG002","otherNumAffected":28,"otherNumAtRisk":28,"seriousNumAffected":8,"seriousNumAtRisk":28,"title":"Randomized to 90 mg/m^2 Bendamustine-Rituximab"},{"deathsNumAffected":5,"deathsNumAtRisk":28,"description":"Treatment Assignment Code 2 (TAC 2) Rituximab + Pentostatin\n\nPentostatin: 28 participants to pentostatin 4 mg/m\\^2 days 1 and 15 of each cycle.\n\nRituximab: Rituximab 375 mg/m\\^2 on day 1, 15 for 6 x 28-day cycles\n\nAcetaminophen: Treatment of infusion-related symptoms with acetaminophen is recommended.\n\nDiphenhydramine: Treatment of infusion-related symptoms with diphenhydramine is recommended.\n\nEpinephrine: Epinephrine should be available for immediate use in the event of a hypersensitivity reaction to Rituximab.\n\nAntihistamines: Antihistamines should be available for immediate use in the event of a hypersensitivity reaction to Rituximab.\n\nCorticosteroids: Corticosteroids should be available for immediate use in the event of a hypersensitivity reaction to Rituximab.\n\nBronchodilators: Additional treatment with bronchodilators may be indicated.\n\nIntravenous (IV) Saline: Additional treatment with intravenous (IV) saline may be indicated.","id":"EG003","otherNumAffected":28,"otherNumAtRisk":28,"seriousNumAffected":7,"seriousNumAtRisk":28,"title":"Randomized to Pentostatin-Rituximab"},{"deathsNumAffected":0,"deathsNumAtRisk":1,"description":"Treatment Assignment Code 5 (TAC 5) Rituximab + Bendamustine at 90 mg/m\\^2 or Rituxan + Pentostatin After initial tolerability studies are completed. 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