Posttherapy [18F] fluorodeoxyglucose positron emission tomography in carcinoma of the cervix: response and outcome.

PURPOSE The aim of this study was to evaluate response to therapy using posttherapy molecular imaging with [(18)F] fluorodeoxyglucose (FDG), and to compare the response with patient outcome. PATIENTS AND METHODS This was a retrospective medical record review of 152 patients with carcinoma of the cervix. All patients underwent a pre- and posttreatment whole-body positron emission tomography (PET) imaging scan with FDG. Patients were treated with external irradiation and intracavitary brachytherapy, and most received concurrent weekly cisplatin. Posttherapy whole-body FDG-PET was performed 1 to 12 months (mean, 3 months) after completion of treatment. RESULTS The posttherapy PET did not show any abnormal FDG uptake in 114 patients, and their 5-year cause-specific survival estimate was 80%. There was persistent (in the irradiated region) abnormal FDG uptake in the cervix or lymph nodes in 20 patients. Their 5-year cause-specific survival estimate was 32%. New anatomic sites (in unirradiated regions) of abnormal FDG uptake were present in 18 patients, and none were alive at 5 years. A Cox proportional hazards model of survival outcome indicated that any abnormal posttherapy FDG uptake (persistent or new) was the most significant prognostic factor for developing metastatic disease and death from cervical cancer when compared with pretreatment- and treatment-related prognostic factors (P <.0001). CONCLUSION Posttherapy abnormal FDG uptake (persistent or new) as detected by whole-body PET measures tumor response and might be predictive of tumor recurrence and death from cervical cancer. Prospective validation of these results is warranted.

[1]  L. Kostakoglu,et al.  18F-FDG PET evaluation of the response to therapy for lymphoma and for breast, lung, and colorectal carcinoma. , 2003, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[2]  M. Rotman,et al.  Radiation therapy with and without extrafascial hysterectomy for bulky stage IB cervical carcinoma: a randomized trial of the Gynecologic Oncology Group. , 2003, Gynecologic oncology.

[3]  C. Choi,et al.  Detection of early recurrence with 18F-FDG PET in patients with cervical cancer. , 2003, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[4]  A. Berchuck,et al.  The role of PET scanning in the detection of recurrent cervical cancer. , 2003, Gynecologic oncology.

[5]  D. Cox Regression Models and Life-Tables , 1972 .

[6]  E. Kaplan,et al.  Nonparametric Estimation from Incomplete Observations , 1958 .

[7]  N. Breslow A generalized Kruskal-Wallis test for comparing K samples subject to unequal patterns of censorship , 1970 .

[8]  R. Hicks,et al.  A comparison of MRI and PET scanning in surgically staged loco-regionally advanced cervical cancer: Potential impact on treatment , 2001, International Journal of Gynecologic Cancer.

[9]  P. Grigsby,et al.  Posttherapy surveillance monitoring of cervical cancer by FDG-PET. , 2003, International journal of radiation oncology, biology, physics.

[10]  Y. Saga,et al.  Abnormal Fragile Histidine Triad Expression in Advanced Cervical Cancer and Evaluation of Its Utility as a Prognostic Factor , 2003, Oncology.

[11]  F Dehdashti,et al.  Lymph node staging by positron emission tomography in patients with carcinoma of the cervix. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[12]  C. Perez,et al.  Short‐term persistence of carcinoma of the uterine cervix after radiation. An indicator of long‐term prognosis , 1986, Cancer.

[13]  J. Wharton,et al.  Posttherapy surveillance of women with cervical cancer: an outcomes analysis. , 2000, Gynecologic oncology.

[14]  L. Adler,et al.  Positron emission tomography for evaluating para-aortic nodal metastasis in locally advanced cervical cancer before surgical staging: a surgicopathologic study. , 1999, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.