High liposomal doxorubicin tumour tissue distribution, as determined by radiopharmaceutical labelling with 99mTc-LD, is associated with the response and survival of patients with unresectable pleural mesothelioma treated with a combination of liposomal doxorubicin and cisplatin

Background There are currently no available biomarkers for advanced pleural mesothelioma that determine which patients could benefit from a specific chemotherapy regimen. Methods Based on the results of a previously published phase II study, we associated the 99m Technetium-labelled liposomal doxoru...

Full description

Saved in:
Bibliographic Details
Published inCancer chemotherapy and pharmacology Vol. 74; no. 1; pp. 211 - 215
Main Authors Arrieta, Oscar, Medina, Luis-Alberto, Estrada-Lobato, Enrique, Ramírez-Tirado, Laura-Alejandra, Mendoza-García, Víctor-Osvaldo, de la Garza-Salazar, Jaime
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer Berlin Heidelberg 01.07.2014
Springer
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Background There are currently no available biomarkers for advanced pleural mesothelioma that determine which patients could benefit from a specific chemotherapy regimen. Methods Based on the results of a previously published phase II study, we associated the 99m Technetium-labelled liposomal doxorubicin ( 99m Tc-LD) uptake value (75 % cut-off) with the response rate, progression-free survival and overall survival of patients treated with a combination of liposomal doxorubicin and cisplatin. Results Patients with tumours exhibiting increased 99m Tc-LD uptake showed better response rates, progression-free survival and overall survival than those exhibiting lower uptake 73.3 versus 15 % ( p  < 0.001); 6.9 versus 3.2 months ( p  = 0.033) and 23 versus 6.6 months ( p  = 0.001), respectively. Conclusion 99m Tc-DL uptake in tumour tissue could define a set of patients who would benefit from this chemotherapy regimen.
ISSN:0344-5704
1432-0843
DOI:10.1007/s00280-014-2477-x