| attribute | type | cardinality | unique | required | doc |
|---|
| absolute-leukocyte-count | long | one | | | The absolute leukocyte count expressed in number of cells per microliter |
| absolute-monocyte-count | long | one | | | The absolute monocyte count expressed in number of cells per microliter |
| bmi | float | one | | | The body mass index of the subject. Unless more information is available,
such observations should be connected to the baseline timepoint |
| bor | clinical-observation.bor | one | | | The best overall response (RECIST) of the subject. Such observations should be connected to the End of Study (EOS) timepoint |
| ca19-9 | float | one | | | CA19-9 (Cancer Antigen 19-9) measurement from blood, in U/mL |
| ctc | float | one | | | CTC (Ciculating Tumor Cells) measurement from blood, in CTC/7.5 mL whole blood |
| dcb | boolean | one | | | Whether this patient has experienced Durable Clinical Benefit. Such observations should be connected to the End of Study (EOS) timepoint |
| dfi | float | one | | | The length of time (in months) the length of time after primary treatment for a cancer ends
that the patient survives without any signs or symptoms of that cancer. Such observations should
be connected to the End of Study (EOS) timepoint |
| dfi-event | boolean | one | | | If DFI observation is censored (use false as the value) or connected to an event (use true) |
| dfi-reason | clinical-observation.event-reason | one | | | The reason (e.g. progression, censoring etc.) supplied for clinical observation DFI.
Refers to entities in the :clinical-observation.event-reason namespace.
See https://candel.parkerici.org/schema/#representing-data-for-survival-analysis-eg-pfs-os-etc for more information
about modeling survival data |
| disease-stage | clinical-observation.disease-stage | one | | | The stage of the disease. Refers to entities in the 'disease.stage' namespace. This is a clinical-observation
in order to allow the possibility for re-staging (even though technically tumor stage is not a time-varying
concept) |
| id | string | one | | | The id of the clinical observation. Must be unique within this dataset (but not within the entire database) |
| ir-recist | clinical-observation.ir-recist | one | | | The irRECIST (Immune Related Response Evaluation Critera in Solid Tumors) score for this observation,
refers to idents in the 'ir.recist' namespace |
| ldh | float | one | | | Lactate Dehydrogenase (LDH) measurement in blood, expressed in U/L |
| metastasis-gdc-anatomic-sites | gdc-anatomic-site | many | | | The GDC anatomic site(s) at which metastasis have been observed |
| metastatic | boolean | one | | | Indicates that the disease has become metastatic |
| os | float | one | | | The overall survival of the subject in months. Such observations should be connected to the End of Study (EOS) timepoint. |
| os-event | boolean | one | | | If OS observation is censored (use false as the value) or connected to an event (use true) |
| os-reason | clinical-observation.event-reason | one | | | The reason (e.g. progression, censoring etc.) supplied for clinical observation OS.
Refers to entities in the :clinical-observation.event-reason namespace.
See https://candel.parkerici.org/schema/#representing-data-for-survival-analysis-eg-pfs-os-etc for more information
about modeling survival data |
| pfs | float | one | | | The progression free survival of the subject in months. Such observations should be connected to the End of Study (EOS) timepoint |
| pfs-event | boolean | one | | | If PFS observation is censored (use false as the value) or connected to an event (use true) |
| pfs-reason | clinical-observation.event-reason | one | | | The reason (e.g. progression, censoring etc.) supplied for clinical observation PFS.
Refers to entities in the :clinical-observation.event-reason namespace.
See https://candel.parkerici.org/schema/#representing-data-for-survival-analysis-eg-pfs-os-etc for more information
about modeling survival data |
| psa | float | one | | | PSA (Prostate-specific antigen) measurement from blood, in ng/mL |
| rano | clinical-observation.rano | one | | | RANO (Response Assessment in Neuro-Oncology) assessment for brain tumor patients (MRI-based) |
| recist | clinical-observation.recist | one | | | The RECIST (Response Evaluation Critera in Solid Tumors) score for this observation,
refers to idents in the 'recist' namespace |
| recurrence | boolean | one | | | Indicates that the disease has recurred |
| study-day | study-day | one | | | The study-day at which this observation was performed |
| subject | subject | one | | | The subject that this clinical observation was performed in |
| timepoint | timepoint | one | | | The timepoint at which this observation was performed |
| ttf | float | one | | | The time to treatment failure of the subject in months. Such observations should be connected to the End of Study (EOS) timepoint |
| ttf-event | boolean | one | | | If TTF observation is censored (use false as the value) or connected to an event (use true) |
| ttf-reason | clinical-observation.event-reason | one | | | The reason (e.g. progression, censoring etc.) supplied for clinical observation TTF.
Refers to entities in the :clinical-observation.event-reason namespace.
See https://candel.parkerici.org/schema/#representing-data-for-survival-analysis-eg-pfs-os-etc for more information
about modeling survival data |
| tumor-sum-diam | float | one | | | The sum of the tumor diameters in mm |
| tumor-sum-diam-perc-change | float | one | | | The percent change in the tumor sum of diameters. Must be a number in [-1 1] |
| uid | [[* string]] | one | yes | | Synthetic unique ID for clinical observation |