Deployment of cisplatin in Veterans with oropharyngeal cancer: toxicity and impact on oncologic outcomes

Author:

Soliman Ola1,Wilde David C.1,Kemnade Jan O.23,Sabichi Anita L.23,Chen George45,Chen Albert45,Little Samantha N.6,Huang Andrew T.16ORCID,Hernandez David J.16ORCID,Sandulache Vlad C.167ORCID

Affiliation:

1. Bobby R. Alford Department of Otolaryngology Head and Neck Surgery Baylor College of Medicine Houston Texas USA

2. Hematology Oncology Section, Medical Care Line Michael E. DeBakey Veterans Affairs Medical Center Houston Texas USA

3. Department of Internal Medicine, Section of Hematology/Oncology Baylor College of Medicine Houston Texas USA

4. Department of Radiation Oncology Baylor College of Medicine Houston Texas USA

5. Radiation Oncology Section, Diagnostic and Therapeutic Care Line Michael E. DeBakey Veterans Affairs Medical Center Houston Texas USA

6. ENT Section, Operative Care Line Michael E. DeBakey Veterans Affairs Medical Center Houston Texas USA

7. Center for Translational Research on Inflammatory Diseases Michael E. DeBakey Veterans Affairs Medical Center Houston Texas USA

Abstract

AbstractObjectiveCisplatin forms the backbone of systemic chemotherapy treatment for oropharyngeal squamous cell carcinoma (OPSCC). The ideal cisplatin dosing regimen remains yet to be fully defined for achieving optimal efficacy and toxicity profiles in patients with comorbidity.MethodsWe retrospectively reviewed oncologic and toxicity data for patients with OPSCC treated at the Michael E. DeBakey Veterans Affairs Medical Center between 2000 and 2020 who initiated curative intent, definitive chemo‐radiation with one of three single agent regimens: high dose (HD) cisplatin, low dose (LD) cisplatin or cetuximab.ResultsPatients with HPV‐associated tumors and nonsmokers demonstrated improved overall and disease‐free survival along with locoregional and distant metastatic control regardless of chemotherapy regimen. Regardless of regimen selection, patients which received a cumulative cisplatin dose ≥200 mg/m2 had a lower rate of distant metastasis. The HD regimen resulted in a greater fraction (75% vs. 50%) of patients receiving a cumulative cisplatin dose ≥200 mg/m2 and a comparable measured toxicity burden compared to the LD regimen.ConclusionsBoth HD and LD cisplatin regimens can be safely delivered to a Veteran OPSCC patient population which should allow for straightforward application of conclusions drawn from completed and active clinical trials testing cisplatin regimens.Level of Evidence4.

Publisher

Wiley

Subject

General Medicine

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