Treatment-related toxicity from prior therapy > grade 
Participants must have fully recovered (grade =<  or baseline or deemed irreversible) from any clinically significant acute toxicity related to prior therapy (with the exception of lymphopenia, which is common after therapy with temozolomide); patients who discontinued bevacizumab previously due to a bevacizumab-related toxicity will not be allowed to participate
Participant has not adequately recovered from toxicity of previous therapy
Participants must have recovered from any acute toxicity associated with prior therapy
Patient must have recovered to Grade  toxicity from prior cancer therapy
Any anti-cancer treatment (except for radiation therapy) within  days, or any investigational agent within  days prior to the first dose of study drug; participants should have recovered from any toxicity related to previous anti-cancer treatment to Common Toxicity Criteria (CTC) grade  or .
Participants who have not recovered to eligibility levels from prior toxicity or adverse events as a result of previous treatment prior to the study.
Toxicity related to any prior therapy must either have returned to =< grade  or baseline
Patients must have recovered from any acute toxicity related to prior therapy, including surgery; toxicity should be =< grade  or returned to baseline
Radiation therapy =<  weeks prior to study entry; patients who have received prior radiotherapy must have recovered from toxicity (=< grade ) induced by this treatment (except for alopecia)
Patients must have recovered from any acute toxicity related to prior therapy, including surgery; toxicity should be =< grade  or returned to baseline
Patients must have recovered from toxicity related to prior therapy to at least grade  (defined by CTCAE .) or baseline level. Chronic stable grade  peripheral neuropathy secondary to neurotoxicity from prior therapies may be considered on a case by case basis by the Principal Investigator.
Patient must have completed prior chemotherapy at least  weeks (washout period) prior to randomization and recovered from toxicity to Grade  or baseline
Patients must have recovered from toxicity of prior therapy
Patients must have recovered from any acute toxicity related to prior therapy, including surgery; toxicity should be =< grade  or returned to baseline
Any toxicity from prior therapy must have recovered to ? Grade  (except alopecia).
Recovered (returned to ? grade  as per CTCAE v.) from prior treatment-related toxicity.
Prior chemotherapy provided patients have been off previous anti-cancer therapy for at least  days and recovered from all treatment related toxicity
Patients must be at least  weeks from any prior treatments and have recovered (to < grade ) from acute toxicity attributed to this prior treatment, unless considered chronic
Not recovered from toxicity of any prior chemotherapy to grade ? .
Toxicity related to prior therapy must either have returned to =< grade , baseline, or deemed irreversible
Non-hematological toxicity related to prior therapy must either have returned to =< grade , baseline, or deemed irreversible
Fully recovered from toxicity due to prior therapy
Toxicity related to prior therapy must either have returned to =< grade , baseline, or been deemed irreversible
Toxicity related to prior therapy must either have returned to less than or equal to grade , baseline, or been deemed irreversible
Patients must have recovered from toxicity of prior therapy
Patients who have had chemotherapy, targeted therapy, or radiotherapy, and have not recovered from acute toxicity to their pretreatment baseline or to a grade  level within  weeks ( weeks for nitrosoureas or mitomycin C) prior to entering the study \r\n* Note: patients with chronic residual prior therapy-related toxicity (e.g. vitiligo, alopecia, low grade neuropathy), or in the consensus opinion of the Cancer Immunotherapy Trials Network (CITN)/Cancer Therapy Evaluation Program (CTEP) investigators would not impact the safety of the patient or the integrity of the study, are not excluded\r\n* Note: for resolution of autoimmune toxicity from prior immune therapy, patients must be off steroids for at least  days without relapse of autoimmune toxicity, or it must be at least  days from their last dose of infliximab or related immunosuppressive therapy without relapse of autoimmune toxicity
Patients must have recovered from any VEGF blocking drug-related toxicity (proteinuria, hypertension, hepatotoxicity, and pancreatic toxicity)
Subjects who have not recovered to within one grade level (not to exceed grade ) of their baseline following a significant adverse event or toxicity attributed to prior anti-cancer treatment are excluded
Have recovered from any acute toxicity related to prior therapy.
Patients must have recovered from any acute toxicity associated with prior therapy by the start of study treatment
Patients should have discontinued any and all other therapy for CLL >=  hours prior to start of study therapy and recovered from any toxicity due to these therapies to grade =< 
Recovery from acute toxicity related to prior therapy, including surgery and radiation, or no toxicity >= grade 
Patients must have recovered from any acute toxicity related to prior therapy, including surgery; toxicity should be =< grade 
Participants must have recovered to grade  toxicity from prior therapy
Patients must have recovered from toxicity of prior therapy
Patients must have recovered from the toxicity of prior therapy to less than grade 
Patients must have recovered to =< grade  in terms of toxicity from prior treatments (excluding neuropathy which can be =< grade )
Received any anti-cancer or investigational therapy within  days prior to the first dose of study drug or has not recovered to less than Grade  clinically significant adverse effect(s)/toxicity(ies) of any previous therapy
Patients must have recovered from acute toxicity (to grade  or less) of all previous therapy prior to enrollment. Treatment may start earlier if necessitated by the patient's medical condition (e.g. progressive disease) following discussion with the Investigator.
Recovery from acute toxicity related to prior therapy, including surgery and radiation, or no toxicity >= grade 
Patients must have recovered from any acute toxicity related to prior therapy, including surgery; toxicity should be =< grade  or returned to baseline
Prior hormonal/endocrine therapy =<  weeks prior to study entry (except for letrozole, which does not need to be interrupted); patients must have recovered from toxicity > grade , except for alopecia
Prior HER-targeted therapy <  weeks prior to study entry; patients must have recovered from toxicity > grade , except for alopecia
Grade >  treatment-related toxicity from prior therapy
Must have recovered from acute toxicity from prior treatment
Patients must be at least  weeks from any prior treatments and have recovered (to < grade ) from acute toxicity attributed to this prior treatment
Time lapse of  to  days between the end of onco-specific treatment and start of vaccination. Patients must have recovered from any acute toxicity produced by previous therapy.
Have not recovered (to baseline or Grade ?) from toxicity associated with prior treatment.
If patient has received previous systemic treatment, at least  weeks must have elapsed since the last chemotherapy, radiotherapy or immunotherapy and the beginning of protocol therapy and the patient must have recovered from toxicity due to the previous therapy (i.e., toxicity has resolved to baseline or is deemed irreversible)
Grade >  treatment-related toxicity from prior therapy
Discontinuation of prior anticancer therapy for ?  days prior to CD and recovered to ? CTCAE grade  (or baseline) from any acute or chronic toxicity associated with prior therapy.
Grade >  treatment-related toxicity from prior therapy
Patients who have toxicity from last prior therapy that has not recovered to at least Grade , with the exception of Grade  alopecia
Patients must have recovered (grade  or baseline) from any clinically significant toxicity associated with prior therapy
Patients must have recovered from any acute toxicity related to prior therapy, including surgery; toxicity should be =< grade  or returned to baseline
The subject has not recovered from toxicity due to all prior therapies (i.e., return to pretherapy baseline or to grade  or )
Failure to have recovered from clinically significant effects of prior chemotherapy (defined as toxicity greater than Grade  with the exception of alopecia)
Participants who have not recovered from clinically significant adverse effect(s)/toxicity(s) of the previous therapy.
Patients must have recovered from toxicity of prior therapy
Patients must have recovered from any acute toxicity related to prior therapy, including surgery; toxicity should be =< grade  or returned to baseline
Recovered from toxicity of any prior therapy to grade  or better
Not recovered from toxicity due to all prior therapies.
Participants must have recovered to grade  toxicity from prior therapy