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Oxygen and Cancer: friend or foe? Part 1: Scientific part Dirk de Ruysscher Part 2: Organisational part Harald Moonen Cancer = Genetic disease with 6 features The 6 Hallmarks of Cancer HYPOXIA = LACK OF OXYGEN Tumor hypoxia Hypoxia Hypoxia 1 mm size Tumor hypoxia Abnormal vasculature is a prime cause of hypoxia in cancer Colon xenograft Normal colon Corrosion castings Two types of hypoxia blood vessel oxygen glucose conc Distance from vessel Heterogeneity in Oxygenation a) b) c) d) Amount (%) amongst patients In severity In space In time Hypoxia tolerance/angiogenesis Hypoxia tolerance varies amongst tumors blood vessel oxygen glucose conc Distance from vessel Tumour hypoxia, does it exist in human tumours? pO2 measurements indicate most tumors are hypoxic 20 Normal tissue Relative frequency (%) Relative frequency (%) Nordsmark et al. Acta Oncol 1994 15 10 5 0 0 20 40 60 80 Oxygen partial pressure (mmHg) 20 Tumour 15 10 5 0 0 20 40 60 80 Median Oxygen Levels of Human Tumors Tumor Type Median pO2 (mmHg) Reference Glioblastoma 5.6 (14 pts) Collingridge et al, 1999 Head & Neck 7.4 (41 pts) 4.6 (63 pts) Rudat et al, 2000 Brizel et al, 1999 Lung 12.8 (26 pts) Le & Stevens (pers. comm.) Breast 10.0 (15 pts) Vaupel et al, 2002 2.7 (7 pts) Koong et al, 2000 10.0 (51 pts) 5.0 (74 pts) Knocke et al, 1999 Fyles et al, 1998 Prostate 2.4 (59 pts) 4.5 (55 pts) Movsas et al, 2001 Parker et al, 2004 Soft Tissue Sarcoma 6.2 (34 pts) Brizel et al, 1996 Pancreas Cervix Cf. normal = 30-60 mmHg (A) Baseline [18F]-fluorodeoxyglucose (FDG) positron emission tomography (PET) of patient with T2N2b squamous cell carcinoma of the pyriform fossa with left nodal mass (A) Baseline [18F]-fluorodeoxyglucose (FDG) positron emission tomography (PET) of patient with T2N2b squamous cell carcinoma of the pyriform fossa with left nodal mass. (B) (B) [18F]-fluoromisonidazole (FMISO) -PET at baseline, nonhypoxic primary tumor, and hypoxic node. (C) C) FDG-PET 12 weeks after chemoboost, complete response in nonhypoxic primary tumor, and poor response in hypoxic node. Residual tumor in nodal mass was confirmed pathologically after neck dissection. Rischin, D. et al. J Clin Oncol; 24:2098-2104 2006 Copyright © American Society of Clinical Oncology Prognostic value of F-MISO PET Rajendran, J. G. et al. Clin Cancer Res 2006;12:5435-5441 Copyright ©2006 American Association for Cancer Research Tumour hypoxia, does it matter? The clinical importance of tumor hypoxia 1. Resistance to radiotherapy 2. Resistance to chemotherapy 3. Contribution to ‘malignancy’ Cure = min kill of 109 cells Cure = min kill of 109 cells 90% cell death: Partial Remission, no cure 99,9% cell death: Complete remission, no cure 99,9999999% cell death: Complete remission, Local control, Cure if no metastasis Cell death N°1 = Mitotic death Stem cells? Dividing cells Unfit cells First clinical demonstration of hypoxia-mediated radioresistance 1909 Gottwald Schwarz Vienna 1880-1959 In vitro effect of hypoxic conditions on radiation-induced cellular lethality 10 OER (Oxygen enhancement ratio) = Radiation dose in hypoxia/ Radiation dose in air Surviving fraction 1 0.1 OER = 2.8 0.01 oxic Hypoxic 0.001 0 5 10 15 20 25 30 Radiation dose (Gy) Cells are much more sensitive to x-rays in the presence of molecular oxygen than in its absence. The ratio of doses under hypoxia to those under oxia necessary to produce the same level of cell killing is close to 3. G. Steel, Basic Clinical Radiobiology 1997, second edition Impact of hypoxia on survival in patients with cervical cancer and definitive radiotherapy Radiotherapy 1.0 pO2 > 10mmHg, n = 19 0.8 0.6 0.4 pO2 < 10mmHg, n = 23 0.2 Log-rank p = 0.0638 0 0 10 20 30 40 Time (months) Höckel M. et al. Cancer Res 56, 4509-4515 (1996) 50 60 70 80 blood vessel cytotoxic drug resistance to radiation drug conc Distance from vessel Impact of pretreatment on prognosis in surgically treated patients with cervical cancer Overall survival 1.0 Surgery 0.8 pO2 > 10 mm Hg, n = 22 0.6 0.4 0.2 Höckel M. et al, 1996 pO2 < 10 mm Hg, n=25 Log-rank n = 0.0107 0 0 10 20 30 40 50 60 Time (months) 70 80 Treatment of hypoxic cells: One example: To kill hypoxic cells with a “bioreductive drug” Non toxic prodrug Toxic drug Hypoxia Mechanism Tirapazamin • Selectivity for tumors: • in hypoxia: TPZ radical is formed which causes DNA breaks • in aerobic conditions: TPZ radical is reoxidized towards the parent compound with the production of superoxide radicals which are moderately cytotoxic Exploit hypoxia: tirapazamine, a bioreductive drug • Tirapazamine - a hypoxia selective cytotoxin Tirapazamine, Cisplatin, and Radiation versus Fluorouracil, Cisplatin, and Radiation in patients with locally advanced head and neck cancer: a randomized phase II trial of the Trans-Tasman Radiation Oncology Group (TROG 98.02). Rischin D et al. JCO 05 Jan 1;23(1):79-87. Effect on normal tissues Rischin D et al. Tirapazamine, Cisplatin, and Radiation versus Fluorouracil, Cisplatin, and Radiation in patients with locally advanced head and neck cancer: a randomized phase II trial of the Trans-Tasman Radiation Oncology Group (TROG 98.02). JCO 05 Jan 1;23(1):79-87. Time to local failure (Kaplan-Meier method) by treatment arm and hypoxia in the primary tumor (censored times are indicated as tick marks on the curves) Rischin, D. et al. J Clin Oncol; 24:2098-2104 2006 extra 2 Gy during the same fraction 2 Gy Does hemoglobin has a prognostic value in human cancer ? Hb is associated with locoregional control of head and neck cancer by RT 80 67.8% Locoregional Failure (%) 65.9% Low Hb 60 High Hb 51.6% 48.3% 40 20 p = 0.0026 Males Females < 14.5 < 13.0 g/dl 14.5 13.0 g/dl Low Hb High Hb 0 0 1 2 3 4 Years from randomization 5 6 7 Lee et al. (RTOG 85-27), IJROBP 42:1069, 1998 Overgaard (1988) Squamous Ca larynx/pharynx 1112 patients Oxidative damage: Plays a role in carcinogenesis Tumour Hypoxia: - related to treatment resistance - related to tumour aggressiveness BUT ALSO - a unique therapeutic opportunity!