Although the number of studies focusing on overall survival after radiosurgery for brain metastases is impressive, much less is known about factors affecting local control. Tumor volume/diameter, volume of edema, large (> 15) number of lesions, concurrent chemotherapy and other factors are listed by various authors but without consistency and the findings usually are not reproduced by others.1,2,3,4,5 Of course, assuming that metastatic tumors contain a constant number of clonogenic cells per volume unit, there is indeed a risk that larger tumors may be treated less effectively. This is because lower doses are used to kill larger number of cancer stem cells per tumor. According to the RTOG 9005 protocol, brain metastases exceeding 3 cm in diameter were treated with a single dose of 15 Gy as opposed to 24 Gy for tumors smaller than 2 cm.6 This results with almost five times more stem cells treated with less than two thirds of the dose delivered to a smaller tumor. Alternatively, fractionated schemes of still uncertain efficacy can be implemented. Their postulated equivalence to single fraction schedules in terms of biological dose is based on radiobiological calculations but the assumptions taken, need confirmation in clinical studies. The first studies aimed at detailed analysis of the effect of the dose normalized to volume of the lesion and probability of local control were made by Amsbaugh
The aim of our study was to assess the association between physical and biological dose delivered per volume unit of a metastatic tumor as well as clinical factors with local control in patients with brain metastases after robotic stereotactic radiosurgery.
All patients treated with the CyberKnife system for cerebral metastases between 2011 and 2016 were retrospectively evaluated to find those with follow-up imaging studies allowing for evaluation of local control. No selection was made in terms of pathology of the tumor, prior treatment or primary tumor status. This resulted with identification of 69 patients for further evaluation.
Patients were immobilized with thermoplastic masks for treatment. CT and MR images were made and the target volume and critical structures were defined on registered images. Usually, no additional margin was added to the GTV. Patients were qualified to a single fraction or hypofractionated treatment after individual assessment of the target volume and proximity of organs at risk. Single doses were prescribed following the RTOG 9005 study. If V12 exceeded 10 cm3 or dose constraints for critical structures were violated, fractionated treatment was prescribed. The dose was specified to isodose encompassing the target, usually between 78 and 90%. All patients were treated with the CyberKnife VSI system.
Biologically effective dose (BED) was calculated assuming the alpha/beta value of 10. The total physical dose (TD) and BED were normalized to the tumor volume to allow better evaluation of the dose effect. Prescription dose was taken as reference for calculation. Threshold values of BED and BED/cm3 were determined after a stepwise analysis and further included into statistical analysis as categorical variables. Age, gender, pathology, primary tumor status, WBRT use and other variables potentially associated with local control and survival were also analyzed. MR imaging after treatment was performed usually every 3-4 months during the first year and every 6-12 months thereafter. Local control (LC) was defined as lack of progression (complete or partial response or stable disease) of the irradiated lesion. Any increase in lesion size without evidence of radiation-induced necrosis was qualified as local progression. Local progression-free survival (LPFS) was defined as time between treatment and the first imaging showing progression of the irradiated lesion. Local progression (LP) was defined as growth of the irradiated lesion irrespective of the status of other lesions. Distant progression-free survival defined as time to development of new brain metastases (outside the irradiated lesions) was not evaluated.
Basic characteristics of the study population
Median (range) | |
---|---|
Age | 58 (32–84) |
KPS | 80 (70–100) |
Number of lesions (1-9) | 1 (1–9) |
Number of patients | |
1 | 40 |
2 | 12 |
3 | |
4 | |
5 | |
6 | |
9 | |
Gender (M/F) | 22/47 |
WBRT before SRS | |
Yes | 34 |
No | 35 |
Location of the primary tumour | |
Lung | 23 |
Breast | 20 |
Kidney | |
Skin (melanoma) | |
Colon | |
Unknown primary | |
Uterine corpus | |
Other = One case of each: intestinal sarcoma, thyroid cancer, uterine cervix carcinoma, esophageal, gastric, oral cavity, ovarian, and bladder cancer; F = female; KPS = Karnofsky performance status; M = male; NED = no evidence of disease; SRS = stereotactic radiosurgery; WBRT = whole brain radiotherapy | |
Disease status | |
Stable/NED | 42 |
Progressive | 27 |
Primary tumor controlled | |
Yes | 62 |
No | 7 |
Extracranial metastases | |
Present | 39 |
No | 30 |
Kaplan-Meier method and log-rank test were used for calculations and intergroup comparisons. Kaplan-Meier estimations were calculated per lesion (progression of the index lesion was an event). If a new lesion occurred, the patient was censored for the purpose of the analysis (only the irradiated lesions were the subject of analysis and it was assumed that dose delivered to an existing lesion will not affect the probability of progression elsewhere in the brain). Patients dying without evidence of progression of the irradiated lesion were censored at the time of death. Cox regression was used for multivariate analysis which was performed on the set of variables significant in the univariate analysis. Mann-Whitney U test was used for intergroup comparisons. The p value < 0.05 was considered significant.
The study follows the principles of the Declaration of Helsinki.
A total of 133 tumors in 69 patients were irradiated and their volumes ranged between 0.001 and 46.99 cm3 (median 1.86). Basic patient characteristics is shown in Table 1.
Median total intracranial tumor volume was 4.1 cm3. The doses used resulted with BED10 values of 11.9 – 81.6 Gy (median 46.2 Gy). Physical doses and BED per 1 cm3 of tumor volume ranged between 0.3 - 1322 Gy (median 11), and 4.6-119733.5 Gy (median 24.3), respectively. Detailed dosimetric characteristics is shown in Table 2.
Median LPFS was 10.7 months. Actuarial 1-year local progression-free survival was 46%. No association between the volume of the tumor and local control could be found. Total dose, BED10 above 59 Gy (Figure 1), presence of a single metastasis (Figure 2), and extracranial progression (Figure 3) were significantly associated with LC variables. Presence of extracranial progression was associated with worse local control whereas higher TD, BED10 > 59 Gy and single metastasis predicted better local outcome. Moreover, negative association with BED10/cm3 (Figure 4), and BED2/cm3 and LC was identified (Table 3).
In multivariate analysis only presence of a single metastasis, BED10 > 59 Gy and extracranial progression retained their significance. Excluding a priori the BED2/cm3 parameter, which can be considered redundant in construction of the Cox model resulted with confirmation of significance of all of the remaining.
Dosimetric and volumetric characteristics of the group
Variable | Median (range) | p |
---|---|---|
Total dose in SRS | 18 Gy (5 | = comparison between groups, Mann-Whitney U test; BED10 = biologically effective dose for alpha/ beta =10; HSRT = hypofractionated stereotactic radiotherapy; SRS – stereotactic radiosurgery |
Total dose in HSRT | 20 Gy (12 | |
Dose per fraction in HSRT | 7.25 Gy (6 | |
BED10 in SRS | 50.4 (7.5 | = comparison between groups, Mann-Whitney U test; BED10 = biologically effective dose for alpha/ beta =10; HSRT = hypofractionated stereotactic radiotherapy; SRS – stereotactic radiosurgery |
BED10 in HSRT | 35.7 (19.2 | |
Lesion volume | 1.74 cm3 (0.001 | |
Single metastasis | 4.68 cm3 (0.05 | = comparison between groups, Mann-Whitney U test; BED10 = biologically effective dose for alpha/ beta =10; HSRT = hypofractionated stereotactic radiotherapy; SRS – stereotactic radiosurgery |
Multiple metastases | 0.96 cm3 (0.001 | |
Total tumor volume | 4.9 cm3 (0.05 | |
Single metastasis volume | 4.68 cm3 (0.05 | = comparison between groups, Mann-Whitney U test; BED10 = biologically effective dose for alpha/ beta =10; HSRT = hypofractionated stereotactic radiotherapy; SRS – stereotactic radiosurgery |
Multiple metastases volume | 4.90 cm3 (0.48 |
Association of selected variables with local control
p | ||
---|---|---|
Variable | univariate | Multivariate |
Single | ||
Gender | 0.2508 | |
Total dose = above | 0.0886 | |
BED10 = above | 0.7026 | |
BED10 > 59 Gy | ||
Fractionation (SRS vs. HSRT) | 0.1265 | |
Tumor volume¶ | 0.1777 | |
Total tumor volume¶ | 0.8950 | |
Chemotherapy before SRS/HSRT | 0.3785 | |
Chemotherapy after SRS/HSRT | 0.2174 | |
Chemotherapy before and after SRS/HSRT | 0.2606 | |
Time between diagnosis of primary and metastases = above | 0.6551 | |
BED10 per 1 ml tumor volume > median (24.3 Gy) | 0.3709 | |
BED10 per 1 ml tumor volume > 36 Gy | 0.3032 | |
Total dose/ml tumor volume > median (11 Gy) | 0.3882 | |
Extracranial metastases | 0.3130 | |
Control of primary tumor | 0.8681 | |
Extracranial progression = progression of primary tumor or any of extracranial metastases; SRS = stereotactic radiosurgery; HSRT = hypofractionated stereotactic radiotherapy; BED10, BED2 = biologically effective dose for alpha/beta =10 and 2, respectively; WBRT = whole brain radiotherapy; RPA = recursive partitioning analysis | ||
RPA class | 0.8627 | |
WBRT use | 0.3918 | |
BED2 | 0.8638 |
The results of analysis prompted to check also the difference in local control between patients with 1-3 and more metastases which was also highly significant (p = 0.0000), with median LPFS of 7.1 and 17.1 months, respectively. All patients with more than 3 metastases failed locally before one year whereas actuarial 1-year LPFS in the group with 1-3 metastases was 68%.
To the best knowledge of the authors this is the first study in which dose normalized to tumor volume is analyzed as a prognostic factor for local control for both single-fraction and hypofractionated regimens. Amsbaugh
BED above 59 Gy10 was associated with improved chances of local control. This parameter retained significance in multivariate analysis indicating that appropriate biologically effective dose increases the probability of local control irrespective of the fractionation method. What is more intriguing, biological doses normalized to tumor volume above 36 Gy10/cm3 (the threshold value calculated for the nervous tissue - BED2 was 60 Gy2/cm3 and was also significant) resulted with significantly worse local control. This phenomenon did not retain significance in multivariate analysis including all variables significant in the univariate analysis. However, in an additionally constructed model without incorporating BED2/cm3 it did. Amsbaugh
Better outcome after larger single dose in terms of probability of local control was confirmed for example by Mohammadi
Our study has drawbacks typical for retrospective evaluations. We cannot exclude patient selection bias and we did not have follow-up imaging available for every patient treated in our center which limited the study sample. We realize also that metastases in a single patients share a lot of common properties important for the prognosis and their independent analysis may be somewhat misleading. On the other hand, it should facilitate demonstration of the dose and volume effect because lesions of various sizes in one patient were often irradiated with different doses.
Our results suggest that local control in the brain can depend on several factors including those not directly related to the local treatment and may be associated also with systemic progression. In turn, this may influence overall survival in much more complex way than we assume. The results suggest also that escalating the dose above certain limits may not be beneficial. The threshold dose for this effect calculated for the nervous tissue is similar to the dose of 60 Gy used in conventional radiotherapy for primary brain tumors. Further escalation did not prove beneficial but was associated with increased risk of adverse effects.14
Hypofractionated treatment schemes have similar efficiency to single fraction treatment in terms of local control and the effect depends on BED, irrespective of fractionation schedule. Effective control of extracranial sites of the disease is associated with probability of local control in the brain which is consistently lower in patients with multiple lesions.