Table 3.
RAM (Year) | Population | Type of Malignancy | Parameters | C Statistics/ HR | Validation Cohort | Advantages/Disadvantages |
---|---|---|---|---|---|---|
Khorana risk score (2008)16 | Derivation cohort, n = 2701 Validation cohort, n = 1365 |
Breast, Lung, Ovarian, Sarcoma, Colon, and Lymphomas | Site of cancer platelet count ≥350 x 109/L haemoglobin ≤100 g/L (10 g/dL) and/or use of erythropoiesis-stimulating agents, leukocyte count ≥11 x 109/L, body mass index (BMI) of 35 kg/m2 or more | 0.7 for both cohorts | More than 55 validation cohorts and several systematic reviews. | Advantages: Good in classifying high-risk. -more predictive when considering a score of ≥2 as a cut-off point for high risk Disadvantages: Suboptimal performance in predicting VTE in low-risk groups |
Vienna Cancer and Thrombosis Study (CATS) Score(2018)17 | n = 819 | Breast, Lung, Stomach, Colorectal, Pancreas, Kidney, Prostate, Brain, Lymphoma, Multiple myeloma | Adds soluble P-selectin and D-dimer to KRS | 1.9 per 1 point increase | Comparison study with no statistical significance2* | Disadvantages: Applicability in p soluble monitoring in a real-life setting might not be feasible |
New Vienna (CATSCORE)18 | CATS cohort, n = 1423 MICA cohort, n = 832 |
Breast, Prostate, Lung, Colorectal, Esophagus, Kidney, Lymphoma, Bladder or urothelial, Uterine, Cervical, Ovarian, Pancreas, Stomach | Site of cancer and D-dimer | 0.66 in CATS 0.68 in MICA |
Comparison study with no statistical significance2* | Advantages: only two factors score Disadvantage: Suboptimal performance in the comparison trial |
PROTECHT Score (2012) | Placebo arm, n = 381 Nadroparin arm, n = 769 |
Gastrointestinal, Lung, Breast, Ovary, Pancreas, Head and Neck | Add gemcitabine, cisplatin, or carboplatin therapy to KRS | NA | 1 study with positive19 2 studies show poor performance2,20 |
Advantages: easy to use, considers treatment-related risk factors Disadvantages: Suboptimal performance in the comparison trial |
CONKO004(2015)21 | n= 312 | NA | Replace BMI in KRS with performance status | NA | Two comparison study with negative outcome*19,20 | Advantage: easy applicability Disadvantages: poor stratification performance |
ONKOTEV Score(2017)22 | n = 843 | Khorana score >2, personal history of VTE, metastatic disease, vascular/lymphatic macroscopic compression | C-statistic:0.719 at 3 months 0.754 at 6 months HR: Score = 1: 3.29 Score = 2: 6.54 Score > 2: 13.74 |
Multiple validation and comparison trials with negative outcome.*2,20 | Advantages: easy to apply, consider tumour-related factors Disadvantages: Suboptimal performance |
|
The COMPASS-CAT score(2016)23 | n = 1023 | Breast, Colorectal, Lung, or Ovarian cancer | Anthracycline or anti-hormonal therapy, time since cancer diagnosis, central venous catheter, stage of cancer, presence of cardiovascular risk factors, recent hospitalization for acute medical illness, personal history of VTE, and platelet count | C statistic: 0.850 | Multiple validation.24–27 | Advantages: Good performance in lung carcinoma,24 moves from traditional KRS Disadvantages: poor calibration. |
Tic-ONCO score(2018)28 | n = 391 | Adds genetic risk score to KS | C-statistic 0.73 HR = 1.69 |
NA | Disadvantages: Application of genetics in a real-life setting is questionable | |
The MDACC CAT model29 | n= 548 | Breast, Gastrointestinal non-pancreas, Pancreas, Genitourinary non-kidney Kidney, Gynaecological Lung and head/neck Lymphoma | Presence of metastasis, use of platinum-based chemotherapy, the use of ESAs and malignancies of origin in the gastrointestinal, gynecologic, and head-neck/lung organs | C-index: 0.74 | NA | Advantages: readily available information Disadvantages: lack of external validation |
Notes: *Comparison studies was done between Khorana, PROTECHT, CONKO, CATScore and ONKOTEV.
Abbreviations: MICA, Multinational Cohort Study; CATS, Vienna Cancer and thrombosis study; HR, hazards ratio; C-statistic /C-index, concordance statistic; NA, not available.