Retinoblastoma screening: Difference between revisions

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Latest revision as of 23:59, 29 July 2020

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sahar Memar Montazerin, M.D.[2] Simrat Sarai, M.D. [3]

Overview

Early diagnosis of retinoblastoma is necessary to obtain the best outcomes for preservation of the vision and the eye. In 2018, a group of experts in clinical retinoblastoma care and ophthalmic pathology and genetics suggested a risk-stratified schedule for ophthalmic screening examinations. Estimated risk of retinoblastoma development is calculated according to the relativity of individuals to the family member with retinoblastoma.

Screening

In 2018, a group of experts in clinical retinoblastoma care and ophthalmic pathology and genetics suggested a risk-stratified schedule for ophthalmic screening examinations.^[1]
This panel of experts recommended that all children with an elevated risk of retinoblastoma (above the population risk) should be screened via regular fundoscopic examinations.
To schedule a screening plan, the risk of tumor development must be determined using the infant relationship to the family member with retinoblastoma.
The table below is an estimate of patients' risk for the development of retinoblastoma depending on the relation of the patient to the affected individual:


Relative of patient	Bilateral involvement (100%)	Unilateral involvement (15%)
Offspring (infant)	50	7.5
Parent	5	0.8
Sibling	2.5	0.4
Niece/nephew	1.3	0.2
Aunt/uncle	0.1	0.007
First cousin	0.05	0.007

The above table adopted from Ophthalmology journal ^[1]

Next step in assessing the risk of these children is to estimate the approximate relative risk of retinoblastoma development according to the percentage mentioned in the above table.

Relatives are categorized into three categories:
- High risk: Those with a risk percentage > 7.5%
- Intermediate risk: Those with a risk percentage between 1% and 7.5% (including 7.5%)
- Low risk: Those with a risk percentage < 1%
American Association of Ophthalmic Oncologists and Pathologists (AAOOP) guideline recommends scheduled eye examination for the screening of children at high risk of developing retinoblastoma. Screening should be initiated at birth and continued till the age of 7 years.^[1]
No further examination is required after the age of 7 years except for those who are known carriers of the RB1 gene mutation.
For those who are carries of the RB1 gene mutation, screening should be continued indefinitely after the age of 7 years and should be done annually or every 2 years.

The following table is the recommended eye examination schedule for unaffected children of families with retinoblastoma depending on their age and risk percentage of tumor development:


Risk category or Age	High risk	Intermediate risk	Low risk

Birth to 8 weeks	Every 2 - 4 weeks	Monthly	Monthly
> 8 - 12 weeks	Monthly	Monthly	Monthly
> 3 - 12 months	Monthly	Every 2 months	Every 3 months
> 12 - 24 months	Every 2 months	Every 3 months	Every 4 months
> 24 - 36 months	Every 3 months	Every 3 months	Every 6 months
> 36 - 48 months	Every 4 months	Every 4 - 6 months	Every 6 months
> 48 - 60 months	Every 6 months	Every 4 - 6 months	Annually
5 - 7 years	Every 6 months	Annually	Annually

This table is adopted from Ophthalmology journal^[1]

The schedule presented above is general guideline for at-risk children when no lesions of concern have been noted. Some children may require more frequent examinations.

The American Association of Ophthalmic Oncologists and Pathologists (AAOOP) guideline also suggests a single dilated fundus examination to evaluate for asymptomatic spontaneously regressed retinoblastoma or retinoma in all first-degree relatives of a patient with retinoblastoma, including older siblings if the RB1 genetic analysis of the relatives is not done.

Genetic Testing for Children with Retinoblastoma

Genetic testing for children with Retinoblastoma

Not available

Blood: RB1 mutation(+)
(germline mutation)

Blood: RB1 mutation(-)
Tumor: RB1 mutation(+)

Blood: RB1 mutation(-)
Tumor: RB1 mutation(-)

Blood: RB1 mutation(-)
Tumor: not available

Ophthalmic screening for all
the relatives with greater risk than the population

Assessment of relatives
for familial retinoblastoma

Ophthalmic screening and genetic analysis
not required for first degree relatives

No need for genetic analysis of first degree relatives

Relatives with RB1 mutation

Relatives without RB1 mutation

Ophthlamic screening for future offspring unless negative for parent's mutation

Future offspring of affected child require ophthalmic screening

Ophthalmic screening for children as high risk

Ophthalmic screening not required

The above table is the recommended genetic analysis guidline for families with affected individuals and adopted from Ophthalmology journal^[1]

References

↑ ^1.0 ^1.1 ^1.2 ^1.3 ^1.4 Skalet, Alison H.; Gombos, Dan S.; Gallie, Brenda L.; Kim, Jonathan W.; Shields, Carol L.; Marr, Brian P.; Plon, Sharon E.; Chévez-Barrios, Patricia (2018). "Screening Children at Risk for Retinoblastoma". Ophthalmology. 125 (3): 453–458. doi:10.1016/j.ophtha.2017.09.001. ISSN 0161-6420.

[SkaletGombos2018-1] 1.0 ^1.1 ^1.2 ^1.3 ^1.4 Skalet, Alison H.; Gombos, Dan S.; Gallie, Brenda L.; Kim, Jonathan W.; Shields, Carol L.; Marr, Brian P.; Plon, Sharon E.; Chévez-Barrios, Patricia (2018). "Screening Children at Risk for Retinoblastoma". Ophthalmology. 125 (3): 453–458. doi:10.1016/j.ophtha.2017.09.001. ISSN 0161-6420.

[1]

@@ Line 3: / Line 3: @@
 {{CMG}}; {{AE}} {{Sahar}} {{Simrat}}
 ==Overview==
-According to the United States Preventive Services Task Force, screening for retinoblastoma is not recommended in the general population. However, children with an increased risk of retinoblastoma such as those with a known 13q deletion or [[family history]] should be evaluated by an [[ophthalmologist]] shortly after birth. Dilated fundus examinations are recommended in siblings and offspring of patients with retinoblastoma.<ref name="RothschildLévy2011">{{cite journal|last1=Rothschild|first1=P-R|last2=Lévy|first2=D|last3=Savignoni|first3=A|last4=Lumbroso-Le Rouic|first4=L|last5=Aerts|first5=I|last6=Gauthier-Villars|first6=M|last7=Esteve|first7=M|last8=Bours|first8=D|last9=Desjardins|first9=L|last10=Doz|first10=F|last11=Lévy-Gabriel|first11=C|title=Familial retinoblastoma: fundus screening schedule impact and guideline proposal. A retrospective study|journal=Eye|volume=25|issue=12|year=2011|pages=1555–1561|issn=0950-222X|doi=10.1038/eye.2011.198}}</ref>
+Early [[diagnosis]] of retinoblastoma is necessary to obtain the best outcomes for preservation of the [[vision]] and the eye. In 2018, a group of experts in clinical retinoblastoma care and [[ophthalmic]]
+[[pathology]] and [[genetics]] suggested a risk-stratified schedule for [[ophthalmic]] [[screening]] [[Examination|examinations]]. Estimated risk of retinoblastoma development is calculated according to the relativity of individuals to the family member with retinoblastoma.
 ==Screening==
-*Children with a family history of retinoblastoma are at increased risk of developing retinoblastoma and require screening plan for the early diagnosis of the tumor.<ref name="Dhar2011">{{cite journal|last1=Dhar|first1=Shweta U.|title=Outcomes of Integrating Genetics in Management of Patients With Retinoblastoma|journal=Archives of Ophthalmology|volume=129|issue=11|year=2011|pages=1428|issn=0003-9950|doi=10.1001/archophthalmol.2011.292}}</ref>
+* In 2018, a group of experts in clinical retinoblastoma care and [[ophthalmic]] [[pathology]] and [[genetics]] suggested a risk-stratified schedule for [[ophthalmic]] [[Screening (medicine)|screening]] [[Examination|examinations]].<ref name="SkaletGombos2018">{{cite journal|last1=Skalet|first1=Alison H.|last2=Gombos|first2=Dan S.|last3=Gallie|first3=Brenda L.|last4=Kim|first4=Jonathan W.|last5=Shields|first5=Carol L.|last6=Marr|first6=Brian P.|last7=Plon|first7=Sharon E.|last8=Chévez-Barrios|first8=Patricia|title=Screening Children at Risk for Retinoblastoma|journal=Ophthalmology|volume=125|issue=3|year=2018|pages=453–458|issn=01616420|doi=10.1016/j.ophtha.2017.09.001}}</ref>
-*To schedule the screening plan, first, the risk of tumor development must be determined using the infant relationship to the family member with retinoblastoma.
+* This panel of experts recommended that all [[Child|children]] with an elevated risk of retinoblastoma (above the population risk) should be [[Screening (medicine)|screened]] via regular [[Fundoscopy|fundoscopic examinations]].
-*The table below is an estimate of patients risk for the development of retinoblastoma depending on the relativity of patient to the affected relatives.
+*To schedule a [[screening]] plan, the risk of [[tumor]] development must be determined using the [[infant]] relationship to the family member with retinoblastoma.
-*Risk of retinoblastoma development in the general population has been estimated at 0.007%.
+*The table below is an estimate of [[Patient|patients']] risk for the development of retinoblastoma depending on the relation of the [[patient]] to the affected individual:
 {| border="3"
-|+ Risk of carrying mutated gene in the relatives of a patient with retinoblastoma (Patient)(%)
+|+
-! Relative of patient !! Bilateral involvement (100%) !! Unilateral involvement (15%)
+! style="background: #4479BA; width: 150px;" | {{fontcolor|#FFF| Relative of patient}} !! style="background: #4479BA; width: 150px;" | {{fontcolor|#FFF| Bilateral involvement (100%)}} !! style="background: #4479BA; width: 150px;" | {{fontcolor|#FFF| Unilateral involvement (15%)}}
 |-
-! Offspring (infant)
+! style="padding: 5px 5px; background: #DCDCDC; " |Offspring (infant)
-| 50  || 7.5
+| style="padding: 5px 5px; background: #F5F5F5;" align="center" | 50  || style="padding: 5px 5px; background: #F5F5F5;" align="center" | 7.5
 |-
-! Parent
+! style="padding: 5px 5px; background: #DCDCDC; " | Parent
-|5
+| style="padding: 5px 5px; background: #F5F5F5;" align="center" |5
-|0.8
+| style="padding: 5px 5px; background: #F5F5F5;" align="center" |0.8
 |-
-! Sibling
+! style="padding: 5px 5px; background: #DCDCDC; " | Sibling
-|2.5
+| style="padding: 5px 5px; background: #F5F5F5;" align="center" |2.5
-|0.4
+| style="padding: 5px 5px; background: #F5F5F5;" align="center" |0.4
 |-
-! Niece/nephew
+! style="padding: 5px 5px; background: #DCDCDC; " | Niece/nephew
-|1.3
+| style="padding: 5px 5px; background: #F5F5F5;" align="center" |1.3
-|0.2
+| style="padding: 5px 5px; background: #F5F5F5;" align="center" |0.2
 |-
-! Aunt/uncle
+! style="padding: 5px 5px; background: #DCDCDC; " | Aunt/uncle
-|0.1
+| style="padding: 5px 5px; background: #F5F5F5;" align="center" |0.1
-|0.007
+| style="padding: 5px 5px; background: #F5F5F5;" align="center" |0.007
 |-
-! First cousin
+! style="padding: 5px 5px; background: #DCDCDC; " | First cousin
-|0.05
+| style="padding: 5px 5px; background: #F5F5F5;" align="center" |0.05
-|0.007
+| style="padding: 5px 5px; background: #F5F5F5;" align="center" |0.007
 |}
 {|
-! colspan="2" style="background:#DCDCDC;" align="center" + |The above table adapted from Ophthalmology journal <ref name="SkaletGombos2018">{{cite journal|last1=Skalet|first1=Alison H.|last2=Gombos|first2=Dan S.|last3=Gallie|first3=Brenda L.|last4=Kim|first4=Jonathan W.|last5=Shields|first5=Carol L.|last6=Marr|first6=Brian P.|last7=Plon|first7=Sharon E.|last8=Chévez-Barrios|first8=Patricia|title=Screening Children at Risk for Retinoblastoma|journal=Ophthalmology|volume=125|issue=3|year=2018|pages=453–458|issn=01616420|doi=10.1016/j.ophtha.2017.09.001}}</ref>
+! colspan="2" style="background:#DCDCDC;" align="center" + |The above table adopted from Ophthalmology journal <ref name="SkaletGombos2018">{{cite journal|last1=Skalet|first1=Alison H.|last2=Gombos|first2=Dan S.|last3=Gallie|first3=Brenda L.|last4=Kim|first4=Jonathan W.|last5=Shields|first5=Carol L.|last6=Marr|first6=Brian P.|last7=Plon|first7=Sharon E.|last8=Chévez-Barrios|first8=Patricia|title=Screening Children at Risk for Retinoblastoma|journal=Ophthalmology|volume=125|issue=3|year=2018|pages=453–458|issn=01616420|doi=10.1016/j.ophtha.2017.09.001}}</ref>
 |-
 |}
-Next step in assessing the risk of these children is to estimate the approximate relative risk of retinoblatoma development according to the percentge mentioned in the afromentioned table.
+* Next step in assessing the risk of these [[Child|children]] is to estimate the approximate relative risk of retinoblastoma development according to the percentage mentioned in the above table.
 *Relatives are categorized into three categories:
-**High risk: those with risk percentage > 7.5%
+**'''High risk:''' Those with a risk percentage > 7.5%
-**Intermediate risk: those with risk percentage between and 1% and 7.5% (including 7.5%).
+**'''Intermediate risk:''' Those with a risk percentage between 1% and 7.5% (including 7.5%)
-**Low risk: those with risk percentage < 1%.
+**'''Low risk:''' Those with a risk percentage < 1%
-The following table is the recommended eye examination schedule for unaffected children of families with retinoblastoma depending on their age and risk percentage of tumor development.
+*American Association of [[Ophthalmic]] [[Oncologists]] and [[Pathologists]] (AAOOP) [[Medical guideline|guideline]] recommends scheduled [[eye examination]] for the [[screening]] of children at high risk of developing retinoblastoma. [[Screening (medicine)|Screening]] should be initiated at [[birth]] and continued till the age of 7 years.<ref name="SkaletGombos2018">{{cite journal|last1=Skalet|first1=Alison H.|last2=Gombos|first2=Dan S.|last3=Gallie|first3=Brenda L.|last4=Kim|first4=Jonathan W.|last5=Shields|first5=Carol L.|last6=Marr|first6=Brian P.|last7=Plon|first7=Sharon E.|last8=Chévez-Barrios|first8=Patricia|title=Screening Children at Risk for Retinoblastoma|journal=Ophthalmology|volume=125|issue=3|year=2018|pages=453–458|issn=01616420|doi=10.1016/j.ophtha.2017.09.001}}</ref>
-{| style="border: 0px; font-size: 90%; margin: 3px; width: 600px" align=center
+*No further [[Eye examination|examination]] is required after the age of 7 years except for those who are known carriers of the [[RB1]] [[gene]] [[mutation]].
-|valign=top|
+*For those who are carries of the [[RB1]] [[gene]] [[mutation]], [[screening]] should be continued indefinitely after the age of 7 years and should be done annually or every 2 years.
+* The following table is the recommended [[eye examination]] schedule for unaffected [[Child|children]] of families with retinoblastoma depending on their age and risk percentage of [[tumor]] development:
+{| style="border: 0px; font-size: 90%; margin: 3px; width: 600px" align="center"
+| valign="top" |
 |+
 ! style="background: #4479BA; width: 200px;" | {{fontcolor|#FFF|Risk category or Age}}
@@ Line 57: / Line 63: @@
 Birth to 8 weeks
 | style="padding: 5px 5px; background: #F5F5F5;" |
-*Every 2-4 weeks
+*Every 2 - 4 weeks
 | style="padding: 5px 5px; background: #F5F5F5;" |
 *Monthly
@@ Line 64: / Line 70: @@
 |-
 | style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" |
->8-12 weeks
+> 8 - 12 weeks
 | style="padding: 5px 5px; background: #F5F5F5;" |
 *Monthly
@@ Line 73: / Line 79: @@
 |-
 | style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" |
->3 to 12 months
+> 3 - 12 months
 | style="padding: 5px 5px; background: #F5F5F5;" |
 *Monthly
@@ Line 82: / Line 88: @@
 |-
 | style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" |
->12 to 24 months
+> 12 - 24 months
 | style="padding: 5px 5px; background: #F5F5F5;" |
 *Every 2 months
@@ Line 91: / Line 97: @@
 |-
 | style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" |
->24 to 36 months
+> 24 - 36 months
 | style="padding: 5px 5px; background: #F5F5F5;" |
 *Every 3 months
@@ Line 100: / Line 106: @@
 |-
 | style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" |
->36 to 48 months
+> 36 - 48 months
 | style="padding: 5px 5px; background: #F5F5F5;" |
 *Every 4 months
 | style="padding: 5px 5px; background: #F5F5F5;" |
-*Every 4-6 months
+*Every 4 - 6 months
 | style="padding: 5px 5px; background: #F5F5F5;" |
 *Every 6 months
 |-
 | style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" |
->48 to 60 months
+> 48 - 60 months
 | style="padding: 5px 5px; background: #F5F5F5;" |
 *Every 6 months
 | style="padding: 5px 5px; background: #F5F5F5;" |
-*Every 4-6 months
+*Every 4 - 6 months
 | style="padding: 5px 5px; background: #F5F5F5;" |
 *Annually
 |-
 | style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" |
-to 7 years
+- 7 years
 | style="padding: 5px 5px; background: #F5F5F5;" |
 *Every 6 months
@@ Line 127: / Line 133: @@
 |}
 {|
-! colspan="2" style="background:#DCDCDC;" align="center" + |The above table is the recommended management guideline for childhood screening of<br>families with affected individuals and adapted from Ophthalmology journal<ref name="SkaletGombos2018">{{cite journal|last1=Skalet|first1=Alison H.|last2=Gombos|first2=Dan S.|last3=Gallie|first3=Brenda L.|last4=Kim|first4=Jonathan W.|last5=Shields|first5=Carol L.|last6=Marr|first6=Brian P.|last7=Plon|first7=Sharon E.|last8=Chévez-Barrios|first8=Patricia|title=Screening Children at Risk for Retinoblastoma|journal=Ophthalmology|volume=125|issue=3|year=2018|pages=453–458|issn=01616420|doi=10.1016/j.ophtha.2017.09.001}}</ref>
+! colspan="2" style="background:#DCDCDC;" align="center" + |This table is adopted from Ophthalmology journal<ref name="SkaletGombos2018">{{cite journal|last1=Skalet|first1=Alison H.|last2=Gombos|first2=Dan S.|last3=Gallie|first3=Brenda L.|last4=Kim|first4=Jonathan W.|last5=Shields|first5=Carol L.|last6=Marr|first6=Brian P.|last7=Plon|first7=Sharon E.|last8=Chévez-Barrios|first8=Patricia|title=Screening Children at Risk for Retinoblastoma|journal=Ophthalmology|volume=125|issue=3|year=2018|pages=453–458|issn=01616420|doi=10.1016/j.ophtha.2017.09.001}}</ref>
 |-
 |}
+*The schedule presented above is general [[Medical guideline|guideline]] for at-risk [[Child|children]] when no [[Lesion|lesions]] of concern have been noted. Some [[Child|children]] may require more frequent [[Eye examination|examinations]].
+* The American Association of [[Ophthalmic]] [[Oncologists]] and [[Pathologists]] (AAOOP) [[Medical guideline|guideline]] also suggests a single dilated [[Fundus (eye)|fundus]] [[Physical examination|examination]] to evaluate for [[asymptomatic]] spontaneously regressed retinoblastoma or retinoma in all first-degree relatives of a [[patient]] with retinoblastoma, including older siblings if the [[RB1]] [[genetic analysis]] of the relatives is not done.
+===[[Genetic testing|Genetic Testing]] for Children with Retinoblastoma===
+{{familytree/start}}
+{{familytree | | | | | | | | | | | | | | | A01 | | | | | |A01=[[Genetic testing]] for children with Retinoblastoma}}
+{{familytree | | | | | | | | | | | | | | | |!| | | }}
+{{familytree | |,|-|-|-|-|-|v|-|-|-|-|-|-|-|+|-|-|-|-|v|-|-|-|.| | }}
+{{familytree | |!| | | | | |!| | | | | | | |!| | | | |!| | | |!| | | }}
+{{familytree | D01 | | | | D02 | | | | | | D03 | | | D04 | | D05 |D01=Not available|D02=[[Blood]]: [[RB1]] [[mutation]](+)<br>([[germline mutation]])|D03=Blood: [[RB1]] [[mutation]](-)<br>[[Tumor]]: [[RB1]] [[mutation]](+)|D04=[[Blood]]: [[RB1]] [[mutation]](-)<br>[[Tumor]]: [[RB1]] [[mutation]](-)|D05=[[Blood]]: [[RB1]] [[mutation]](-)<br>[[Tumor]]: not available}}
+{{familytree | |!| | | | | |!| | | | | | | |!| | | | |!| | | |!| }}
+{{familytree | E01 | | | | E02 | | | | | | E03 | | | |`| E04 |'| |E01=Ophthalmic [[screening]] for all<br>the relatives with greater risk than the population |E02=Assessment of relatives<br>for familial retinoblastoma|E03=Ophthalmic [[screening]] and [[genetic analysis]]<br>not required for first degree relatives|E04=No need for [[genetic analysis]] of first degree relatives}}
+{{familytree | | | | | |,|-|^|-|.| | | | | |!| | | | | | |!| }}
+{{familytree | | | | | F01 | | F02 | | | | F03 | | | | | F04 |F01=Relatives with [[RB1]] [[mutation]]|F02=Relatives without [[RB1]] [[mutation]]|F03=Ophthlamic [[screening]] for future offspring unless negative for parent's [[mutation]]|F04=Future offspring of affected child require ophthalmic [[screening]]}}
+{{familytree | | | | | |!| | | |!| | | |}}
+{{familytree | | | | | G01 | | G02 | | |G01=Ophthalmic [[screening]] for children as high risk|G02=Ophthalmic [[screening]] not required}}
+{{familytree/end}}
+{|
+! colspan="2" style="background:#DCDCDC;" align="center" + |The above table is the recommended genetic analysis guidline for families with affected individuals and adopted from Ophthalmology journal<ref name="SkaletGombos2018">{{cite journal|last1=Skalet|first1=Alison H.|last2=Gombos|first2=Dan S.|last3=Gallie|first3=Brenda L.|last4=Kim|first4=Jonathan W.|last5=Shields|first5=Carol L.|last6=Marr|first6=Brian P.|last7=Plon|first7=Sharon E.|last8=Chévez-Barrios|first8=Patricia|title=Screening Children at Risk for Retinoblastoma|journal=Ophthalmology|volume=125|issue=3|year=2018|pages=453–458|issn=01616420|doi=10.1016/j.ophtha.2017.09.001}}</ref>
+|-
+|}
 ==References==
 {{reflist|2}}
+[[Category:Medicine]]
+[[Category:Oncology]]
+[[Category:Up-To-Date]]
+[[Category:Surgery]]