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Study to Determine the Feasibility of Sentinel Node Biopsy in Patients With Anal Cancer

R-SeNSAR Feasibility Study: The Role of Sentinel Node Biopsy in Patients With Anal Cancer

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02162641
Acronym
R-SeNSAR
Enrollment
0
Registered
2014-06-13
Start date
2014-09-30
Completion date
2015-05-31
Last updated
2015-06-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Squamous Cell Carcinoma of the Anus

Brief summary

The purpose of this study is assess the technical and operational feasibility of a specialised biopsy technique, sentinel lymph node biopsy (SLNB), in patients with anal cancer.

Detailed description

SLNB is based on the premise that lymphatic dissemination from a tumour occurs in a stepwise fashion, with initial involvement of a primary node, called the sentinel node, before dissemination to the remainder of the lymphatic chain. If the sentinel node is histologically negative, then the remainder of the nodes in the same anatomic region will be at a lower (assumed to be minimal) risk of containing metastases. SLNB is part of standard care for patients with malignant melanoma and with breast cancer but has yet to be prospectively evaluated in patients with anal cancer. Currently, the standard way to treat patients with anal cancer is to deliver a combination of chemotherapy and radiation to the tumour at the anus together with 'preventative' (prophylactic) radiotherapy to the lymph glands of the groin and pelvis. There is a growing perception for the need to reduce the morbidity of radiotherapy i.e. current regimens over-treat the patient and one approach is to reduce radiotherapy volume and/or dose where there is an absence or very low risk of nodal metastases. This feasibility study is a vital first step in informing the design of a larger study examining the role of SLNB in clinical decision-making and outcomes for patients with anal cancer. In this trial eligible patients will attend for lymphoscintigraphy, to locate the lymph node, before sentinel lymph node removal by surgery. Detection rate of the sentinel node(s) will be the key outcome for the study.

Interventions

PROCEDURESentinel lymph node biopsy

Sponsors

The Christie NHS Foundation Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with squamous cell carcinoma (SCC) of the anus (any T size and/or those with recurrent disease) * Equivocal lymph node involvement on standard CT staging or magnetic resonance (MR) staging or PET-CT scan, as determined by the anal cancer multidisciplinary team (MDT) * Age \>= 18 years * Written informed consent provided by the patient

Exclusion criteria

* Patients with unequivocal lymph node involvement on standard CT staging or MR staging, as determined by the anal cancer MDT. * Unfit for surgical biopsy * Patients undergoing palliative treatment * Previous pelvic or inguinal area radiotherapy * Other coincident cancers * Previous inguinal surgery (e.g. hernia repair) with mesh insertion

Design outcomes

Primary

MeasureTime frame
The proportion of nodes detected will be expressed per inguinal nodal basin and per number of patientsDay 0 (Day of SLNB)

Secondary

MeasureTime frameDescription
Micro-metastatic disease within sentinel nodesDays 7 to 10
Surgical complicationsUp to 15 weeks after SLNBTo include wound healing assessment and assessment of pain
Delays in receiving radiotherapy treatment15 weeks after SLNBAny delay greater than 37 days from presentation to treatment

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026