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Rituximab dramatically enhanced cytotoxic task. No clients discontinued therapy. There have been no treatment-related serious adverse occasions. Three patients had progressed because of the end of followup. After a median (interquartile range) followup of 59.4 (43.8-70.9) months, 85% of patients remained progression free. No fatalities happened. Quality-of-life improved through the study. Post-induction LAK cells with rituximab appear safe in the long run. Larger studies tend to be war
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