TAME (T-A-M End-Result) System | Cancer Therapy Adverse Events

Purpose: To evaluate a cancer therapy regimen using the TAME (T-A-M End-result) system.

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Evaluation

Are you evaluating a cancer therapy regimen?

Yes

Number of patients in the study cohort

Total number of Grade 3 or 4 acute adverse events

Number of patients without any Grade 3 or 4 acute toxic events

Total number of Grade 3 or 4 chronic, long-term adverse events

Total number of deaths

Results

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Results Interpretation and Description References Next Steps

Data complete?

Evaluation appropriate?

Percent of cohort without acute toxic events

T value

which indicates

A value

M value

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Interpretation and Description

References

Next Steps in Evaluation

Diagnosis

Risk Factors
Criteria For Diagnosis
- Advanced Stage Hodgkin Disease | Score for Treatment-Related Mortality (TRM)
Severity, Prognosis, Stage
- Tool for Predicting Acute Chemotherapy-Induced Nausea and Vomiting (CINV)
- Advanced Stage Hodgkin Disease | Score for Treatment-Related Mortality (TRM)
Complications

Therapy

Selection
- Anticipatory Nausea Index for Cancer Chemotherapy
Dosage Calculations
- Predicting Cycle One Serious Drug-Related Toxicity (SDRT) in Phase I Oncology Trial
Prevention
- Emetic Effect of Chemotherapeutic Agents

Monitoring

Response To Therapy
Adverse Effects
Drug Levels
- Predicting Cycle One Serious Drug-Related Toxicity (SDRT) in Phase I Oncology Trial
Overdose And Reversal
- Predicting Cycle One Serious Drug-Related Toxicity (SDRT) in Phase I Oncology Trial

Specialty

Hematology Oncology

Objective

adverse effects

ICD-10

T45.1 - Poisoning, antineoplastic and immunosuppressive drugs

Info

Purpose: To evaluate a cancer therapy regimen using the TAME (T-A-M End-result) system.

Specialty: Hematology Oncology

Objective: adverse effects

ICD-10: T45.1,

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