Background: Biomarkers for cyclin-dependent kinase 4/6 inhibitors, such as palbociclib, for patients with hormone receptor-positive/HER2-negative metastatic breast cancer are lacking. Thymidine kinase is a proliferation marker downstream of the cyclin-dependent kinase 4/6 pathway. We prospectively investigated the prognostic role of serum thymidine kinase activity (sTKa), in patients treated with Palbociclib + fulvestrant.Patients and methods: PYTHIA was a phase II, single-arm, multicentre, trial that enrolled 124 post-menopausal women with endocrine-resistant hormone receptor-positive/HER2-negative metastatic breast cancer. Serum samples were collected pre-treatment (pre-trt; n = 122), at day 15 of cycle 1 (D15; n = 108), during the one week-off palbociclib before initiating cycle 2 (D28; n = 108) and at end of treatment (n = 76). sTKa was determined centrally using Divitum (R), a refined ELISA-based assay with a limit of detection of 20 Divitum Units (Du)/L. The primary study endpoint was progression-free survival, assessed for its association with pre-and on-treatment sTKa.Results: Data from 122 women were analysed. Pre-treatment sTKa was not associated with clinical characteristics and moderately correlated with tissue Ki-67. Palbociclib + fulvestrant markedly suppressed sTKa levels at D15, with 83% of patients recording levels below limit of detection. At D28, sTKa showed a rebound in 60% of patients. At each timepoint, higher sTKa was associated with shorter progression-free survival (each p < 0.001), with the strongest effect at D15.Conclusions: STKa is an independent prognostic biomarker in patients treated with palbociclib. High pre-treatment sTKa and its incomplete suppression during treatment may identify patients with poorer prognosis and primary resistance. This warrants validation in prospective compar-ative trials. (c) 2022 Elsevier Ltd. All rights reserved.

Serum thymidine kinase activity in patients with hormone receptor-positive and HER2-negative metastatic breast cancer treated with palbociclib and fulvestrant / Malorni, Luca; Tyekucheva, Svitlana; Hilbers, Florentine S; Ignatiadis, Michail; Neven, Patrick; Colleoni, Marco; Henry, Stéphanie; Ballestrero, Alberto; Bonetti, Andrea; Jerusalem, Guy; Papadimitriou, Konstantinos; Bernardo, Antonio; Seles, Elena; Duhoux, Francois P; MacPherson, Iain R; Thomson, Alastair; Davies, David Mark; Bergqvist, Mattias; Migliaccio, Ilenia; Gebhart, Géraldine; Zoppoli, Gabriele; Bliss, Judith M; Benelli, Matteo; McCartney, Amelia; Kammler, Roswitha; De Swert, Heidi; Ruepp, Barbara; Fumagalli, Debora; Maibach, Rudolf; Cameron, David; Loi, Sherene; Piccart, Martine; Regan, Meredith M. - In: EUROPEAN JOURNAL OF CANCER. - ISSN 1879-0852. - ELETTRONICO. - 164:(2022), pp. 0-0. [10.1016/j.ejca.2021.12.030]

Serum thymidine kinase activity in patients with hormone receptor-positive and HER2-negative metastatic breast cancer treated with palbociclib and fulvestrant

Benelli, Matteo;
2022

Abstract

Background: Biomarkers for cyclin-dependent kinase 4/6 inhibitors, such as palbociclib, for patients with hormone receptor-positive/HER2-negative metastatic breast cancer are lacking. Thymidine kinase is a proliferation marker downstream of the cyclin-dependent kinase 4/6 pathway. We prospectively investigated the prognostic role of serum thymidine kinase activity (sTKa), in patients treated with Palbociclib + fulvestrant.Patients and methods: PYTHIA was a phase II, single-arm, multicentre, trial that enrolled 124 post-menopausal women with endocrine-resistant hormone receptor-positive/HER2-negative metastatic breast cancer. Serum samples were collected pre-treatment (pre-trt; n = 122), at day 15 of cycle 1 (D15; n = 108), during the one week-off palbociclib before initiating cycle 2 (D28; n = 108) and at end of treatment (n = 76). sTKa was determined centrally using Divitum (R), a refined ELISA-based assay with a limit of detection of 20 Divitum Units (Du)/L. The primary study endpoint was progression-free survival, assessed for its association with pre-and on-treatment sTKa.Results: Data from 122 women were analysed. Pre-treatment sTKa was not associated with clinical characteristics and moderately correlated with tissue Ki-67. Palbociclib + fulvestrant markedly suppressed sTKa levels at D15, with 83% of patients recording levels below limit of detection. At D28, sTKa showed a rebound in 60% of patients. At each timepoint, higher sTKa was associated with shorter progression-free survival (each p < 0.001), with the strongest effect at D15.Conclusions: STKa is an independent prognostic biomarker in patients treated with palbociclib. High pre-treatment sTKa and its incomplete suppression during treatment may identify patients with poorer prognosis and primary resistance. This warrants validation in prospective compar-ative trials. (c) 2022 Elsevier Ltd. All rights reserved.
2022
164
0
0
Goal 3: Good health and well-being
Malorni, Luca; Tyekucheva, Svitlana; Hilbers, Florentine S; Ignatiadis, Michail; Neven, Patrick; Colleoni, Marco; Henry, Stéphanie; Ballestrero, Alber...espandi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1352419
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