Adjusting for patient selection suggests the addition of docetaxel to 5-fluorouracil-cisplatin induction therapy may offer survival benefit in squamous cell cancer of the head and neck Journal Article


Authors: Pignon, J. P.; Syz, N.; Posner, M.; Olivares, R.; Le Lann, L.; Yver, A.; Dunant, A.; Lewin, F.; Dalley, D. N.; Paccagnella, A.; Taylor, S. G.; Domenge, C.; Bourhis, J.; Mazumdar, M.
Article Title: Adjusting for patient selection suggests the addition of docetaxel to 5-fluorouracil-cisplatin induction therapy may offer survival benefit in squamous cell cancer of the head and neck
Abstract: When induction chemotherapy is used in locally advanced squamous cell cancer of the head and neck (SCCHN), patients often receive cisplatin-5- fluorouracil (PF) followed by radical loco-regional therapy. Phase II studies of docetaxel-cisplatin-5-fluorouracil (TPF) induction therapy, with or without leucovorin (L), have achieved high survival rates versus those reported in phase III PF trials. However, the distribution of prognostic factors may vary between phase II and phase III study populations, making the extrapolation of phase II TPF/L results to phase III PF populations difficult This study used a patient selection standardization method and Cox model to adjust for potential selection bias. Thus, the survival benefit from adding docetaxel into PF induction regimens in SCCHN could be more accurately assessed. The TPF/L dataset comprised 195 patients from six phase II trials. The PF dataset of 585 patients was derived from five large randomized trials included in the Meta-Analysis of Chemotherapy in Head and Neck Cancer (MACH-NC) database. TPF/L and PF datasets differed significantly concerning the distribution of several prognostic factors. Adjusting for these differences, the relative risk of death in the PF versus TPF/L datasets was 1.85 (95% confidence interval 1.37-2.49), corresponding to a 20% 2-year survival benefit (p < 0.0001). Sensitivity analyses confirmed that this improved 2-year survival rate of TPF/L over PF was robust, irrespective of the distribution of studied prognostic factors between treatment datasets. We conclude that this improved survival might be due either to docetaxel's pharmacologic effect or to uncontrolled prognostic factors. © 2004 Lippincott Williams & Wilkins.
Keywords: adult; cancer survival; aged; major clinical study; clinical trial; squamous cell carcinoma; cisplatin; fluorouracil; patient selection; methodology; accuracy; phase 2 clinical trial; antineoplastic combined chemotherapy protocols; drug effect; docetaxel; standardization; population research; head and neck cancer; head and neck neoplasms; randomized controlled trials; folinic acid; taxoids; phase 3 clinical trial; head and neck carcinoma; pooled analysis; neoplasms, squamous cell; clinical trials, phase ii; clinical trials, phase iii; humans; prognosis; human; male; female; priority journal; article
Journal Title: Anti-Cancer Drugs
Volume: 15
Issue: 4
ISSN: 0959-4973
Publisher: Lippincott Williams & Wilkins  
Date Published: 2004-04-01
Start Page: 331
End Page: 340
Language: English
DOI: 10.1097/00001813-200404000-00004
PROVIDER: scopus
PUBMED: 15057136
DOI/URL:
Notes: Anti-Cancer Drugs -- Cited By (since 1996):39 -- Export Date: 16 June 2014 -- CODEN: ANTDE -- Source: Scopus
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  1. Madhu Mazumdar
    127 Mazumdar