Description

Stojadinovic et al identified predictors for disease-specific survival (DSS) in patients with adrenocortical carcinoma. These can help identify patients who may benefit from aggressive or novel therapies. The authors are from Memorial Sloan-Kettering Cancer Center in New York.


 

Parameters:

(1) distant metastasis status

(2) tumor invasion of veins, capsule or adjacent organs

(3) tumor necrosis

(4) mitotic rate

(5) atypical mitosis

(6) overexpression of mdm-2 by immunohistochemistry

 

Parameter

Finding

Points

distant metastasis

absent

0

 

present

1

tumor invasion

absent

0

 

into veins, capsule and/or adjacent organs

1

tumor necrosis

absent

0

 

present

1

mitotic rate in areas with greatest mitotic activity

<= 5 mitoses in 50 high powered fields (HPF)

0

 

> 5 mitoses in 50 HPF

1

atypical mitosis

absent

0

 

present

1

expression of mdm-2

no overexpression

1

 

overexpression present

0

 

where:

• A high powered field indicates use of a 40x objective. An Olympus U-D0 model was used; the area of the field was not stated.

• mdm-2 was from clone 2A10, using a 1:500 diluted, provided by Dr A Levine of Rockefeller University. The staining protocol is given on page 942. Over-expression is defined as > 50% nuclei staining.

• In the original version risk was assigned to overexpression (based on text in column 1 on page 946). However, adrenal cortical carcinomas are mdm-2 negative, so the risk should be assigned to "negative" overexpression.

 

number of risk factors present =

= SUM(points for all 6 parameters)

 

Interpretation:

• minimum number of risk factors: 0

• maximum number of risk factors: 6

• Disease-specific survival was higher with low numbers of risk factors.

Number of Risk Factors

5 Year Disease Specific Survival

0

not stated

1 or 2

84%

3 or 4

37%

5 or 6

9%

 

Conclusions of the paper:

(1) Predicting prognosis for a patient depends on a meticulous morphologic evaluation, mitotic count and staging of the tumor.

(2) The tumors show a significant molecular complexity and heterogeneity, indicating that targeted therapy needs to be individualized for each patient.

 

Limitations:

• Staining for mdm-2 is likely to be available at only a few centers, at least for the near term. However, the other parameters should be sufficient to determine the relative prognosis for the patient.

 


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