Pembrolizumab plus platinum and taxanes as first-line and as neoadjuvant/induction therapies in PF-unfit patients with PDL1-positive squamous cell carcinoma of the head and neck

Poster abstract

Purpose/Objective

Pembrolizumab (P) is approved in the first-line (1L) setting in patients with squamous cell carcinoma of the head and neck (SCCHN) with a CPS ≥ 1 and has shown promising activity in the locally-advanced (LA) setting. However, there are no alternatives for patients who are platinum-5FU (PF)-unfit and in need of a rapid tumor response. Taxanes are active agents in SCCHN that could effectively substitute 5FU as shown in Keynote-B10, Frail-Immune and DEPEND trials [1-3]. We evaluated the combination of pembrolizumab plus platinum and taxanes (PCT) +/- prophylactic (p) G-CSF in PF-unfit patients at our institution.

Material/Methods

Retrospective study of patients diagnosed with SCCHN and treated with PCT at Hospital Clínico Universitario San Carlos, Madrid (Spain). A descriptive study, as well as objective response rate (ORR), progression-free survival (PFS), overall survival (OS) and safety in the 1L and in the LA setting, were analyzed.

Results

Within the period August 2019 – October 2023, 18 patients (1L: n=6; LA: n=12) were identified. Among 1L: Male/Female: 2/4; age: 65y (56-86). Subsite: oral cavity (OC): n=5, larynx (n=1). Median CPS: 40 (5-80). No. combo PCT cycles: 6 (2-9). No. maintenance P cycles: 4 (1-8). ORR: 67% (2 CR, 2 PR, 2 SD). After a median follow-up (F-U) of 9 months (m) (1-25), median PFS and OS were 8 m (4.7 - 11.3) and NR (NR-NR), respectively. pG-CSF in 4/6 pts. G3/4 toxicity: G3 neutropenia: 4/6, G3 thrombopenia: 1/6. There were no toxic deaths. Among LA: Male/Female: 8/4; age: 72y (47-96). P + wkCBDCA-paclitaxel: n=10/12; P + 3wkCBDCA-paclitaxel: n=1/12, P + 3wkCDDP-docetaxel: n=1/12. Subsite: oropharynx: n=3, OC: n=5, CUP: n=1, Sinonasal: n=3. Median CPS: 30 (3-100). No. combo PCT cycles: 3 (2-4). No. maintenance P cycles: 0 (0-4). ORR after PCT (n=10): 90% (4 CR, 5 PR, 1 PD). Post-PCT Tx: Surgery: n=3; CRTx: n=5; Maint P: n=6. After a median follow-up (F-U) of 4 m (0-34), median PFS and OS were 6 m (NR - NR) and NR (NR-NR), respectively. pG-CSF in 6/12 pts. G3/4 toxicity: G3 neutropenia: 6/12, G3 thrombopenia: 4/12, G3 pneumonia: 1/12, G3 IR-colitis: 1/12, G4 IR-transaminitis: 1/12. There were no toxic deaths.

Updated results for the LA population (as of March 2024) will be presented at the meeting.

Conclusion

PCT and particularly weekly PCT +/- pG-CSF is a highly effective and safe chemoimmunotherapy option for PF-unfit patients in need of a rapid response and a positive CPS, both in the 1L and LA settings. Trials with weekly PCT should be conducted in comorbid and/or elderly patients with LA and R/M SCCHN  not candidates for high-dose CT and in need of rapid response.

Authors
1,2Santiago Cabezas-Camarero, 3,4,5Miguel Sotelo-Lezama, 6Óscar De-la-Sen, 6Alejandro Encinas-Bascones, 6Farzin Falahat, 6Almudena Alonso-Ovies, 6Elisa Varela-Reyes, 6Miguel Alonso-Juarranz, 6Manuel de Pedro-Marina, 7Jesús Gimeno-Hernández, 7Maria Cruz Iglesias-Moreno, 8Elena Cerezo-Druet, 8Fernando Puebla, 1,2Pedro Pérez-Segura
1IDISSC, IDISSC, Madrid, Spain. 2Hospital Clinico Universitario San Carlos, Medical Oncology, Madrid, Spain. 3Aliada Cancer Center, Medical Oncology, Lima, Peru. 4Clinica San Felipe, Medical Oncology, Lima, Peru. 5Hospital María Auxiliadora, Medical Oncology, Lima, Peru. 6Hospital Clinico Universitario San Carlos, Craniomaxillofacial Surgery, Madrid, Spain. 7Hospital Clinico Universitario San Carlos, ENT Head and Neck Surgery, Madrid, Spain. 8Hospital Clinico Universitario San Carlos, Radiation Oncology, Madrid, Spain
Bibliographic references

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