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                                    | Effective Date: 08/01/2011 | Title: Xiaflex (Collagenase Clostridium Histolyticum) |  
                                    | Revision Date: 10/01/2019 | Document: BI300:00 |  
                                    | CPT Code(s): J0775 
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                                    | Public Statement 
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                                    | 
Effective Date: 
 
a)   
This policy will apply to 
all services performed on or after the above revision date which will become the 
new effective date. 
b)   
For all services referred 
to in this policy that were performed before the revision date, contact customer 
service for the rules that would apply. 
	
	Xiaflex is covered 
	only for the treatment of Dupuytren’s contracture.
	Dupuytren`s 
	contracture, a progressive fibro-proliferative disorder, is characterized by 
	nodule formation and contracture of the palmar fascia, and may result in 
	flexion deformity of the fingers and loss of hand function.  The disease is 
	common in men older than 40 years; and in persons who smoke, use alcohol, or 
	have diabetes mellitus.  The symptoms 
	of Dupuytren`s contracture are often mild and painless and do not require 
	treatment. In some patients, however, it may progress to the next stage, in 
	which cords of fibrous tissue form in the palm and run into the fingers or 
	thumb, eventually, pulling them into a permanently flexed position, making 
	it difficult to perform activities of daily living.  
3. Xiaflex requires prior authorization for diagnosis 
of Peyronie’s Disease (PD). 
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                                    | Medical Statement 
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                                    | 
	
	Collagenase 
	clostridium histolyticum (Xiaflex) injections are considered medically 
	necessary for the treatment of adults with Dupuytren`s contracture with a 
	palpable cord.
	.  
	 Xiaflex for the treatment of Peyronie’s disease requires prior 
	authorization and is covered when all of the following criteria are met: 
-      
Diagnosis of PD with both 
a palpable plaque and curvature deformity of ≥ 30 degrees at the start of 
therapy; 
-      
 Prescribed by or in consultation with a 
healthcare provider experienced in the treatment of male urological diseases; 
-      
 Age ≥ 18 years; 
-      
Dose does not exceed 0.58 
mg per injection (one vial per injection). 
-      
Approval duration: 3 
months (up to 2 injections) 
Request for continuation 
of Xiaflex for Peyronie’s disease require all of the following criteria: 
1.   
Member has previously met 
initial approval criteria;  
2.   
There is documented 
curvature deformity of ≥15 degrees remaining since last treatment cycle; 
 
3.   
Last treatment cycle was 
≥ 6 weeks ago. 
4.   
 Member has received < 4 treatment cycles 
(i.e. < 8 injections [2 injections per cycle]); 
5.   
 If request is for a dose increase, new 
dose does not exceed 0.58 mg per injection (one vial per injection). Approval 
duration: 3 months (up to 2 injections) 
Codes 
Used In This BI: J0775
Collagenase, clost hist inj 
Addendum:
 
1.   
Effective 01/10/2019: 
Xiaflex is covered with prior authorization for diagnosis of Peyronie’s disease 
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                                        | Background 
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                                        | 
Dupuytren’s 
contracture initially can be managed with observation and non-surgical therapy. 
 It will regress without treatment in about 10% of patients.  Injection of 
steroids into the nodule has been shown to reduce the need for surgery.  
Surgical referral should be made when metacarpophalangeal (MCP) joint 
contracture reaches 30 degrees or when proximal interphalangeal (PIP) joint 
contracture occurs at any degree.  In-office percutaneous needle aponeurotomy is 
an alternative to surgery (Trojian and Chu, 2007). 
Swartz and 
Lalonde (2008) stated that treatment of Dupuytren`s disease is offered to 
symptomatic patients with painful nodular or disabling contracture.  Limited 
fasciectomy of the involved abnormal structures followed by hand therapy is 
standard treatment, but it is associated with serious potential complications.  
Moreover, recurrence is common.  New treatments include the injection of 
clostridial collagenase, which works by breaking down the excessive build-up of 
collagen in the hand. 
In a phase II 
open-label clinical trial, Badalamente and Hurst (2000) examined the clinical 
safety and effectiveness of clostridial collagenase injection as a non-surgical 
treatment of Dupuytren`s disease.  A total of 35 patients entered the study (3 
women and 32 men).  The mean age was 65 years.  The first 6 patients were 
treated following a dose escalation protocol and received 300, 600, 1200, 2400, 
4800, and 9600 units (U) collagenase injected into the cord that was causing 
contracture of the MCP joint.  There were no beneficial clinical effects of 
these injections.  The remaining 29 patients had collagenase injections at a 
dose level of 10,000 U into cords that are causing contractures of 34 MCP 
joints, 9 PIP joints, and 1 thumb.  Twenty-eight of the 34 MCP joint 
contractures corrected to normal extension (0 degrees) and 2 of the 34 MCP joint 
contractures corrected to 5 degrees of normal extension, with full range of 
motion, within 1 to 14 days of injection.  In patients with PIP joint 
contractures, 4 of the 9 joints corrected to normal (0 degrees).  One PIP joint 
corrected to within 10 degrees of normal and 2 corrected to within 15 degrees of 
normal.  There were 2 failures; these patients required surgery.  The mean 
follow-up period was 20.0 +/- 5.6 months for the MCP joints and 14.1 +/- 6.6 
months for the PIP joints.  Clostridial collagenase injection of Dupuytren`s 
cords causing MCP and PIP joint contractures appears to have merit as 
non-surgical treatment of this disorder.  The authors stated that pending 
further placebo, double-blind studies, collagenase injection to treat 
Dupuytren`s disease may be a safe and effective alternative to surgical 
fasciectomy. 
Badalamente 
et al (2002) reported that in a series of controlled phase II clinical trials, 
excessive collagen deposition in Dupuytren`s disease has been targeted by a 
unique non-operative method using clostridial collagenase injection therapy to 
lyse and rupture finger cords causing MCP and/or PIP joint contractures.  A 
total of 49 patients were treated in a random, placebo-controlled trial of one 
dose of collagenase versus placebo at 1 center.  Subsequently 80 patients were 
treated in a random, placebo-controlled, dose-response study of collagenase at 2 
test centers.  The results of these studies indicated that non-operative 
collagenase injection therapy for Dupuytren`s disease is both a safe and 
effective method of treating this disorder in the majority of patients as an 
alternative to surgical fasciectomy. 
In a 
prospective, randomized, double-blind, placebo-controlled, multi-center study, 
Hurst et al (2009) examined the effects of injectable collagenase clostridium 
histolyticum for the treatment of Dupuytren`s contracture.  These 
investigators enrolled 308 patients with joint contractures of 20 degrees or 
more.  The primary MCP or PIP joints of these patients were randomly assigned to 
receive up to 3 injections of collagenase clostridium histolyticum (at a dose of 
0.58 mg per injection) or placebo in the contracted collagen cord at 30-day 
intervals.  One day after injection, the joints were manipulated. The primary 
end point was a reduction in contracture to 0 to 5 degrees of full extension 30 
days after the last injection.  Twenty-six secondary end points were evaluated, 
and data on adverse events were collected.  Collagenase treatment significantly 
improved outcomes.  More cords that were injected with collagenase than cords 
injected with placebo met the primary end point (64.0 % versus 6.8 %, p < 
0.001), as well as all secondary end points (p < or = 0.002).  Overall, the 
range of motion in the joints was significantly improved after injection with 
collagenase as compared with placebo (from 43.9 to 80.7 degrees versus from 45.3 
to 49.5 degrees, p < 0.001).  The most commonly reported adverse events were 
localized swelling, pain, bruising, pruritus, and transient regional lymph-node 
enlargement and tenderness.  Three treatment-related serious adverse events were 
reported: 2 tendon ruptures and 1 case of complex regional pain syndrome.  No 
significant changes in flexion or grip strength, no systemic allergic reactions, 
and no nerve injuries were observed.  The authors concluded that collagenase 
clostridium histolyticum injection significantly reduced contractures and 
improved the range of motion in joints affected by advanced Dupuytren`s disease. 
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                                        | Reference 
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                                        | 
	
	Badalamente MA, Hurst LC. Enzyme 
	injection as nonsurgical treatment of Dupuytren`s disease. J Hand Surg Am. 
	2000;25(4):629-636. 
	Badalamente MA, Hurst LC, Hentz 
	VR. Collagen as a clinical target: Nonoperative treatment of Dupuytren`s 
	disease. J Hand Surg Am. 2002;27(5):788-798. 
	National Institute for Clinical 
	Excellence (NICE). Needle fasciotomy for Dupuytren’s contracture. 
	Interventional Procedure Guidance 43. London, UK: NICE; February 2004.
	
	Trojian TH, Chu SM. Dupuytren`s 
	disease: diagnosis and treatment. Am Fam Physician. 2007;76(1):86-89. 
	
	Swartz WM, Lalonde DH. MOC-PS(SM) 
	CME article: Dupuytren`s disease. Plast Reconstr Surg. 2008;121(4 Suppl):1-10.
	
	Jordan GH. The use of 
	intralesional clostridial collagenase injection therapy for Peyronie`s 
	disease: A prospective, single-center, non-placebo-controlled study. J Sex 
	Med. 2008; 5(1):180-187. 
	Hurst LC, Badalamente MA, Hentz 
	VR, et al. Injectable collagenase clostridium histolyticum for Dupuytren`s 
	contracture. N Engl J Med. 2009;361(10):968-979. 
	U.S. Food and Drug 
	Administration. FDA approves Xiaflex for debilitating hand condition. FDA 
	News. Silver Spring, MD; FDA; February 2, 2010. Available at: 
	
	
	http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm199736.htm. 
	Accessed Mar. 23 2011. 
	Auxilium Pharmaceuticals, Inc. 
	Xiaflex (collagenase clostridium histolyticum). Prescribing 
	Information. Malvern, PA; Auxilium; February, 2010. Available at: 
	
	
	http://www.xiaflex.com/docs/pi_medguide_combo.pdf. 
	Accessed Mar. 23 2011.
	Keilholz L, Seegenschmiedt MH, 
	Sauer R. Radiotherapy for prevention of disease progression in early-stage 
	Dupuytren`s contracture: Initial and long-term results. Int J Radiat Oncol 
	Biol Phys. 1996;36(4):891-897. 
	Seegenschmiedt MH, Olschewski T, 
	Guntrum F. Radiotherapy optimization in early-stage Dupuytren`s contracture: 
	First results of a randomized clinical study. Int J Radiat Oncol Biol Phys. 
	2001;49(3):785-798. 
	Foucher G, Medina J, Navarro R. 
	Percutaneous needle aponeurotomy: Complications and results. J Hand Surg Br. 
	2003;28(5):427-431. 
	Trojian TH, Chu SM. Dupuytren`s 
	disease: Diagnosis and treatment. Am Fam Physician. 2007;76(1):86-89. 
	
	Cheng HS, Hung LK, Tse WL, Ho PC. 
	Needle aponeurotomy for Dupuytren`s contracture. J Orthop Surg (Hong Kong). 
	2008;16(1):88-90. 
	Lellouche H. Dupuytren`s 
	contracture: Surgery is no longer necessary. Presse Med. 
	2008;37(12):1779-1781. 
	Oxfordshire NHS Trust. Surgery 
	for Dupuytren’s contracture. Interim Treatment Threshold Statement. 
	Priorities Forum Policy Statement. Oxford, UK: NHS; October 15, 2009. 
	
	Betz N, Ott OJ, Adamietz B, et 
	al. Radiotherapy in early-stage Dupuytren`s contracture. Long-term results 
	after 13 years. Strahlenther Onkol. 2010;186(2):82-90. 
	Manet MP, Roulot E, Teyssedou JP, 
	et al. Dupuytren`s contracture: Needle aponeurotomy is an alternative to 
	surgery. Rev Med Interne. 2010 Sep 7. [Epub ahead of print] 
	National Institute for Health and 
	Clinical Excellence (NICE). Radiation therapy for early Dupuytren’s disease. 
	Interventional Procedure Guidance 368. London, UK: NICE; November 2010. 
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                                    | Application to Products 
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                                    | This policy applies to all health plans administered by QualChoice, both those insured by QualChoice and those that are self-funded by the sponsoring employer, unless there is indication in this policy otherwise or a stated exclusion in your medical plan booklet.  Consult the individual plan sponsor Summary Plan Description (SPD) for self-insured plans or the specific Evidence of Coverage (EOC) for those plans insured by QualChoice.  In the event of a discrepancy between this policy and a self-insured customer’s SPD or the specific QualChoice EOC, the SPD or EOC, as applicable, will prevail.  State and federal mandates will be followed as they apply. 
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                                    | Changes: QualChoice reserves the right to alter, amend, change or supplement benefit interpretations as needed. |  |