NF1 PN: prevalent, progressive, and debilitating1-3
PN are a common manifestation of NF1 that occur early, may progress over time, and are potentially debilitating1-3
Up to
50%
of all patients with
NF1 have PN2,3*
Results from the NCI NF1 Natural History study showed over 5.6 years4†:
82% of patients with NF1 PN had tumor progression ≥20%
The median growth rate was 16% per year (-3% to 136%)
In general, PN grew continuously
*Using whole-body MRI.3
†The NF1 Natural History study began in 2008 and is an ongoing study. Ninety-two patients with NF1-related PN between the ages of 3 and 18 years who had at least 2 volumetric scans were included in the analysis above as the age- and period-matched external control for the SPRINT study.5
MOA=mechanism of action; MRI=magnetic resonance imaging; NCI=National Cancer Institute; NF1=neurofibromatosis type 1; PN=plexiform neurofibromas.
NF1 PN: a growing concern
In patients with NF1 PN, PN volume growth rates can exceed weight or height growth rates6-8‡
In the NCI NF1 Natural History study, PN typically continued to grow.5§
Percentage change in target PN volume, Natural History study5
‡Based on 2 longitudinal studies, including 49 patients with 61 tumors and 70 patients with 80 tumors.6,7
§The NCI NF1 Natural History study began in 2008 and is an ongoing study. 92 patients with NF1-related PN between the ages of 3 and 18 years who had at least 2 volumetric scans were included in the analysis above as the age- and period-matched external control for the SPRINT study.5
PN typically grow fastest in the first 10 years of life.2 Early action is crucial.9
PN are a significant cause of morbidity in pediatric patients with NF11,2
Visible deformities throughout the body1
Airway compromise1,9
Motor dysfunction1,9
- Weakness
- Difficulty walking
- Numbness
Vision impairment10
PN-related pain throughout the body1
Bladder/bowel dysfunction1
PN are a significant cause of morbidity in pediatric patients with NF11,2
Vision impairment12
Visible deformities throughout the body1
Airway compromise1,6
PN-related pain throughout the body1
Bladder/bowel dysfunction1
Motor dysfunction1,6
- Weakness
- Difficulty walking
- Numbness
Some internal PN are seen only on MRI. Advanced imaging plays an essential role in diagnosing and disease management.1,9
In a study of 78 patients11:
99% of target PN were associated with ≥1 morbidity
89.2% of patients had at least 1 target PN-related morbidity during the 24-month follow-up period
The burden of NF1 PN can go beyond physical symptoms
Data suggest that children with NF1 PN suffer from worse12:
Anxiety
Stigma
Depressive symptoms
Meaning and purpose
Psychological stress
Well-being
Peer relationships
In a study of caregivers and patients, caregivers' behavioral ratings showed that13:
Larger tumor volumes and anxiety symptoms predicted greater pain interference
Greater pain interference, worse depressive symptoms, and disease complications predicted poorer QoL
QoL=quality of life.
The surgical dilemma in NF1 PN
Not all PN require intervention, but when feasible, surgery is an effective means of resection and debulking NF1 PN14
Surgery can be challenging, and not all PNs may be operable or fully resectable due to1:
- Continuous growth within and throughout the nerve sheath
- Proximity to vital organs, which can occur initially or as the PN progresses
- Poorly defined margins
- Challenging locations such as the head, neck, spine, or trunk
- Hypervascularity, which can increase the risk of bleeding
PN regrowth is common after surgery
From 2 retrospective analyses
Rates of PN regrowth after surgery range from 20%-68%, depending on extent of resection.15,16‖
‖Based on a review of inpatient and outpatient records of 121 patients who had 302 procedures on 168 tumors over a 20-year period at a single large pediatric referral center and a retrospective review of 96 patients who had 186 subtotal or partial resections on 130 tumors over a 10-year follow-up period at an NF center.15,16
¶In the 2012 study by Prada CE, Rangwala FA, Martin LJ, et al, subtotal resection was defined as 50%-80% excision.15
NF=neurofibromatosis.
PN grow fastest during the first 10 years of life and typically continue to grow2,9
PN morbidities can worsen over time9
PN are highly variable and have the potential to cause life-altering clinical complications9
Not all PNs may be operable or fully resectable with surgery1
Discover Koselugo—the FIRST and ONLY FDA-approved therapy for pediatric patients with NF1 and symptomatic, inoperable PN.17,18
FDA=Food and Drug Administration.
WARNINGS AND PRECAUTIONS
Cardiomyopathy. A decrease in left
ventricular ejection fraction (LVEF) ≥10% below baseline occurred
in pediatric
patients who received Koselugo in SPRINT with some
experiencing decreased LVEF below the institutional lower limit of normal
(LLN), including one patient with Grade 3. All patients with decreased
LVEF were asymptomatic and identified during routine echocardiography.
The safety of Koselugo has not been established in patients with a history
of impaired LVEF or a baseline ejection fraction that is below the institutional
LLN. Assess ejection fraction by echocardiogram prior to initiating treatment,
every 3 months during the first year of treatment, every 6 months thereafter,
and as clinically indicated. Withhold, reduce dose, or permanently discontinue
Koselugo based on severity of adverse reaction. In patients who interrupt
Koselugo for decreased LVEF, obtain an echocardiogram or a cardiac MRI
every 3 to 6 weeks. Upon resolution of decreased LVEF, obtain an echocardiogram
or a cardiac MRI every 2 to 3 months.
Ocular Toxicity. Blurred vision,
photophobia, cataracts, and ocular hypertension
occurred. Retinal
pigment epithelial detachment (RPED) occurred in the pediatric population
during treatment with single agent Koselugo and resulted in permanent discontinuation.
Conduct ophthalmic assessments prior to initiating Koselugo, at regular
intervals during treatment, and for new or worsening visual changes. Permanently
discontinue Koselugo in patients with retinal vein occlusion (RVO). Withhold
Koselugo in patients with RPED, conduct ophthalmic assessments every 3
weeks until resolution, and resume Koselugo at a reduced dose.
Gastrointestinal Toxicity. Diarrhea
occurred, including Grade 3. Diarrhea resulting in permanent discontinuation,
dose interruption or dose reduction occurred. Advise patients to start
an anti-diarrheal agent (eg, loperamide) and to increase fluid intake immediately
after the first episode of diarrhea. Withhold, reduce dose, or permanently
discontinue Koselugo based on severity of adverse reaction.
Skin Toxicity. Rash occurred in 91% of 74 pediatric patients. The most frequent rashes included dermatitis acneiform (54%), maculopapular rash (39%), and eczema (28%). Grade 3 rash occurred, in addition to rash resulting in dose interruption or dose reduction. Monitor for severe skin rashes. Withhold, reduce dose, or permanently discontinue Koselugo based on severity of adverse reaction.
Increased Creatine Phosphokinase (CPK). Increased CPK occurred, including Grade 3 or 4 resulting in dose reduction. Increased CPK concurrent with myalgia occurred, including one patient who permanently discontinued Koselugo for myalgia. Obtain serum CPK prior to initiating Koselugo, periodically during treatment, and as clinically indicated. If increased CPK occurs, evaluate for rhabdomyolysis or other causes. Withhold, reduce dose, or permanently discontinue Koselugo based on severity of adverse reaction.
Increased Levels of Vitamin E and Risk of Bleeding. Koselugo capsules contain
vitamin E which can inhibit platelet
aggregation and antagonize vitamin K-dependent clotting factors. Supplemental
vitamin E is not recommended if daily vitamin E intake (including the amount
of vitamin E in Koselugo and supplement) will exceed the recommended or
safe limits due to increased risk of bleeding. An increased risk of bleeding
may occur in patients who are coadministered vitamin-K antagonists or anti-platelet
antagonists with Koselugo. Monitor for bleeding in these patients and increase
international normalized ratio (INR) in patients taking a vitamin-K antagonist.
Perform anticoagulant assessments more frequently and adjust the dose of
vitamin K antagonists or anti-platelet agents as appropriate.
Embryo-Fetal Toxicity. Based on
findings
from animal studies, Koselugo can cause fetal harm when
administered during pregnancy. In animal studies, administration of selumetinib
to mice during organogenesis caused reduced fetal weight, adverse structural
defects, and effects on embryo-fetal survival at approximate exposures
>5 times the human exposure at the clinical dose of 25 mg/m2 twice daily.
Advise patients of reproductive potential of the potential risk to a fetus
and to use effective contraception during treatment with Koselugo and for
1 week after the last dose.
ADVERSE REACTIONS
Common adverse reactions ≥40% include vomiting, rash (all), abdominal pain, diarrhea, nausea, dry skin, musculoskeletal pain, fatigue, pyrexia, acneiform rash, stomatitis, headache, paronychia, and pruritus.
DRUG INTERACTIONS
Effect of Other Drugs on Koselugo
Concomitant use of Koselugo with a strong or moderate CYP3A4 inducer decreased selumetinib plasma concentrations, which may reduce Koselugo efficacy. Avoid concomitant use with Koselugo.
SPECIAL POPULATIONS
Pregnancy & Lactation. Verify the
pregnancy status of patients of reproductive potential prior to
initiating Koselugo. Due to the potential for adverse reactions in a breastfed
child, advise patients not to breastfeed during treatment with Koselugo
and for 1 week after the last dose.
INDICATION
KOSELUGO is indicated for the treatment of pediatric patients 2 years of age and older with neurofibromatosis type 1 (NF1) who have symptomatic, inoperable plexiform neurofibromas (PN).
To report SUSPECTED ADVERSE REACTIONS, contact AstraZeneca
1-800-236-9933
or at
https://us-aereporting.astrazeneca.com
or FDA at
1-800-FDA-1088 or
www.fda.gov/
medwatch.
Please see full Prescribing Information for Koselugo® (selumetinib).
References:
1. Korf BR, Rubenstein AE. Neurofibromatosis: A Handbook for Patients, Families, and Health Care Professionals. Thieme Medical Publishers; 2005.
2. Anderson JL, Gutmann DH. Neurofibromatosis type 1. In: Islam MP, Roach SE, eds. Handbook of Clinical Neurology. 3rd series; vol 132. Elsevier B.V.; 2015:75-86.
3. Miller DT, Freedenberg D, Schorry E, et
al. Health supervision for children with neurofibromatosis type 1. Pediatrics. 2019;143(5):e20190660. doi:10.1542/peds.2019-0660
4. Data on File, REF-36656, AstraZeneca Pharmaceuticals LP.
5. Data on File, REF-75729, AstraZeneca Pharmaceuticals LP.
6. Dombi E, Ardern-Holmes SL, Babovic-Vuksanovic D, et al.
Recommendations for imaging tumor response in neurofibromatosis clinical trials.
Neurology. 2013;81(21)(suppl 1):S33-S40. doi:10.1212/01.wnl.
0000435744.57038
.af
7. Akshintala S, Baldwin A, Liewehr DJ, et
al. Longitudinal evaluation of peripheral nerve sheath tumors in
neurofibromatosis type 1: growth analysis of plexiform neurofibromas and
distinct nodular lesions. Neuro Oncol. 2020;22(9):1368-1378.
doi:10.1093/neuonc/noaa053
8. Akshintala S, Baldwin A, Liewehr DJ, et
al. Longitudinal evaluation of peripheral nerve sheath tumors in
neurofibromatosis type 1: growth analysis of plexiform neurofibromas and
distinct nodular lesions (Supplementary). Neuro Oncol.
2020;22(9):1368-1378. doi:10.1093
/neuonc/noaa053
9. Gross AM, Singh G, Akshintala S, et al. Association of plexiform neurofibroma volume changes and development of clinical morbidities in neurofibromatosis 1. Neuro Oncol. 2018;20(12):1643-1651. doi:10.1093/neuonc/noy067
10. Avery RA, Katowitz JA, Fisher MJ, et al. Orbital/periorbital plexiform neurofibromas in children with neurofibromatosis type 1: multidisciplinary recommendations for care. Ophthalmology. 2017;124(1):123-132. doi:10.1016/j.ophtha.2016.09.020
11. Wolkenstein P, Chaix Y, Werle NE, et al. French cohort
of children and adolescents with neurofibromatosis type 1 and symptomatic inoperable
plexiform neurofibromas: CASSIOPEA study. Eur J Med Genet.
2023;66(5):104734. doi:10.1016/
j.ejmg.2023.104734
12. Lai JS, Jensen SE, Charrow J, Listernick R. Patient reported
outcomes measurement information system and quality of life in neurological
disorders measurement system to evaluate quality of life for children and adolescents
with neurofibromatosis type 1 associated plexiform neurofibroma. J Pediatr. 2019;206:190-196. doi:10.1016/
j.jpeds.2018.10.019
13. Wolters PL, Burns KM, Martin S, et al. Pain interference
in youth with neurofibromatosis type 1 and plexiform neurofibromas and relation
to disease severity, social-emotional functioning, and quality of life. Am J Med Genet A. 2015;167A(9):2103-2113. doi:10.1002/
ajmg.a.37123
14. Armstrong AE, Belzberg AJ, Crawford JR, Hirbe AC, Wang
ZJ. Treatment decisions and the use of MEK inhibitors for children with neurofibromatosis
type 1-related plexiform neurofibromas. BMC Cancer.
2023;23(1):553. doi:10.1186/
s12885-023-10996-y
15. Prada CE, Rangwala FA, Martin LJ, et al. Pediatric plexiform
neurofibromas: impact on morbidity and mortality in neurofibromatosis type
1. J Pediatr. 2012;160(3):461-467. doi:10.1016/
j.jpeds.2011.08.051
16. Needle MN, Cnaan A, Dattilo J, et al. Prognostic signs
in the surgical management of plexiform neurofibroma: the Children's Hospital
of Philadelphia experience, 1974-1994. J Pediatr.
1997;131(5):678-682. doi:10.1016/
s0022-3476(97)70092-1
17. Koselugo. Package insert. AstraZeneca Pharmaceuticals LP.
18. Koselugo (selumetinib) approved in US for paediatric patients with neurofibromatosis type 1 plexiform neurofibromas. AstraZeneca. April 13, 2020. Accessed December 4, 2023. https://www.astrazeneca.com/media-centre/press-releases/2020/koselugo-selumetinib-approved-in-us-for-paediatric-patients-with-neurofibromatosis-type-1-plexiform-neurofibromas.html#