TY - JOUR
T1 - Predictive value of early F-18-fluoro-deoxyglucose positron emission tomography in chemosensitive relapsed lymphoma
AU - Schot, B
AU - van Imhoff, G
AU - Pruim, J
AU - Sluiter, W
AU - Vaalburg, W
AU - Vellenga, E
PY - 2003/10
Y1 - 2003/10
N2 - F-18-fluoro-deoxyglucose (FDG) positron emission tomography (PET) might be a better tool than computerized tomography (CT) in predicting long-term treatment outcome in patients with relapsed chemosensitive lymphoma who are candidates for autologous stem cell transplantation (ASCT). We studied patients with recurrent or persistent aggressive non-Hodgkin's lymphoma (NHL) and Hodgkin's disease (HD), who were treated with three courses of second-line induction chemotherapy [DHAP-VIM (dexamethasone, cytarabine, cisplatin followed by etoposide, iphosphamide and methotrexate)-DHAP], followed by myeloablative therapy and ASCT if chemosensitive. FDG-PET was performed in parallel to conventional diagnostic methods before starting, and after two courses of, second-line therapy. Of 68 relapsed lymphoma patients, 46 chemosensitive patients (33 NHL and 13 HD) were included, of whom 39 were transplanted. After DHAP-VIM, the second PET scan was normalized in 15/46 patients; progression-free survival at 2 years was 62% for PET-negative patients versus 32% for PET-positive patients (P = 0.048). The relative risk for progressive disease in patients with 90% reduction of intensity of abnormal FDG uptake after two courses of reinduction therapy was correlated with a favourable outcome.
AB - F-18-fluoro-deoxyglucose (FDG) positron emission tomography (PET) might be a better tool than computerized tomography (CT) in predicting long-term treatment outcome in patients with relapsed chemosensitive lymphoma who are candidates for autologous stem cell transplantation (ASCT). We studied patients with recurrent or persistent aggressive non-Hodgkin's lymphoma (NHL) and Hodgkin's disease (HD), who were treated with three courses of second-line induction chemotherapy [DHAP-VIM (dexamethasone, cytarabine, cisplatin followed by etoposide, iphosphamide and methotrexate)-DHAP], followed by myeloablative therapy and ASCT if chemosensitive. FDG-PET was performed in parallel to conventional diagnostic methods before starting, and after two courses of, second-line therapy. Of 68 relapsed lymphoma patients, 46 chemosensitive patients (33 NHL and 13 HD) were included, of whom 39 were transplanted. After DHAP-VIM, the second PET scan was normalized in 15/46 patients; progression-free survival at 2 years was 62% for PET-negative patients versus 32% for PET-positive patients (P = 0.048). The relative risk for progressive disease in patients with 90% reduction of intensity of abnormal FDG uptake after two courses of reinduction therapy was correlated with a favourable outcome.
KW - relapsed lymphoma
KW - autologous stem cell transplantation
KW - F-18-fluorodeoxyglucose (FDG)
KW - positron emission tomography (PET)
KW - prognosis
KW - NON-HODGKINS-LYMPHOMA
KW - STEM-CELL TRANSPLANTATION
KW - BONE-MARROW TRANSPLANTATION
KW - RESIDUAL MASS
KW - FDG-PET
KW - COMBINATION CHEMOTHERAPY
KW - F-18 FLUORODEOXYGLUCOSE
KW - AGGRESSIVE LYMPHOMA
KW - MALIGNANT-LYMPHOMA
KW - PROGNOSTIC VALUE
M3 - Article
SN - 0007-1048
VL - 123
SP - 282
EP - 287
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 2
ER -