Clinical value of metabolic tumor volume by PET/CT in extranodal natural killer/T cell lymphoma

Abstract This study investigated whether metabolic tumor volume (MTV) by PET/CT as indicator of extent of lymphoma burden would be a prognostic factor in stage IE /IIE extranodal natural killer/T cell lymphoma (ENKTCL). Eighty patients with stage IE /IIE ENKTCL in the upper aerodigestive tract under...

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Veröffentlicht in:Leukemia research 2013-01, Vol.37 (1), p.58-63
Hauptverfasser: Song, Moo-Kon, Chung, Joo-Seop, Shin, Ho-Jin, Moon, Joon-Ho, Ahn, Jae-Sook, Lee, Ho-Sup, Lee, Sang-Min, Lee, Gyeong-Won, Kim, Seong-Jang, Lee, Seok-Mo
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Sprache:eng
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Zusammenfassung:Abstract This study investigated whether metabolic tumor volume (MTV) by PET/CT as indicator of extent of lymphoma burden would be a prognostic factor in stage IE /IIE extranodal natural killer/T cell lymphoma (ENKTCL). Eighty patients with stage IE /IIE ENKTCL in the upper aerodigestive tract underwent PET/CT at diagnosis were enrolled and 32 patients received upfront radiotherapy (RTx). MTV was measured on PET/CT images by the extranodal region above SUV, 2.5. Receiver operating curve analyses indicated that an MTV of 35.2 cm3 was the ideal cut-off to distinguish between low and high MTV groups. Clinical outcomes were compared according to several prognostic factors (age, stage, high performance status [PS], high International Prognostic Index, elevated lactate dehydrogenase [LDH], local tumor invasiveness [LTI], high MTV and up-front RT). High PS, elevated LDH, LTI, high MTV and upfront RT were associated with survivals. In multivariate analysis, high MTV (PFS, HR = 4.170, 95% CI = 1.714–10.147, p = 0.002; OS, HR = 4.102, 95% CI = 1.617–10.408, p = 0.003) and up-front RT (PFS, HR = 0.410, 95%CI = 0.178–0.946, p = 0.037; OS, HR = 0.365, 95% CI = 0.152–0.872, p = 0.023) were significant independent prognostic factors. Upfront RTx and extent of tumor burden, as measured by the MTV, had significant prognostic value in patients with ENKTCL.
ISSN:0145-2126
1873-5835
DOI:10.1016/j.leukres.2012.09.011