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Chmura, Steven J.

https://orcid.org/0000-0001-8851-7108

Mayo Clinic

University of Chicago

Citations 5

Neuro-oncology at the American Society for Clinical Oncology 2022 Annual Meeting
Lukas, Rimas V. , Chmura, Steven J. , Mammoser, Aaron, Smith, Sonali M. , Parney, Ian F. , Li, Jing

Neuro-Oncology Practice | September 10, 2022 | Volume: 9 | Issue: 6 | Pages: 552-558

10.1093/nop/npac071 Get It

Abstract In the following brief report, we highlight the advances in the neuro-oncology space from the ASCO 2022 Annual Meeting. We put into context the phase 2 and 3 trials and how these may alter the standard of care going forward. In addition, we highlight some other earlier work that will lead to future and potentially practice-changing trials.
Hippocampal Avoidance During Whole-Brain Radiotherapy Plus Memantine for Patients With Brain Metastases: Phase III Trial NRG Oncology CC001
Brown, Paul D. , Gondi, Vinai , Pugh, Stephanie L. , Tomé, Wolfgang A. , Bovi, Joseph , Robinson, Clifford G. , Konski, André , Khuntia, Deepak , Grosshans, David R. , Benzinger, Tammie L.S. , Devisetty, Kiran , Shah, Sunjay, Usuki, Kenneth Y., Anderson, Bethany , Yoon, Harold, Li, Jing , Chmura, Steven J. , Shi, Wenyin , Deshmukh, Snehal, Kachnic, Lisa A. , Oncology, for NRG, Robinson, Clifford , Benzinger, Tammie L S , Shi, Wenyin , Wefel, Jeffrey S. , Armstrong, Terri S. , Bruner, Deborah Watkins , Gilbert, Mark R. , Roberge, David , Kundapur, Vijayananda , Stea, Baldassarre , Laack, Nadia N. , Kruser, Tim J. , Mehta, Minesh P. , Oncology, for NRG

Journal of Clinical Oncology | February 14, 2020 | Volume: 38 | Issue: 10 | Pages: 1019-1029

10.1200/jco.19.02767 Get It

PURPOSE Radiation dose to the neuroregenerative zone of the hippocampus has been found to be associated with cognitive toxicity. Hippocampal avoidance (HA) using intensity-modulated radiotherapy during whole-brain radiotherapy (WBRT) is hypothesized to preserve cognition. METHODS This phase III trial enrolled adult patients with brain metastases to HA-WBRT plus memantine or WBRT plus memantine. The primary end point was time to cognitive function failure, defined as decline using the reliable change index on at least one of the cognitive tests. Secondary end points included overall survival (OS), intracranial progression-free survival (PFS), toxicity, and patient-reported symptom burden. RESULTS Between July 2015 and March 2018, 518 patients were randomly assigned. Median follow-up for alive patients was 7.9 months. Risk of cognitive failure was significantly lower after HA-WBRT plus memantine versus WBRT plus memantine (adjusted hazard ratio, 0.74; 95% CI, 0.58 to 0.95; P = .02). This difference was attributable to less deterioration in executive function at 4 months (23.3% v 40.4%; P = .01) and learning and memory at 6 months (11.5% v 24.7% [ P = .049] and 16.4% v 33.3% [ P = .02], respectively). Treatment arms did not differ significantly in OS, intracranial PFS, or toxicity. At 6 months, using all data, patients who received HA-WBRT plus memantine reported less fatigue ( P = .04), less difficulty with remembering things ( P = .01), and less difficulty with speaking ( P = .049) and using imputed data, less interference of neurologic symptoms in daily activities ( P = .008) and fewer cognitive symptoms ( P = .01). CONCLUSION HA-WBRT plus memantine better preserves cognitive function and patient-reported symptoms, with no difference in intracranial PFS and OS, and should be considered a standard of care for patients with good performance status who plan to receive WBRT for brain metastases with no metastases in the HA region.
NCOG-01. PRESERVATION OF NEUROCOGNITIVE FUNCTION (NCF) WITH HIPPOCAMPAL AVOIDANCE DURING WHOLE-BRAIN RADIOTHERAPY (WBRT) FOR BRAIN METASTASES: PRELIMINARY RESULTS OF PHASE III TRIAL NRG ONCOLOGY CC001
Gondi, Vinai , Pugh, Stephanie L. , Brown, Paul D. , Bovi, Joseph , Benzinger, Tammie, Khuntia, Deepak , Grosshans, David R. , Konski, André , Robidoux, André, Devisetty, Kiran , Shah, Sunjay, Usuki, Kenneth Y., Anderson, Bethany , Yoon, Harold, Li, Jing , Chmura, Steven J. , Kachnic, Lisa A. , Wefel, Jeffrey S. , Gilbert, Mark R. , Robinson, Clifford G. , Benzinger, Tammie L S , Tomé, Wolfgang A. , Armstrong, Terri S. , Bruner, Deborah Watkins , Kundapur, Vijayananda , Stea, Baldassarre , Laack, Nadia N. , Kruser, Tim J. , Shi, Wenyin , Mehta, Minesh P.

Neuro-Oncology | November 5, 2018 | Volume: 20 | Issue: suppl_6 | Pages: vi172-vi172

10.1093/neuonc/noy148.716 Get It

A randomized phase II study of anti-PD1 antibody [MK-3475 (Pembrolizumab)] alone versus anti-PD1 antibody plus stereotactic body radiation therapy in advanced merkel cell carcinoma (Alliance A091605).
Chmura, Steven J. , Allred, Jacob B., Salama, Joseph K. , Al‐Hallaq, Hania , Hsu, Charles C., Kozloff, M., Luke, Jason J. , Yom, Sue S. , Münster, Pamela N. , Schwartz, Gary K.

Journal of Clinical Oncology | September 5, 2018 | Volume: 36 | Issue: 15_suppl | Pages: TPS9599-TPS9599

10.1200/jco.2018.36.15_suppl.tps9599 Get It

Concurrent Chemotherapy and Intensity-Modulated Radiation Therapy for Anal Canal Cancer Patients: A Multicenter Experience
Salama, Joseph K. , Mell, Loren K. , Schomas, David A., Miller, Robert C. , Devisetty, Kiran , Jani, Ashesh B. , Mundt, Arno J., Roeske, John C. , Liauw, Stanley L. , Chmura, Steven J. , Liauw, Stanley L

Journal of Clinical Oncology | October 9, 2007 | Volume: 25 | Issue: 29 | Pages: 4581-4586

10.1200/jco.2007.12.0170 Get It

Purpose To report a multicenter experience treating anal canal cancer patients with concurrent chemotherapy and intensity-modulated radiation therapy (IMRT). Patients and Methods From October 2000 to June 2006, 53 patients were treated with concurrent chemotherapy and IMRT for anal squamous cell carcinoma at three tertiary-care academic medical centers. Sixty-two percent were T1-2, and 67% were N0; eight patients were HIV positive. Forty-eight patients received fluorouracil (FU)/mitomycin, one received FU/cisplatin, and four received FU alone. All patients underwent computed tomography–based treatment planning with pelvic regions and inguinal nodes receiving a median of 45 Gy. Primary sites and involved nodes were boosted to a median dose of 51.5 Gy. All acute toxicity was scored according to the Common Terminology Criteria for Adverse Events, version 3.0. All late toxicity was scored using Radiation Therapy Oncology Group criteria. Results Median follow-up was 14.5 months (range, 5.2 to 102.8 months). Acute grade 3+ toxicity included 15.1% GI and 37.7% dermatologic toxicity; all acute grade 4 toxicities were hematologic; and acute grade 4 leukopenia and neutropenia occurred in 30.2% and 34.0% of patients, respectively. Treatment breaks occurred in 41.5% of patients, lasting a median of 4 days. Forty-nine patients (92.5%) had a complete response, one patient had a partial response, and three had stable disease. All HIV-positive patients achieved a complete response. Eighteen-month colostomy-free survival, overall survival, freedom from local failure, and freedom from distant failure were 83.7%, 93.4%, 83.9%, and 92.9%, respectively. Conclusion Preliminary outcomes suggest that concurrent chemotherapy and IMRT for anal canal cancers is effective and tolerated favorably compared with historical standards.