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RESEARCH PRODUCT

The Greta Study: Generating Real-World Evidence about Bevacizumab Treatment of Metastatic Colorectal Cancer by Linking Cancer Registries and Healthcare Databases in Italy

Giovanna TagliabueGiovanni CorraoSandro BarniPaolo RicciMc De CeglieMatteo FranchiR. TuminoAntonietta CaputoWalter Mazzucco

subject

Oncologymedicine.medical_specialtyBevacizumabBEVACIZUMAB TREATMENT OF METASTATIC COLORECTAL CANCER CANCER REGISTRIESbusiness.industryColorectal cancerHealth PolicyPublic Health Environmental and Occupational HealthCancerSettore MED/42 - Igiene Generale E Applicatamedicine.diseaseReal world evidenceInternal medicineHealth caremedicinebusinessmedicine.drug

description

OBJECTIVES: Based on the results of randomized clinical trials, bevacizumab plus chemotherapy is currently recommended as first­line treatment for metastatic colorectal cancer (mCRC). However, scant real­world data are available about effectiveness of bevacizumab­containing therapy used in patients with mCRC in Italy. The GRETA observational cohort study was designed for comparing overall survival (OS) of mCRC patients treated with first­line bevacizumab plus chemotherapy (B+CT), as compared to CT alone, in the real­world setting of Italian clinical practice, by linking cancer registries and healthcare utilization (HCU) databases. METHODS: Incident mCRC patients were identified during the period 2010­2012 from five population­based cancer registries, representing the 5.4% of the entire Italian population. Cases were linked to Regional HCU databases, in order to obtain the entire pathway of health services provided to each patient. Patients who started a first­line treatment with either B+CT or CT alone were included in the study cohort. A propensity score (PS) method was applied in order to take into account residual confounding. RESULTS: A study cohort of 480 subjects was selected, of which 101 received first­line B+CT and 379 CT alone. The median OS was 22.5 and 14.6 months in patients treated with or without bevacizumab, respectively (p=0.011). The corresponding adjusted hazard ratio (HR) was 0.82 (95% CI 0.62­1.08). The HR resulting from the PS matched analysis was 0.86 (95% CI 0.56­1.33). The gain in median OS was 8.3 months among patients aged less than 70 years (p=0.087) and 4.3 months among those aged 70 years or older (p=0.221). CONCLUSIONS: Despite not statistically significant, the addition of bevacizumab to CT showed a beneficial effect on OS, in the real­world clinical practice of mCRC patients in Italy. The gain in OS is comparable to that from the pivotal trial.

https://doi.org/10.1016/j.jval.2017.08.010