Abstract:Objective: To prospectively evaluate the feasibility, safety, and survival of laparoscopic surgical staging in patients with locally advanced cervical cancer. Methods: From Oct 2001 to Jul 2006, a total of 83 consecutive patients were eligible for inclusion and underwent laparoscopic surgical staging. Results: Three patients with intraoperative great vessel injury and 1 patient in whom the colpotomizer was unable to be inserted were excluded. Laparoscopic surgical staging was feasible in 95.2% (79/83). Immedia… Show more
“…Nodal status was determined by magnetic resonance imaging of the pelvis 6 positron emission tomography except for 36 patients who also underwent laparoscopic lymph node staging as a part of our previous clinical trial. 14,15 HPV status was evaluated from the cervical smear collected prior to radiotherapy using the Hybrid Capture II system (HC2; Digene Corporation, Gaithersburg, MD). HC2 test uses an RNA probe mixture of 13 high-risk HPV types and detects HPV types of 16,18,31,33,35,39,45, 51, 52, 56, 58, 59 and 68.…”
Section: Study Population Hpv Dna Test and Radiotherapymentioning
Human papillomavirus (HPV) DNA is considered as a hallmark of cervical cancer. We investigated whether persistent HPV DNA at the cervix is associated with local recurrence after radiotherapy in patients with locally advanced cervical cancer. A total of 156 patients with HPV-positive cervical cancer (International Federation of Gynecology and Obstetrics stage IB-IVB) treated with radiotherapy between July 2003 and December 2006 were analyzed. HPV DNA was measured prior to radiotherapy and after completion of radiotherapy. The results of HPV DNA test at postradiotherapy 1, 3, 6 and 12 months were analyzed individually for association with local recurrence-free survival (LRFS). In addition, the result of any last follow-up HPV test within 24 months postradiotherapy was defined as the overall status of HPV at 24 months and was also analyzed for association with LRFS. HPV DNA was cleared in 127 patients (81.4%) and persistent in 29 patients (18.6%) by 24 months. In 18 patients with local recurrences, 14 patients (78%) showed positive HPV tests at 1-3 months. Among the various time points analyzed, a positive HPV test at 3 months was the most accurate predictor of local recurrence. Multivariate analysis indicated that overall status of HPV at 24 months, low HPV viral load and histologic grade as being significantly related to poor LRFS. In HPV-positive cervical carcinoma treated primarily with radiotherapy, persistent HPV DNA within 24 months after treatment indicates a high risk of local recurrence. Diagnostic accuracy of HPV test was highest at 3 months.Cervical cancer is a significant health problem worldwide, ranking second highest in cancer incidence and fourth highest in site-specific cause of cancer death in women.1,2 While concurrent chemoradiotherapy is the main treatment modality for locally advanced cervical cancer, treatment failure in the central pelvis occurs in approximately 20-25% of patients. 3,4 Cytological tests are commonly inaccurate in detecting locally persistent or recurrent disease because the effect of radiation on the cells may result in ambiguous cell morphology in the early postradiotherapy period.5 Because positive high-risk human papillomavirus (HPV) DNA is considered as an important tool in the diagnosis of both preinvasive and invasive cervical cancer, the usefulness of the HPV test has often also been considered as a method of post-treatment surveillance. Previous studies have examined the effectiveness of the HPV DNA test as a clinically useful marker for detecting residual disease or recurrence after conservative surgical procedures for cervical intraepithelial neoplasia 6-8 and also after radiotherapy. [9][10][11][12] In terms of radiotherapy outcome, several past studies showed that HPV persistence is associated with high rates of local recurrence and poor overall survival in patients with cervical cancer. 10,11 However, the status of HPV DNA was only examined at a single time point after radiotherapy in those studies, and hence, the pattern of HPV clearance after radiotherapy and...
“…Nodal status was determined by magnetic resonance imaging of the pelvis 6 positron emission tomography except for 36 patients who also underwent laparoscopic lymph node staging as a part of our previous clinical trial. 14,15 HPV status was evaluated from the cervical smear collected prior to radiotherapy using the Hybrid Capture II system (HC2; Digene Corporation, Gaithersburg, MD). HC2 test uses an RNA probe mixture of 13 high-risk HPV types and detects HPV types of 16,18,31,33,35,39,45, 51, 52, 56, 58, 59 and 68.…”
Section: Study Population Hpv Dna Test and Radiotherapymentioning
Human papillomavirus (HPV) DNA is considered as a hallmark of cervical cancer. We investigated whether persistent HPV DNA at the cervix is associated with local recurrence after radiotherapy in patients with locally advanced cervical cancer. A total of 156 patients with HPV-positive cervical cancer (International Federation of Gynecology and Obstetrics stage IB-IVB) treated with radiotherapy between July 2003 and December 2006 were analyzed. HPV DNA was measured prior to radiotherapy and after completion of radiotherapy. The results of HPV DNA test at postradiotherapy 1, 3, 6 and 12 months were analyzed individually for association with local recurrence-free survival (LRFS). In addition, the result of any last follow-up HPV test within 24 months postradiotherapy was defined as the overall status of HPV at 24 months and was also analyzed for association with LRFS. HPV DNA was cleared in 127 patients (81.4%) and persistent in 29 patients (18.6%) by 24 months. In 18 patients with local recurrences, 14 patients (78%) showed positive HPV tests at 1-3 months. Among the various time points analyzed, a positive HPV test at 3 months was the most accurate predictor of local recurrence. Multivariate analysis indicated that overall status of HPV at 24 months, low HPV viral load and histologic grade as being significantly related to poor LRFS. In HPV-positive cervical carcinoma treated primarily with radiotherapy, persistent HPV DNA within 24 months after treatment indicates a high risk of local recurrence. Diagnostic accuracy of HPV test was highest at 3 months.Cervical cancer is a significant health problem worldwide, ranking second highest in cancer incidence and fourth highest in site-specific cause of cancer death in women.1,2 While concurrent chemoradiotherapy is the main treatment modality for locally advanced cervical cancer, treatment failure in the central pelvis occurs in approximately 20-25% of patients. 3,4 Cytological tests are commonly inaccurate in detecting locally persistent or recurrent disease because the effect of radiation on the cells may result in ambiguous cell morphology in the early postradiotherapy period.5 Because positive high-risk human papillomavirus (HPV) DNA is considered as an important tool in the diagnosis of both preinvasive and invasive cervical cancer, the usefulness of the HPV test has often also been considered as a method of post-treatment surveillance. Previous studies have examined the effectiveness of the HPV DNA test as a clinically useful marker for detecting residual disease or recurrence after conservative surgical procedures for cervical intraepithelial neoplasia 6-8 and also after radiotherapy. [9][10][11][12] In terms of radiotherapy outcome, several past studies showed that HPV persistence is associated with high rates of local recurrence and poor overall survival in patients with cervical cancer. 10,11 However, the status of HPV DNA was only examined at a single time point after radiotherapy in those studies, and hence, the pattern of HPV clearance after radiotherapy and...
“…First, pathologic confirmation of LN metastasis is available, enabling a more tailored radiotherapy. 8 Because imaging studies, such as CT, MRI, or PET, are inaccurate for predicting LN metastases, primary radiotherapy may result in undertreatment (resulting from a false negative) and overtreatment (resulting from a false positive). 20 As such, radiotherapeutic overtreatment is associated with complications including bowel perforation, and an accurate diagnosis via surgical staging and tailored radiotherapy is essential.…”
Section: Discussionmentioning
confidence: 99%
“…In our institution, a prospective study conducted between 2001 and 2006 demonstrated the feasibility and safety of this strategy. 8 Because radiotherapy and pelvic LND are known risk factors for lymphedema, patients treated with both modalities are expected to experience this complication more frequently. 9 Nevertheless, no previous study has compared the incidence of lymphedema or LEE in cervical cancer patients considering the use of primary versus pretreatment laparoscopic staging followed by radiotherapy.…”
Patients with cervical cancer who underwent radiotherapy after laparoscopic surgical staging more commonly experienced LEE and related symptoms than patients who underwent primary radiotherapy. As LEE decreases patients' quality of life, it should be considered during patient consultation and surveillance.
“…1 Lymph nodes (LNs) metastasis is an important prognostic factor in not only that it is the most significant prognostic factor in early-stage cervical cancer but also that the field of RT depend on the extent of LN involvement. 2 However, the current clinical International Federation of Gynecology and Obstetrics (FIGO) staging system does not consider LN status, 3 which results in some discrepancies between FIGO stage and prognosis. In addition, preoperative imaging studies were not known to be satisfactorily sensitive for detecting LN metastasis in cervical cancer.…”
Objective: This study was designed to evaluate the survival benefit of laparoscopic surgical staging (LSS)-guided tailored radiation therapy (RT) in locally advanced cervical cancer (LACC). Methods: We retrospectively reviewed 89 LACC patients' medical records who primarily received non-surgical treatment, of which pretreatment LSS was performed in 20 (LSS group) and primary chemoradiation therapy (CCRT) without LSS (CCRT group) was carried out in 69 from January 2000 to January 2006. We analyzed clinical characteristics, pretreatment imaging study results and survival outcomes including disease free survival (DFS) and overall survival (OS) to compare them between the two groups. Results: There were as many as eight cases (40%) of LSS related complications. The mean time interval between LSS and RT or CCRT was 26.6 days (±18.8 days). Six out of twenty (30%) in LSS group and 10 out of 69 (14.5%) in CCRT group received extended field RT when paraaortic lymph nodes (LNs) were positive based on the pathologic findings after LSS and the results of imaging studies, respectively. Three-year DFS and OS were both better in 33 imaging-negative CCRT group patients than those in 4 imaging-negative/pathology-positive (false negative) patients after LSS (3-year DFS, 50% vs. 87%, p=0.022; 3-year OS, 50% vs. 84%, p=0.033). The 5-year DFS rates were 52% and 55% in LSS group and in CCRT group, respectively (p=0.28). The 5-year OS rates were 68% in LSS group and 62% in CCRT group without significant difference between the two groups (p=0.79).
Conclusion:We found that LSS-based RT tailoring did not show survival benefit in LACC despite inaccuracy of imaging-based RT tailoring. Further studies are required to find new method to overcome this inaccuracy and improve survival outcomes.
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