Abstract 275P
Background
First-line TP-Ex-like regimen (taxane-platinum-cetuximab) in recurrent and/or metastatic squamous cell carcinoma of head and neck (R/M SCCHN) followed by 2nd-line immunotherapy represents one of the standards of care. We report our experience from 2 tertiary care institutions of India.
Methods
This is a retrospective analysis of 54 consecutive patients of platinum-sensitive R/M SCCHN treated between August 2017 and May 2020 with 1st-line weekly combination paclitaxel 80mg/m2, carboplatin AUC2 and cetuximab 400mg/m2 loading followed by 250mg/m2 (PCC) for upto maximum 12 weeks. Non-progressive patients were then started on cetuximab maintenance. Patients were further treated with 2nd-line nivolumab or oral metronomic chemotherapy (OMCT) on progression as per feasibility. Overall Response rates (ORR), progression-free survival 1 and 2 (PFS-1 & PFS-2), overall survival (OS) and safety were evaluated.
Results
The median age of the study population was 56.5 years with 48 males; 30/24 had oral/non-oral primaries; ECOG PS was 1/2 in 32/22 cases; 50 patients had local disease while 34 had distant metastasis; 41 had history of tobacco abuse; 7/6 patients had renal/cardiac dysfunction respectively. The ORR and median PFS-1 was 79.7% and 7.031 months respectively. Out of the 33 patients who progressed, 19/10/4 received 2nd-line nivolumab, OMCT or best supportive care respectively. The ORR to 2nd-line nivolumab / OMCT was 36.8%/10% and the median PFS-2 was 6.5 / 2 months respectively. The median OS of the entire cohort was 15.014 months while that of the selected 2nd-line nivolumab cohort was 20.4 months. Grade III/IV adverse events on 1st-line therapy included neutropenia (31.4%), anemia (35.1%), thrombocytopenia (7.4%), febrile neutropenia (11.1%) and skin reaction (16.6%) and there were no grade III/IV treatment related toxicities in 2nd-line.
Conclusions
First-line weekly PCC is an effective regimen for palliative therapy of platinum-sensitive R/M SCCHN with acceptable toxicity profile. Addition of 2nd-line nivolumab on progression further improves the outcomes.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
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