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Table 1.  

All HNSCC Patients Patients with R/M HNSCC
Low performance status Low performance status
Extent of prior treatment Lack of response to prior chemotherapy
Substance abuse (tobacco, alcohol, betel quid) Prior radiation therapy
Low reported quality of life Hypopharynx or oral cavity primary site
Lack of private medical insurance (in the United States) Weight loss > 5%
  Well/moderate tumor cell differentiation
  Malignant hypercalcemia (end-stage disease)

Factors Associated With Inferior Overall Survival for Patients With HNSCC

Abbreviation: R/M HNSCC, recurrent and/or metastatic head and neck squamous cell cancer.

Table 2.  

Authors (y) No. of Subjects Treatment Groups Response Rate (%) Median Overall Survival (mo) Reference
Jacobs et al. (1992) 249 Cisplatin + 5-FU 32* 5.5 16
Cisplatin 17 5.0
5-FU 13 6.1
Forastiere et al. (1992) 227 Cisplatin + 5-FU 32* 6.6 20
Carboplatin + 5-FU 21 5.0
Cisplatin 10 5.6
Clavel et al. (1994) 382 CABO 34*   17
Cisplatin + 5-FU 31 6.7
Cisplatin 15  
Gibson et al. (2005) 218 Cisplatin + 5-FU 27 8.7 23
Cisplatin + paclitaxel 26 8.1
Burtness et al. (2005) 117 Cisplatin + cetuximab 26* 9.2 45
Cisplatin + placebo 10 8.0
Vermorken et al. (2008) 442 Platinum + 5-FU + cetuximab 36* 10.1§ 46
Platinum + 5-FU 20 7.4

Selected Randomized Phase III Trials of Cisplatin-Containing Regimens for Patients With Recurrent or
Metastatic Head and Neck Squamous Cell Carcinoma

Abbreviations: 5-FU, 5-fluorouracil; CABO, cisplatin, methotrexate, bleomycin, and vincristine.
*Higher response rates were statistically significant.
In both arms, substitution of carboplatin for cisplatin was allowed, at investigator’s discretion. In the experimental arm, maintenance cetuximab was allowed until disease progression or unacceptable toxicity.
Overall survival was 29 weeks (6.7 months) for the entire study, with no significant differences among groups.
§Higher overall survival was statistically significant.

CME

Current Recommendations for Systemic Therapy of Recurrent and/or Metastatic Head and Neck Squamous Cell Cancer

  • Authors: Matthew G. Fury, MD, PhD; David G. Pfister, MD
  • CME Released: 6/1/2011
  • THIS ACTIVITY HAS EXPIRED FOR CREDIT
  • Valid for credit through: 6/1/2012, 11:59 PM EST
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Target Audience and Goal Statement

This activity is intended for oncologists, otolaryngologists, and other physicians who care for patients with R/M HNSCC.

The goal of this activity is to evaluate treatment approaches to incurable R/M HNSCC.

Upon completion of this activity, participants will be able to:

  1. Distinguish prognostic factors for survival in cases of R/M HNSCC
  2. Evaluate different therapeutic approaches to patients with R/M HNSCC
  3. Analyze the use of cytotoxic agents in the management of R/M HNSCC
  4. Analyze the use of cetuximab in the management of R/M HNSCC


Disclosures

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Author(s)

  • Matthew G. Fury, MD, PhD

    Head and Neck Medical Oncology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY

    Disclosures

    Disclosure: Matthew G. Fury, MD, PhD, has disclosed the following relevant financial relationships:
    Participated in funded or unfunded research on a technology, process, or product development for: Novartis Pharmaceuticals Corporation; Genentech Inc.; Bristol-Myers Squibb Company
    Served as an advisory board member, speakers bureau member, expert witness, or consultant for: Boehringer Ingelheim Pharmaceuticals, Inc.

  • David G. Pfister, MD

    Head and Neck Medical Oncology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY

    Disclosures

    Disclosure: David G. Pfister, MD, has disclosed the following relevant financial relationships:
    Participated in funded or unfunded research on a technology, process, or product development for: Novartis Pharmaceuticals Corporation; Imclone

Editor(s)

  • Kerrin M. Green, MA

    Assistant Managing Editor, Journal of the National Comprehensive Cancer Network

    Disclosures

    Disclosure: Kerrin M. Green, MA, has disclosed no relevant financial relationships.

CME Author(s)

  • Charles P. Vega, MD

    Associate Professor; Residency Director, Department of Family Medicine, University of California, Irvine

    Disclosures

    Disclosure: Charles P. Vega, MD, has disclosed no relevant financial relationships.

CME Reviewer(s)

  • Nafeez Zawahir, MD

    CME Clinical Director, Medscape, LLC

    Disclosures

    Disclosure: Nafeez Zawahir, MD, has disclosed no relevant financial relationships.

  • Sarah Fleischman

    CME Program Manager, Medscape, LLC

    Disclosures

    Disclosure: Sarah Fleischman has disclosed no relevant financial relationships.


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    Medscape, LLC staff have disclosed that they have no relevant financial relationships.

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CME

Current Recommendations for Systemic Therapy of Recurrent and/or Metastatic Head and Neck Squamous Cell Cancer

Authors: Matthew G. Fury, MD, PhD; David G. Pfister, MDFaculty and Disclosures
THIS ACTIVITY HAS EXPIRED FOR CREDIT

CME Released: 6/1/2011

Valid for credit through: 6/1/2012, 11:59 PM EST

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Abstract

For palliation of patients with recurrent and/or metastatic head and neck squamous cell cancer (R/M HNSCC), the major classes of commonly used cytotoxic chemotherapeutic agents are platinum agents (cisplatin, carboplatin), taxanes (paclitaxel, docetaxel), and antimetabolic agents (methotrexate, 5-fluorouracil). Cetuximab, a monoclonal antibody directed against the extracellular domain of the epidermal growth factor receptor, also shows modest activity against R/M HNSCC. Because the overall management of patients with R/M HNSCC often involves multidisciplinary input, this review focuses on data that help guide decision-making in scenarios in which palliative chemotherapy is planned. Avenues for ongoing research are also presented. (JNCCN 2011;9:681–690)