1 / 29

The Efficacy of Pentoxifylline / Tocopherol Combination in the Treatment of Osteoradionecrosis

The Efficacy of Pentoxifylline / Tocopherol Combination in the Treatment of Osteoradionecrosis. Marc Hayashi, DMD Monica Pellecer , DDS UCLA Hospital Dentistry Clinic April 12, 2014. Learning Objectives. Summarize the radiation-induced fibroatrophic pathogenesis model of ORN

talisa
Download Presentation

The Efficacy of Pentoxifylline / Tocopherol Combination in the Treatment of Osteoradionecrosis

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. The Efficacy of Pentoxifylline/Tocopherol Combination in the Treatment of Osteoradionecrosis Marc Hayashi, DMD Monica Pellecer, DDSUCLA Hospital Dentistry Clinic April 12, 2014

  2. Learning Objectives • Summarize the radiation-induced fibroatrophic pathogenesis model of ORN • Understand the rationale for utilizing pentoxifylline and tocopherol in the management of ORN • Evaluate the effectiveness and safety of pentoxifylline and tocopherol

  3. Osteoradionecrosis (ORN) • Consequence of radiation therapy in head and neck cancer treatment • “Bone necrosis that can occur in association with radiation treatment for cancer in the absence of recurrent or metastatic disease” • Incidence of 5-15% • Mandible more than maxilla • Trismus, pain, xerostomia, dysgeusia, dysphagia • Superficial to pathological fracture

  4. Osteoradionecrosis (ORN) • Most important risk factor: surgical trauma • Other factors: periodontal disease, denture irritation, spontaneous • Incidence increases w/ increased dosage • More common w/ brachytherapy

  5. Treatment • Conservative tx often employed • Abx, local wound irrigation, debridement and gentle sequestrectomy

  6. Treatment • Established ORN: HBO often considered tx of choice • Recent insights to pathophysiology of ORN • Radiation-induced fibroatrophic process (RIF)

  7. Hyperbaric Oxygen Therapy • Based on three H principle (Marx) • Hypoxia, Hypocellularity, Hypovascularity as cause of ORN • HBO alone can arrest ORN, but not resolve it • Aggressive surgical management required in most cases • Marx’s initial study, 41/58 patients (70% required resection and grafting) • Mixed success rates

  8. Review Article • “Hyperbaric Oxygen Therapy for Radionecrosis of the Jaw: A Randomized, Placebo-Controlled, Double-Blind Trial From the ORN96 Study Group.” • Annane et al. J ClinOncol2004 • At 1 year, 19% had recovered in HBO arm, 32% in placebo arm • No benefit for overt mandibularosteoradionecrosis

  9. Review Article • “Paradigm shifts in the management of osteoradionecrosis of the mandible.” • Jacobson et al. Oral Oncology 2010 • HBO alone has minimal if any benefit in the treatment of advanced ORN • Advanced ORN requires aggressive surgical therapy • Some benefit to HBO in early/intermediate ORN

  10. Update to Pathophysiology of ORN • Radiation-induced fibroatrophic process (RIF) as outlined by Delanian et al • Targeted treatment • Antioxidant pathway • Pentoxifylline and Tocopherol (Vitamin E) • 3 successive clinical and histopathologic phases

  11. Pathophysiology • Pre-Fibrotic Phase • First few months after XRT, asymptomatic • Endothelial cells (EC) release chemokines • Chronic non-specific inflammation, increasing vascular permeability and edema formation • Vascular thrombosis, causing necrosis of microvessels with localized ischemia • CT exposed, triggering fibroblastic activation • Fibroblasts differentiate to myofibroblasts

  12. Pathophysiology • Constitutive Phase • Organized fibrotic sequelae, thickening and hardening of the tissues • RIF tissues made of fibroblasts/myofibroblasts and ECM • Combined damage to EC and CT cells, with increased action of cytokines, leads to persistent state of RIF • Myofibroblasts persist, radiation induced fibrous swellings

  13. Pathophysiology • Late Fibroatrophy Phase • Lasts 5-30 years after XRT • Retractile atrophy, gradual destruction of tissues within field • Density increases by successive remodeling of ECM deposits • Tissues are friable, developing poorly vascularized and cellularisedfibroatrophy • Subject to late reactivated inflammation after physicochemical trauma

  14. Suryawanshi A, Kumar SN, Dolas RS, Khindria R, Pawar V, Singh M. Review Article: Maxillofacial osteoradionecrosis. Journal of Dental Research and Review. 2014:1:1:42-49.

  15. PENTOCLO • Delanian et al • Pentoxifylline-Tocopherol-Clodronate (PENTOCLO) combination demonstrated impressive results in resolving ORN • Well tolerated, no adverse effects noted • Most recent trial, all 54 patients treated achieved complete recovery in a median 9 months

  16. PENTO • Pentoxifylline • Methylxanthine derivative • Decreases blood viscosity, increases erythrocyte flexibility, increases tissue oxygen levels • Opposes certain inflammatory mediators (TNF-α) • Shown to accelerate healing w/ late radiation-related injuries • GI and allergy related issues

  17. PENTO • Tocopherol (Vitamin E) • Methylated phenol compound • Antioxidant properties, decreasing oxidative damage from XRT • Protects cell membranes against lipid peroxidation • Partly inhibits TGF-beta1 and procollagen gene expression

  18. PENTO • In combination, demonstrated positive synergistic effect on inflammation progression and fibrosis • Delanian et al determined dose to be 800mg Pentoxifylline and 1,000 IU Tocopherol per day • Total duration of treatment time not yet determined • <12 months, partial rebound effect • >2-3 years, appeared necessary for advanced cases

  19. Method • Chart review of hospital dentistry group • 13 patients • All had exposed bone after cancerocidal doses of XRT for oropharyngeal cancers • Pentoxifylline 400mg BID and Tocopherol 1000 IU QD • All XRT over 60Gy; 9 additionally received Chemo • Reviewed chart entries, noting improvement/resolution or worsening/adverse effects • Ethical approval obtained from IRB

  20. Results • 12 Male: 1 Female • Age: 45-79 • 12 in mandible, 1 in maxilla • 6 spontaneous, 4 extractions, 3 periodontal • 7 had h/o EtOH/Tob use

  21. Results (continued) • 11 patients healed • One currently undergoing treatment • One demonstrated no improvement after 22 months, opting for segmental resection • No adverse effects noted • Avg. treatment time: 13.5 months • Treatment Time Range: 1-33 months

  22. Results

  23. Discussion • 11/13 of our patients resolved (84%) • No adverse effects noted, well tolerated • Limitations: • Small sample size • Staging of ORN lesions w/ Epstein system or SOMA score • Clodronate not utilized

  24. Conclusion • Medical approach appears safe and efficacious • Tolerance and compliance satisfactory • Further randomized and controlled clinical trials are necessary to validate our findings

  25. Thank You • Dr. Monica Pellecer • Dr. Eric Sung • Dr. Evelyn Chung

  26. References • Annane D, Depondt J, Aubert P, Villart M, Gehanno P, Gajdos P, Chvret S. Hyperbaric Oxygen Therapy for Radionecrosis of the Jaw: A Randomized, Placebo-Controlled, Double-Blind Trial From the ORN96 Study Group. J ClinOncol. 2004;22:4893-4900. • Beumer J, Curtis TA. Radiation therapy of head and neck tumors: Oral Effects and Dental Manifestations. Maxillofacial Rehabilitation. St. Louis, CV Mosby, 1979, pp 23-89. • Beumer J, Harrison R, Sanders B, Kurrasch M. Osteoradionecrosis: Predisposing factors and outcomes of therapy. Head and Neck Surgery 1984;6:819-827. • Chiao TB, Lee AJ. Role of Pentoxifylline and Vitamin E in Attenuation of Radiation-Induced Fibrosis. The Annals of Pharmacotherapy 2005;39:516-522. • Delanian S, Lefaix J-L. Complete healing of severe osteoradionecrosis with treatment combining pentoxifylline, tocopherol and clodronate. The British Journal of Radiology 2002;75:467-469. • Delanian S, Chatel C, Porcher R, Depondt J, Lefaix J-L. Complete restoration of refractory mandibularosteoradionecrosis by prolonged treatment with a pentoxifylline-tocopherol-clodronate combination (PENTOCLO): A phase II trial. Int J RadiatOncolBiol Phys 2011;80:3:832-839. • Delanian S, Depondt J, Lefaix J-L. Major healing of refractory mandible osteoradionecrosis after treatment combining pentoxifylline and tocopherol: A phase II trial. Head Neck 2005;27:114-123. • Delanian S, Lefaix J-L. The radiation-induced fibroatrophic process: therapeutic perspective via the antioxidant pathway. Radiotherapy and Oncology 2004;73:119-131. • Epstein JB, Wong FL, Stevenson-Moore P. Osteoradionecrosis: Clinical Experience and a Proposal for Classification. J Oral MaxillofacSurg 1987;45:104-110. • Epstein J, van derMeij E, McKenzie M, Wong F, Lepawsky M, Stevenson-Moore P. Postradiationosteoradionecrosis of the mandible: A long-term follow-up study. Oral Surg Oral Med Oral Pathol Oral RadiolEndod 1997;83:657-62. • Fritz GW, Gunsolley JC, Abubaker O, Laskin DM. Efficacy of Pre- and Postirradiation Hyperbaric Oxygen Therapy in the Prevention of PostextractionOsteoradionecrosis: A Systematic Review. J Oral MaxillofacSurg 2010;68:2653-2660.

  27. References (continued) • Futran ND, Trotti A, Gwede CG. Pentoxifylline in the Treatment of Radiation-Related Soft Tissue Injury: Preliminary Observations. The Laryngoscope 1997;107:391-395. • Jacobson AS, Buchbinder D, Hu K, Urken ML. Paradigm shifts in the management of osteoradionecrosis of the mandible. Oral Oncology 2010;46:795-801. • Kahenasa N, Sung EC, Nabili V, Kelly J, Gerret N, Nishimura I. Resolution of pain and complete healing of mandibularosteoradionecrosis using pentoxifylline and tocopherol: a case report. Oral Surg Oral Med Oral Pathol Oral Radiol 2012;113:e18-e23. • Lyons A, Ghazali N. Osteoradionecrosis of the jaws: current understanding of its pathophysiology and treatment. British Journal of Oral and Maxillofacial Surgery 2008;46:653-660. • Marx RE. A new concept in the treatment of osteoradionecrosis. J Oral MaxillofacSurg 1983;41:351-357. • Marx RE. Osteoradionecrosis: A New Concept of Its Pathophysiology. J Oral MaxillofacSurg 1983;41:283-288. • Mcleod NMH, Pratt CA, Brennan PA. Pentoxifylline and tocopherol in the management of patients with osteoradionecrosis, the Portsmouth experience. British Journal of Oral and Maxillofacial Surgery 2012;50:41-44. • Shaw RJ, Dhanda J. Hyperbaric oxygen in the management of late radiation injury to the head and neck. Part I: treatment. Br J Oral MaxillofacSurg(2010),doi:10.1016/j.bjoms.2009.10.036.1-7. • Singh N, Scully C, Joyston-Bechal S. Oral Complications of Cancer Therapies: Prevention and Management. Clinical Oncology 1996;8:15-24. • Spiegelberg L, Djasim UM, van Neck HW, Wolvius EB, van derWal KG. Hyperbaric Oxygen Therapy in the Management of Radiation-Induced Injury in the Head and Neck Region: A Review of the Literature. J Oral MaxillofacSurg 2010;68:1732-1739. • Suryawanshi A, Kumar SN, Dolas RS, Khindria R, Pawar V, Singh M. Review Article: Maxillofacial osteoradionecrosis. Journal of Dental Research and Review. 2014:1:1:42-49. • Vissink A, Burlage FR, Spijkervet FKL, Jansma J, Coppes RP. Prevention and Treatment of the Consequences of Head and Neck Radiotherapy. Crit Rev Oral Biol Med 2003;14(3):213-225.

More Related