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Role of Antisecretory Factor in Curative Radiochemotherapy for Anal Carcinoma

A Randomized Phase 2 Double-blind Placebo-controlled Trial Investigating the Effect of Salovum™ and SPC-flakes on Radiochemotherapy Induced Toxicity in Curative Treatment of Anal Carcinoma

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05351931
Acronym
SALFLAC
Enrollment
38
Registered
2022-04-28
Start date
2022-06-30
Completion date
2024-03-31
Last updated
2022-04-28

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

Conditions

Anal Cancer

Keywords

Radiochemotherapy, Adverse event, Antisecretory factor

Brief summary

Curative radiochemotherapy (RCT) for anal carcinoma (AC) is associated with considerable acute and long-term toxicity. The acute toxicity derives from the combined effects of radiation and chemotherapy and is dominated by localized skin mucositis, diarrhoea and pain from radiation and nausea, fatigue, anemia/leukopenia, diarrhoea and general skin dryness from chemotherapy. Cholera induced diarrhoea, as well as other forms of diarrhoea-inducing agents, has been shown to elicit a stimulated, endogenous production of a protein, named antisecretory factor (ASF). This protein has been chemically characterized in detail. ASF acts by modulating secretion of water and ions but also counteracts inflammatory processes. With this background the present study will investigate if induction of endogenous ASF by intake of SPC-flakes might be beneficial in AC patients to prevent RCT induced adverse events (AEs) and if administration of ASF from Salovum provides additional benefit (explorative).

Detailed description

Curative RCT for AC is associated with considerable acute and long-term toxicity. The acute toxicity derives from the combined effects of radiation and chemotherapy and is dominated by localized skin mucositis, diarrhoea and pain from radiation and nausea, fatigue, anemia/leukopenia, diarrhoea and general skin dryness from chemotherapy. These adverse effects are treated symptomatically with mostly modest effect and sometimes leads to the need for in-patient care and temporary stop of the RCT. Long-term toxicity is caused by radiation fibrosis and is dominated by impaired anal sphincter function leading to faeces incontinence, pelvic pain and reduced sexual function. Thus, new ways to efficiently counteract the RCT induced adverse effects are urgently needed. Cholera induced diarrhoea, as well as other forms of diarrhoea-inducing agents, has been shown to elicit a stimulated, endogenous production of a protein, named antisecretory factor (ASF). This protein has been chemically characterized in detail. ASF acts by modulating secretion of water and ions but also counteracts inflammatory processes . ASF is also produced by hens fed on a diet of fermented grains or a specific diet of sugars and amino acids, leading to an accumulation of the ASF protein in the egg yolk. Spray dried yolk in the form of a powder is commercialized as Salovum registered by the EU authorities as Food for specific medical purposes, i e is not adrug from a regulatory perspective. Salovum rapidly increase the plasma (P-) ASF-concentration. Another way to increase ASF and, thus, to achieve benefit, is to induce its production/conversion by ingestion of oat flakes, specially processed (similar to malting) to contain the proper mix of sugars and amino acids. Such flakes are also commercially available (named SPC flakes) as Food for specific medical purposes and has been recommended or considered for a number of secretory pathological conditions, e g for treatment of Mb Meniére. With this background the present study will investigate if induction of endogenous ASF by intake of SPC-flakes might be beneficial in AC patients to prevent RCT induced adverse events (AEs) and if administration of ASF from Salovum provides additional benefit (explorative).

Interventions

DIETARY_SUPPLEMENTSalovum and SPC-flakes or corresponding placebo

Salovum and SPC-flakes are foods approved for specific medical purposes.

Sponsors

Lantmännen AB
CollaboratorUNKNOWN
Sjöbergstiftelsen
CollaboratorUNKNOWN
Onkologiska klinikens forskningsfond
CollaboratorUNKNOWN
Swedish Cancer Society
CollaboratorOTHER
Uppsala University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Placebo similar to active study products

Intervention model description

Randomized parallel two groups

Eligibility

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

Inclusion criteria

1. Age ≥ 18 years. 2. Histologically confirmed diagnosis of AC irrespective of tumour p16-status. 3. Planned for curative RCT according to national care programme schedule B 4. WHO performance status of 0 or 1. 5. For patients planned for schedule C, they must be unsuitable for or not consenting to participation in the SWANCA trial. 6. Able to understand study information and questionnaires and provide signed informed consent.

Exclusion criteria

1. Patients with stoma. 2. Contraindications to the investigational product, e g known or suspected hypersensitivity to the investigational products or expected inability to their use in accordance with the protocol. 3. Contraindications to curative RCT in accordance with AC national care programme. 4. Lack of suitability for participation in the study, e g expected difficulties to follow the protocol procedures, as judged by the investigator. 5. Prior exposure to Salovum or SPC-flakes.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of diarrhoea, fecal urgency, anal skin toxicity/mucositis and anal pain CTCAEv5.0 ≥ grade 2 during and up to 6 months after RCT. Anal skin toxicity/mucositis is to be verified by photos.Through study completion, approximately 6 monthsTreatment related toxicity

Secondary

MeasureTime frameDescription
Incidence and severity of other AEs according to CTCAEv5.0 during and up to 6 months after RCT.Through study completion, approximately 6 monthsOther treatment related toxicity
Change from baseline in patient reported hQoL and abdominal symptoms assessed by EORTC QLQ- 30 and the ANL27 subscale questionnaires as well as the Bristol Stool Form Scale.Through study completion, approximately 6 monthsPROMS
Increase in plasma (P)-ASF concentration from baseline to the day of start of RCT and to the end of treatment.Days -1, 6 and 42Pharmacodynamic outcome and compliance check
Differences in primary and secondary endpoints between Salovum and placebo subgroups.Through study completion, approximately 6 monthsAssessment of added value of Salovum
Tumour response rate according to RECIST v1.1 and clinical examination at 2, 3 (radiology) and 6 months after stop of RCT.Through study completion, approximately 6 monthsAssessment of benefit, if any, from study products on clinical outcome
Disease free and overall survival at 3 and 6 months after stop of RCT.At 3 and 6 months after stop of treatmentAssessment of benefit, if any, from study products on clinical outcome
Relationships between P-ASF concentration, biomarkers reflecting inflammation and adverse events.Through study completion, approximately 6 monthsBiomarker assessments

Other

MeasureTime frameDescription
Incidence of AEs CTCAEv5.0 grade ≥ 2 considered probably related to investigational products/placebo.Through study completion, approximately 6 monthsAdverse effects from study products

Contacts

Primary ContactPeter Nygren, MD
peter.nygren@igp.uu.se+46704250719

Outcome results

None listed

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