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+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+Patients must have fully recovered from the acute toxic effects of all prior anti-cancer chemotherapy
+Patients who relapse on frontline therapy in phases other than maintenance must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+Patients must have fully recovered from the acute toxic effects of all prior anti-cancer therapy
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study.
+Patients must have fully recovered (Eastern Cooperative Oncology Group [ECOG] -) from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+Patients must have fully recovered from the acute toxic effects of chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+Subjects must have fully recovered from the acute toxic effects of all prior anti-cancer therapy
+Patients must have recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy or radiotherapy prior to entering this study
+Recovered from the toxic effects of all prior chemotherapy before entering this study
+INCLUSION - TREATMENT: Recovered from acute toxic effects of prior chemotherapy at least one week before entering this study
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study.
+The patient must have failed at least one prior therapy besides surgery- radiation or chemotherapy (either cytotoxic or biologic agent)-prior to study registration; patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+INCLUSION - FUSION: Recovered from acute toxic effects of prior chemotherapy at least one week before entering the study
+Prior Therapy- Patients must have fully recovered from the acute toxic effects of all prior anti- cancer chemotherapy and be within the following timelines:
+Patients must be fully recovered from all acute effects of prior surgical intervention
+Fully recovered from acute toxic effects of any prior chemotherapy, biological modifiers or radiotherapy
+All patients must, in the opinion of the study PI, have sufficiently recovered from significant acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+INCLUSION - TREATMENT: Recovered from the acute toxic effects of all prior chemotherapy
+Patients who relapse on therapy other than standard ALL maintenance must have fully recovered from the acute toxic effects of all prior anti-cancer therapy, defined as resolution of all such toxicities to ? grade  or lower per the inclusion/exclusion criteria prior to entering this study
+Participants must have fully recovered from the acute toxic effects of all prior anticancer therapies or must adhere to post-treatment conditions as follows:
+Patients must have received prior therapy other than surgery and must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, biologic therapy or radiotherapy prior to study entry
+All subjects must, in the opinion of the study PI, have sufficiently recovered from significant acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+Participants must have fully recovered from the acute toxic effects of all prior anticancer treatments prior to study drug administration:
+All subjects must, in the opinion of the study PI, have sufficiently recovered from significant acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+Patients may have been previously treated for a plexiform neurofibroma but must have fully recovered from the acute toxic effects of all prior chemotherapy or radiotherapy prior to entering this study
+Patients must have recovered from the acute toxic effects of all prior therapy to =< grade  before entering this study
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+Patient must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, radiotherapy, or surgery prior to study entry.
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+Patient must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+ELIGIBILITY CRITERIA- LYMPHODEPLETION/INFUSION OF tvs-CTL: Must have fully recovered from the acute toxic effects of all prior therapy including chemotherapy, radiotherapy and immunotherapy
+Patients must have fully recovered from the acute toxic effects of all prior anti-cancer chemotherapy or radiation to grade  or less
+Patients must have fully recovered from the acute toxic effects of all prior anti-cancer chemotherapy:
+Patient must, in the opinion of the study principal investigator (PI) or designee, have fully recovered from significant acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to enrollment onto this study
+Patients must have recovered from the acute toxic effects of all prior anticancer chemotherapy
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+Prior Therapy- Patients must have fully recovered from the acute toxic effects of all prior anti- cancer chemotherapy and be within the following timelines:
+Recovered from acute toxic effects of prior chemotherapy at least one week before entering this study
+Recovered from the acute toxic effects of all prior chemotherapy at least one week and  days from prior chemotherapy before entering this study
+Subjects must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy or radiotherapy prior to entering this study
+Recovered from the acute toxic effects of all prior chemotherapy at least  weeks before entering this study
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study.
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+Patients must have recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, stem cell transplant or radiotherapy prior to entering this study; all prior treatment-related toxicities must have resolved to =< grade  prior to enrollment
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to study enrollment
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+Patients who relapse on therapy other than standard ALL maintenance therapy must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+All patients must have fully recovered from the acute toxic effects of all prior anti-cancer chemotherapy
+Recovered from the acute toxic effects of all prior chemotherapy at least a week before entering this study
+Recovered from the toxic effects of all prior chemotherapy before entering this study
+Subject has recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to first dose. All prior treatment-related toxicities must have resolved to ? Grade  prior to enrollment.
+Recovered from acute toxic effects of all prior chemotherapy at least one week and  days from prior chemotherapy before entering this study
+Subjects may have been previously treated for a plexiform neurofibroma or other tumor/malignancy, but must have fully recovered from the acute toxic effects of all prior chemotherapy or radiotherapy prior to entering this study
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy
+Patients must have fully recovered from the acute toxic effects of all prior anti-cancer therapy (toxicity < grade )
+Subjects must have fully recovered from the acute toxic effects of all previous chemotherapy, immunotherapy, or radiotherapy treatment before enrollment.
+Participants must have fully recovered from the acute toxic effects of all prior anti-cancer therapy
+Fully recovered from acute toxic effects of any prior chemotherapy, biological modifiers or radiotherapy
+Patients must have recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study; no chemotherapy or radiotherapy may be given within  weeks prior to the start of protocol treatment
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiation therapy prior to entering this study
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study.
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study.
+Patients must have received prior therapy other than surgery and must have fully recovered from the acute treatment related toxicities of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+Prior therapy: \r\n* The patients malignancy must have relapsed after or failed to respond to frontline curative therapy and/or there must not be any potentially curative treatment options available at the time of study entry\r\n* There is no limit to the number of prior treatment regimens; however, patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to study enrollment; acute toxicity of any previous therapy must have resolved to grade  or less, unless specified elsewhere
+Patients must have recovered from the toxic effects of all prior chemotherapy before entering this study
+Participants must have fully recovered from the acute toxic effects of all prior therapy prior to first administration of study drug
+Patients must have fully recovered from the acute toxic effects of all prior anticancer chemotherapy
+PRIOR THERAPY Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study.
+Prior Therapy: Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study. Myelosuppressive Chemotherapy:
+Patients must have fully recovered from the acute toxic effects of all previous chemotherapy, immunotherapy, or radiotherapy prior to study enrollment.
+Participants must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study; at least  days must have elapsed from prior chemotherapy; at least  days must have elapsed since receiving biological therapy
+Patients must have fully recovered from the acute effects of all prior therapy
+Patients must have fully recovered from the acute toxic effects of all prior chemotherapy prior to entering study; three () weeks must have elapsed since the administration of prior chemotherapy
+Diseases refractory/relapsed after one or more systemic cytotoxic therapies; patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study.
+Patient must have fully recovered from the acute toxic effects of all prior chemotherapy or radiation prior to entering this study