Radiochemotherapy +/- Durvalumab for Locally-advanced Anal Carcinoma. a Multicenter, Randomized, Phase II Trial of the German Anal Cancer Study Group

NCT ID: NCT04230759

Last Updated: 2024-09-19

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 180 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-01-07
• Study Completion Date: 2027-03-31

Brief Summary

The RADIANCE multicenter, randomized phase II trial will assess the efficacy of durvalumab, a PD-L1 immune checkpoint inhibitor, in combination with primary mitomycin C (MMC)/5-fluorouracil (5-FU)-based radiochemotherapy (RCT) in patients with locally-advanced anal squamous cell carcinoma (ASCC).

Detailed Description

Anal squamous cell carcinomas (ASCC) are increasing in frequency across the developed world. There is a strong rationale for combining the PD-L1 immune checkpoint inhibitor durvalumab with radiochemotherapy (RCT) in patients with ASCC. First, although primary RCT with concurrent mitomycin C and 5-fluorouracil (MMC/5-FU) is the standard treatment for ASCC, the 3-year DFS in patients with locally-advanced disease is only in the range of 60%. Second, approximately 80-90% of patients with ASCC are human papilloma virus (HPV)-positive, which is associated with higher tumor "immunogenicity" in this malignancy that is known to correlate with better response to RCT as well as PD-1/PD-L1 immune checkpoint inhibitors. Also, PD-L1 expression was observed in 33%-62% of patients with locally advanced non-metastatic ASCC that correlated with tumor stage. Third, inhibition of the PD-1/PD-L1 axis showed encouraging responses in recurrent/metastatic ASCC in two phase Ib/II trials. Fourth, several data indicate complementary roles between R(C)T and immunotherapy. Fifth, R(C)T can induce PD-L1 upregulation with resulting dysfunction in CD8+ T-cells, and addition of anti-PD-L1 to R(C)T can overcome T-cell suppression to reinvigorate immune surveillance. First clinical studies have demonstrated promising findings for the combination of RCT and immunotherapies. Thus, based on the above data, RCT combined with durvalumab is expected to be more effective than primary RCT alone. Altogether, the hereby proposed RADIANCE multicenter, randomized phase II trial aims to improve the current standard treatment by incorporating durvalumab to the primary MMC/5-FU-based RCT in patients with locally-advanced ASCC (T2=>4cm Nany, stage IIB-IIIC).

Conditions

Anal Cancer; Anal Carcinoma; Anal Cancer Stage III; Anal Cancer Stage II

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

5FU+Mitomycin C

Radiochemotherapy for anal cancer

Group Type: ACTIVE_COMPARATOR

Chemotherapy

Intervention Type: DRUG

Patients receive chemotherapy cycles as followed:

Mitomycin-C 12 mg/m², day 1 (maximum single dose 20 mg) 5-FU: 1000 mg/m² per day, continuous i.v. infusion, on day 1-4 and 29-32

Radiation

Intervention Type: RADIATION

PTV\_A (primary tumor): T1-T2\<4cm N+: 28 x 1.9 Gy=53.2 Gy, five fractions per week or PTV\_A (primary tumor): T2\>=4cm, T3-4 Nany: 31 x 1.9 Gy=58.9 Gy, five fractions per week PTV\_N (involved node): 28 x 1.8 Gy=50.4 Gy, five fractions per weeks PTV\_Elec (elective node): 28 x 1.43 Gy=40.0 Gy, five fractions per week

5FU+Mitomycin C+Durvalumab

Radiochemotherapy with Durvalumab for anal cancer

Group Type: EXPERIMENTAL

Chemotherapy

Intervention Type: DRUG

Patients receive chemotherapy cycles as followed:

Mitomycin-C 12 mg/m², day 1 (maximum single dose 20 mg) 5-FU: 1000 mg/m² per day, continuous i.v. infusion, on day 1-4 and 29-32

Radiation

Intervention Type: RADIATION

PTV\_A (primary tumor): T1-T2\<4cm N+: 28 x 1.9 Gy=53.2 Gy, five fractions per week or PTV\_A (primary tumor): T2\>=4cm, T3-4 Nany: 31 x 1.9 Gy=58.9 Gy, five fractions per week PTV\_N (involved node): 28 x 1.8 Gy=50.4 Gy, five fractions per weeks PTV\_Elec (elective node): 28 x 1.43 Gy=40.0 Gy, five fractions per week

Durvalumab

Intervention Type: DRUG

1500 mg, 1h-civ, every 4 weeks (q4w) applied on day -14 (that is 14 days prior to initiation of RCT), day 15 (during RCT), and thereafter q4w (+/- 3d) for a total of 12 doses

Interventions

Chemotherapy

Patients receive chemotherapy cycles as followed:

Mitomycin-C 12 mg/m², day 1 (maximum single dose 20 mg) 5-FU: 1000 mg/m² per day, continuous i.v. infusion, on day 1-4 and 29-32

Intervention Type: DRUG

Radiation

PTV\_A (primary tumor): T1-T2\<4cm N+: 28 x 1.9 Gy=53.2 Gy, five fractions per week or PTV\_A (primary tumor): T2\>=4cm, T3-4 Nany: 31 x 1.9 Gy=58.9 Gy, five fractions per week PTV\_N (involved node): 28 x 1.8 Gy=50.4 Gy, five fractions per weeks PTV\_Elec (elective node): 28 x 1.43 Gy=40.0 Gy, five fractions per week

Intervention Type: RADIATION

Durvalumab

1500 mg, 1h-civ, every 4 weeks (q4w) applied on day -14 (that is 14 days prior to initiation of RCT), day 15 (during RCT), and thereafter q4w (+/- 3d) for a total of 12 doses

Intervention Type: DRUG

Other Intervention Names

all brands of 5-fluorouracil (5-FU) are allowed; all brands of Mitomycin C (MMC) are allowed; PD-L1 inhibitor

Eligibility Criteria

Inclusion Criteria

• Histologically-confirmed ASCC (both genders) of the anal canal or the anal margin
• UICC-Stage IIB-IIIC including T2>4cm Nany (IIB: T3N0M0; IIIA: T1-2N1M0; IIIB: T4N0M0; IIIC: T3-4N1M0; T2>4cm Nany) according to proctoscopy, pelvic MRI, CT scan of thorax and abdomen, all within 30 days prior to recruitment
• Age ≥ 18 years, no upper age limit
• ECOG-Performance score 0-1
• History/physical examination within 30 days prior to recruitment
• Written informed consent and any locally-required authorization (e.g. EU Data Privacy Directive in the EU) obtained from the patient prior to performing any protocol-related procedures, including screening evaluations
• Life expectancy of > 12 months
• Body weight >30kg
• Hemoglobin ≥9.0 g/dl
• Leukocytes >3.5 x 10 ^9/l
• Absolute neutrophil count (ANC) 1.5 x 10 9/l (> 1500 per mm3)
• Platelet count ≥100 x 109/l (>100,000 per mm3)
• Serum bilirubin ≤1.5 x institutional upper limit of normal (ULN). (This will not apply to patients with confirmed Gilbert's syndrome (persistent or recurrent hyperbilirubinemia that is predominantly unconjugated in the absence of hemolysis or hepatic pathology), who will be allowed only in consultation with their physician.
• AST (SGOT), ALT (SGPT), AP ≤ 3x institutional ULN
• Calculated creatinine CL>40 mL/min by the Cockcroft-Gault formula creatinine clearance
• Female subject of childbearing potential should have a negative serum pregnancy within 72 hours prior to receiving the first dose of durvalumab. A highly sensitive pregnancy test must be used.
• Female subjects of childbearing potential must be willing to use a highly effective contraceptive measure as defined in the Clinical Trial Facilitation Group (CTFG) guideline ("Recommendations related to contraception and pregnancy testing in clinical trials"). Highly effective contraception is required from screening to 90 days after the last dose of durvalumab. (Note: Abstinence is acceptable if this is the usual lifestyle and preferred contraception for the subject.)
• Male subjects of childbearing potential must agree to use a highly effective method of contraception, starting from screening to 90 days after the last dose of durvalumab. (Note: Abstinence is acceptable if this is the usual lifestyle and preferred contraception for the subject.) Male patients should refrain from fathering a child or donating sperm during the study and for 180 days after the last dose of durvalumab + any drug combination therapy or 90 days after the last dose of durvalumab monotherapy, whichever is the longer time period.
• Patient is willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations including follow up.
• For HIV-positive patients: running combined antiretroviral therapy (CART) on a stable dose at study entry and undetectable HIV-viral load (HIV Viral load <50 copies/mL and CD4>200/mircoliter). Patients will be closely monitored and CART management will be performed according to appropriate labelling guidance of the antiviral therapy. CART should be on a stable dose at study entry.

• Patients with Grade ≥2 neuropathy will be evaluated on a case-by-case basis after consultation with the Study Chairman.
• Patients with irreversible toxicity not reasonably expected to be exacerbated by treatment with durvalumab may be included only after consultation with the Study Chairman
• Any concurrent chemotherapy, biologic, or hormonal therapy for cancer treatment, other than the study medication. Concurrent use of hormonal therapy for non-cancer-related conditions (e.g., hormone replacement therapy) is acceptable.
• Previous radiotherapy treatment to the pelvis or radiotherapy treatment to more than 30% of the bone marrow or with a wide field of radiation within 4 weeks of the first dose of study drug
• Major surgical procedure (as defined by the Investigator) within 28 days prior to the first dose of durvalumab.
• History of allogenic organ transplantation.
• Active or prior documented autoimmune or inflammatory disorders (including inflammatory bowel disease [e.g., colitis or Crohn's disease], diverticulitis [with the exception of diverticulosis], systemic lupus erythematosus, Sarcoidosis syndrome, or Wegener syndrome [granulomatosis with polyangiitis, Graves' disease, rheumatoid arthritis, hypophysitis, uveitis, etc]). The following are exceptions to this criterion:

• Patients with vitiligo or alopecia
• Patients with hypothyroidism (e.g., following Hashimoto syndrome) stable on hormone replacement
• Any chronic skin condition that does not require systemic therapy
• Patients without active disease in the last 5 years may be included but only after consultation with the study chairman
• Patients with celiac disease controlled by diet alone
• Uncontrolled intercurrent illness, including but not limited to, ongoing or active infection, symptomatic congestive heart failure, uncontrolled hypertension, unstable angina pectoris, cardiac arrhythmia, interstitial lung disease, serious chronic gastrointestinal conditions associated with diarrhoea, or psychiatric illness/social situations that would limit compliance with study requirement, substantially increase risk of incurring AEs or compromise the ability of the patient to give written informed consent
• History of leptomeningeal carcinomatosis or any other metastatic disease
• History of active primary immunodeficiency
• Active infection including tuberculosis (clinical evaluation that includes clinical history, physical examination and radiographic findings, and TB testing in line with local practice), hepatitis B (known positive HBV surface antigen (HBsAg) result), hepatitis C. Patients with a past or resolved HBV infection (defined as the presence of hepatitis B core antibody [anti-HBc] and absence of HBsAg) are eligible. Patients positive for hepatitis C (HCV) antibody are eligible only if polymerase chain reaction is negative for HCV RNA.
• Receipt of live attenuated vaccine within 30 days prior to the first dose of durvalumab. Note: Patients, if enrolled, should not receive live vaccine whilst receiving durvalumab and up to 30 days after the last dose of durvalumab.
• Known allergy or hypersensitivity to any of the study/investigational drugs or any of the study/investigational drug excipients and/or radiochemotherapy with 5-FU and Mitomycin C.
• Female patients who are pregnant or breastfeeding or male or female patients of reproductive potential who are not willing to employ effective birth control from screening to 90 days after the last dose of durvalumab.

Exclusion Criteria

• UICC-Stage I-IIA ASCC defined as cT1N0M0 or cT2 <4cm N0M0 disease
• Second malignancy other than basalioma or cervical/genital/ neoplasia in situ
• History of another primary malignancy except for:

• Malignancy treated with curative intent and with no known active disease ≥5 years before the first dose of durvalumab and of low potential risk for recurrence
• Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease
• Adequately treated carcinoma in situ without evidence of disease
• Known DPD-deficiency
• Participation in another clinical study with an investigational product during the last 12 months
• Concurrent enrolment in another clinical study, unless it is an observational (non-interventional) clinical study or during the follow-up period of an interventional study
• Any previous treatment with other immunotherapy, a PD1 or PD-L1 inhibitor
• QT interval corrected for heart rate (QTc) ≥470 ms
• Current or prior use of immunosuppressive medication within 14 days before the first dose of durvalumab, with the exceptions of intranasal and inhaled corticosteroids or systemic corticosteroids at physiological doses, which are not to exceed 10 mg/d of prednisone, or an equivalent corticosteroid. In case of recent introduction of CART, inclusion will be possible provided subjects had at least 4 weeks of treatment prior to inclusion.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Goethe University

OTHER

Sponsor Role: lead

Responsible Party

Daniel Martin

PD MD

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Univeritätsklinik für Strahlentherapie-Radioonkologie

Graz, , Austria

Institut für Radioonkologie und Strahlentherapie

Darmstadt, Darmstadt, Germany

Klinik und Poliklinik für Strahlentherapie und Radioonkologie

Dresden, Dresden, Germany

Klinik für Strahlenheilkunde, Universitätsklinikum Freiburg

Freiburg im Breisgau, Freiburg, Germany

Klinik und Poliklinik für Strahlentherapie

Essen, Hesse, Germany

UKSH Campus Kiel

Kiel, Kiel, Germany

Universitätsklinikum Leipzig

Leipzig, Leipzig, Germany

Universitätsklinikum Magdeburg

Magdeburg, Magdeburg, Germany

Universitätsmedizin Mainz

Mainz, Mainz, Germany

Uniklinikum Marburg

Marburg, Marburg, Germany

Kliniken Maria Hilf GmbH Mönchengladbach

Mönchengladbach, Mönchengladbach, Germany

LMU Klinikum der Universität München

München, München, Germany

Technische Universität München

München, München, Germany

Universitätsklinikum Regensburg

Regensburg, Regensburg, Germany

Universitätsklinikum Rostock

Rostock, Rostock, Germany

Radioonkologie und Strahlentherapie

Berlin, State of Berlin, Germany

Universitätsklinik Tübingen

Tübingen, Tübingen, Germany

Universitätsklinikum Würzburg

Würzburg, Würzburg, Germany

OnkoLibri GbR

Berlin, , Germany

University Hospital Goethe University Frankfurt

Frankfurt, , Germany

Universitätsmedizin Göttingen

Goettigen, , Germany

Asklepios Klinik Altona

Hamburg, , Germany

Hospital Barmherzige Brüder

Regensburg, , Germany

Klinikum Stuttgart

Stuttgart, , Germany

UniversitätsSpital Zürich

Zurich, Canton of Zurich, Switzerland

Countries

Austria; Germany; Switzerland

Other Identifiers

2018-003005-25

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

70113615

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

ESR-17-13077

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

2024-513914-36-00

Identifier Type: CTIS

Identifier Source: secondary_id

RADIANCE

Identifier Type: -

Identifier Source: org_study_id