Face to face with oral isotretinoin: a closer look at the spectrum of therapeutic outcomes and why some patients need repeated courses.

Oral isotretinoin, available in the United States for four decades, has been used for the treatment of recalcitrant nodular and deep inflammatory acne vulgaris. This drug revolutionized the management of patients affected by severe inflammatory disease due to its ability to markedly induce acne clearance coupled with prolonged durations of remission after completion of a course of therapy, usually over approximately five months. Over time, it has become recognized that prolonged remission correlates with achieving a threshold cumulative exposure range of approximately 120 to 150 mg/kg of oral isotretinoin. Lesser exposures have demonstrated a higher risk of earlier recurrence of acne vulgaris and a greater likelihood that the patient will require retreatment. As the oral bioavailability of oral isotretinoin is variable, and highly dependent on administration with food, it is very conceivable that earlier relapse may occur if patients have often ingested oral isotretinoin on an empty stomach, thus leading to lesser actual cumulative drug exposure despite the daily dose administered. This article provides an overview on the dosing of oral isotretinoin, reported data on factors that influence relapse after oral isotretinoin therapy, and the potential impact of coadministration with food.

[1]  A. Gewirtzman,et al.  High‐dose isotretinoin in acne vulgaris: improved treatment outcomes and quality of life , 2012, International journal of dermatology.

[2]  E. Wolpert,et al.  Systemic isotretinoin therapy normalizes exaggerated TLR-2-mediated innate immune responses in acne patients , 2012, The Journal of investigative dermatology.

[3]  The state of family nutrition and physical activity: are we making progress? , 2011, Journal of the American Dietetic Association.

[4]  Yan Liu,et al.  Do Breakfast Skipping and Breakfast Type Affect Energy Intake, Nutrient Intake, Nutrient Adequacy, and Diet Quality in Young Adults? NHANES 1999–2002 , 2010, Journal of the American College of Nutrition.

[5]  T. Nicklas,et al.  The relationship of breakfast skipping and type of breakfast consumption with nutrient intake and weight status in children and adolescents: the National Health and Nutrition Examination Survey 1999-2006. , 2010, Journal of the American Dietetic Association.

[6]  H. Gollnick,et al.  Large‐scale worldwide observational study of adherence with acne therapy , 2010, International journal of dermatology.

[7]  A. Layton The use of isotretinoin in acne , 2009, Dermato-endocrinology.

[8]  B. Dréno,et al.  Isotretinoin therapy and the incidence of acne relapse: a nested case–control study , 2009, The British journal of dermatology.

[9]  D. Thiboutot,et al.  Neutrophil gelatinase-associated lipocalin mediates 13-cis retinoic acid-induced apoptosis of human sebaceous gland cells. , 2008, The Journal of clinical investigation.

[10]  J. Strauss,et al.  Guidelines of care for acne vulgaris management. , 2007, Journal of the American Academy of Dermatology.

[11]  I. Haryati,et al.  Profile of acne patients in the Philippines requiring a second course of oral isotretinoin , 2005, International journal of dermatology.

[12]  G. Rampersaud,et al.  Breakfast habits, nutritional status, body weight, and academic performance in children and adolescents. , 2005, Journal of the American Dietetic Association.

[13]  G. Plewig,et al.  Influence of oral isotretinoin treatment on the composition of comedonal lipids. Implications for comedogenesis in acne vulgaris , 2004, Archives of Dermatological Research.

[14]  H. Gollnick,et al.  Management of acne: a report from a Global Alliance to Improve Outcomes in Acne. , 2003, Journal of the American Academy of Dermatology.

[15]  C. Chastang,et al.  Predictive Factors for Failure of Isotretinoin Treatment in Acne Patients: Results from a Cohort of 237 Patients , 1999, Dermatology.

[16]  G. Wolde‐Tsadik,et al.  Recurrence rates after the first course of isotretinoin. , 1998, Archives of dermatology.

[17]  H. Gollnick,et al.  Roaccutane treatment guidelines: results of an international survey. , 1997, Dermatology.

[18]  W. Cunliffe,et al.  Isotretinoin for acne vulgaris—10 years later; a safe and successful treatment , 1993, The British journal of dermatology.

[19]  W. Cunliffe,et al.  Isotretinoin for the treatment of acne vulgaris: which factors may predict the need for more than one course? , 1993, The British journal of dermatology.

[20]  W. Cunliffe,et al.  Oral isotretinoin: patient selection and management , 1993 .

[21]  W. Cunliffe,et al.  Guidelines for optimal use of isotretinoin in acne. , 1992, Journal of the American Academy of Dermatology.

[22]  W. Cunliffe,et al.  Isotretinoin--an explanation for its long-term benefit. , 1987, Dermatologica.

[23]  R. N. Brogden,et al.  Isotretinoin. A review of its pharmacological properties and therapeutic efficacy in acne and other skin disorders. , 1984, Drugs.

[24]  H. Schell,et al.  Relapse Rate of Acne Conglobata after Stopping Isotretinoin , 1984 .

[25]  J. Strauss,et al.  Isotretinoin therapy for acne: results of a multicenter dose-response study. , 1984, Journal of the American Academy of Dermatology.

[26]  W. Colburn,et al.  Food Increases the Bioavailability of Isotretinoin , 1983, Journal of clinical pharmacology.

[27]  W. Cunliffe,et al.  A dose‐response study of 13‐cis‐retinoic acid in acne vulgaris , 1983, The British journal of dermatology.

[28]  J. Strauss,et al.  The treatment of severe cystic acne with 13-cis-retinoic acid. Evaluation of sebum production and the clinical response in a multiple-dose trial. , 1980, Journal of the American Academy of Dermatology.

[29]  W. Cunliffe,et al.  13-CIS RETINOIC ACID AND ACNE , 1980, The Lancet.

[30]  J. Strauss,et al.  Prolonged remissions of cystic and conglobate acne with 13-cis-retinoic acid. , 1979, The New England journal of medicine.