J Martínez-Trufero1, A Lozano Borbalas2, I Pajares Bernad3, M Taberna Sanz4, E Ortega Izquierdo3, B Cirauqui Cirauqui5, J Rubió-Casadevall6, M Plana Serrahima4, J M Ponce Ortega7, I Planas Toledano8, J Caballero9, J Marruecos Querol10, L Iglesias Docampo11, J Lambea Sorrosal12, J C Adansa13, R Mesía Nin4. 1. Medical Oncology Department, University Hospital Miguel Servet, Av. Isabel la Católica 1-3, 50009, Zaragoza, Spain. jmtrufero@seom.org. 2. Radiation Oncology Service, Institut Català D'Oncologia (ICO) Hospitalet, Barcelona, Spain. 3. Medical Oncology Department, University Hospital Miguel Servet, Av. Isabel la Católica 1-3, 50009, Zaragoza, Spain. 4. Medical Oncology Service, Institut Català D'Oncologia (ICO) Hospitalet, Barcelona, Spain. 5. Medical Oncology Service, Institut Català D'Oncologia (ICO) Badalona, Barcelona, Spain. 6. Medical Oncology Service, Institut Català D'Oncologia (ICO) Girona, University Hospital Josep Trueta, Girona, Spain. 7. Radiation Oncology Service, University Hospital Miguel Servet, Zaragoza, Spain. 8. Radiation Oncology Service, Institut Català D'Oncologia (ICO) Badalona, Barcelona, Spain. 9. Medical Oncology Service, University and Polytechnic Hospital La Fe, Valencia, Spain. 10. Radiation Oncology Service, Institut Català D'Oncologia (ICO) Girona, University Hospital Josep Trueta, Girona, Spain. 11. Medical Oncology Service, University Hospital 12 de Octubre, Madrid, Spain. 12. Medical Oncology Service, University Hospital Lozano Blesa, Zaragoza, Spain. 13. Biomedical Research Institute of Salamanca, Salamanca, Spain.
Abstract
BACKGROUND: Sequential treatment of Panitumumab (Pb) plus Paclitaxel (Px) as induction treatment (IT) followed by concurrent bioradiotherapy (Bio-RT) with Pb may be an alternative for locally advanced squamous cell carcinoma of the head and neck (LA-SCCHN) in patients ineligible for high-dose cisplatin therapy. METHODS: Phase II, single-arm, multicentre study, with two-stage design, in patients ≥ 18 years with stage III-IVa-b LA-SCCHN unfit for platinum. Patients received Px + Pb (9 weeks) as IT followed by Bio-RT + Pb. Primary endpoint: overall response rate (ORR) after IT, defined as: more than 70% of patients achieving complete response (CR) or partial response (PR) to IT. Secondary end-points: progression-free survival, organ preservation rate, safety profile. RESULTS: Study ended prematurely (51 patients) due to slow recruitment. ORR: 66.7% (95% CI: 53.7-79.6), 8 (15.7%) CR and 26 (51.0%) PR. 39 patients (76%) completed radiotherapy (RT). Pb and/or Px-related adverse events (AEs) grade 3-4: 56.9% during IT and 63.4% during the concomitant phase, of which most common were skin toxicity (33.3%). Five deaths occurred during treatment, two of them (3.9%) were Pb and/or Px-related. CONCLUSIONS: Although underpowered, ORR was higher than the pre-specified boundary for considering the treatment active. Although Px + Pb as IT provides some benefit, the safety profile is worse than expected. To consider Pb + Px as IT as an alternative for platinum-unsuitable LA-SCCHN, further research/investigation would be needed.
BACKGROUND: Sequential treatment of Panitumumab (Pb) plus Paclitaxel (Px) as induction treatment (IT) followed by concurrent bioradiotherapy (Bio-RT) with Pb may be an alternative for locally advanced squamous cell carcinoma of the head and neck (LA-SCCHN) in patients ineligible for high-dose cisplatin therapy. METHODS: Phase II, single-arm, multicentre study, with two-stage design, in patients ≥ 18 years with stage III-IVa-b LA-SCCHN unfit for platinum. Patients received Px + Pb (9 weeks) as IT followed by Bio-RT + Pb. Primary endpoint: overall response rate (ORR) after IT, defined as: more than 70% of patients achieving complete response (CR) or partial response (PR) to IT. Secondary end-points: progression-free survival, organ preservation rate, safety profile. RESULTS: Study ended prematurely (51 patients) due to slow recruitment. ORR: 66.7% (95% CI: 53.7-79.6), 8 (15.7%) CR and 26 (51.0%) PR. 39 patients (76%) completed radiotherapy (RT). Pb and/or Px-related adverse events (AEs) grade 3-4: 56.9% during IT and 63.4% during the concomitant phase, of which most common were skin toxicity (33.3%). Five deaths occurred during treatment, two of them (3.9%) were Pb and/or Px-related. CONCLUSIONS: Although underpowered, ORR was higher than the pre-specified boundary for considering the treatment active. Although Px + Pb as IT provides some benefit, the safety profile is worse than expected. To consider Pb + Px as IT as an alternative for platinum-unsuitable LA-SCCHN, further research/investigation would be needed.
Entities:
Keywords:
Comorbidity; EGFR tyrosine kinase inhibitor; Head and neck neoplasms; Induction chemotherapy; Panitumumab; Squamous cell carcinoma
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