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Vulvar CancerNCT00315159

Conservative Management With Isolated Sentinel Lymph Node Biopsy in Vulvar Cancer Patients.

A study testing Sentinel Node Biopsy in people with Vulvar Cancer, run by Women and Infants Hospital of Rhode Island at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to evaluate a less invasive procedure for the evaluation of the inguinal (groin) nodes in patients with a primary squamous cell carcinoma of the vulva. Each patient will undergo a sentinel lymph node dissection as well as resection of the primary tumor on the vulva. Read more about this study

Who is it for?
Ages 18 years and older, women only
Conditions the study is for
Vulvar Cancer
What is being tested?
Sentinel Node Biopsy
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
74 participants
Where
1 siteUnited States
Study dates
Aug 2003to May 2014
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patient of any age 18 years or over.
  • Biopsy proven squamous cell carcinoma of the vulva.
  • Depth of invasion 1mm or greater.
  • Patients with groins clinically negative for nodal metastasis.
  • Patients that are candidates for groin dissections.

Who cannot join

  • Any patient below the age of 18
  • Patients with clinically suspicious groin nodes for metastatic disease.
  • Patients with non-squamous cell vulvar lesions.
  • Depth of invasion less than 1mm.
  • Patients refusing to sign an informed consent form.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Women and Infants' Hospital of Rhode Island

    Providence, Rhode Island, 02905

Other trials in United States

About this study

Official title: Conservative Management With Isolated Sentinel Lymph Node Biopsy in Vulvar Cancer Patients With Sentinel Lymph Nodes Determined to be Negative for Metastatic Disease.

The purpose of this study is to evaluate a less invasive procedure for the evaluation of the inguinal (groin) nodes in patients with a primary squamous cell carcinoma of the vulva. Each patient will undergo a sentinel lymph node dissection as well as resection of the primary tumor on the vulva. Patients who are determined to have sentinel nodes that are negative for metastatic disease will not receive a full groin dissection. Patients who have sentinel lymph nodes that contain metastasis will undergo a complete inguinal dissection. The study will evaluate the long-term outcomes in patients who receive only a sentinel lymph node dissection without a complete dissection. All patients entered onto the study will have a biopsy proven squamous cell carcinoma of the vulva. Each patient will be enrolled by a Gynecologic Oncologist practicing out of Women \& Infants Hospital

Read the detailed description

Conservative Management with Isolated Sentinel Lymph Node Biopsy in Vulvar Cancer Patients with Sentinel Lymph Nodes Determined to be Negative for Metastatic Disease.

Introduction The American Cancer Society estimates there will be 4000 new cases of vulvar cancer for the year 2003(1). The majority of these patients will undergo surgical therapy with groin node dissection to assess the inguinal nodal chain for evidence of metastatic disease. For many years there has been a search for a less radical surgical approach to evaluating the inguinal lymphatic basin. The classic approach to vulvar cancer was an en-bloc resection of the vulva and groins with a single incision. This approach led to complication rates as high as 69% for chronic leg edema and 85 % for wound breakdown(2). In an effort to reduce the morbidity of groin node dissections, the triple incision technique was introduced(3). A GOG study evaluating limited surgery with wide local excision and superficial groin node dissection reported rates of chronic lymphedema of 19% and wound infection and or separation of 29%(4). In their report on penile carcinoma the concept of a sentinel node as the first group of nodes in the inguinal lymphatic chain was put forth by Cabanas et al.(5). Morton and colleagues advanced the technique of sentinel node lymphatic mapping in patients with cutaneous melanoma(6). In 1994 Levenback et al, described of the use of isosulfan blue dye for the detection of sentinel nodes in the inguinal lymphatic chain(7). To date, a number of studies have been performed evaluating the utility of sentinel node technology and its application in vulvar malignancies (Table 1)(7-20). For melanoma, the sentinel node dissection has become the standard of care for the evaluation of the lymphatic basins. Many cancer centers, including Women and Infants' Hospital, use sentinel node dissection for the evaluation of axillary nodes in breast cancer patients as their standard of care. This technology has decreased the rate of chronic arm edema in breast cancer patients.

Inguinal node metastasis in patients with squamous cell carcinoma of the vulva is reported to be as high as 27%(21). Consequently, a large number of patients may undergo a potentially morbid procedure without any gain. Non-invasive methods for the evaluation of the inguinofemoral nodes such as CT, MRI and PET scans have not yet been proven reliable. Sentinel node biopsy utilizing Tc-99m sulfur colloid and isosulfan blue dye allows for evaluation of nodal status in patients with vulvar malignancies through minimally invasive surgery. Our study, at Women and Infants' Hospital, employed Tc-99m sulfur colloid and isosulfan blue dye to identify sentinel nodes in the inguinal lymphatic chain of patients with primary squamous cell carcinoma of the vulva. Twenty nine patients were enrolled and 107 sentinel nodes were studied with no false negative SLN being reported(22) There are over 175 patients in the reported literature who have undergone a SLN dissection for the evaluation of the inguinal lymphatic basin for metastatic disease. To date there have been no false negative SLN reported. We feel the SLN dissection has been proven to be reliable and safe procedure both at our institution and others around the world. Further studies need to be performed in order to evaluate the use of SLN dissection alone in patients with pathologic negative sentinel nodes for metastasis. This study will evaluate the use of sentinel node dissection alone and management of these patients who potentially do not need or will benefit from a full inguinal node dissection.

Sentinel Node Concept Sentinel node dissection was first applied for the evaluation of inguinal nodal basins in patients with penile cancer(23). The sentinel node concept is based on the belief that certain anatomical areas are drained by individual nodal chains with the first lymph node in this chain being the sentinel node. It has been shown the sentinel node is predictive of the status of the lymphatic basin for the presence of metastatic disease to non-sentinel nodes. The use of both lymphazurin blue dye and technetium-99m sulfur colloid has been shown to reliably identify sentinel nodes in many cancers such ad melanoma, breast and colon. This technology has also been studied in patients with vulvar malignancies and has been shown to detect a sentinel node 100% of the time(22). With a limited number of sentinel nodes obtained from a lymphatic basin a more complete pathologic evaluation of the lymph node can be performed. The use of ultra-staging (serial sectioning) allows for smaller metastasis and micrometastasis to be reliably detected. Sentinel lymph node technology will allow for a more complete surgical and pathologic evaluation of the inguinal lymphatic basins with a potential benefit of avoiding a complete inguinal node dissection for patients with a SLN determined to be negative for metastatic disease.

Study Design

This is a prospective trial examining conservative management of patients with inguinal sentinel nodes that have been deemed negative for metastatic disease in patients with primary squamous cell carcinoma of the vulva.

Number of Patients:

The goal of this study is to enroll 100 patients over a 5 year period and follow each for a total of three years.

Sentinel Lymph Node Technique:

Each patient will undergo two intradermal peritumoral injections with a total of 2-3 mCi of unfiltered technetium-99m sulfur colloid in a volume of 1cc, within 24 hours prior to surgery. These injections will take place in the nuclear medicine suite at Rhode Island Hospital under Dr. Richard Noto's supervision. Following the injection of the Tc-99m sulfur colloid a lymphoscintigram will be performed to detect the presence of a sentinel node. Intra-operatively, 5 to 10 minutes prior to the groin dissection, 3 cc of isosulfan blue dye will be injected at the peritumoral edge in a manner and location similar to the Tc-99m sulfur colloid injection. An inguinal dissection will then performed before the radical excision of the vulvar tumor. Prior to the groin node incision, a hand held collimated gamma counter will be used to identify the location of the sentinel node. This area will be marked with ink on the skin surface. An inguinal incision will be made and the inguinal lymphatic beds will be dissected to identify blue afferent lymphatic tracts and/or blue stained lymph nodes. A hand held collimated gamma counter will be used to detect any lymph nodes with increased activity, defined as a count greater than 5 % of that at the injection site, through the groin incision. Also, any lymph node with a blue lymphatic tract leading to it or stained blue will be considered a sentinel node. As well, any lymph node identified with the hand held gamma counter as taking up the Tc-99m sulfur colloid will be considered a hot sentinel node. Each sentinel node will be evaluated with a 10 second gamma count and labeled as hot and blue, hot and non-blue or cold and blue. With completion of the sentinel node groin node dissection, the lymphatic beds will be re-scanned with the gamma counter to ensure all sentinel nodes have been removed. Once the SLN groin dissection is complete the incision will be closed and a full groin dissection will be done at a separate sitting pending the pathologic evaluation of the sentinel lymph node. The remainder of the surgery for the treatment of the primary tumor will then be completed with a current standard of care procedure depending on the size and location of the tumor.

Pathologic Analysis of Sentinel Lymph Nodes:

Each sentinel lymph node will be serially sectioned at 2mm intervals parallel to the long axis and totally submitted for histologic evaluation in one or more blocks. From each block, five slides will be cut at 100 micron intervals and stained with hematoxylin and eosin. A parallel slide at each level will be cut and held for batch cytokeratin AE1/AE3 immunohistochemical staining if negative for metastasis by initial H\&E staining. The largest dimension of each metastasis will be measured and recorded in order to track the presence of micrometastasis defined as a metastatic focus less than 2mm in size.

Patient Management Protocol:

Patients enrolled on to the sentinel lymph node protocol will undergo a sentinel lymph node dissection as described above followed by a radical excision of the primary tumor. Patients with sentinel nodes found to contain metastatic disease from the primary vulvar malignancy will under go a complete inguinal lymph node dissection as per standard care. Patients with sentinel lymph nodes deemed negative for metastatic disease based on ultra-staging and H\&E staining will be followed with conservative management (no further groin node dissection). Each of these patients will be followed clinically at 3 month intervals for the first three years for a total study follow up period of three years. Any patient determined to have a groin recurrence will be treated with current standard of care modalities as appropriate for their recurrence. Published data documenting a 5-7% unanticipated groin failures in patients with negative lymphadenectomies will be used as the comparative outcomes (25).

Conditions
Vulvar Cancer
Being tested
Sentinel Node Biopsy
Keywords
Squamous, Cell, Carcinoma, Vulva, Sentinel Node
Medical subject headings
Vulvar Neoplasms, Carcinoma

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Sentinel Node BiopsyProcedure or surgery

    Inguinal sentinel node biopsy will be performed.

Study groups in NCT00315159
Study groupRoleWhat they receive
No interventionNo interventionPatients with negative SLN will be followed on no intervention arm
Receives: Procedure: Sentinel Node Biopsy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Determination of inguinal recurrence rates in patients with negative sentinel lymph node biopsy alone.

    Measured: Three years

Secondary outcomes (1)
  1. Ability to detect inguinal sentinel nodes in vulvar cancer patients.

    Measured: Three years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Apr 2006 (estimated)
  2. Study startAug 2003
  3. Primary completionMay 2014
  4. Study completionMay 2014

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
74 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00315159
Sponsor's protocol ID
03-0031
Status last verified
Jan 2015
First submitted
13 Apr 2006
Last updated
12 Jan 2015
Results posted
No
Data monitoring committee
Yes

Publications

  • Jemal A, Murray T, Samuels A, Ghafoor A, Ward E, Thun MJ. Cancer statistics, 2003. CA Cancer J Clin. 2003 Jan-Feb;53(1):5-26. doi: 10.3322/canjclin.53.1.5.

    PubMed 12568441
  • Jemal A, Murray T, Ward E, Samuels A, Tiwari RC, Ghafoor A, Feuer EJ, Thun MJ. Cancer statistics, 2005. CA Cancer J Clin. 2005 Jan-Feb;55(1):10-30. doi: 10.3322/canjclin.55.1.10.

    PubMed 15661684
  • Podratz KC, Symmonds RE, Taylor WF, Williams TJ. Carcinoma of the vulva: analysis of treatment and survival. Obstet Gynecol. 1983 Jan;61(1):63-74.

    PubMed 6823350
  • Hacker NF, Leuchter RS, Berek JS, Castaldo TW, Lagasse LD. Radical vulvectomy and bilateral inguinal lymphadenectomy through separate groin incisions. Obstet Gynecol. 1981 Nov;58(5):574-9.

    PubMed 7301232
  • Cabanas RM. An approach for the treatment of penile carcinoma. Cancer. 1977 Feb;39(2):456-66. doi: 10.1002/1097-0142(197702)39:23.0.co;2-i.

    PubMed 837331
  • Morton DL, Wen DR, Wong JH, Economou JS, Cagle LA, Storm FK, Foshag LJ, Cochran AJ. Technical details of intraoperative lymphatic mapping for early stage melanoma. Arch Surg. 1992 Apr;127(4):392-9. doi: 10.1001/archsurg.1992.01420040034005.

    PubMed 1558490
  • Levenback C, Burke TW, Morris M, Malpica A, Lucas KR, Gershenson DM. Potential applications of intraoperative lymphatic mapping in vulvar cancer. Gynecol Oncol. 1995 Nov;59(2):216-20. doi: 10.1006/gyno.1995.0011.

    PubMed 7590476
  • Levenback C, Morris M, Burke TW, Gershenson DM, Wolf JK, Wharton JT. Groin dissection practices among gynecologic oncologists treating early vulvar cancer. Gynecol Oncol. 1996 Jul;62(1):73-7. doi: 10.1006/gyno.1996.0192.

    PubMed 8690296
  • Levenback C. Intraoperative lymphatic mapping and sentinel node identification: gynecologic applications. Recent Results Cancer Res. 2000;157:150-8. doi: 10.1007/978-3-642-57151-0_13.

    PubMed 10857169
  • Levenback C, Coleman RL, Ansink A, van der Zee AG. Re: Terada et al.: Sentinel node dissection and ultrastaging in squamous cell cancer of the vulva. Gynecol Oncol 76:40-44, 2000. Gynecol Oncol. 2000 Jun;77(3):484-5. doi: 10.1006/gyno.2000.5832. No abstract available.

    PubMed 10831370
  • Levenback C, Coleman RL, Burke TW, Bodurka-Bevers D, Wolf JK, Gershenson DM. Intraoperative lymphatic mapping and sentinel node identification with blue dye in patients with vulvar cancer. Gynecol Oncol. 2001 Nov;83(2):276-81. doi: 10.1006/gyno.2001.6374.

    PubMed 11606084
  • Decesare SL, Fiorica JV, Roberts WS, Reintgen D, Arango H, Hoffman MS, Puleo C, Cavanagh D. A pilot study utilizing intraoperative lymphoscintigraphy for identification of the sentinel lymph nodes in vulvar cancer. Gynecol Oncol. 1997 Sep;66(3):425-8. doi: 10.1006/gyno.1997.4798.

    PubMed 9299256
  • Terada KY, Coel MN, Ko P, Wong JH. Combined use of intraoperative lymphatic mapping and lymphoscintigraphy in the management of squamous cell cancer of the vulva. Gynecol Oncol. 1998 Jul;70(1):65-9. doi: 10.1006/gyno.1998.5035.

    PubMed 9698476
  • de Hullu JA, Doting E, Piers DA, Hollema H, Aalders JG, Koops HS, Boonstra H, van der Zee AG. Sentinel lymph node identification with technetium-99m-labeled nanocolloid in squamous cell cancer of the vulva. J Nucl Med. 1998 Aug;39(8):1381-5.

    PubMed 9708512
  • Echt ML, Finan MA, Hoffman MS, Kline RC, Roberts WS, Fiorica JV. Detection of sentinel lymph nodes with lymphazurin in cervical, uterine, and vulvar malignancies. South Med J. 1999 Feb;92(2):204-8. doi: 10.1097/00007611-199902000-00008.

    PubMed 10071668

Questions about this trial

What is this clinical trial studying?

A study testing Sentinel Node Biopsy in people with Vulvar Cancer, run by Women and Infants Hospital of Rhode Island at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 12 Jan 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Determination of inguinal recurrence rates in patients with negative sentinel lymph node biopsy alone. (time frame: Three years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00315159, which also lists 24 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Jan 2015.

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