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. 2021 Apr 28;26(7):e1288–e1289. doi: 10.1002/onco.13792

Trend in Stereotactic Radiation Therapy Use for Management of Bone and Brain Metastases in Patients with Renal Cell Carcinoma in Australia

Wee Loon Ong 1,2,3,4,9, Shankar Siva 1,5, Roger L Milne 6,7,8,10, Farshad Foroudi 2, Jeremy L Millar 9,11
PMCID: PMC8265356  PMID: 33844360

Short abstract

Adding to the limited literature on the subject, this letter to the editor focuses on the trend in the use of stereotactic radiation therapy for metastatic renal cell carcinoma.


Paciotti et al. recently reported an increasing trend in the use of stereotactic radiation therapy (SRT) for metastatic renal cell carcinoma (mRCC) using data from the U.S. National Cancer Database (NCDB) [1]. We have found similar—yet in some ways different—trends in Australia that will expand the evidence base in this rapidly evolving field.

We used data from the population‐based Victorian Radiotherapy Minimum Dataset in Australia to identify radiation therapy (RT) courses delivered between 2012 and 2017 in patients with mRCC and limited our analyses to RT to bone and brain metastases, as these are the most common metastatic sites of mRCC [1]. The RT techniques were classified as SRT versus non‐SRT for bone metastases based on reporting by individual institutions, whereas the definition for stereotactic radiosurgery (SRS) for brain metastases was defined according to an earlier Australian study [2].

There were 425 patients who received 733 RT courses for bone metastases in our cohort—of these, 3% of RT courses were SRT (Table‐1). The Cochran‐Armitage test for trend showed marked increase in SRT use from 0% in 2012 to 10% in 2017 (p < .001), consistent with that seen in the U.S. [1]. In multivariable logistic regressions (employing robust standard error (SE) by clustering patients who had multiple courses of RT), factors independently associated with increased likelihood of SRT use for bone metastases were as follows: more recent year of RT (odds ratio [OR], 2.49; 95% confidence interval [CI], 1.53–4.06; p < .001), younger age at time of RT (OR, 0.94; 95% CI, 0.90–0.99; p = .02), female (OR, 4.9; 95% CI, 1.16–21.0; p = .03), and treatment in private institutions (OR, 7.61; 95% CI, 2.18–26.5; p = .001). One hundred thirty‐two patients received 184 RT courses for brain metastases—of these, 53% of RT courses were SRS (Table 1). There was an 8% absolute increase in SRS use over time, from 55% in 2012 to 63% in 2017 (p = .06). There was no statistically significant association between the different factors and SRS use for brain metastases in multivariable analyses. No SRT or SRS was delivered in regional institutions.

Table 1.

Factors associated with stereotactic radiation therapy/stereotactic radiosurgery use for bone and brain metastases in metastatic renal cell carcinoma

Characteristics Bone metastases Brain metastases
Non‐SRT, n (%) SRT, n (%) p value a Non‐SRS, n (%) SRS, n (%) p value a
Number of RT courses (%) 712 (97) 21 (2.9) 86 (47) 98 (53)
Year of RT
2012 102 (100) 0 (0) <.001 b 5 (45) 6 (55) .06 b
2013 124 (100) 0 (0) 15 (75) 5 (25)
2014 119 (97) 4 (3.3) 9 (43) 12 (57)
2015 144 (98) 3 (2.0) 18 (46) 21 (54)
2016 124 (98) 3 (2.4) 21 (47) 24 (53)
2017 99 (90) 11 (10) 18 (38) 30 (63)
Age at RT, years
Mean ± SD 67.3 ± 11.3 62.2 ± 9.0 67.6 ± 10.9 63.3 ± 11.3
<60 183 (96) 7 (4) .09 19 (35) 35 (65) .07
60–69 224 (96) 10 (4) 30 (47) 34 (53)
70–79 305 (99) 4 (1) 37 (56) 29 (44)
Sex
Male 524 (98) 13 (2) .2 60 (46) 74 (54) .68
Female 188 (96) 8 (4) 26 (49) 27 (51)
Socioeconomic status
First quintile (lowest) 138 (99) 1 (0.7) .04 10 (56) 8 (44) .09
Second quintile 119 (97) 4 (3.3) 11 (50) 11 (50)
Third quintile 164 (97) 5 (3.0) 23 (52) 21 (48)
Fourth quintile 133 (99) 1 (0.8) 20 (61) 13 (39)
Fifth quintile (highest) 158 (94) 10 (6.0) 22 (34) 43 (66)
Remoteness of residence
Major cities 472 (96) 19 (4) .02 56 (42) 77 (58) .04
Regional/remote 240 (99) 2 (1) 30 (59) 21 (41)
Treatment institution type
Public 480 (99) 5 (1) <.001 51 (40) 76 (60) .008
Private 232 (94) 16 (6) 35 (61) 22 (39)
Treatment institution location
Metropolitan 531 (96) 21 (3.8) .008 62 (39) 98 (61) <.001
Regional 181 (100) 0 (0) 24 (100) 0 (0)
a

p values based on Pearson's chi‐squared test.

b

p value based on Cochran‐Armitage test for trend.

Abbreviations: RT, radiation therapy; SRT, stereotactic radiation therapy; SRS, stereotactic radiosurgery.

These data, while smaller in number compared with the U.S. NCDB, are to the best of our knowledge the only Australian population‐based series to date, adding to the very limited real‐life literature in SRT/SRS use for mRCC [1]. Although SRT for bone metastases is only gaining traction in more recent years in our cohort, SRS use for brain metastases is already relatively common for mRCC, and in fact its use is more common compared with brain metastases from other primary cancers [2]. In comparison with Paciotti et al., we did not find patients’ socioeconomic and remoteness of residence to be associated with SRT/SRS use in multivariate analyses, suggesting that patients in our cohort most likely had access to metropolitan centres in Victoria providing SRT/SRS services.

With technological advancement and increasing experience with SRT/SRS, in conjunction with increasing efficacy of targeted systemic therapy and immunotherapies for mRCC [3], we anticipate that SRT/SRS will be an integral modality in treatment for mRCC in combination with systemic therapies [4]. However, it is important to ensure equal and easy access to SRT/SRS services for all patients with cancer who will benefit from it.

Disclosures

The authors indicated no financial relationships.

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Editor's Note: See the Letter article, “Temporal Trends and Predictors in the Use of Stereotactic Body Radiotherapy for Treatment of Metastatic Renal Cell Carcinoma in the U.S” by Marco Paciotti, Andrew L. Schmidt, Praful Ravi, et al., on page e905 on 26:5 issue.

References

  • 1. Paciotti M, Schmidt A, Ravi P et al. Temporal trends and predictors in the use of stereotactic body radiotherapy for treatment of metastatic renal cell carcinoma in the United States. The Oncologist 2021;26:e905–e906. [DOI] [PMC free article] [PubMed] [Google Scholar]
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