1. ¹Department of Pathology, VU Medical Center, Amsterdam, The Netherlands
2. ²Gadjah Mada University, School of Medicine/Sardjito Academic Hospital, Yogyakarta, Indonesia
3. ³UMR 8126, Institut Gustave Roussy, Villejuif, France
4. ⁴Department of Otolaryngology of the Antoni van Leeuwenhoekhuis/The Dutch Cancer Institute, Amsterdam, The Netherlands

Correspondence: Dr JJ Oudejans, MD, PhD, Department of Pathology, VU Medical Centre, De Boelelaan 1117, Amsterdam 1081 HV, The Netherlands. E-mail: jj.oudejans@azvu.nl

Received 6 December 2004; Revised 25 January 2005; Accepted 25 January 2005; Published online 1 April 2005.

Abstract

Poor prognosis in nasopharyngeal carcinoma patients may result from resistance to the apoptosis-inducing effect of radio- and/or chemotherapy. Apoptosis depends on proper activation of caspase 3, resulting in cleavage of key proteins like PARP-1. To investigate whether disruption of the apoptosis pathway results in therapy-resistant tumour cells, we investigated whether absence of caspase 3 activation in tumour biopsies of nasopharyngeal carcinoma patients is related to poor clinical outcome. Moreover, we investigated whether absence of caspase 3 activation is related to loss of procaspase 3 expression or expression of the apoptosis regulators p53, bcl-2 and XIAP. We studied 36 Indonesian nasopharyngeal carcinoma patients without evidence of distant metastases who were treated with curative intent by radiotherapy only. Activation of caspase 3 and expression of the different markers were determined using specific antibodies. Levels of caspase 3 activation were determined by quantifying positively staining tumour cells. Nasopharyngeal carcinoma-derived C15 and C17 tumour cells were used as control. Absence of caspase 3 activation was strongly related to a poor clinical response to radiotherapy and to a higher T and N stage, resulting in a particularly poor clinical outcome with regard to progression-free (P<0.0001) and overall survival time (P<0.0001). Absence of caspase 3 activation was significantly correlated to loss of expression of procaspase 3 (P=0.04). In nasopharyngeal carcinoma patients treated with curative intent, absence of active caspase 3-positive neoplastic cells predicts rapid fatal outcome, and is associated with poor response to radiotherapy and high T and N stage at time of presentation.