Final results of the randomized phase II DeLOS-II trial: Induction chemotherapy (IC) followed by radiotherapy (R) vs. cetuximab (E) plus IC and R for functional larynx preservation in resectable laryngeal and hypopharyngeal cancer (LHSCC).

Authors

null

Andreas Dietz

University of Leipzig, Leipzig, Germany

Andreas Dietz , Gunnar Wichmann , Michael Flentje , Rudolf Hagen , Oliver Koelbl , Frank Schreiber , Volker Schilling , Georg Maschmeyer , Ursula Schroeder , Christian Sittel , Thomas Lenarz , Jens Peter Klussmann , Orlando Guntinas-Lichius , Claudia Rudack , Thomas Foerg , Martin Westhofen , Hans Juergen Welkoborsky , Dirk Esser , Swantje Held , Ulrich Keilholz

Organizations

University of Leipzig, Leipzig, Germany, Department of Otolaryngology, Head and Neck Surgery, University Hospital Leipzig, Leipzig, Germany, Universitat Würzburg, Wurzburg, Germany, ENT Department University Würzburg, Würzburg, Germany, Dpt. for Radiation Oncology, University of Regensburg, Regensburg, Germany, ENT Department, Klinikum Kassel, Kassel, Germany, ENT Clinic Vivantes, Berlin, Neuköln, Germany, Potsdam Klinikum, Potsdam, Germany, ENT Department University Lübeck, Lübeck, Germany, ENT Department Katharinen Hospital, Stuttgart, Germany, ENT Department MHH Hannover, Hannover, Germany, ENT Department University Gießen, Gießen, Germany, University Hospital Jena, Head and Neck Surgery, Jena, Germany, ENT Department University Münster, Münster, Germany, Department Radiation Oncology, Vincentius Clinic, Karlsruhe, Germany, ENT Department University Aachen, Aachen, Germany, ENT Clinic, Nordstadt, Hannover, Germany, ENT Department, Helios Clinic, Erfurt, Germany, ClinAssess GmbH, Leverkusen, Germany, Department for Hemato-Oncology, Comprehensive Cancer Center, Charité-University Medicine, Berlin, Germany

Research Funding

Pharmaceutical/Biotech Company

Background: To evaluate the impact of E added throughout IC and R on the rate of two-year functional laryngectomy free survival (fLFS). Methods: Untreated patients (pts) with stage III/IV LHSCC, amenable to resection by total laryngectomy, were randomized to three cycles of IC with TPF (docetaxel and cisplatin 75 mg/m² day 1 and F 750 mg/m²/day on days 1-5) followed by R (69,6Gy) without (arm A) or with (arm B) standard dose of cetuximab for 16 weeks throughout IC and R. In case of non-response after the first IC cycle, salvage laryngectomy was performed. The primary objective was a 2-year fLFS rate above 35% (lower bound of 80%-CI) in the experimental arm. Results: Of180 pts randomized (7.2007-9.2012), 173 fulfilled ITT criteria. Due to 4 therapy related deaths among the first 64 randomized pts, F was omitted from IC in 2.2009 with no further treatment related deaths in the remaining 112 pts. Table 1 summarizes rates of response, laryngectomy, fLFS and OS. The primary objective of an fLFS above 35% was met, however, the control arm also met objectives. 31.8% (arm A) and 22.7% (arm B) of patients did not respond to first cycle IC. Conclusions: IC with TPFE/TPE was feasible and showed a trend towards being more effective compared to TPF/TP in terms of rates of fLFS and OS. The early response rate to IC of 77.3% and the 1 and 2 year fLFS rates of 63.6% and 46.6%, respectively compare very well to previous larynx preservation trials and suggest effective treatment selection and stratification by early response evaluation to IC. Clinical trial information: NCT00508664

Efficacy and outcome data.

Arm A TP(F) –> RArm B TP(F) –> R
plus cetuximab
OR (95%CI)
Localisation:::
    Larynx4442
    Hypopharynx4146
TPF3031
    TP5557
ORR* (n = 126)::
    TPF94.7%80.0%
    TP79.1%94.9%
Laryngectomy25.9%33.0%
fLFS at 6 months65.9%77.3%0.5680 (0.2905-1.1105)
fLFS at 1 year55.3%63.6%0.7068 (0.3842-1.3001)
fLFS at 2 years44.7%46.6%0.9268 (0.5094-1.6863)
OS at 2 years68.2%69.3%0.9508 (0.4997-1.8091)

OR: Odds Ratio; *at final examination

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Abstract Details

Meeting

2016 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Head and Neck Cancer

Track

Head and Neck Cancer

Sub Track

Advanced/Metastatic Disease

Clinical Trial Registration Number

NCT00508664

Citation

J Clin Oncol 34, 2016 (suppl; abstr 6025)

DOI

10.1200/JCO.2016.34.15_suppl.6025

Abstract #

6025

Poster Bd #

347

Abstract Disclosures