If requires pheresis to collect blood, partial thromboplastin time (kaolin) (PTTK) < 1.5 upper limit normal
Partial thromboplastin (PT) or partial thromboplastin time (PTT) < 1.5 x institutional upper limit
Partial thromboplastin time (PTT) within 1.5x upper limit of normal;
Partial thromboplastin time =< 1.66 times upper limit of normal
Partial thromboplastin time (PTT) at enrollment per institutional range
Partial thromboplastin time (PTT) < 1.5 x upper limit of normal (ULN)
Prothrombin and partial thromboplastin times =< 1.2 x upper limit of normal (ULN) prior to biopsy
Partial thromboplastin time (PTT) =< 1.5 x ULN
Prothrombin and partial thromboplastin times =< 1.2 x normal prior to biopsy
Partial thromboplastin time (PTT) < IULN
Partial thromboplastin time (PTT) < 1.5 x upper limit of normal (ULN)
Partial thromboplastin time (PTT) < 1.5 x ULN
Partial thromboplastin time =< 1.5 x institutional ULN obtained within 14 days of first treatment
Partial thromboplastin time (PTT) =< 1.5 x upper limit of normal (ULN)
Partial thromboplastin time (PTT) =< 1.5 x institutional ULN
Partial thromboplastin time (PTT) < 1.3 x ULN
Partial thromboplastin time (PTT) =< institution's upper limit of normal, unless receiving therapeutic low molecular weight heparin
Partial thromboplastin time (PTT) < 70 seconds (sec)
Partial thromboplastin time (PTT) =< 1.2 x ULN
Partial thromboplastin time (PTT) must be =< 2 X upper normal limit of institution's normal range; subjects on anticoagulant (such as coumadin) must have a PTT =< 5 X upper normal limit of institution's normal range
Or partial thromboplastin time [PTT] > 100 sec
Partial thromboplastin time (PTT) within normal limits (+/- 15%)
Partial bladder or partial kidney removal (eg, partial cystectomy or partial nephrectomy)
Partial thromboplastin time (PTT) =< 48 seconds (1.25 x ULN)
Partial thromboplastin time (PTT) must be =< 1.5 × upper normal limit of institution's normal range
Partial thromboplastin time (PTT) =< 1.5 x ULN
Partial thromboplastin time (PTT) < 1.5 x the upper limit of institution’s normal range
Partial thromboplastin time (PTT) =< 1.2 x IULN (if not receiving anticoagulation therapy)
Partial Thromboplastin Time (PTT) ?1.5x upper limit of normal (ULN) unless receiving therapeutic anticoagulation.
Partial thromboplastin time (PTT) =< 1.5 times the upper limit of normal
Partial thromboplastin time > 50 seconds (secs)
Partial thromboplastin time (PTT) =< 1.2 x institutional ULN
Partial thromboplastin time =< 1.66 times upper limit of normal
Partial thromboplastin time 5 seconds above ULN.
Partial thromboplastin time (PTT) < 1.5 x ULN for institution unless patient is on planned therapy with heparin or heparin-like products obtained =< 14 days prior to registration
Partial thromboplastin time (PTT) less than or equal to 1.3 x ULN
Partial thromboplastin time (PTT) < 1.5 times upper limit of normal within 14 days before enrollment
Partial thromboplastin time (PTT) =< 1.5 times the upper limit of normal
Partial thromboplastin time (PTT) =< 60
Partial thromboplastin time (PTT) =< 1.5 X institutional upper limit of normal
Partial thromboplastin time (PTT) < 1.5 x upper limit of normal (ULN)
Partial thromboplastin time (PTT) >= 45 seconds
Partial thromboplastin time (PTT) must be =< 1.5 × upper normal limit of institution's normal range
Partial thromboplastin time (PTT) < 1.2 times institutional upper limit of normal
Prothrombin and partial thromboplastin times =< 1.2 x normal prior to biopsy
Partial thromboplastin time (PTT) =< 2 x normal outside the setting of stable chronic anticoagulation therapy
Abnormal laboratory values as defined by protocol for creatinine, creatinine clearance, aspartate transaminase (AST) or alanine transaminase (ALT), total bilirubin, international normalized ration (INR), partial thromboplastin time (PTT) or activated partial thromboplastin time (aPPT), unless these abnormalities are due to underlying lymphoma
Partial thromboplastin time (PTT) =< 1.5 X institutional ULN unless patients are on therapeutic anticoagulation with warfarin
EXPANSION COHORT ONLY: Partial thromboplastin time (PTT) =< 1.5 X institutional ULN unless patients are on therapeutic anticoagulation with warfarin
Partial thromboplastin time (PTT) =< 1.2 times the ULN unless the patient is receiving therapeutic anticoagulation
Partial thromboplastin time (PTT) =< 1.2 x upper limit of normal (ULN) unless the patient is receiving therapeutic anticoagulation
Subject has acceptable coagulation studies (obtained ? 14 days prior to starting Cycle 1 Day 1) partial thromboplastin time (PTT) < 1.2 x ULN and INR ? 1.5 x ULN.
Partial thromboplastin time (PTT) < 1.2 x institutional upper limits of normal
Partial thromboplastin time (PTT) > 80
Partial thromboplastin time ? 1.5 X upper limit
Partial thromboplastin time (PTT) or activated (a)PTT =< 1.5 x upper limit of normal (ULN) per institutional laboratory range
Partial thromboplastin time (PTT) < 1.2 times the upper limit of normal
Partial thromboplastin time (PTT) =< 1.2 X ULN
Partial thromboplastin time (PTT) within normal limits (WNL)
Partial thromboplastin time (PTT) =< 60
Partial thromboplastin time (PTT) < 1.5 times the upper limit of normal (heparin, lovenox or alternative anticoagulants are acceptable)
Partial thromboplastin time (PTT) =< 2 x upper limit of normal (ULN)
PTT (partial thromboplastin time) =< 1 x ULN
Partial thromboplastin time less than 4.0 times below or above the upper or lower limit range
Partial thromboplastin time (PTT) =< 1.2 X ULN (evaluated within 28 days of randomization)
Partial thromboplastin time less than 2.5 times below or above the upper or lower limit range; for those patients receiving Coumadin or another anticoagulant the upper limit for partial thromboplastin time must not exceed 6 times the upper limit of the normal range
Pre-treatment laboratory tests for patients receiving fluorine F 18 fluorothymidine ([18F]FLT) must be performed within 21 days prior to baseline imaging; these laboratory tests must be less than 4.0 times below or above the upper or lower limit range for the respective laboratory test for entry into the study (unless not clinically relevant); 2.5 x for prothrombin time and partial thromboplastin time; for those patients receiving Coumadin or another anticoagulant the upper limit for prothrombin time or partial thromboplastin time must not exceed 6 times the upper limit of the normal range; the initial 4.0 x value will be critical for liver function test results which can be extremely variable, and a 4.0 x above the upper normal range is still acceptable for inclusion in this study; urinalysis abnormalities will not preclude the patient from being enrolled and studied; the baseline and subsequent laboratory testing will include liver enzymes (serum glutamic oxaloacetic transaminase [SGOT], serum glutamate pyruvate transaminase [SGPT], anaplastic lymphoma kinase [ALK]), bilirubin (total), serum electrolytes, complete blood count (CBC) with platelets prothrombin time, partial thromboplastin time, blood urea nitrogen (BUN), and creatinine
For the follow-up scanning sessions after therapy has been instituted and within 7 days prior to the second [18F]FLT study the laboratory assessments will be required due to the use of [18F]FLT; these studies should also be less than 4.0 times below or above the upper or lower limit range for the respective laboratory study (unless not clinically relevant); 2.5 x for prothrombin time and partial thromboplastin time; however at the discretion of the study principal investigator (PI) the second imaging sessions can occur if laboratory values are not within the 4 X upper limit of normal (unless not clinically relevant); for those patients receiving Coumadin or another anticoagulant the upper limit for prothrombin time or partial thromboplastin time must not exceed 6 times the upper limit of the normal range; for the assessments at subsequent imaging time points the laboratory tests as described for baseline assessment will again be obtained
internal normalized ratio and partial thromboplastin time <1.5x upper limit of normal