Para-Aortic Lymph Nodal Staging and Evaluation of Treatment Outcome by 18F-Fluorodeoxyglucose Positron Emission Tomography (FDG-PET) in Advanced Cancer Cervix

The recruitment status of this study is unknown because the information has not been verified recently.
Verified July 2008 by Tata Memorial Hospital.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Tata Memorial Hospital
ClinicalTrials.gov Identifier:
NCT00193752
First received: September 13, 2005
Last updated: July 14, 2008
Last verified: July 2008
  Purpose

18F-fluorodeoxyglucose Positron Emission Tomography (FDG-PET) Imaging has been extensively used in the evaluation of various malignancies and is rapidly being recognized as a mandatory investigations. 18F-fluorodeoxyglucose Positron Emission Tomography (FDG-PET) Imaging has also been tried in cervical cancers with excellent results for detection of both pelvic and extra-pelvic disease in terms of sensitivity and specificity. Till date, PET Imaging has been reported to have highest sensitivity and specificity for detection of disease and treatment failures compared to other non-invasive investigations available. Treatment decisions (Localized RT Vs Extended RT) will be according to the results of PET Scans. The treatment response, outcome and follow-up will be labelled according to the PET Scan results and will be directed for treatment accordingly.


Condition Intervention Phase
Cancer of Cervix
Other: PET IMAGING
Phase 2

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Para-Aortic Lymph Nodal Staging and Evaluation of Treatment Outcome by 18F-Fluorodeoxyglucose Positron Emission Tomography (FDG-PET) in Advanced Cancer Cervix

Resource links provided by NLM:


Further study details as provided by Tata Memorial Hospital:

Primary Outcome Measures:
  • PET Scan for Para-Aortic Staging in Carcinoma Cervix [ Time Frame: 5 years ] [ Designated as safety issue: No ]
  • Clinical (FIGO), MRI, and PET - Abdomen and Pelvis Correlation [ Time Frame: 5 years ] [ Designated as safety issue: No ]
  • Volumetric Correlation of Local Disease by PET and MRI [ Time Frame: 5 years ] [ Designated as safety issue: No ]
  • Radiotherapy Response Evaluation and Post therapy Surveillance by serial PET Scans [ Time Frame: 5 years ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • overall survival [ Time Frame: 5 years ] [ Designated as safety issue: No ]

Estimated Enrollment: 100
Study Start Date: September 2005
Estimated Study Completion Date: September 2010
Intervention Details:
    Other: PET IMAGING
    PET imaging in cervical cancers to predict, prognosticate outcome in cervical cancers
  Hide Detailed Description

Detailed Description:

BACKGROUND AND RATIONALE:

Carcinoma Cervix is the commonest malignancy and a leading cause of cancer mortality seen in Indian women. At Tata Memorial Hospital, Carcinoma Cervix constitutes approximately 10% of all cancers (1). Nearly 85% of the patients present with advanced stages (FIGO Stage II/III). The main stay of treatment has traditionally been radical radiation therapy with 80-90% of patients requiring radiation in their lifetime and over decades the survival rates have achieved a plateau of 30 - 55% at 5 years. In patients with advanced stages (stages IIB to IVA), 15 - 38% have para-aortic lymph nodal metastases (2). Identification of para-aortic nodal status allows modification of radiation therapy fields to include this nodal disease, which, because of intestinal morbidity, is not routinely included in the treatment field by most of the Radiation Oncologists. Extended field radiation therapy that includes the para-aortic nodes is associated with a 31% to 50% 5 year-survival, depending on the location and extent of para-aortic nodal metastasis and the likelihood of controlling the pelvic disease (3-5) Therefore, in advanced cervical cancer, it has been reported that progression-free survival is significantly related to para-aortic lymph node metastasis (6-8). In a collective series of Gynecologic Oncology Group protocols, Para aortic nodal status was the most significant indication of recurrence (6).

A number of noninvasive modalities have been used to evaluate the status of para-aortic nodal metastasis. The introduction of Computed Tomographic (CT) Scanning in the mid-1970s provided a method of para-aortic nodal disease evaluation (9). CT Scanning has been widely used for clinical staging, but its sensitivity for nodal metastasis is only 44% (10). In contrast to CT, which primarily relies on the morphologic criteria, FDG-PET can non-invasively assess metabolic activity in cancers and metastatic lesions. The differentiation capability for malignant lesions of FDG-PET is not compromised by using morphologic size criteria. Even malignant lesions less than 1 cm in diameter that manifest high FDG uptake can be differentiated from nonmalignant tissue by using PET. Therefore, FDG-PET can detect metastatic para-aortic lymph nodes in patients with advanced cervical cancer whose lymph nodes have not been abnormally enlarged.

Many published data have previously reported the clinical value of 18F FDG PET for imaging the primary tumor, staging the nodal and visceral involvement, and also detecting a recurrent disease (11-19). Rose et al. (11) used FDG-PET for evaluating nodal metastasis in locally advanced cervical cancer before surgical staging, with a sensitivity of 75% and a specificity of 92% to detect the metastases of para-aortic lymph nodes. They found that the accuracy of FDG-PET was greater than that of CT in detecting the para-aortic lymph nodal metastasis. In a similar series, Wu et al. have reported a sensitivity of 85.7%, a specificity of 94.4%, and an accuracy of 92% with FDG PET to detect para-aortic lymph nodal metastasis in patients with advanced cervical cancer and negative abdominal CT findings. Grigsby et al. (12) demonstrated that FDG-PET detects more abnormal lymph node regions than does CT, and that FDG-PET findings are a better predictor of survival than those of CT in patients with cervical cancer.

Magnetic Resonance Imaging (MRI) has also been reviewed in evaluating both the primary disease at cervix and also para-aortic nodal staging. MRI has been recognized as an important imaging modality for the management of cervical cancer because of its multiplanar capability, distinct tissue contrast characteristics using various pulse sequences, and excellent tissue contrast, particularly between tumor and surrounding normal tissues. However, PET findings were most often compared to CT results, while MRI is nowadays considered as the modality of choice for staging the primary tumor (20,21). Only one study by Narayan et al. has compared the respective value of MRI and PET for staging loco-regionally advanced cervical cancer (22). Their study found that the primary tumor was similarly detected by the two imaging techniques with a sensitivity of 100%. On the other hand, except for small-volume metastases, PET had a sufficiently high positive predictive value (91%) in the pelvis and para-aortic region, to obviate lymph node sampling. More recent studies have shown that the 3D quantitative imaging-based method of tumor size assessment using MRI is highly accurate in determining actual tumor size and extent (23-27) and may be superior to clinical palpation in predicting local tumor control (23,25,28) Conversely, MRI accuracy was insufficient for nodal management. If MRI remains the modality of choice for evaluating the loco-regional status of the primary tumor, metabolic imaging i.e FDG PET seems particularly useful for staging, in one session, extra pelvic nodal metastases. Thus, PET may have a significant impact on treatment decision-making.

Identification of para-aortic nodal status allows modification of radiation therapy fields to include this nodal disease. Stehman et al. previously demonstrated the prognostic importance of para-aortic nodal status in locally advanced cervical carcinoma (6). In advanced cervical cancer, it has been reported that progression-free survival is significantly related to para-aortic lymph node metastasis (6-8). Recent studies have shown a survival benefit in patients with positive para-aortic nodes treated by extended-field irradiation and concurrent radio-sensitizing chemotherapy (29-31).

PET is also of great value for optimally confirming a complete remission and detecting a recurrence non-invasively in post-treatment follow-up. More recently, positron emission tomography (PET) with the glucose analogue, 18 F-fluorodeoxyglucose (FDG) has demonstrated promising results in evaluating tumor response and predicting survival after primary treatment with radiation therapy or chemotherapy for several tumor types, including head-and-neck cancer, breast cancer, seminoma, colorectal cancer, lymphoma, and lung cancer (33-40). Recently, Grigsby et al have reported the role of FDG PET in posttherapy surveillance monitoring in a series of 75 patients with cervical cancer. They have concluded that FDG-PET is a valuable tool to evaluate the response of both at primary and its lymph node disease after radiation therapy and chemotherapy and for the Post-Rx surveillance of patients to detect asymptomatic recurrence (41).

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

Patients with hisotologically proven cervical cancers with FIGO II-IIIB eligible for the study will be invited for the study

Criteria

Inclusion Criteria:

  • Histologically proven squamous carcinoma or adenocarcinoma of cervix
  • Performance index WHO grade 0 or 1
  • Patients below 65 years of age
  • FIGO Stage IIB / IIIB
  • Normal ECG and Cardiovascular system
  • Normal hematological parameters
  • Normal renal and liver function tests
  • Normal Blood Sugar levels / Controlled Diabetes

Exclusion Criteria:

  • Co-morbid conditions like medical renal disease
  • Past History of Phobia for MRI Examination
  • Medical or Psychological condition that would preclude Investigations / Treatment
  • H/o Previous treatment / Pregnancy
  • Patient unreliable for treatment completion and follow-up Investigations.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00193752

Contacts
Contact: Shyamkishore J Shrivastava, MD, DNB(RT) +91-22-2417 7163 sshyam@mtnl.net.in
Contact: Umesh M Mahantshetty, MD, DNB (RT) +91-22-2417 7168 drumeshm@yahoo.com

Locations
India
Tata Memorial Hospital Recruiting
Mumbai, Maharastra, India, 400 012
Contact: Shyamkishore J Shrivastava, MD, DNB (RT)    +91-22-2417 7163    sshyam@mtnl.net.in   
Contact: Umesh M Mahantshetty, MD, DNB (RT)    +91-22-2417 7168    drumeshm@yahoo.com   
Principal Investigator: Shyamkishore J Shrivastava, MD, DNB (RT)         
Sponsors and Collaborators
Tata Memorial Hospital
Investigators
Principal Investigator: Shyamkishore J Shrivastava, MD, DNB (RT) Professor & Head, Radiation Oncology, Tata Memorial Hospital
  More Information

No publications provided

Responsible Party: Dr SK Shrivastava, Tata Memorial Hospital
ClinicalTrials.gov Identifier: NCT00193752     History of Changes
Other Study ID Numbers: TMH/205/2004/Cx_PET STUDY
Study First Received: September 13, 2005
Last Updated: July 14, 2008
Health Authority: India: Department of Atomic Energy

Keywords provided by Tata Memorial Hospital:
FDG-PET Imaging
Cervical Cancer
Post-treatment evaluation
Para-aortic Nodal Staging
Extended field Radiation
Extended field IMRT
Cancer of the Cervix
Cervix Cancer

Additional relevant MeSH terms:
Uterine Cervical Neoplasms
Uterine Neoplasms
Genital Neoplasms, Female
Urogenital Neoplasms
Neoplasms by Site
Neoplasms
Uterine Cervical Diseases
Uterine Diseases
Genital Diseases, Female
Fluorodeoxyglucose F18
Radiopharmaceuticals
Diagnostic Uses of Chemicals
Pharmacologic Actions
Molecular Mechanisms of Pharmacological Action

ClinicalTrials.gov processed this record on September 14, 2014