Meningioma Flashcards

1
Q

What % of all primary CNS tumors do meningiomas account for in adults?

A

36%. Meningioma is the most common benign 1st-degree CNS tumor. (Central Brain Tumor Registry of the United States, 2016 update) Autopsy studies suggest prevalence of subclinical meningiomas in up to 3% of the general population

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the age and sex predilection for meningiomas?

A

The incidence of meningiomas increases with age (mean age at Dx 62, incidence peaks in the 8th decade). Females are more commonly affected than males (2:1).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are some risk factors for meningiomas?

A

Prior RT (RR 10, median interval to development 20 yrs), NF-2 (5%–15% risk of multiple meningiomas), and HRT in women (RR 2).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Which protein is defective in NF-2, and to what else does NF-2 predispose?

A

Merlin; bilat acoustic neuromas/ependymomas and juvenile subcapsular cataracts

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What histologic features can be seen in meningiomas?

A

Psammoma bodies and calcifications

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

List 5 negative prognostic factors for meningiomas.

A

Negative prognostic factors for meningiomas:

  1. High grade
  2. Young age
  3. Chromosome alterations
  4. Poor PS
  5. STR
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is the grade classification of meningiomas?

A

WHO grade I (benign), grade II (atypical), and grade III

anaplastic/malignant

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

According to the 2007 WHO classification, what criterion upgrades an otherwise grade I meningioma to grade II?

A

Brain invasion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is the prevalence of grades II–III meningiomas?

A

6% and 4%, respectively. 90% are grade I.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Name the histologies associated with WHO grades II–III meningiomas.

A

Grade II: atypical, clear cell, chordoid

Grade III: anaplastic, rhabdoid, papillary

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Of grade I meningiomas, which histologic subtype is most aggressive?

A

The angioblastic subtype is the most aggressive grade I meningioma.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the OS difference b/t atypical and anaplastic meningiomas?

A

Atypical 12 yrs vs. anaplastic 3.3 yrs (Yang SY et al., J Neurol Neurosurg Psychiatry 2008)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What are some prognostic factors identified for anaplastic meningiomas?

A

Brain invasion, adj RT, extent of resection, and p53 overexpression (Yang SY et al., J Neurol Neurosurg Psychiatry 2008)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is the most common Sx at presentation for meningiomas?

A

HA is the most common presenting Sx.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is the appearance of meningiomas on CT/MRI?

A

Homogeneously and intensely enhancing mass, +/– dural tail

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What % of meningiomas exhibit a dural tail? In what other tumors/lesions can dural tails be seen?

A

60%. Dural tails can also be seen in chloroma, lymphoma, and sarcoidosis.

17
Q

What proportion of incidentally found meningiomas remain stable on imaging?

A

Two-thirds. The majority remain stable on imaging.

18
Q

For meningiomas, with what are slower growth rates associated?

A

Slower growth rates are associated with older pts and calcifications.

19
Q

What surgical grading system is used in meningiomas? For what does it predict?

A

Simpson grade (I/GTR–V/decompression) predicts the likelihood of LR.

20
Q

In what anatomic regions is GTR more difficult to achieve for meningioma resection?

A

Cavernous sinus, petroclival region, postsagittal sinus, and optic nerve

21
Q

How is optic sheath meningioma diagnosed?

A

Optic sheath meningioma is diagnosed clinically/radiographically by a neuroophthalmologist/
MRI (no Bx).

22
Q

What are the Tx paradigms for meningiomas?

A

Meningioma Tx paradigms:
If incidental/asymptomatic: observation
If grade I and symptomatic/progressive: Sg + RT (if STR)
If grade II (high risk) or III: Sg + RT

23
Q

For which types of meningioma is RT the primary Tx modality?

A

Optic nerve sheath and cavernous sinus (inaccessible regions)

24
Q

When should observation be considered?

A

Observation should be considered with incidental/asymptomatic and stable lesions. Consider Sg for large (≥30 mm) lesions, if accessible.

25
Q

When is RT utilized after Sg for meningiomas?

A

RT should be utilized after Sg if there is recurrent Dz or STR or if there is anaplastic histology or brain invasion.

26
Q

What is the avg time to recurrence after Sg for meningiomas?

A

4 yrs is the avg time to recurrence after Sg.

27
Q

What are the 10-yr recurrence rates with Sg alone after either GTR or STR of meningioma?

A

10-yr recurrence rates with Sg alone are ∼10% after GTR and 60% after STR.

28
Q

Is there a benefit to upfront RT after STR for grade I meningioma?

A

This is controversial (upfront control rates are considered equivalent to salvage rates). RTOG 0539 showed RT benefit for WHO II (post-STR) and all WHO III tumors (Rogers L et al., NeuroOncol 2017) and may address this question in its low-risk cohort.

29
Q

What are the RT doses employed for meningiomas?

A

RT doses are 45–54 Gy for benign and 60 Gy for malignant tumors (CTV = GTV + 1–2 cm).

30
Q

Is there any RT dose–response data for meningiomas?

A

Yes. Goldsmith BJ et al. showed improved PFS with doses >52 Gy. (J Neurosurg 1994)

31
Q

What are typical SRS doses used for meningiomas?

A

Typical SRS doses range from 12–16 Gy to 50% IDL at the tumor margin (depending on location/size).

32
Q

What is the 5-yr LC rate for meningiomas after SRS?

A

The 5-yr LC rate is ∼95% for grade I tumors. For grades II–III, it is 68% and 0%, respectively. (Stafford SL et al., Neurosurgery 2001)

33
Q

What poor prognostic factors have been identified in pts receiving SRS for meningiomas?

A

Male sex, previous Sg, tumors located in parasagittal/falx/convexity regions (Pollock BE et al., Neurosurgery 2012)

34
Q

Should the dural tail be covered in the RT field?

A

In general, no; however this is controversial. Some studies have shown improved 5-yr DFS when the dural tail was included in SRS Rx isodose. (DiBiase SJ et al., IJROBP 2004)

35
Q

What is the surgical complication rate after resection for meningiomas?

A

After resection, the surgical complication rate is 2%–30% depending on the location/type; 1%–14% mortality (worse in the elderly).

36
Q

If observed, pts with meningiomas should get MRIs at what intervals?

A

At 3 mos, 6 mos, and 12 mos, then every 6–12 mos for 5 yrs, then every 1–3 yrs if stable (NCCN 2018)

37
Q

What is the toxicity rate for SRS if doses >16 Gy are used?

A

There is temporary toxicity in 10% of pts and permanent toxicity in 6% of pts. Perilesional edema is observed in 15%. (Kullova A et al., J Neurosurg 2007)

38
Q

How are optic nerve sheath/cavernous sinus meningioma pts followed?

A

These pts should be followed with serial MRIs, neuro-ophthalmology exams, and regular endocrinology exams.