PQA 04 - PQA 04 Palliative Care and Central Nervous System Poster Q&A
2573 - Feasibility and Outcomes of Navigated Transcranial Magnetic Stimulation Based Diffusion Tensor Imaging Tractography of Motor Pathways in Patients Undergoing Stereotactic Radiosurgery
J. McDonald1, J. K. Bronk1, M. Muir2, H. Michener3, D. Mackin4, W. Talpur1, T. Beckham1, A. J. Ghia1, S. L. McGovern1, C. Wang1, K. D. Woodhouse1, D. N. Yeboa1, M. Farhat1, A. M. Elliott1, J. Li1, S. Prabhu2, S. Prinsloo2,3, and C. Chung1; 1Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, 2Department of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, TX, 3Department of Palliative, Rehabilitation, and Integrative Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, 4Department of Radiation Physics, The University of Texas MD Anderson Cancer Center, Houston, TX
Purpose/Objective(s):There are no stereotactic radiosurgery (SRS) dose constraint guidelines for the motor cortex and tracts as this region of interest (ROI) is difficult to delineate using conventional imaging techniques and anatomic landmarks. Navigated transcranial magnetic stimulation (nTMS) is a novel non-invasive tool using electromyographic signal and magnetic resonance diffusion tensor imaging (DTI) to functionally map cortical motor tracts (MT). While nTMS is used to identify the MT before tumor resection, it has not been implemented in SRS planning. The objectives of this study were to (i) determine the feasibility of performing nTMS-based DTI in patients with previously SRS treated brain metastases in or near the MT, (ii) measure concordance of nTMS seeded MT (TMS-MT) versus anatomically seeded MT (A-MT) and (iii) evaluate the relationship between radiation dose to TMS-MT and patient outcomes measured by objective hand function testing and patient reported outcomes (PROs).Materials/
Methods: 15 patientswith brain metastasesproximal toanatomically defined MTpreviously treated with single-fraction SRSwere enrolled onan IRB-approved cross-sectional study. At a median4.9 monthsafter SRS, patients underwent nTMS testingof the upper extremities and brainDTI. Functional outcomes testing (GripDynamometer) and quality-of-life (QOL)PROs (EQ-5D-5L) were acquired. Tractography was generatedon treatment planning software and imported as anROIinto the treatment planning system for volumetric and dosimetric evaluation. Results: Functional testing, PRO questionnaires, and nTMS scheduling was successful for 15/15 (100%) of enrolled patients andTMS-MT was successful in 14/15(93.3%).Examination of size and location ofA-MT versus TMS-MTrevealed that A-MT were larger (median volume 17.85cc versus 7.1cc for TMS-MT). There was a medianvolumetricoverlap of4.16cc (32.1%) between the TMS-MT and A-MT on the patient’s treated side (range 16.4-46.3%).Strength deficitsoccurred in 5/10 (50%) patients treated unilaterally(unaffected extremity testing measures used as a baseline control), and 60% of patients experienced coordination deficits.Median Dmax to TMS-MT was 12.5Gy for patients with deficits in grip strength compared to 4.2Gy for those without detected deficits.For all patients, a decrease in EQ5D5L score trended linearly with increase inDmaxto the TMS-MT. Conclusion: In this completed feasibility study,nTMS testing in the radiation oncology clinic met criteria for feasibility. Dmax to the TMS-MT correlated withmagnitude ofnegative impact in motor function and overall QOL.Thenotable differences in location and size of the TMS-MTvs. A-MTsuggest thatadditional functional imaging may improveMT delineation to inform clinical decision making and SRS treatment planning.