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<sup>18</sup>F-FDG PET After 2 Cycles of ABVD Predicts Event-Free Survival in Early and Advanced Hodgkin Lymphoma

Juliano J. CerciDepartment of Nuclear Medicine, Heart Institute (InCor), University of São Paulo Medical School, São Paulo, Brazil. [email protected]Luís Fernando PracchiaKorea Institute of Radiological & Medical Sciences, Seoul, Republic of KoreaCamila C.G. LinardiDivision of Hematology, Clinical Hospital of the University of Sao Paulo Medical School, Sao Paulo, Brazil;Felipe Arriva PitellaDepartment of Nuclear Medicine, Heart Institute (InCor), University of Sao Paulo Medical School, Sao Paulo, Brazil;Dominique DelbekeDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, Tennessee;Marisa IzakiDepartment of Nuclear Medicine, Heart Institute (InCor), University of Sao Paulo Medical School, Sao Paulo, Brazil;Evelinda TrindadeHealth Technology Assessment/Executive Direction, Heart Institute (InCor), University of Sao Paulo Medical School, Sao Paulo, BrazilJosé SoaresDepartment of Nuclear Medicine, Heart Institute (InCor), University of Sao Paulo Medical School, Sao Paulo, Brazil;Valéria BuccheriDivision of Hematology, Clinical Hospital of the University of Sao Paulo Medical School, Sao Paulo, Brazil;José Cláudio MeneghettiDepartment of Nuclear Medicine, Heart Institute (InCor), University of Sao Paulo Medical School, Sao Paulo, Brazil;
2010en
ABI

Аннотация

UNLABELLED: Our objective was to assess the prognostic value of (18)F-FDG PET after 2 cycles of chemotherapy using doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) in Hodgkin lymphoma (HL) patients overall and in subgroups of patients with early and advanced stages and with low and high risks according to the International Prognostic Score (IPS). METHODS: One hundred fifteen patients with newly diagnosed HL were prospectively included in the study. All underwent standard ABVD therapy followed by consolidation radiotherapy in cases of bulky disease. After 2 cycles of ABVD, the patients were evaluated with PET (PET2). Prognostic analysis compared the 3-y event-free survival (EFS) rate to the PET2 results, clinical data, and IPS. RESULTS: Of the 104 evaluated patients, 93 achieved complete remission after first-line therapy. During a median follow-up of 36 mo, relapse or disease progression was seen in 22 patients. Treatment failure was seen in 16 of the 30 PET2-positive patients and in only 6 of the 74 PET2-negative patients. PET2 was the only significant prognostic factor. The 3-y EFS was 53.4% for PET2-positive patients and 90.5% for PET2-negative ones (P < 0.001). When patients were categorized according to low or high IPS risk and according to early or advanced stage of disease, PET2 was also significantly associated with treatment outcome. CONCLUSION: PET2 is an accurate and independent predictor of EFS in HL. A negative interim (18)F-FDG PET result is highly predictive of treatment success in overall HL patients, as well as in subgroups with early or advanced-stage disease and with low or high IPS risk.

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