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STEREOTACTIC RADIOSURGERY AND
RADIOTHERAPY OF PITUITARY ADENOMAS
Clinical White Paper

Pituitary adenomas (PAs) are the third most common intracranial tumors in surgical practice, accounting for
approximately 10 to 25% of all intracranial neoplasms 1. Radiological series suggest that unsuspected PAs
may be present in one out of six people and autopsy specimens reveal a prevalence of 14% 2.
Histopathologically, PAs are mostly benign lesions located on the anterior lobe of the pituitary gland 3.
Because of their invasive growth tendency, these adenomas may cause significant morbidity in affected
patients, expressed by visual, endocrinologic and neurologic symptoms 4,5.

Figure: Details of a typical pituitary adenoma treatment plan
Pituitary adenomas can be classified as endocrine active or
endocrine inactive6. Endocrine-active adenomas prevail when
the secreted amount of biologically active hormones exceeds
the normal blood level values. Approximately 70% of all newly
diagnosed PAs are endocrine active, mostly stimulating the
7
secretion of prolactin, the growth hormone, and corticotropin .
Endocrine-inactive or non-functioning adenomas represent 30%
of all PAs and do have secretory granules, but they either
produce undetectable small amounts of normal hormones or
secrete abnormal hormones that are not recognized by
8
biological receptors .
Where endocrine-active tumors may produce symptoms due to
excessive secretion of particular hormones and also by some
mass effect on neighboring structures, non-functioning tumors
only do so by the mass effect.
Successful management of PAs requires the dual attainment of
lifelong local tumor control and, for those tumors which are
hormonally active, normalization of excess hormone secretion.
Historically, surgery has been established as the standard for
pituitary treatment. However, even with improved surgical
techniques, complete tumor removal is challenging with reported
9
recurrence rates in the range of 3 to 18% . Adjuvant
conventional radiotherapy has been employed as a treatment
option for PAs since 190910.

Over the years, combinations of surgery, radiotherapy and
medical therapy proved effective for the treatment of PAs.
The individualized therapeutic approach depends nowadays
on tumor and patient characteristics, as well as clinician
experience and preference.
The successful control of the majority of tumors comes at the
price of treatment-related toxicity. Hypopituitarism is the most
common case of radiation-induced pituitary deficiency and
can result in complications such as optic nerve atrophy,
11
blindness, secondary tumor growth and dementia .
Radiation-induced hypopituitarism may be induced from
direct exposure of the pituitary gland and the hypothalamus
and can be prevented by assuring superior target dose
conformality and a steep dose fall-off. This is achieved by
single fraction stereotactic radiosurgery (SRS) or fractionated
stereotactic radiotherapy (SRT), two techniques that
maximize the sparing of critical organs and minimize
12-18
.
morbidity without compromising local tumor control
Most studies limit the use of SRS to small spherical lesions in
close proximity to organs at risk12,13 and chose SRT for all
other lesions to benefit from the radiobiological effects of
19
fractionation .
An overview of some recent studies, evaluating the efficiency
of SRS and SRT treatments for PAs, is presented in the table
below.
The mean treatment dose ranges from 15 to 21 Gy for SRS
and from 45 to 52 Gy for SRT, typically split up in fractions of
1.8 Gy. Depending on the collimator, the dose is delivered by
13,16,18
multiple, non-coplanar arcs or beams, either conformal
15
or intensity-modulated .
The achieved mean local control for both SRS and SRT
treatments is 96% with an average hormonal response rate of
80%. Newly initiated hormonal replacement therapy, as a
result of radiation-induced pituitary deficiency, was required in
5 to 40% of all cases.

This wide range of values reflects the various positions of the
lesions with respect to the organs at risk. Patients with
lesions close the pituitary gland or the hypothalamus are
more likely to suffer radiation-induced toxicity.
From the summarized results it can be concluded that SRS
and SRT, either as a primary treatment or in combination
with surgery, represent an effective, safe and minimally
invasive option for controlling the growth of PAs and reducing
hormone production.

Overview of the recent clinical literature on SRS and SRT for pituitary adenomas
Institution

Year

#
Lesions

% Prior
Surgery

Mean
Volume
(cm³)

Mean
Dose
(Gy)

#
Fractions

% Local
Control

%
Tumor
Response

%
Hormonal
Response

% Pituitary
Deficiency

12

Brigham and Women´s
Hospital, Boston

1998

18

88

1.90

15

1

100 at 47
months

22

50

30

12

Brigham and Women´s
Hospital, Boston

1998

30

88

5.70

45

25

85 at 34
months

20

62

21

Kangnam St. Mary´s
Hospital, Seoul

1998

24

96

NA

21

1

96 at 49
months

63

84

29

University of
Heidelberg

2001

62

11

30.2

50

28

93 at 39
months

30

60

5

University of
Heidelberg

2004

5

100

3.50

15

1

100 at 38
months

60

100

8

13

University of
Heidelberg

2004

20

95

26.2

52

29

100 at 61
months

25

80

8

16

Polyclinique Courlancy,
Reims

2005

110

81

4.20

50

28

99 at 82
months

89

100

37

17

National University,
Seoul

2005

68

96

6.20

50

28

98 at 30
months

38

NA

6

Author

Mitsumori

Mitsumori

14

Yoon

Milker-

18

Zabel

Milker-

13

Zabel

MilkerZabel

Colin

Paek

Because local control doesn´t necessarily imply a reduction of tumor volume, tumor response indicates the percentage of adenomas that present a measurable
reduction of the tumor volume after irradiation. Similarly, hormonal response is defined as a quantitative reduction of the initial hormonal level. The wide range of
values for the pituitary deficiency reflects the various positions of the lesions with respect to the organs at risk. Patients with lesions close the pituitary gland or the
hypothalamus are more likely to suffer radiation-induced toxicity.
References
[1]
[2]
[3]
[4]
[5]
[6]
[7]
[8]
[9]

Scheithauer B.W. et al., Neurosurg 59, 341, 2006
Ezzat S. et al., Cancer 101, 613, 2004
Dworakowska D. et al., Best Pract Res Cl En 23, 525, 2009
Milker-Zabel S. et al., Int J Radiat Oncol Biol Phys 50(5), 1279, 2001
Daly A.F. et al., Best Pract Res Cl En 23, 543, 2009
Wilson C.B., Cancer medicine. Lea & Febiger, Philadelphia 1993, pp. 1131–1137
Lindholm J. et al., J Clin Endocr Metab 86, 117, 2001
Sauer R., Therapy of malignant brain tumors. Springer-Verlag 1987, pp. 195–276
Davis D.H. et al., J Neurosurg 79, 70, 1993

Europe | +49 89 99 1568 0 | de_sales@brainlab.com
North America | +1 800 784 7700 | us_sales@brainlab.com
Latin America | +55 11 3355 3370 | br_sales@brainlab.com

RT_WP_E_PITUITARY_APR11

[10]
[11]
[12]
[13]
[14]
[15]
[16]
[17]
[18]
[19]

Beclere A., Arch Roentgen Radiol 14, 147, 1909
Rush S. et al., Int J Radiat Oncol Biol Phys Biol Phys 37, 1031, 1997
Mitsumori M. et al., Int J Radiat Oncol Biol Phys 42(3), 573, 1998
Milker-zabel S. et al., Int J Radiat Oncol Biol Phys 59(4), 1088, 2004
Yoon S.C. et al., Int J Radiat Oncol Biol Phys 41(4), 849, 1998
Mackley H.B. et al., Int J Radiat Oncol Biol Phys 67(1), 232, 2007
Colin P. et al., Int J Radiat Oncol Biol Phys 62(2), 333, 2005
Paek S.H. et al., Int J Radiat Oncol Biol Phys 61(3), 795, 2005
Milker-zabel S. et al., Int J Radiat Oncol Biol Phys 50(5), 1279, 2001
Tome W.A. et al., Technol Cancer Res Treat 1, 153, 2002

Asia Pacific | +852 2417 1881 | hk_sales@brainlab.com
Japan | +81 3 3769 6900 | jp_sales@brainlab.com

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Stereotactic Radiosurgery and Radiotherapy of Pituitary Adenomas Clinical White Paper

  • 1. STEREOTACTIC RADIOSURGERY AND RADIOTHERAPY OF PITUITARY ADENOMAS Clinical White Paper Pituitary adenomas (PAs) are the third most common intracranial tumors in surgical practice, accounting for approximately 10 to 25% of all intracranial neoplasms 1. Radiological series suggest that unsuspected PAs may be present in one out of six people and autopsy specimens reveal a prevalence of 14% 2. Histopathologically, PAs are mostly benign lesions located on the anterior lobe of the pituitary gland 3. Because of their invasive growth tendency, these adenomas may cause significant morbidity in affected patients, expressed by visual, endocrinologic and neurologic symptoms 4,5. Figure: Details of a typical pituitary adenoma treatment plan Pituitary adenomas can be classified as endocrine active or endocrine inactive6. Endocrine-active adenomas prevail when the secreted amount of biologically active hormones exceeds the normal blood level values. Approximately 70% of all newly diagnosed PAs are endocrine active, mostly stimulating the 7 secretion of prolactin, the growth hormone, and corticotropin . Endocrine-inactive or non-functioning adenomas represent 30% of all PAs and do have secretory granules, but they either produce undetectable small amounts of normal hormones or secrete abnormal hormones that are not recognized by 8 biological receptors . Where endocrine-active tumors may produce symptoms due to excessive secretion of particular hormones and also by some mass effect on neighboring structures, non-functioning tumors only do so by the mass effect. Successful management of PAs requires the dual attainment of lifelong local tumor control and, for those tumors which are hormonally active, normalization of excess hormone secretion. Historically, surgery has been established as the standard for pituitary treatment. However, even with improved surgical techniques, complete tumor removal is challenging with reported 9 recurrence rates in the range of 3 to 18% . Adjuvant conventional radiotherapy has been employed as a treatment option for PAs since 190910. Over the years, combinations of surgery, radiotherapy and medical therapy proved effective for the treatment of PAs. The individualized therapeutic approach depends nowadays on tumor and patient characteristics, as well as clinician experience and preference. The successful control of the majority of tumors comes at the price of treatment-related toxicity. Hypopituitarism is the most common case of radiation-induced pituitary deficiency and can result in complications such as optic nerve atrophy, 11 blindness, secondary tumor growth and dementia . Radiation-induced hypopituitarism may be induced from direct exposure of the pituitary gland and the hypothalamus and can be prevented by assuring superior target dose conformality and a steep dose fall-off. This is achieved by single fraction stereotactic radiosurgery (SRS) or fractionated stereotactic radiotherapy (SRT), two techniques that maximize the sparing of critical organs and minimize 12-18 . morbidity without compromising local tumor control Most studies limit the use of SRS to small spherical lesions in close proximity to organs at risk12,13 and chose SRT for all other lesions to benefit from the radiobiological effects of 19 fractionation . An overview of some recent studies, evaluating the efficiency of SRS and SRT treatments for PAs, is presented in the table below.
  • 2. The mean treatment dose ranges from 15 to 21 Gy for SRS and from 45 to 52 Gy for SRT, typically split up in fractions of 1.8 Gy. Depending on the collimator, the dose is delivered by 13,16,18 multiple, non-coplanar arcs or beams, either conformal 15 or intensity-modulated . The achieved mean local control for both SRS and SRT treatments is 96% with an average hormonal response rate of 80%. Newly initiated hormonal replacement therapy, as a result of radiation-induced pituitary deficiency, was required in 5 to 40% of all cases. This wide range of values reflects the various positions of the lesions with respect to the organs at risk. Patients with lesions close the pituitary gland or the hypothalamus are more likely to suffer radiation-induced toxicity. From the summarized results it can be concluded that SRS and SRT, either as a primary treatment or in combination with surgery, represent an effective, safe and minimally invasive option for controlling the growth of PAs and reducing hormone production. Overview of the recent clinical literature on SRS and SRT for pituitary adenomas Institution Year # Lesions % Prior Surgery Mean Volume (cm³) Mean Dose (Gy) # Fractions % Local Control % Tumor Response % Hormonal Response % Pituitary Deficiency 12 Brigham and Women´s Hospital, Boston 1998 18 88 1.90 15 1 100 at 47 months 22 50 30 12 Brigham and Women´s Hospital, Boston 1998 30 88 5.70 45 25 85 at 34 months 20 62 21 Kangnam St. Mary´s Hospital, Seoul 1998 24 96 NA 21 1 96 at 49 months 63 84 29 University of Heidelberg 2001 62 11 30.2 50 28 93 at 39 months 30 60 5 University of Heidelberg 2004 5 100 3.50 15 1 100 at 38 months 60 100 8 13 University of Heidelberg 2004 20 95 26.2 52 29 100 at 61 months 25 80 8 16 Polyclinique Courlancy, Reims 2005 110 81 4.20 50 28 99 at 82 months 89 100 37 17 National University, Seoul 2005 68 96 6.20 50 28 98 at 30 months 38 NA 6 Author Mitsumori Mitsumori 14 Yoon Milker- 18 Zabel Milker- 13 Zabel MilkerZabel Colin Paek Because local control doesn´t necessarily imply a reduction of tumor volume, tumor response indicates the percentage of adenomas that present a measurable reduction of the tumor volume after irradiation. Similarly, hormonal response is defined as a quantitative reduction of the initial hormonal level. The wide range of values for the pituitary deficiency reflects the various positions of the lesions with respect to the organs at risk. Patients with lesions close the pituitary gland or the hypothalamus are more likely to suffer radiation-induced toxicity. References [1] [2] [3] [4] [5] [6] [7] [8] [9] Scheithauer B.W. et al., Neurosurg 59, 341, 2006 Ezzat S. et al., Cancer 101, 613, 2004 Dworakowska D. et al., Best Pract Res Cl En 23, 525, 2009 Milker-Zabel S. et al., Int J Radiat Oncol Biol Phys 50(5), 1279, 2001 Daly A.F. et al., Best Pract Res Cl En 23, 543, 2009 Wilson C.B., Cancer medicine. Lea & Febiger, Philadelphia 1993, pp. 1131–1137 Lindholm J. et al., J Clin Endocr Metab 86, 117, 2001 Sauer R., Therapy of malignant brain tumors. Springer-Verlag 1987, pp. 195–276 Davis D.H. et al., J Neurosurg 79, 70, 1993 Europe | +49 89 99 1568 0 | de_sales@brainlab.com North America | +1 800 784 7700 | us_sales@brainlab.com Latin America | +55 11 3355 3370 | br_sales@brainlab.com RT_WP_E_PITUITARY_APR11 [10] [11] [12] [13] [14] [15] [16] [17] [18] [19] Beclere A., Arch Roentgen Radiol 14, 147, 1909 Rush S. et al., Int J Radiat Oncol Biol Phys Biol Phys 37, 1031, 1997 Mitsumori M. et al., Int J Radiat Oncol Biol Phys 42(3), 573, 1998 Milker-zabel S. et al., Int J Radiat Oncol Biol Phys 59(4), 1088, 2004 Yoon S.C. et al., Int J Radiat Oncol Biol Phys 41(4), 849, 1998 Mackley H.B. et al., Int J Radiat Oncol Biol Phys 67(1), 232, 2007 Colin P. et al., Int J Radiat Oncol Biol Phys 62(2), 333, 2005 Paek S.H. et al., Int J Radiat Oncol Biol Phys 61(3), 795, 2005 Milker-zabel S. et al., Int J Radiat Oncol Biol Phys 50(5), 1279, 2001 Tome W.A. et al., Technol Cancer Res Treat 1, 153, 2002 Asia Pacific | +852 2417 1881 | hk_sales@brainlab.com Japan | +81 3 3769 6900 | jp_sales@brainlab.com