Subject: Isotretinoins PA 118-A P08-2024_R
| Isotretinoins (All Oral) |
|
ABSORICA
(isotretinoin)
|
|
ABSORICA LD
(isotretinoin)
|
|
ACCUTANE
(isotretinoin)
|
|
AMNESTEEM
(isotretinoin)
|
|
CLARAVIS
(isotretinoin)
|
|
MYORISAN
(isotretinoin)
|
|
ZENATANE
(isotretinoin)
|
Policy:
Indications
FDA-approved Indications
Absorica, Absorica LD
Absorica and Absorica LD are indicated for the treatment of severe recalcitrant nodular acne in non-pregnant patients 12 years of age and older with multiple inflammatory nodules with a diameter of 5 mm or greater. Because of significant adverse reactions associated with its use, Absorica and Absorica LD are reserved for patients with severe nodular acne who are unresponsive to conventional therapy, including systemic antibiotics.
Limitations of Use
If a second course of Absorica/Absorica LD therapy is needed, it is not recommended before a two-month waiting period because the patient’s acne may continue to improve following a 15 to 20-week course of therapy.
Accutane, Amnesteem, Claravis, Myorisan, Zenatane
Isotretinoin is indicated for the treatment of severe recalcitrant nodular acne. Nodules are inflammatory lesions with a diameter of 5 mm or greater. The nodules may become suppurative or hemorrhagic. “Severe,” by definition, means “many” as opposed to “few or several” nodules. Because of significant adverse effects associated with its use, isotretinoin should be reserved for patients with severe nodular acne who are unresponsive to conventional therapy, including systemic antibiotics. In addition, isotretinoin is indicated only for those patients who are not pregnant, because isotretinoin can cause life-threatening birth defects.
A single course of therapy for 15 to 20 weeks has been shown to result in complete and prolonged remission of disease in many patients. If a second course of therapy is needed, it should not be initiated until at least 8 weeks after completion of the first course, because experience has shown that patients may continue to improve while off isotretinoin. The optimal interval before retreatment has not been defined for patients who have not completed skeletal growth.
Compendial Uses
Acne – refractory9
Cutaneous T-Cell Lymphoma (CTCL) (e.g., mycosis fungoides, Sézary syndrome)7
Keratosis follicularis (Darier Disease) – severe9
Lamellar ichthyosis – severe skin involvement7
Neuroblastoma9
Pityriasis rubra pilaris7
Rosacea – severe refractory9
Squamous Cell Cancers – to reduce the development of precancers and skin cancers in high risk patients9
Transient acantholytic dermatosis (Grover’s Disease) – severe9
Coverage Criteria
Acne Vulgaris, Rosacea
Authorization may be granted when the patient has a diagnosis of severe recalcitrant nodular acne vulgaris, refractory acne vulgaris, OR severe refractory rosacea when ALL of the following criteria are met:
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The patient has tried and had an inadequate treatment response to ANY topical acne product AND an oral antibiotic [Note: Topical products include salicylic acid, benzoyl peroxide, azelaic acid, adapalene, tretinoin, tazarotene, clindamycin, erythromycin, or metronidazole for rosacea. Oral antibiotics include minocycline, doxycycline, tetracycline, erythromycin, trimethoprim-sulfamethoxazole, trimethoprim, azithromycin.]
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Treatment will be limited to 40 weeks (2 courses) or less AND with at least 8 weeks between each course
Neuroblastoma, Cutaneous T-cell Lymphoma (CTCL), Squamous Cell Cancers, Grover’s Disease, Darier Disease, Lamellar Ichthyosis, Pityriasis Rubra Pilaris
Authorization may be granted when the patient has a diagnosis of neuroblastoma, cutaneous T-cell lymphoma (CTCL) (e.g., mycosis fungoides, Sézary syndrome), is at high risk for developing skin cancer (squamous cell cancers), transient acantholytic dermatosis (Grover’s Disease), keratosis follicularis (Darier Disease), lamellar ichthyosis, OR pityriasis rubra pilaris
Duration of Approval (DOA)
Place of Service:
Outpatient
The above policy is based on the following references:
- Absorica, Absorica LD [package insert]. Cranbury, NJ: Sun Pharmaceutical Industries, Inc.; June 2023.
- Accutane [package insert]. Scottsdale, AZ: JG Pharma Inc.; December 2023.
- Amnesteem [package insert]. Morgantown, WV: Mylan Pharmaceuticals Inc.; August 2022.
- Claravis [package insert]. North Wales, PA: Teva Pharmaceuticals USA, Inc.; August 2022.
- Myorisan [package insert]. Gurnee, IL: Akorn Operating Company LLC.; December 2022.
- Zenatane [package insert]. Princeton, NJ: Dr. Reddy’s Laboratories, Inc.; September 2022.
- Lexicomp Online, AHFS DI (Adult and Pediatric) Online. Waltham, MA: UpToDate, Inc.; 2024. https://online.lexi.com. Accessed July 3, 2024.
- Lexicomp Online, Lexi-Drugs Online. Waltham, MA: UpToDate, Inc.; 2024. https://online.lexi.com. Accessed July 3, 2024.
- Micromedex® (electronic version). Merative, Ann Arbor, Michigan, USA. Available at: https://www.micromedexsolutions.com/ (cited: 07/02/2024).
- Reynolds RV, Yeung H, Cheng CE, et al. Guidelines of care for the management of acne vulgaris. J Am Acad Dermatol. 2024;90(5):1006.e1-1006.e30.
- National Institute of Arthritis and Musculoskeletal and Skin Diseases. http://www.niams.nih.gov/Health_Info/Rosacea/default.asp#6. Accessed July 3, 2024.
- Granulomatous Rosacea. National Center for Advancing Translational Sciences: Genetic and Rare Diseases Information Center. https://rarediseases.info.nih.gov/diseases/6548/granulomatous-rosacea. Accessed July 3, 2024.
- Del Rosso JQ, Thiboutot D, Gallo R, et al. Consensus recommendations from the american acne & rosacea society on the management of rosacea, Part 3: A status report on systemic therapies. CUTIS. 2014;93:134-38.
- Neuroblastoma Treatment. National Cancer Institute at the National Institute of Health. https://cancer.gov/types/neuroblastoma/hp/neuroblastoma-treatment-pdq#_707_toc. Accessed July 3, 2024.
- National Comprehensive Cancer Network. Clinical Practice Guidelines in Oncology. Squamous Cell Skin Cancer. Version 1.2024. November 9, 2023. Available at: www.NCCN.org. Accessed July 3, 2024.
- National Comprehensive Cancer Network. Clinical Practice Guidelines in Oncology. Primary Cutaneous Lymphomas. Version 2.2024. May 6, 2024. Available at: www.NCCN.org. Accessed July 3, 2024.
- NIH National Center for Advancing Translational Sciences. Grover’s Disease. https://rarediseases.info.nih.gov/diseases/6551/grovers-disease. Accessed July 3, 2024.
- American Osteopathic College of Dermatology. Grover's Disease. http://www.aocd.org/?page=GroversDisease. Accessed July 3, 2024.
- NIH National Center for Advancing Translational Sciences. Genetic and Rare Diseases Information Center. Darier disease. https://rarediseases.info.nih.gov/diseases/6243/darier-disease. Accessed July 3, 2024.
- Darier Disease. American Osteopathic College of Dermatology. http://www.aocd.org/skin/dermatologic_diseases/darier_disease.html. Accessed July 3, 2024.
- NIH National Center for Advancing Translational Sciences. Genetic and Rare Diseases Information Center. Lamellar ichthyosis. https://rarediseases.info.nih.gov/diseases/10803/lamellar-ichthyosis. Accessed July 3, 2024.
- NIH National Center for Advancing Translational Sciences. Genetic and Rare Diseases Information Center. Pityriasis rubra pilaris. https://rarediseases.info.nih.gov/diseases/7401/pityriasis-rubra-pilaris. Accessed July 3, 2024.
- Pityriasis Rubra Pilaris. American Osteopathic College of Dermatology. http://www.aocd.org/?page=PityriasisRubraPil. Accessed July 3, 2024.
Copyright Aetna Inc. All rights reserved. Pharmacy Clinical Policy Bulletins are developed by Aetna to assist in administering plan benefits and constitute neither offers of coverage nor medical advice. This Clinical Policy Bulletin contains only a partial, general description of plan or program benefits and does not constitute a contract. Aetna does not provide health care services and, therefore, cannot guarantee any results or outcomes. Participating providers are independent contractors in private practice and are neither employees nor agents of Aetna or its affiliates. Treating providers are solely responsible for medical advice and treatment of members. This Clinical Policy Bulletin may be updated and therefore is subject to change.
December 19, 2024