Abstract
Background
The EXTREME (Erbitux in First-Line Treatment of Recurrent and Metastatic Head and Neck Squamous Cell Carcinoma) protocol is generally considered the gold standard in palliative first-line treatment. However, there is some disagreement about its effectivity, toxicity, and applicability in daily clinical routine. The purpose of this cross-sectional survey was to describe the palliative treatment offered in German-speaking countries.
Methods
From November 2013 to July 2014, 204 departments of otorhinolaryngology (ORL) in Germany, Austria, and the German-speaking parts of Switzerland were contacted and invited to take part in a web-based survey on the treatment of HNSCC.
Results
In all, 62 of 204 treatment centers (30.4 %) participated in the survey. Of these, 58 departments offered palliative systemic therapy to their patients; 19 of 58 (32.8 %) treated patients undergoing palliative chemotherapy in their own ORL departments, while 40 of 58 (69 %) upheld a cooperation with medical oncologists in the same hospital and 24 of 58 (41.4 %) with medical oncologic practices. Many of these treatment centers offered multiple locations for treatment. Of the 58 departments, 56 provided an institutional standard for first-line palliative treatment, 13 for second-line, and two for third-line treatment. In 42 of 58 departments the EXTREME protocol was the institutional standard of care for first-line treatment. Moreover, 12 of 58 departments mentioned an individual protocol and two of 58 the inclusion in clinical trials as their local standard. The assessment of patients who could be treated with the first-line standard ranged from 0 to 95 % with a mean of 44.5 %.
Conclusion
Palliative systemic therapy seems to be well standardized for first-line treatment, whereas there is little standardization in second- and third-line treatments. A large variation was found regarding the estimate of the applicability of the institutional standard. Reasons for this could be the physicians’ individual experience as well as the varying assessment regarding the toxicity of palliative systemic therapy.
Zusammenfassung
Einleitung
Für die palliative Erstlinientherapie wird meist das EXTREME-Protokoll als Standard angesehen. Es besteht aber Uneinigkeit über Effektivität, Toxizität und Anwendbarkeit in der klinischen Routine. Das Ziel dieser Querschnittsumfrage war die Darstellung der palliativen Behandlungslandschaft im deutschsprachigen Raum.
Methoden
Von 11/2013 bis 07/2014 wurden 204 HNO-Kliniken in Deutschland, Österreich und der deutschsprachigen Schweiz kontaktiert und zur Teilnahme an einer webbasierten Umfrage zur Tumortherapie von Plattenepithelkarzinomen im Kopf-Hals-Bereich (HNSCC) aufgefordert.
Ergebnisse
Von 204 HNO-Kliniken partizipierten 62 (30,4 %). 58 Kliniken bieten medikamentöse Palliativtherapien an. 19/58 Kliniken führen medikamentöse Palliativtherapien direkt in der HNO-Klinik durch, 40/58 kooperieren mit internistischen Onkologen in der eigenen Klinik, 24/58 mit niedergelassenen Onkologen. Viele Kliniken bieten mehrere Behandlungsorte an. Interne Behandlungsstandards halten 56/58 Kliniken für die Erstlinien-, 13/58 für die Zweitlinien-, 2/58 für die Drittlinientherapie vor. Als institutioneller Erstlinienstandard wurde von 42/58 Kliniken das EXTREME-Protokoll, von 12/58 ein individuelles Protokoll und von 2/58 der Einschluss in klinische Studien genannt. Die Einschätzung, wie viele Patienten den Erstlinienstandard erhalten können, reichte von 0–95 % mit einem Mittelwert von 44,5 %.
Schlussfolgerung
Unsere Umfrage ergab eine recht standardisierte Behandlung in der Erstlinientherapie, während Zweit- und Drittlinientherapie kaum standardisiert sind. Die Einschätzung der Anwendbarkeit der institutionellen Standardprotokolle variiert stark. Gründe dafür könnten einerseits die individuelle Erfahrung der Therapeuten, andererseits unterschiedliche Einschätzungen bezüglich der Toxizität der medikamentösen Palliativtherapie darstellen.
Similar content being viewed by others
References
Argiris A, Karamouzis M, Gooding WE et al (2010) Pemetrexed (P) and bevacizumab (B) in patients (pts) with recurrent or metastatic (R/M) squamous cell carcinoma of the head and neck (SCCHN): Final results and correlation with TS, MTHFR, and VEGF gene polymorphisms. J Clin Oncol 28:5533 (Meeting Abstracts)
Baghi M, Hambek M, Wagenblast J et al (2006) A phase II trial of docetaxel, cisplatin and 5‑fluorouracil in patients with recurrent squamous cell carcinoma of the head and neck (SCCHN). Anticancer Res 26:585–590
Chauvergne J, Cappelaere P, Fargeot P et al (1988) A randomized study comparing cisplatin alone or combined in the palliative treatment of carcinoma of the head and neck. Analysis of a series of 209 patients. Bull Cancer 75:9–22
Greenhalgh J, Bagust A, Boland A et al (2009) Cetuximab for the treatment of recurrent and/or metastatic squamous cell carcinoma of the head and neck. Health Technol Assess 13(Suppl 3):49–54
Guntinas-Lichius O, Ruhlow S, Veelken F et al (2009) Quality of life during first-line palliative chemotherapy for recurrent and metastatic head and neck cancer with weekly cisplatin and docetaxel. J Cancer Res Clin Oncol 135:901–908
Knoedler M, Gauler TC, Gruenwald V et al (2013) Phase II study of cetuximab in combination with docetaxel in patients with recurrent and/or metastatic squamous cell carcinoma of the head and neck after platinum-containing therapy: a multicenter study of the Arbeitsgemeinschaft Internistische Onkologie. Oncology 84:284–289
Kurzweg T, Mockelmann N, Laban S et al (2012) Current treatment options for recurrent/metastatic head and neck cancer: a post-ASCO 2011 update and review of last year’s literature. Eur Arch Oto-Rhino-Laryngol 269(10):2157–2167
Machiels JP, Subramanian S, Ruzsa A et al (2011) Zalutumumab plus best supportive care versus best supportive care alone in patients with recurrent or metastatic squamous-cell carcinoma of the head and neck after failure of platinum-based chemotherapy: an open-label, randomised phase 3 trial. Lancet Oncol 12:333–343
Peron J, Polivka V, Chabaud S et al (2014) An effective and well-tolerated strategy in recurrent and/or metastatic head and neck cancer: successive lines of active chemotherapeutic agents. BMC Cancer 14:504
Sabichi AL, Kies MS, Glisson BS et al (2010) A phase II study of sorafenib in combination with carboplatin and paclitaxel in patients with metastatic or recurrent squamous cell cancer of the head and neck (SCCHN). J Clin Oncol 28:5532 (Meeting Abstracts)
Schopper S, Laban S, Guldenzoph B et al (2012) New aspects in the therapy of recurrence and metastasis of head and neck cancer: Highlights from the 2012 ASCO meeting. HNO 60:957–961
Schornagel JH, Verweij J, De Mulder PH et al (1995) Randomized phase III trial of edatrexate versus methotrexate in patients with metastatic and/or recurrent squamous cell carcinoma of the head and neck: a European Organization for Research and Treatment of Cancer Head and Neck Cancer Cooperative Group study. J Clin Oncol 13:1649–1655
Seiwert TY, Clement PM, Cupissol D et al (2010) BIBW 2992 versus cetuximab in patients with metastatic or recurrent head and neck cancer (SCCHN) after failure of platinum-containing therapy with a cross-over period for progressing patients: Preliminary results of a randomized, open-label phase II study. J Clin Oncol 28:5501 (Meeting Abstracts)
Vermorken JB, Mesia R, Rivera F et al (2008) Platinum-based chemotherapy plus cetuximab in head and neck cancer. N Engl J Med 359:1116–1127
Vermorken JB, Peyrade F, Krauss J et al (2014) Cisplatin, 5‑fluorouracil, and cetuximab (PFE) with or without cilengitide in recurrent/metastatic squamous cell carcinoma of the head and neck: results of the randomized phase I/II ADVANTAGE trial (phase II part). Ann Oncol 25:682–688
Vermorken JB, Stohlmacher-Williams J, Davidenko I et al (2013) Cisplatin and fluorouracil with or without panitumumab in patients with recurrent or metastatic squamous-cell carcinoma of the head and neck (SPECTRUM): an open-label phase 3 randomised trial. Lancet Oncol 14:697–710
Vermorken JB, Trigo J, Hitt R et al (2007) Open-label, uncontrolled, multicenter phase II study to evaluate the efficacy and toxicity of cetuximab as a single agent in patients with recurrent and/or metastatic squamous cell carcinoma of the head and neck who failed to respond to platinum-based therapy. J Clin Oncol 25:2171–2177
Williamson SK, Moon J, Huang CH et al (2010) Phase II evaluation of sorafenib in advanced and metastatic squamous cell carcinoma of the head and neck: Southwest Oncology Group Study S0420. J Clin Oncol 28:3330–3335
Winquist E, Al-Rasheedy I, Nichols AC et al (2014) Temporal changes in the efficacy of chemotherapy for recurrent or metastatic squamous cell carcinoma of the head and neck: A systematic review and meta-analysis. Cancer Treat Rev 40:1073–1079
Acknowledgements
We would like to thank all participating treatment centers for their time in completing this survey and their detailed responses.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
S. Laban, J. Kimmeyer, T. K. Hoffmann, C.-J. Busch, J. A. Veit, N. Möckelmann, and T. Kurzweg state that there are no conflicts of interest. R. Knecht is a member of the scientific advisory board for Merck Serono, Sanofi Aventis, Boehringer Ingelheim, and Bayer Healthcare Leverkusen.
The accompanying manuscript does not include studies on humans or animals.
Additional information
Dieser Beitrag ist als eine Originalarbeit anzusehen und aus formalen Gründen im Leitthema dieser Ausgabe eingeordnet.
This article should be considered an original contribution and has been classified for technical reasons as a main topic.
Rights and permissions
About this article
Cite this article
Laban, S., Kimmeyer, J., Knecht, R. et al. Palliative treatment standards for head and neck squamous cell carcinoma. HNO 64, 487–493 (2016). https://doi.org/10.1007/s00106-016-0187-x
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00106-016-0187-x
Keywords
- Palliative therapy, systemic
- Squamous cell carcinoma, head and neck
- Otorhinolaryngology
- Treatment protocols
- Clinical trial