Prognostic Model for Intracranial Progression after Stereotactic Radiosurgery: A Multicenter Validation Study

被引:1
|
作者
Carpenter, David J. [1 ]
Natarajan, Brahma [2 ]
Arshad, Muzamil [3 ]
Natesan, Divya [4 ]
Schultz, Olivia [3 ]
Moravan, Michael J. [5 ]
Read, Charlotte [1 ,6 ]
Lafata, Kyle J. [1 ,6 ,7 ]
Giles, Will [1 ]
Fecci, Peter [8 ]
Mullikin, Trey C. [1 ]
Reitman, Zachary J. [1 ]
Kirkpatrick, John P. [1 ,8 ]
Floyd, Scott R. [1 ]
Chmura, Steven J. [3 ]
Hong, Julian C. [9 ,10 ,11 ,12 ]
Salama, Joseph K. [1 ,13 ]
机构
[1] Duke Univ, Dept Radiat Oncol, Med Ctr, Durham, NC 27710 USA
[2] Univ Carolina Chapel Hill, Dept Med, Chapel Hill, NC 27599 USA
[3] Univ Chicago, Dept Radiat Oncol, Chicago, IL 60637 USA
[4] Univ Carolina Chapel Hill, Dept Radiat Oncol, Chapel Hill, NC 27599 USA
[5] Vet Affairs St Louis Hlth Care Syst, Radiat Oncol Clin Serv, St Louis, MO 63110 USA
[6] Duke Univ, Dept Radiol, Med Ctr, Durham, NC 27710 USA
[7] Duke Univ, Dept Elect & Comp Engn, Durham, NC 27710 USA
[8] Duke Univ, Dept Neurosurg, Med Ctr, Durham, NC 27710 USA
[9] Univ Calif San Francisco, Dept Radiat Oncol, San Francisco, CA 94143 USA
[10] Univ Calif San Francisco, Bakar Computat Hlth Sci Inst, San Francisco, CA 94143 USA
[11] Univ Calif San Francisco, Joint Program Computat Precis Hlth, San Francisco, CA 94143 USA
[12] Univ Calif Berkeley, Berkeley, CA 94720 USA
[13] Durham VA Hlth Care Syst, Radiat Oncol Clin Serv, Durham, NC 27710 USA
关键词
stereotactic radiosurgery; intracranial progression; brain metastases; RECURSIVE PARTITIONING ANALYSIS; BRAIN METASTASES; RADIATION-THERAPY; BREAST-CANCER; SURVIVAL; DIAGNOSIS;
D O I
10.3390/cancers14215186
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary To optimize surveillance for patients with brain metastases following stereotactic radiosurgery (SRS), we sought to validate a previously published nomogram estimating post-SRS intracranial progression (IP) risk. Among 890 patients completing an initial SRS course across two institutions 7/2017-12/2020, 53% were deemed high-risk for IP. Freedom from IP was superior for low-risk patients (p < 0.001), with a median of 13.9 months (95% CI 11.1-17.1 months) versus 7.6 months (95% CI 6.4-9.3 months) for high-risk patients. This large multisite cohort supports the use of an IP nomogram as a quick, simple means of stratifying patients into low- and high-risk groups for post-SRS IP. Stereotactic radiosurgery (SRS) is a standard of care for many patients with brain metastases. To optimize post-SRS surveillance, this study aimed to validate a previously published nomogram predicting post-SRS intracranial progression (IP). We identified consecutive patients completing an initial course of SRS across two institutions between July 2017 and December 2020. Patients were classified as low- or high-risk for post-SRS IP per a previously published nomogram. Overall survival (OS) and freedom from IP (FFIP) were assessed via the Kaplan-Meier method. Assessment of parameters impacting FFIP was performed with univariable and multivariable Cox proportional hazard models. Among 890 patients, median follow-up was 9.8 months (95% CI 9.1-11.2 months). In total, 47% had NSCLC primary tumors, and 47% had oligometastatic disease (defined as <= 5 metastastic foci) at the time of SRS. Per the IP nomogram, 53% of patients were deemed high-risk. For low- and high-risk patients, median FFIP was 13.9 months (95% CI 11.1-17.1 months) and 7.6 months (95% CI 6.4-9.3 months), respectively, and FFIP was superior in low-risk patients (p < 0.0001). This large multisite BM cohort supports the use of an IP nomogram as a quick and simple means of stratifying patients into low- and high-risk groups for post-SRS IP.
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页数:15
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