RADIANCE – Radiochemotherapy with or without Durvalumab in the treatment of anal squamous cell carcinoma: a randomized multicenter phase II trial
Abstract: Purpose
Anal squamous cell carcinomas (ASCC) are increasing in frequency across the developed world. The 3-year disease-free survival (DFS) in patients with locally-advanced disease is approximately 60% after primary radiochemotherapy (RCT). There is a strong rationale for combining immunotherapy with RCT in patients with ASCC due to its association with human papilloma virus (HPV) infection.
Methods/design
RADIANCE is an investigator initiated, prospective, multicenter, randomized phase II trial testing the addition of Durvalumab, a PD-L1 immune checkpoint inhibitor, to standard RCT in 178 patients with locally advanced ASCC (T2 ≥ 4 cm Nany, cT3-4 and/or cN+). In the control arm, patients will be treated with standard mitomycin C (MMC)/5-fluorouracil (5-FU)-based RCT. Intensity-modulated radiotherapy (IMRT) will be applied as follows: PTV_A (primary tumor) T1-T2 < 4 cm N+: 28 × 1.9 Gy = 53.2 Gy; or T2 ≥ 4 cm, T3-4 Nany: 31 × 1.9 Gy = 58.9 Gy; PTV_N (involved node): 28 × 1.8 Gy = 50.4 Gy ; and PTV_Elec (elective node): 28 × 1.43 Gy = 40.0 Gy over a period of 5,5–6 weeks. Concomitant chemotherapy will be administered using MMC with 5-FU during weeks 1 and 5 of radiotherapy (MMC 12 mg/m2, day 1 [maximum single dose 20 mg]; 5-FU 1000 mg/m2 days 1–4 and 29–32). In the experimental arm, Durvalmab (1500 mg absolute dose, intravenously) will be combined with the same RCT as in the control arm. Immunotherapy with Durvalumab will start 14 days before initiation of standard RCT, administered every four weeks (q4w) thereafter for a total of twelve doses. The primary endpoint is disease-free survival (DFS) after 3 years.
Discussion
As ASCC is considered an immunogenically “hot” tumor due to its association with HPV infection, the combination of RCT with Durvalumab may improve tumor control and long-term clinical outcome in this patient collective compared to RCT alone
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
Clinical and translational radiation oncology. - 23 (2020) , 43-49, ISSN: 2405-6308
- Schlagwort
-
Darmkrebs
Immuntherapie
Radiochemotherapie
- Ereignis
-
Veröffentlichung
- (wo)
-
Freiburg
- (wer)
-
Universität
- (wann)
-
2020
- Urheber
-
Martin, Daniel
Balermpas, Panagiotis
Gollrad, Johannes Michael
Weiß, Christian
Valentini, Chiara
Stuschke, Martin
Schäfer, Henning Sebastian
Henkenberens, Christoph
Debus, Jürgen
Krug, David
Kuhnt, Thomas
Brunner, Thomas B.
Bostel, Tilman
Engenhart, Rita
Nestle, Ursula
Combs, Stephanie
Belka, Claus
Hautmann, Matthias Günther
Hildebrandt, Guido
Gani, Cihan
Polat, Bülent
Rödel, Claus
Fokas, Emmanouil
- DOI
-
10.1016/j.ctro.2020.04.010
- URN
-
urn:nbn:de:bsz:25-freidok-1670313
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:54 MESZ
Datenpartner
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Martin, Daniel
- Balermpas, Panagiotis
- Gollrad, Johannes Michael
- Weiß, Christian
- Valentini, Chiara
- Stuschke, Martin
- Schäfer, Henning Sebastian
- Henkenberens, Christoph
- Debus, Jürgen
- Krug, David
- Kuhnt, Thomas
- Brunner, Thomas B.
- Bostel, Tilman
- Engenhart, Rita
- Nestle, Ursula
- Combs, Stephanie
- Belka, Claus
- Hautmann, Matthias Günther
- Hildebrandt, Guido
- Gani, Cihan
- Polat, Bülent
- Rödel, Claus
- Fokas, Emmanouil
- Universität
Entstanden
- 2020
Ähnliche Objekte (12)