Added-value of SPECT/CT in Patients Undergoing LM/SL for Gynecological Cancers

This study has been completed.
Sponsor:
Collaborator:
University of Western Ontario, Canada
Information provided by (Responsible Party):
Irina Rachinsky, Lawson Health Research Institute
ClinicalTrials.gov Identifier:
NCT00773071
First received: July 25, 2008
Last updated: June 7, 2012
Last verified: June 2012
  Purpose

Nodal staging is a key-step in pre-treatment assessment of gynecological cancers. In recent years, lymphatic mapping and sentinel lymphadenectomy (LM/SL) as a minimally invasive pelvic lymph nodes staging has been successfully evaluated in women with early stage of vulvar cancer, cervical cancer, and endometrial cancer. Such a technique may offer several valuable advantages: a) it is readily applicable in clinical routine using a safe, inexpensive, and reproducible protocol; b) it may help to avoid the cost and the morbidity of unnecessary lymphadenectomy in the majority of cases with uninvolved sentinel lymph nodes; c) it has the potential to guide the surgeon to nodal regions that are not routinely dissected (i.e. pre-sacral, para-aortic nodes) and to identify micro-metastases that would have been ignored otherwise; d) it also offers the basis for sophisticated pathological analysis to detect sub-microscopic nodal metastases using either immunohistochemical or molecular biological techniques.

So far, within the abdomen and the pelvis, the LM/SL technique alone is often blinded to the accurate localization of SLNs. The integration of computed tomography (CT) to single photon emission computed tomography (SPECT) devices in a single gantry (SPECT/CT) has allowed a significant gain in terms of diagnostic accuracy and anatomic precision; clinical examples include malignant melanoma, head and neck cancer, breast cancer, and bladder cancer. In a seminal series of 26 patients with cervical cancer (Zhang et al., 2006), SPECT/CT was recently found superior to conventional planar imaging for detection of SLN and accurate localization. A more recent study (Kushner al., 2007) has also highlighted the technical feasibility and the clinical added-value of a low-dose SPECT/CT in a series of 20 patients with early stage cervical cancer (IA2-IIA) who underwent LM/SL.

In the light of the encouraging data from literature and our own preliminary clinical experience, we hypothesized that the use of LM/SL plus SPECT/CT may be of clinical interest in patients with gynecological cancers.


Condition Intervention
Cervical Cancer
Vulvar Cancer
Device: SPECT/CT guided LM/SL

Study Type: Interventional
Study Design: Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Diagnostic
Official Title: Added-value of SPECT/CT in Patients Undergoing Lymphatic Mapping and Sentinel Lymphadenectomy (LM/SL) for Gynecological Cancers

Resource links provided by NLM:


Further study details as provided by Lawson Health Research Institute:

Primary Outcome Measures:
  • Sensitivity, predictive value, anatomic localization, and impact on management of SPECT/CT guided LM/SL versus CLND [ Time Frame: 6 months -1 year ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Patient tolerability and operating time for SPECT/CT guided LM/SL versus CLND [ Time Frame: 6 months - 1 year ] [ Designated as safety issue: Yes ]

Enrollment: 15
Study Start Date: April 2008
Study Completion Date: February 2012
Primary Completion Date: February 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: A

Single photon emission computed tomography/computed tomography (SPECT/CT) guided lymphatic mapping and sentinel lymphadenectomy (LM/SL) vs. complete lymph node dissection (CLND)

All cervical cancer and vulvar cancer patients will undergo CLND according to the standard of care in gynecologic cancers as recommended by the International Federation of Gynecology and Obstetrics (FIGO).

Patients with FIGO IA2 and IB1 cervical cancers will be scheduled for radical hysterectomy and pelvic lymph node dissection.

Patients with FIGO IB and II vulvar cancers and those of patients with FIGO III with clinically negative regional lymph nodes will be scheduled for vulvectomy and inguinal lymph node dissection.

Device: SPECT/CT guided LM/SL
Pre-operatively, SLNs will be detected by low-dose SPECT/CT (99mTc-cystein rhenium colloids, 1cc/1mCi). Intra-operatively, a blue-dye (Patent Blue, 2cc) and a gamma-probe guidance will be used to detect the SLN nodes. All blue-stained and/or hot lymph nodes with a radioactivity greater than 10% of the hottest node will be considered as SLNs. Serial sections of SLNs will be analyzed by H-E staining. In cases of negative H-E, the SLNs will be further analyzed by immunochemistry (CKAE1/CKAE3, and high molecular weight Cytokeratin 34BE12). Non-SLNs will be analyzed as usual in routine by H-E.
Other Name: Sentinel lymph node detection

Detailed Description:

This clinical trial is aimed at assessing the utility of a minimally invasive surgery preoperatively guided by a new nuclear medicine imaging procedure called SPECT/CT. In patients suffering from an early stage of gynecological cancer with no clinical evidence of lymph node involvement, there is theoretically no reason to perform systematically an aggressive lymphadenectomy as demonstrated for other types of lymphophilic cancers such as malignant melanoma, breast cancer, and head and neck cancer.

We plan to follow a well known and safe procedure in Nuclear Medicine called lymphatic mapping and sentinel lymphadenectomy (LM/SL). The patient will be injected by the gynecologist referee in the department of Nuclear Medicine. These injections consist of a radioactive tracer routinely used in Nuclear Medicine, which allows the detection of the first nodes draining the primary tumor. The so-called sentinel lymph node (SLN) may be different from the lymph nodes anatomically predefined. As well demonstrated for other cancers, including those mentioned above, we hypothesized that the histological status of the SLN may accurately reflect the histological status of the entire nodal basin. If this assumption is clinically validated, the minimally invasive procedure may avoid the cost and the morbidity of unnecessary complete lymph node dissections in the majority of patients with uninvolved SLNs.

The originality of this clinical trial also relies upon the use of a new hybrid imaging device called SPECT/CT, which allows the ability to obtain in a single study both functional and anatomical information. This is critical to precisely guide the surgeon in his task. No contrast medium will be injected during this study. The radiation exposure remains within the limits accepted worldwide; for instance, the CT dose index (CTDI) will be 3.0 mGy, which is in the order of the yearly natural background radiation exposure (< 2mSv).

In this clinical trial, all patients will be treated according to the standard of care currently applied for gynecological cancers. Therefore, either the hysterectomy or the vulvectomy will be followed by a complete lymph node dissection (CLND).

Overall, the research protocol will be carried out in a 1-day protocol including the SPECT/CT guided LM/SL and the CLND.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients with histologically proven gynecological cancers
  • Patients with FIGO IA2 and IB1 cervical cancers
  • Cervical cancer patients will be scheduled for radical hysterectomy and pelvic lymph node dissection
  • Patients with FIGO IB and II vulvar cancers and those of patients with FIGO III with clinically negative regional lymph nodes
  • Vulvar cancer patients will be scheduled for vulvectomy and inguinal lymph node dissection
  • Informed consent signed by the patient, the gynaecologist, and the nuclear medicine physician referees

Exclusion Criteria:

  • Patients with no histological evidence of gynecological cancer
  • Patient with regionally advanced disease or metastatic disease
  • Patients with clinically and/or radiologically evident regional lymph node metastases
  • Patients who are not scheduled for radical surgery and lymph node dissection
  • Patients with physical and/or psychological contraindications
  • Recent study in Nuclear Medicine with long half-time isotopes (i.e. T ½ >48h; 111In, 67Ga, 201Tl, 131I ) performed within 1 week preceding the LM/SL
  • Pregnant or lactating patients
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00773071

Locations
Canada, Ontario
375, South Street Hospital - Dpt. of Nuclear Medicine
London, Ontario, Canada, N6A4G5
Sponsors and Collaborators
Lawson Health Research Institute
University of Western Ontario, Canada
Investigators
Principal Investigator: Irina Rachinsky, MD, MSc The University of Western Ontario - Nuclear Medicine
Study Chair: Jean-Luc Urbain, MD, PhD The University of Western Ontario - Nuclear Medicine
Study Director: Monique Bertrand, MD, PhD The University of Western ontario - Gynaecology
Study Director: Helen Ettler, MD The University of Western Ontario -Pathology
  More Information

Additional Information:
Publications:

Responsible Party: Irina Rachinsky, Principal Investigator, Lawson Health Research Institute
ClinicalTrials.gov Identifier: NCT00773071     History of Changes
Obsolete Identifiers: NCT00972166
Other Study ID Numbers: R-06-377, 12576
Study First Received: July 25, 2008
Last Updated: June 7, 2012
Health Authority: Canada: Ethics Review Committee

Keywords provided by Lawson Health Research Institute:
Cervical cancer, vulvar cancer, LM/SL, SPECT/CT

Additional relevant MeSH terms:
Uterine Cervical Neoplasms
Vulvar Neoplasms
Uterine Neoplasms
Genital Neoplasms, Female
Urogenital Neoplasms
Neoplasms by Site
Neoplasms
Vulvar Diseases
Uterine Cervical Diseases
Uterine Diseases
Genital Diseases, Female

ClinicalTrials.gov processed this record on August 20, 2014