Minimal Residual Disease–Guided Intermittent Dosing in Patients With Cancer: Successful Treatment of Chemoresistant Anaplastic Large Cell Lymphoma Using Intermittent Lorlatinib Dosing

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Publikace nespadá pod Filozofickou fakultu, ale pod Lékařskou fakultu. Oficiální stránka publikace je na webu muni.cz.
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POKORNÁ Petra KLEMENT Giannoula VAŠÍKOVÁ Alžběta KANDEROVÁ Veronika JEŽOVÁ Marta NOSKOVÁ Kristýna MÚDRY Peter KÝR Michal MERTA Tomáš BAJČIOVÁ Viera KŘENOVÁ Zdenka PÁLOVÁ Hana ZDRAŽILOVÁ DUBSKÁ Lenka SLABÝ Ondřej VALÍK Dalibor ŠTĚRBA Jaroslav

Rok publikování 2022
Druh Článek v odborném periodiku
Časopis / Zdroj JCO PRECISION ONCOLOGY
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
www https://ascopubs.org/doi/full/10.1200/PO.21.00525
Doi http://dx.doi.org/10.1200/PO.21.00525
Klíčová slova intermitent dosing lorlatinib; chemoresistant lymphoma; minimal disseminated disease; pediatric oncology
Popis With the emergence of targeted therapies, the traditional maximum tolerated dosing where toxicities guide the treatment dose is no longer relevant. Especially in the case of tyrosine kinase inhibitors (TKIs), where higher doses lead to therapeutic resistance due to ligand or receptor upregulation and where off-target toxicities plague any increase of dose. In the case of TKIs, where the most effective dose is at the bottom of a U-shaped curve, therapy should be guided by biomarkers, or by minimal residual disease. We present a case of relapsed chemotherapy-refractory ALK-positive anaplastic large cell lymphoma treated with lorlatinib, where we used frequent minimal disseminated disease monitoring to guide the length of on/off therapy periods during intermitted dosing in order to prevent treatment resistance.
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