Model study moduleΒΆ

Tumors from PDX often undergo comprehensive genomic characterization and/or treatment in controlled dosing studies to define therapeutic response and resistance. PDX-MI includes desirable fields in the reporting of these studies that supplement existing guidelines for reporting on in vivo biomedical research ( Meehan et al., 2017).

Field Rec Example PDXNet
Study name or identifier   PDX-123P3 Pertuzmab/Trastuzumab Needs to be unique to attach files
Treatment D pertuzumab in combination with trastuzumab; CHEMBL2007641 List of 1 or more generic drugs
Treatment protocol D trastuzumab (30 mg/kg loading dose, 15 mg/kg weekly); Additional module to capture Drug,Dose,Route,Frequency
Treatment Response D   RECIST Term
Passage D P2 Integer
Metastasis D Yes Yes or No
Metastasized to D Liver Uberon
Metastasis in passage D P3 Integer
Lag time/doubling time D 48h separate elements

Table 2.5. Model study module. Rec: Recommendation; E: essential; D:desirable.

1. Study Name or identifier (if not available could be model + passage + treatment) A way to uniquly identify the study. Human readable or unique ID

2. Treatment List of treatment(s) as generic terms for medications.

3. Treatment protocol For each treatment drug provide drug name, dosage, route and frequency.

4. Treatment response complete response, partial response, stable disease, progressive disease.

5 Model Passage Passage(s) of models used in study. Assumption is P0 modles have tissue directly from patient. P1 is engrafted with tissue from P0 etc.

Tumor OMICS: This was removed. It will be populated based on types of files uploaded for Study/Model.

6,7,8 Development of metastases in strain We will code this as Yes/no; site as uberon; passage as enumeration

9. Lag time/doubling time of tumor We will code this as the number of hours.