AE Toxicity Grading for Transplant Patients

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AE Toxicity Grading for Transplant Patients Marcie Tomblyn, MD, MS Associate Member Director, BMT Clinical Research Moffitt Cancer Center Objectives Why do we care????? Toxicity vs Adverse Event vs Serious Adverse Event Importance of accurate toxicity grading Examples Why is this relevant? Toxicities are common following transplant Knowledge about frequencies of certain toxicities allow us to better counsel our patients We can only learn about frequency of toxicity if we have data Toxicity vs AE vs SAE Toxicity Adverse Event Toxicity: An unplanned, unwanted event which occurs following transplant AE: An unplanned, unwanted event which is possibly related to clinical trial specific therapy **EVENT.. Not a Cause!*** SAE An AE resulting in the following: - Death - persistent disability - Life-threatening - birth defect - Hospitalization (or prolongation of) ADVERSE EVENT TOXICITY An SAE is always an AE and a Toxicity A Toxicity may be an AE and/or SAE SERIOUS ADVERSE EVENT Expectedness and Attribution Only for clinical trials Expected vs Unexpected If it s listed in the trial protocol and/or the consent form expected Attribution Is it related to the investigational therapy of the trial? - Definite - Unlikely - Probable - Unrelated - Possible

Toxicity Grading Common Terminology Criteria Adverse Events Developed by NCI Currently on Version 4.03 Significantly different than v 3.0 Available at http://evs.nci.nih.gov/ftp1/ctcae/ctcae_ 4.03_2010-06-4_QuickReference_5x7.pdf Grading Scale 0: no AE or within normal limits 1: mild 2: moderate 3: severe 4: life-threatening/disabling 5: fatal Common Toxicities after HCT Common occur in >20% of patients Should be easily recognized and graded Examples: Nausea Neutropenic fever Vomiting Fatigue Diarrhea Electrolyte disturbances Mucositis Pancytopenia requiring transfusions Grading Toxicities during Transplant Most toxicities change severity day to day sometimes hour to hour! Assessments often look for most severe in a block of time Ex. Most severe grade of oral mucositis between day 0 day 7 Ideally, assess about the same time each day during HCT Reporting differs based on indication for report: daily nurse assessments vs clinical research vs registry reporting Less Common toxicities Many other issues with our transplant patients Consider assessment by organ systems Pulmonary Cardiac Hepatic GU Still assess with CTC AE criteria

Example 33 yo M with ALL now day +8 after MUD HCT with Flu/Bu conditioning and Tac/MTX for GvHD prophylaxis Temp 101.3F, BP 92/57, HR 124, RR 24, O2 sat 90% on RA and inc to 97% with 2 LPM/NC PE: A&O x4, tachycardic and tachypneic, crackles at the bases bilaterally, abdomen bland, no rash What are the toxicities to be graded and what are the grades? What other information do you need to assist in grading? Toxicities which could be graded. Fever is patient neutropenic? ANC < 500/mcL Hypotension what is the baseline BP? 100 s/60 s Tachycardia Hypoxia Patient is now day +10 He is unable to eat due to mouth pain and exam shows an ulcer on the tongue and some mild mucosal bleeding Blood cultures from day +8 grew Streptococcus viridans and he is on appropriate antibiotics without additional fevers and no longer requiring O2 CIBMTR Registry CIBMTR (registry) Report the infection on form 2100 Trial Reporting (CTN/RCI BMT) Does it fall into a clinically significant infection category?

Now day +16 with an ANC of 600/mcL Bilirubin increasing to 3.4 with abdominal distension and weight has increased to 96kg from admission of 90kg A RUQ ultrasound demonstrates reversal of flow c/w VOD/SOS and ascites Trial Reporting (CTN/RCI BMT Toxicity forms are time-point driven D30, d60, d100, d180, etc Asks not only symptoms but requests potential etiologies On day +22, he develops a confluent maculopapular erythematous rash on his face, back, chest, abdomen, and arms His bilirubin is now 4.2 and his creatinine is 1.6 He has started having diarrhea, about 6 stools per day, with a volume of about 800 ml Patient has a skin biopsy and EGD/Flex sig to assess for GVHD Skin: consistent with GVHD Rectal biopsy with path 3/4 GVHD Gastric biopsy with path 1/4 GVHD Stool cultures are also sent for infectious etiology Negative

Rule of Nines chart to assess percent BSA involved with a rash Trial Reporting (CTN/RCI BMT) GVHD Weekly assessments for reporting agvhd Clinical diagnosis with pathologic confirmation Organ STAGE and Overall GRADE Summary Toxicities Signs and Symptoms Not etiologies Clear criteria for assessment Available on-line in a searchable PDF Reporting of toxicities varies based on reasons for assessment