Status:
RECRUITING
Combination of Spartalizumab, mDCF and Radiotherapy in Patients With Metastatic Squamous Cell Anal Carcinoma
Lead Sponsor:
Centre Hospitalier Universitaire de Besancon
Collaborating Sponsors:
National Cancer Institute, France
Novartis
Conditions:
Squamous Cell Anal Carcinoma
Metastatic Squamous Cell Carcinoma
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
This study evaluates the feasibility of the combination of radiotherapy, chemotherapies (docetaxel, cisplatin and 5-fluorouracil) and spartalizumab (anti-PD-1 therapy) in patients with metastatic squa...
Detailed Description
In SCCA (squamous cell carcinoma of anus) about 15% of patients are diagnosed in metastatic stage, and around 25-40% of patients will experience disease progression after curative intent chemoradiothe...
Eligibility Criteria
Inclusion
- Male or female, aged ≥18 years,
- Performance status Eastern Cooperative Oncology Group World Health Organization (ECOG-WHO) ≤1,
- Histologically proven metastatic or locally advanced recurrent squamous cell carcinoma of anus (SCCA)
- Presence of a evaluable lesion on CT-scan/MRI assessed by RECIST v1.1 criteria,
- Patient eligible to the mDCF regimen
- CT scan performed within 30 days prior inclusion,
- PET scan performed within 30 days prior inclusion
- Life expectancy ≥12 months,
- Adequate organ and marrow function, based upon meeting all of the following laboratory criteria within 14 days before first dose of study treatment:
- Absolute neutrophil count (ANC) ≥ 1500/mm3 (≥ 1.5 GI/L) without granulocyte colony-stimulating factor support.
- White blood cell count ≥ 2500/mm3 (≥ 2.5 GI/L).
- Platelets ≥ 100,000/mm3 (≥ 100 GI/L) without transfusion.
- Hemoglobin ≥ 9 g/dL (≥ 90 g/L).
- Alanine aminotransferase (ALT), aspartate aminotransferase (AST) ≤ 3 x upper limit of normal (ULN), or ≤ 5 x ULN with documented liver metastases.
- Total bilirubin ≤ 1.5 x ULN (for subjects with Gilbert's disease ≤ 3 x ULN).
- Serum albumin ≥ 2.8 g/dl.
- Calculated creatinine clearance ≥ 60 mL/min (using the MDRD formula):
- Urine protein/creatinine ratio (UPCR) ≤ 1 g/g
- Signed and dated informed consent, to participate indicating that the subject has understood the purpose and the procedures required by the study and that he agrees to participate in the study and to comply with the requirements and restrictions inherent in this study
- Patient affiliated to or beneficiary of French social security system
- Ability to comply with the study protocol, in the Investigator's judgment
Exclusion
- HIV positive patient , CD4 count \< 400 cells/mm3 (HIV test mandatory before inclusion)
- Diagnosis of additional malignancy within 2 years prior to the inclusion with the exception for superficial skin cancers, or localized, low grade tumors deemed cured and not treated with systemic therapy,
- Any medical or psychiatric condition or disease, which would make the patient inappropriate for entry into this study,
- Current participation in a study of an investigational agent or in the period of exclusion,
- Receipt of any type of cytotoxic, biologic or other systemic anticancer therapy (including investigational) within 4 weeks before first dose of study treatment,
- Radiation therapy for bone metastasis within 2 weeks, any other radiation therapy within 4 weeks before first dose of study treatment. Systemic treatment with radionuclides within 6 weeks before the first dose of study treatment. Subjects with clinically relevant ongoing complications from prior radiation therapy are not eligible,
- Pregnancy, breast-feeding or absence/refusal of adequate contraception for fertile patients during the period of treatment and for 6 months from the last treatment administration,
- Patient under guardianship, curatorship or under the protection of justice.
- Inability to perform radiotherapy
- Untreated or symptomatic central nervous system (CNS) lesion. However, patients are eligible if: a) all known CNS lesions have been treated with radiotherapy or surgery and b) patient remained without evidence of CNS disease progression ≥ 4 weeks after treatment and c) patients must be off corticosteroid therapy for ≥ 2 weeks
- Use of hematopoietic colony-stimulating growth factors (e.g. G-CSF, GMCSF, M-CSF), thrombopoietin mimetics or erythroid stimulating agents ≤ 2 weeks prior start of study treatment. If erythroid stimulating agents were initiated more than 2 weeks prior to the first dose of study treatment and the patient is on a stable dose, they can be maintained.
- Use of any live vaccines against infectious diseases within 4 weeks of initiation of study treatment
- Elevated Cardiac troponin T (cTnT) or cardiac troponin I (cTnI) elevation \> 2x ULN
- Systemic chronic steroid therapy (\> 10mg/day prednisone or equivalent) or any immunosuppressive therapy 7 days prior to planned date of first dose of study treatment.
- Note: Topical, inhaled, nasal and ophthalmic steroids are allowed. For patients with adrenal insufficiency, replacement dose of prednisone \> 10 mg/ day or equivalent are permitted
- Active, known or suspected autoimmune disease or a documented history of autoimmune disease Note: Patients with vitiligo, controlled type I diabetes mellitus on stable insulin dose, residual autoimmune-related hypothyroidism only requiring hormone replacement or psoriasis not requiring systemic treatment are permitted.
- Allogenic bone marrow or solid organ transplant
- History of severe hypersensitivity reactions to other monoclonal antibodies, which in the opinion of the investigator may pose an increased risk of serious infusion reaction
- Pre-existing neuropathy, hearing problem, or cardiorespiratory pathology, which prevent the administration of cisplatin.
- clinically significant active heart disease or myocardial infarction within 6 months
- recent or concomitant treatment with brivudine
- persistent toxicities related to prior treatment of grade greater than 1
- History or current interstitial lung disease or non-infectious pneumonitis
- History of major surgery within 28 days before treatment
- Active infection
- Active Hepatitis B infection (HBsAg positive)
- Active hepatitis C (HCV RNA positive)
- Pregnant or nursing (lactating) women confirmed by a positive hCG laboratory test within 72 hours prior to initiating study treatment.
- Note: Low levels of hCG may also be considered a tumor marker, therefore if low hCG levels are detected, another blood sample at least 4 days later must be taken to assess the kinetics of the increase and transvaginal ultrasound must be performed to rule out pregnancy.
- Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant, unless they are using highly effective methods of contraception during dosing and for 7.5 months after stopping treatment with Spartalizumab.
- Complete or partial deficit in dihydropyrimidine dehydrogenase (DPD) activity
- Active inflammatory bowel disease Note: In case of a history of inflammatory bowel disease, it is advisable to take the advice of the referring gastroenterologist of the patient to ensure the absence of the evolution of inflammatory bowel disease (inflammatory thrust in progress) before the initiation of docetaxel treatment
Key Trial Info
Start Date :
June 9 2022
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
November 1 2026
Estimated Enrollment :
34 Patients enrolled
Trial Details
Trial ID
NCT04894370
Start Date
June 9 2022
End Date
November 1 2026
Last Update
December 22 2023
Active Locations (5)
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1
Centre Hospitalier Universitaire de Besançon
Besançon, France, 25000
2
Centre Georges-François Leclerc (CGFL)
Dijon, France
3
Hôpital Franco-Britannique
Levallois-Perret, France
4
Centre Léon Bérard
Lyon, France, 69000