Phase 2
N=184
Cilengitide in Recurrent and/or Metastatic Squamous Cell Carcinoma of the Head and Neck (SCCHN)
Squamous Cell Cancer
Bottom Line
View on ClinicalTrials.gov: NCT00705016 ↗Enrolled (actual)
184
Serious AEs
71.4%
Results posted
Apr 2014
Primary outcome: Primary: Progression-free Survival (PFS) Time: Investigator Read — 6.4; 5.6; 5.7 months — p=0.885
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- Cilengitide 2000 mg once weekly (Drug); Cilengitide 2000 mg twice weekly (Drug); Cetuximab (Drug); 5-fluorouracil (5-FU) (Drug); Cisplatin (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Merck KGaA, Darmstadt, Germany
- Primary completion
- Sep 2011
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Progression-free Survival (PFS) Time: Investigator Read |
6.4; 5.6; 5.7 | 0.885 |
| SECONDARY Overall Survival (OS) Time |
12.4; 10.6; 11.6 | 0.800 |
| SECONDARY Best Overall Response (BOR) Rate |
46.8; 26.7; 35.5 | 0.205 |
| SECONDARY Disease Control Rate |
85.5; 73.3; 80.6 | 0.476 |
| SECONDARY Time to Treatment Failure (TTF) |
5.6; 4.5; 4.3 | 0.294 |
| SECONDARY Duration of Response |
5.8; 4.1; 6.4 | 0.391 |
| SECONDARY Safety - Number of Participants Experiencing Any Adverse Event |
61; 59; 61 | — |
Summary
The purpose of this open-label, randomized, controlled, Phase 1/2 study of the integrin inhibitor cilengitide is to evaluate the safety and efficacy of the combination of different regimens of cilengitide added to cisplatin, 5-fluorouracil (5-FU), and cetuximab in participants with recurrent/metastatic squamous cell carcinoma of the head and neck (SCCHN).
The Phase 1 part was conducted in dedicated study centers. In the Phase 2 part of this trial, cilengitide is administered at two different doses to two experimental groups. The third group will only receive cisplatin, 5-FU and cetuximab. In the Phase 1 part of this trial, the dose of cilengitide in combination with cisplatin, 5-FU and cetuximab was determined.
Cilengitide is an experimental anti-cancer substance interacting with so-called integrins. Integrins are protein molecules that are known to be present on the surface of certain cancer cells. Integrins are also found on certain cells that belong to growing blood vessels (endothelial cells). Integrins potentially facilitate the blood vessels' support of the tumor (angiogenesis) as well as the tumor's growth and further spread throughout the body (metastasis). By inhibiting integrins on the tumor cell surface, cilengitide potentially kills cancer cells, and potentially sensitizes cancer cells to other co-administered therapeutics. By inhibiting integrins on the endothelial cell surface, it potentially inhibits the ingrowth of additional blood vessels towards the tumor.
Cilengitide is given as an intravenous infusion (given by a drip in one vein of your arm). If any unacceptable side effect occurs, treatment with the study drug will be stopped.
Eligibility Criteria
Inclusion Criteria
- Histologically or cytologically confirmed diagnosis of SCCHN
- At least one measurable lesion either by computerized tomography (CT) scan or magnetic resonance imaging (MRI)
- Karnofsky performance status (KPS) of greater than or equal to 70 or eastern cooperative oncology group performance status (ECOG PS) of 0-1 at trial entry
Exclusion Criteria
- Prior systemic chemotherapy, except if given as part of a multimodal treatment for locally advanced disease, which was completed more than 6 months prior to trial entry
- Surgery (excluding prior diagnostic biopsy) or irradiation within 4 weeks before trial entry
- Nasopharyngeal Carcinoma
- Documented or symptomatic brain or leptomeningeal metastasis
- Previous treatment with epidermal growth factor receptor (EGFR) targeting therapy or signal transduction inhibitors
Data sourced from ClinicalTrials.gov (NCT00705016). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.