Secondary malignancies and survival of FCR-treated patients with chronic lymphocytic leukemia in Central Europe

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KOSA Fruzsina NEČASOVÁ Tereza SPACEK Martin GIANNOPOULOS Krzysztof HUS Iwona JURKOVÁ Tereza KORIŤÁKOVÁ Eva CHRÁPAVÁ Marika NOVACKOVA Martina KATINOVÁ Ivana KREJČÍ Denisa JUJKA Adam MATRAI Zoltan VALYI-NAGY Istvan ROBAK Tadeusz DOUBEK Michael

Rok publikování 2023
Druh Článek v odborném periodiku
Časopis / Zdroj Cancer Medicine
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
www https://onlinelibrary.wiley.com/doi/10.1002/cam4.5033
Doi http://dx.doi.org/10.1002/cam4.5033
Klíčová slova CLL population; FCR therapy; secondary malignancy; survival
Popis This is the first large-scale cross-country analysis of patients with chronic lymphocytic leukemia (CLL) aimed to evaluate the incidence, types, and key prognostic factors of secondary malignancies, and to assess the impact on overall survival based on retrospective claims data from three Central European countries. We analyzed 25,814 newly diagnosed CLL patients from Czechia, Hungary, and Poland; 10,312 (39.9%) patients were treated for CLL in study periods between 2004 and 2016. Out of the treated patients, 1986 (19.3%) received the FCR therapy in the first line and 779 (7.6%) received FCR in subsequent lines. We observed that 33.7% of treated patients developed secondary malignancies during the study. Based on country estimates, the probability to develop a secondary malignancy within 4 years since starting the first-line FCR therapy ranged between 28.0% and 36.8%. We found the age at diagnosis, male gender, any malignancy prior to the CLL diagnosis, and the CLL treatment to be the key risk factors for developing secondary malignancies. Specifically, the FCR therapy was a statistically significant (p < 0.001) prognostic factor for risk increase with the hazard ratio between 1.46 and 1.60. Across the three Central European countries, we observed consistent results indicating FCR increased the risk of secondary malignancies in CLL patients. We conclude that secondary malignancies are clearly an undervalued burden for CLL patients, caregivers, and the healthcare system. When evaluating new therapies in regulatory and reimbursement decision making, the factor of secondary malignancies deserves deeper considerations.

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