Assessing the impact of FDG-PET in the management of anal cancer

被引:83
|
作者
Nguyen, Brandon T.
Joon, Daryl Lim
Khoo, Vincent [1 ,2 ]
Quong, George
Chao, Michael
Wada, Morikatsu
Joon, Michael Lim
See, Andrew
Feigen, Malcolm
Rykers, Kym
Kai, Cynteen
Zupan, Eddy
Scott, Andrew
机构
[1] Royal Marsden Hosp, NHS Fdn Trust, Dept Acad Radiotherapy, London SW3 6JJ, England
[2] Inst Canc Res, London SW3 6JJ, England
关键词
anal carcinoma; FDG-PET; follow-up; radiotherapy; response; staging;
D O I
10.1016/j.radonc.2008.04.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To assess the utility of FDG-PET in anal cancer for staging and impact on radiotherapy planning (RTP), response and detection of recurrent disease. Methods and materials: Fifty histopathological anal cancer patients were reviewed between 1996 and 2006. The median age was 58 years (range 36-85) with 19 males: 3 1 females. Clinical assessment with CT was compared to PET. Impact on management, disease response, recurrence and metastases was evaluated. Results: The non-PET staging was Stage I(8), Stage II(18), Stage III(22), and Stage IV(2)s. The primary was strongly FDG avid in 98% with non-excised tumors compared to CT (58%). PET upstaged 17% with unsuspected pelvic/inguinal nodal disease. Pre-treatment PET identified 11 additional by involved nodal groups in 48 patients causing RTP amendments in 19%. Post-treatment PETs at median 17 weeks (range 9-28) showed complete responses in 20 (80%) and 5 (20%) partial responses (PR). PRs were biopsy positive in 2 and negative in 3. Fifteen had follow-up scans of which all nine PETs detected recurrences were pathologically confirmed. Conclusions: Anal cancer is FDG-PET avid. PET upstages 17% and changes the RTP in 19%. PET can aid in anal cancer staging and identification of residual disease, recurrent/metastaitic disease but warrants further prospective studies. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:376 / 382
页数:7
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