A phase I study afatinib/carboplatin/paclitaxel induction chemotherapy followed by standard chemoradiation in HPV-negative or high-risk HPV-positive locally advanced stage III/IVa/IVb head and neck squamous cell carcinoma
Christine H Chung, Michelle A Rudek, Hyunseok Kang, Shanthi Marur, Pritish John, Nancy Tsottles, Sarah Bonerigo, Andy Veasey, Ana Kiess, Harry Quon, Anthony Cmelak, Barbara A Murphy, Jill Gilbert, Christine H Chung, Michelle A Rudek, Hyunseok Kang, Shanthi Marur, Pritish John, Nancy Tsottles, Sarah Bonerigo, Andy Veasey, Ana Kiess, Harry Quon, Anthony Cmelak, Barbara A Murphy, Jill Gilbert
Abstract
Introduction: Afatinib is an ErbB family receptor inhibitor with efficacy in head and neck squamous cell carcinoma (HNSCC). A phase I trial was conducted to determine the maximally tolerated dose (MTD) of afatinib in combination with carboplatin and paclitaxel as induction chemotherapy (IC).
Material and methods: Patients with newly diagnosed, locally advanced HPV-negative or HPV-positive HNSCC with a significant smoking history were enrolled. Afatinib alone was given daily for two weeks as lead-in and subsequently given with carboplatin AUC 6mg/mlmin and paclitaxel 175mg/m(2) every 21days as IC. Afatinib was started at a dose of 20mg daily and dose escalated using a modified Fibonacci design. After completion of IC, afatinib was discontinued and patients received concurrent cisplatin 40mg/m(2) weekly and standard radiation. Toxicity was assessed using CTCAE version 4.0.
Results: Seven of nine patients completed afatinib lead-in and IC. Five patients had partial response and two patients had stable disease after IC. Dose level 1 (afatinib 20mg) was well tolerated with one grade 3 (ALT elevation) and one grade 4 (neutropenia) toxicities. However, dose level 2 (afatinib 30mg) was not well tolerated with nine grade 3 (pneumonia, abdominal pain, diarrhea, pancytopenia, and UTI), two grade 4 (sepsis) and one grade 5 (death) toxicities.
Conclusions: The MTD of afatinib given with carboplatin AUC 6mg/mlmin and paclitaxel 175mg/m(2) is 20mg daily. Combination of afatinib at doses higher than 20mg with carboplatin and paclitaxel should be administered with caution due to the toxicities.
Keywords: ABCB1; Afatinib; Carboplatin; Efficacy; Head and neck squamous cell carcinoma; Paclitaxel; Phase I trial; Toxicity.
Conflict of interest statement
Conflict of interest
All other authors have no conflict of interest.
Copyright © 2015 Elsevier Ltd. All rights reserved.
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Source: PubMed