Abstract
Radiation therapy is a cornerstone in the therapeutic management of craniopharyngioma. The close proximity to neighboring eloquent structures pose a particular challenge to radiation therapy. Modern treatment technologies including fractionated 3-D conformal radiotherapy, intensity modulated radiation therapy, and recently proton therapy are able to precisely cover the target while preserving surrounding tissue, Tumor controls between 80 and in access of 90% can be achieved. Alternative treatments consisting of radiosurgery, intracavitary application of isotopes, and brachytherapy also offer an acceptable tumor control and might be given in selected cases. More research is needed to establish the role of each treatment modality.
Keywords: craniopharyngioma, radiotherapy, post-operative
Introduction
Surgery and radiotherapy are the cornerstones in therapeutic management of craniopharyngioma. Radical excision is associated with a risk of mortality or morbidity particularly as hypothalamic damage, visual deterioration, and endocrine complication between 45 and 90% of cases. By contrast, recurrent disease after partial excision alone is observed between in 50 and 91% (Becker et al., 1999). Today less radical surgery in combination with radiation therapy are favored achieving a progression-free survival between 70 and 90% (Fahlbusch et al., 1999; Chiou et al., 2001; Tomita and Bowman, 2005).
New technologies are currently under investigation to achieve a better balance between tumor control and the risk for hazardous effects for surrounding eloquent structures such as the pituitary gland, hypothalamus, optic apparatus, and arteries at the base of the skull.
Role of Radiotherapy/Conventional Technologies
External fractionated radiotherapy is presently standard of care to achieve an optimal progression-free survival after non-radical excision (Wen et al., 1989; Hetelekidis et al., 1993; Merchant et al., 2002; Stripp et al., 2004; Karavitaki et al., 2005; Lin et al., 2008). An excellent long-term outcome of conventional radiotherapy was found in many retrospective series reporting 10 and 20 years progression-free survival up to 95 and 54% (Table 1).
Table 1.
Author | Patients | PFS (%) |
OS (%) |
||
---|---|---|---|---|---|
5 years | 10 years | 5 years | 10 years | ||
Carmel et al. (1982) | 14 | 78 | 78 | 90 | 80 |
Habrand et al. (1999) | 32 | 78 | 56 | 91 | 65 |
Flickinger et al. (1990) | 21 | 95 | 95 | 89 | 89 |
Rajan et al. (1993) | 173 | – | 83 | – | 77 |
Hetelekidis et al. (1993) | 46 | – | 86 | – | 91 |
Mark et al. (1995) | 25 | 96 | – | 96 | 96 |
Varlotto et al. (2002) | 24 | 89.1 (10 years) | 54 (20 years) | 100 (10 years) | 92.3 (20 years) |
Pemberton et al. (2005) | 87 | 77 (10 years) | 66 (20 years) | 86 (10 years) | 76 (20 years) |
PFS, progression-free survival; OS, overall survival.
Modern Technologies in Radiation Therapy
Advances in radiation therapy technologies have opened up new approaches in the radio-oncological management of craniopharyngioma. The selection of the adequate treatment technology is of ongoing debate.
Fractionated conformal radiotherapy/intensity modulated radiation therapy
With the use of modern imaging technologies and treatment planning systems a precise coverage of the tumor area can be achieved by using stereotactic irradiation technologies. Stereotactic irradiation can be given in a single dose as stereotactic radiosurgery or in multiple doses as fractionated stereotactic radiotherapy. The modern systems permit an exact calculation of dose distribution within the tumor and provide a steeper dose gradient to surrounding normal tissue. If a cystic component is present, careful monitoring during radiotherapy is necessary (Winkfield et al., 2009). The results are shown in Table 2.
Table 2.
Author | Patients | Technique | Dose | PFS | OS |
---|---|---|---|---|---|
Combs et al. (2007) | 40 | 3-D conformal fractionated stereotactic radiotherapy | Median 52.2 Gy, range 50.4–56 Gy, 1.8–2 Gy single dose | 100% local control at 5 and 10 years | 5/10 years 79/89% |
Minniti et al. (2007) | 36 | 3-D conformal fractionated stereotactic radiotherapy | 50 Gy in 30–33 fractions | 3–5 years 97/92% | 3/5 years 100% |
Kanesaka et al., 2011 (adults) | 16 | 3-D conformal fractionated stereotactic radiotherapy | 30 Gy in 6 fractions | 3 year local control 82.4% | 3 year 94.1% |
Hashizume et al. (2010) | 10 | FSRT Novalis IMRT | 30–39 Gy in 10–15 fractions (median 33 Gy) | Control rate 100% | Not reported |
Selch et al. (2002) | 16 | 3-D conformal fractionated stereotactic radiotherapy | 55 Gy fractionated | 75% at 3 years | 93% at 3 years |
Proton therapy
The major advantage of proton therapy is the high degree of dose conformity to the target. Beltran et al. (2011) retrospectively evaluated proton treatment plans with IMRT plan. He concluded that compared with photon IMRT proton therapy has the potential to significantly reduce whole brain and body irradiation. Fitzek et al. treated 15 patients with craniopharyngioma with a mix of photon and protons. The tumor control rates at 5 and 10 years were 93 and 85%, respectively (Fitzek et al., 2006). Luu et al. (2006) treated 16 patients. Local control could be achieved in 14 of 15 patients (Luu et al., 2006).
Timing of Radiation Therapy
Often immediate post-operative radiation therapy is favored in order to obviate early tumor progression leading to a functional deterioration caused by tumor growth or the necessity for repeat surgery. Others favor a watch-and-wait strategy fearing the long-term adverse effects of radiation therapy. The recent series of Stripp et al. (2004), Tomita and Bowman (2005), and Moon et al. (2005) showed no differences between progression-free and overall survival between the different approaches (Table 3). However, in the recent series of Lin et al. (2008) early radiation therapy yielded a 100% local control rate at 10 years as compared with 32% when radiation therapy was performed at relapse.
Table 3.
Author (year) | Patients | Early RT | RT at relapse |
---|---|---|---|
Sung et al. (1981) | 10 | – | 70.9%, 10 years OS |
Regine et al. (1993) | 58 | 78%, 20 years OS | 25%, 20 years OS |
Stripp et al. (2004) | 40 | 83%, 10 years OS | 86%, 10 years OS |
Tomita and Bowman (2005) | 30 | 71%, 5 years PFS | 90%, 5 years PFS |
Moon et al. (2005) | 50 | 91.3%, 10 years PFS | 91.2%, 10 years PFS |
Lin et al. (2008) | 31 | 100%, 10 years LC | 32%, 10 years LC |
RT, radiotherapy; OS, overall survival; PFS, progression-free survival; LC, local tumor control.
Other Technologies
Radiosurgery
Stereotactic radiosurgery is an alternative to fractionated treatments in patients with craniopharyngioma harboring smaller lesions. The reported results of radiosurgery, however, suggest that tumor control is inferior to fractionated treatments and might carry the risk for optic neuropathies unless only smaller lesions are treated away from the optic apparatus (Tishler et al., 1993). Minniti et al. (2009) reviewed eight published series and found an average tumor control rate of 90% for solid tumors, 88% for cystic tumors, and 60% for mixed tumors (Table 4).
Table 4.
Author | Patients | Dose | PFS | OS |
---|---|---|---|---|
Kobayashi et al. (2005) | 98 | Marginal dose 11 Gy | 61 and 54% at 5 and 10 years | 94.1 and 91% at 5 and 10 years |
Ulfarsson et al. (2002) | 21 | 3–25 Gy | 34% | n.a. |
Amendola et al. (2003) | 14 | 14 Gy (11–20 Gy) | 86% | All alive 6–86 months |
Chiou et al. (2001) | 10 | Median 16.4 Gy | 58% | n.a. |
Yu et al. (2000) | 46 | Marginal dose 8–18 Gy | 89.5% | n.a. |
Chung et al. (2000) | 31 | 9.5–16 Gy | 87% | n.a. |
Mokry (1999) | 23 | Marginal dose 8–9.7 Gy | 74% | n.a. |
Prasad et al. (1995) | 9 | 13 Gy | 62.5% | n.a. |
n.a., not analyzed.
CyberKnife
CyberKnife includes a compact linear accelerator mounted on a robotic arm combined with the pair of diagnostic X-ray sources permitting an online reproducibility of the incident beams and a subsequent adjustment of the beam with a precision below 1 mm. Lee et al. reported results obtained in 16 patients treated for residual recurrent craniopharyngioma Tumor shrinkage was achieved in 7 of these 11 patients and tumor control in another 3 patients. The overall tumor control was achieved in 91% of patients without complications (Lee et al., 2008).
Interstitial brachytherapy
There is one report from Barlas et al. (2000) in two patients in whom iodine125-seeds were implanted delivering a dose of 67 and 60 Gy to tumor periphery. Response was partially observed in one and tumor completely resolved in the other patient 24 months after treatment. Radiation induced toxicity or recurrence has not been reported 6 years after treatment.
Intracavitary application of isotopes
Approximately 90% of craniopharyngioma display a cystic component often leading to a space occupying clinically relevant effect. There are different series reporting on the intracavitary application of different isotopes such as Rhenium186, Yttrium90, or Phosporus32. The nuclides emit β-rays with a therapeutic range within only a few millimeters. Response rates and cyst controls can be achieved in more than 80% of case. Tumors with a solid component, however, are insufficiently controlled (Voges et al., 1997; Hasegawa et al., 2004). Deterioration of visual function due to ionizing irradiation of the nuclides can occur (Table 5).
Table 5.
Author | Patients | Isotope | Complete remission | Reduction | No change | expansion | Tumor control | Visual impairment |
---|---|---|---|---|---|---|---|---|
Voges et al. (1997) | 62 | Y 90 | 35/78 | 27/78 | 12/78 | 4/78 | 10 years OS | 4/62 |
78 C | Rhe 186 | Solid: 31% | ||||||
P 32 | Cystic: 64% | |||||||
Blackburn et al. (1999) | 6 | Y 90 | 0 | 6 | 1 | 2 | n.a. | 1/5 |
9 C | ||||||||
Hasegawa et al. (2004) | 41 | P 32 | 7 | 24 | 5 | 5 | 10 years: 70% | 3/40 (RT induced) |
41 C | Solid comp.: 32% increase | |||||||
Derrey et al. (2008) | 39 | Rhe 186 | 17 | 17 | 5 | 5 | n.a. | 3/39 |
44 C |
C, cysts; Y 90, Yttrium 90; Rhe 186, Rhenium 186; P 32, Phosphorus 32; OS, overall survival.
Conclusion
Standard treatments today consist of fractionated external irradiation therapy. The recent developments in modern treatment technologies permit an exact delineation of target and non-target surrounding normal tissue (Merchant et al., 2006). Tumor control and overall survival might be improved as compared with the excellent results obtained with conventional treatments at shorter follow-up periods. Longer follow-up periods, however, are warranted. Today the 5-year progression-free survival after modern fractionated irradiation is in the range between 80 and 100%. Good results are achieved with a combined approach (surgery + radiation therapy) using standard fractionation. The recently introduced proton therapy opens up the possibility for a better sparing of normal surrounding tissue. Presently data are, however, limited and the expected improvement of functional outcome remains yet to be proven.
Post-operative radiation therapy is superior to surveillance after non-radical resection in terms of progression-free survival. The impact of different timing on functional outcome is still unknown. The current prospective German study Craniopharyngioma 2007 is addressing this issue in a randomized prospective study.
Radiosurgery as an option for circumscribed small lesions away from the optic apparatus is an attractive option because normal surrounding tissue is excellently spared. Single dose radiotherapy is, however, associated with an inferior tumor control according to retrospective data. CyberKnife as a new technological development utilizing image guided high precision stereotactic radiotherapy is able to use the radiobiologically advantageous fractionation concept. Interstitial treatments like the intracystic application of radioactive colloids might be used in selected cases in which only cystic tumors are present. It is, however, more a historical experience and should not be favored in the area of modern treatment technologies. Brachytherapy is of limited importance and the experiences so far obtained are very scarce. Minimizing the dose to non-target tissue will be the future step to reduce the risk for late effects. Reproducible data in prospective settings including neurocognitive function, quality of life, visual, and endocrinological function are still missing and require further research and evaluation. Table 6 gives an overview of the current technologies.
Table 6.
Technology | Advantages | Disadvantages |
---|---|---|
Conventional 2-D radiotherapy | Reliable clinical data and long follow-up indicating high efficacy of radiotherapy | Poor geometrical precision. No reliable protection of normal surrounding tissue |
Fractionated conformal radiation therapy/IMRT | Excellent adjustment of treatment portals to tumor site. In 3-D. Sparing of normal tissue | Rigid head fixation (relocatable). Few patient numbers and not yet long follow-up |
Fractionated proton therapy | Optimal coverage of tumor site. With maximal sparing of surrounding tissue | Few patient numbers. Limited access, high costs |
Radiosurgery | Only one session. Excellent coverage of tumor. Almost no dose to non-target tissue | Limited clinical settings. Tumor control inferior to fractionated treatments? Low patient numbers. No long follow-up |
Hypofractionated image guided radiosurgery (CyberKnife) | Only few session. The biological advantages of fractionation can be utilized. Excellent coverage of tumor. Almost no dose to non-target tissue | Very few experiences. Role still unclear. No reliable data for tumor control. No long-term follow-up. Only selected clinical settings |
Intracavitary colloid isotope application | High tumor control rates for cystic components | Only cystic tumors. Underdosage in solid components. Leakage possible. Detrimental effects on visual function reported |
Interstitial irradiation (Iodine seeds) | Excellent dose conformity. Optimal protection of normal tissue | Very few clinical data |
Conflict of Interest Statement
The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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