ID | Measure | N | Expected value | Obtained values (year) | ||
---|---|---|---|---|---|---|
2019 | 2020 | 2021 | ||||
F_0a | Multidisciplinary tumourboards assess the completeness of the diagnosticsa | 10,793 | 0% | 8% | 5% | 5% |
F_1 | The percentage of deaths within one year from the diagnosis of a malignant neoplasm, correlated to tumour stage | 505 330 1310 1273 | 0% | I 1% II 2% III 11% IV 29% | I 4% II 15% III 30% IV 51% | I 4% II 14% III 37% IV 59% |
F_2 | The percentage of deaths within 30 days from the date of surgery, correlated to tumour stage | 362 201 545 492 | 0% | I 0% II 0% III 0% IV 0% | I 0% II 0% III 1% IV 5% | I 0,3% II 1% III 2% IV 6% |
F_3 | Percentage of deaths within 30 days from the end of chemotherapy, correlated to tumour stage | 71 139 740 665 | 0% | I 0% II 0% III 6% IV 14% | I 4% II 4% III 11% IV 20% | I 3% II 4% III 12% IV 21% |
F_4 | Percentage of deaths within 30 days from the end of palliative radiotherapy, correlated to tumour stage | 7 17 108 198 | 0% | I - II- III 0% IV 25% | I - II 0% III 15% IV 21% | I 28%b II 0% III 13% IV 22% |
F_5 | Percentage of patients requiring hospitalisation due to complications after surgical treatment | 2205 | 0% | 1% | 1% | 5% |
F_6 | Percentage of patients requiring hospitalisation due to complications after radiotherapy | 50 56 316 265 | 0% | I 0% II 0% III 0% IV 0% | I 0% II 0% III 0% IV 0% | I 0% II 0% III 0% IV 0% |
F_7 | Percentage of patients requiring hospitalisation due to complications after systemic treatment (after 30, 60, 90 days) | 1748 1748 1748 | 0% | 30 d5% 60 d5% 90 d5% | 30 d4% 60 d4% 90 d4% | 30 d2% 60 d2% 90 d2% |
F_8 | Percentage of patients who received chemotherapy during inpatient hospitalisation (according to the WHO ECOG) | 8818c 156 | 20%d | WHO 0–2 84% WHO 3–4 9% | WHO 0–2 74% WHO 3–4 85% | WHO 0–2 54% WHO 3–4 79% |
F_9 | Percentage of stage III and IV cancer patients | 2417 2417 | 0% | III 35% IV 32% | III 37% IV 35% | III 37% IV 36% |
F_10 | Assessment of the completeness of a pathological exam | 2167 1857 | 0% 0% | initial diagnostics0% in-depth 0% diagnostics | initial diagnostics0% in-depth 0,5% diagnostics | initial diagnostics0% in-depth 0,3% diagnostics |
F_11_2 | Percentage of patients with genetic and molecular testing for predictive factors (lung cancer)e | 225 211 | 100% 100% | III 33% IV 77% | III 40% IV 59% | III 35% IV 59% |
F_12_2 | The percentage of surgical procedures performed with minimally invasive surgery (lung cancer) | 724 | 100% | 44% | 49% | 58% |
F_13 | Median time elapsed from the date of registration of the patient for a diagnostic (imaging or pathomorphological) exam to the date of obtaining the result of this exama | N/A | 0 days (d) | PET-CT 7 d H/P 7 d | PET-CT 12 d H/P 18 d | PET-CT 24 d H/P 14 d |
F_14 | Percentage of repeated diagnostic tests over a 6-week period (computed tomography, endoscopy, biopsy, pathomorphological assessment, molecular assessment), shown for each participating centre by tumour type and test type | 3103 1423 194 1092 3822 | 0% | CT 0% Biopsy 0% MolecularN/A Endoscopy0% H/P 0% | CT 0% Biopsy 0% Molecular0% Endoscopy0% H/P 0% | CT 0% Biopsy 0% Molecular0% Endoscopy 0% H/P 0,05% |
F_15 | Percentage of repeated surgical treatments for diagnoses other than breast cancer | 2205 | 0% | 2% | 2% | 6% |
F_22† | Percentage of patients with suspected lung cancer consulted by a pulmonologist within 14 working days from the date of registering the referral with the service provider | 62 | 100% | N/A | 87% | 92% |
F_23 | The proportion of patients with mediastinal lymphadenopathy greaterthan 10 mm who underwent EBUS-TBNA | 217 | 100% | 44% | 60% | 67% |
F_24† | The proportion of patients with suspected lung cancer and pleural effusion diagnosed with fluid aetiology | 25 | 100% | N/A | 4% | 8% |
F_25‡ | The proportion of patients with stage III non-small-cell lung cancer who received concurrent chemoradiotherapy | 516 | 100% | 3% | 1% | 6% |
F_31 | Percentage of diagnostic tests requiring redescription or reverification of the material over a 6-week period (computed tomography, pathomorphological assessment, molecular assessment), shown for each participating centre by tumour type and test type | 3103 194 3822 | 0% | CT 0% Molecular0% H/P 0% | CT 0% Molecular0% H/P 0% | CT 0% Molecular 0% H/P 0% |