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Flampouri, Stella

https://orcid.org/0000-0001-6489-5278

Mayo Clinic

Emory University

Citations 7

Consensus radiation therapy organ at risk constraints for NCTN trials in hematologic malignancies
Sim, Austin J. , Hoppe, Bradford S. , Ballas, Leslie K, Milgrom, Sarah A. , Terezakis, Stephanie A, Ha, Chul S. , Figura, Nicholas , Parikh, Rahul R., Grecula, J.C., Flampouri, Stella , Kelsey, Christopher R, Parikh, Rahul R. , Parikh, Rahul R , Hoppe, Bradford S , Ballas, Leslie K. , Terezakis, Stephanie A , Plastaras, John Peter , Hodgson, David C. , Ryckman, Jeffrey M. , Pinnix, Chelsea C. , Kelsey, Chris R.

JNCI: Journal of the National Cancer Institute | April 7, 2026 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.1093/jnci/djag112 Get It

Abstract Modern radiation therapy (RT) technologies allow for improved sparing of normal tissues, decreasing the risk of both acute and long-term toxicities. Existing RT dose constraints for prospective trials within the National Clinical Trials Network (NCTN) were formulated in the context of solid malignancies. As patients with hematologic malignancies are often treated with lower RT doses and are usually younger with more favorable prognoses, customized dose constraints are needed. The NRG Oncology Hematologic Malignancies Working Group (NRG HEME) commissioned a review of existing organ-at-risk (OAR) constraints from published primary literature, the NRG Center for Innovation in Radiation Oncology (CIRO), and national guidelines. Customized constraints were developed by iterative review by NRG HEME. Final recommendations were approved by radiation oncology representatives from all the lymphoma NCTN groups (NRG Oncology, Children’s Oncology Group, Alliance, ECOG-ACRIN, SWOG, Canadian Cancer Trials Group). For 49 OARs, a strict recommended constraint was determined, of which 20 were not present in CIRO. Of the remaining 29 constraints, 20 were lower, 2 were the same, and 5 used different metrics; 2 were higher than at least 1 CIRO trial constraint. Acceptable variations were determined and unacceptable variations were added for select critical OARs for plan scoring. While doses to OARs without explicit unacceptable variations should not exceed acceptable variations, violations should not be considered for plan quality assessment on trials. This consensus list of standard OAR constraints should be incorporated for all future NCTN trials in hematologic malignancies. Strict dose constraints will minimize long-term toxicities in this patient population.
Proton Pencil Beam Scanning Facilitates the Safe Treatment of Extended Radiation Targets for Hodgkin Lymphoma: A Report from the Proton Collaborative Group Registry
Ebadi, Maryam , Pankuch, Mark , Boyer, Sean, Chang, J. , Stevens, Craig , Hall, Matthew D. , Bates, James E. , Flampouri, Stella , Kole, Adam J. , Mohindra, Pranshu , Rossi, Carl J., Sanghvi, Parag, McGee, L.A. , Rana, Zaker , Tseng, Yolanda D. , Kole, Adam J , Mohindra, Pranshu , McGee, Lisa, Tseng, Yolanda D , Hall, Matthew D , Hasan, Shaakir

Cancers | August 1, 2024 | Volume: 16 | Issue: 15 | Pages: 2736

10.3390/cancers16152736 Get It

Because proton beam therapy (PBT) can lower the dose of radiation to the heart, lungs, and breast, it is an established radiation modality for patients with Hodgkin lymphoma (HL). Pencil beam scanning (PBS) PBT facilitates the treatment of more extensive targets. This may be especially of value for lymphoma patients who require RT to both mediastinal and axillary targets, defined here as extended target RT (ETRT), given the target distribution and need to minimize the lung, heart, and breast dose. Using the Proton Collaborative Group registry, we identified patients with HL treated with PBT to both their mediastinum and axilla, for which DICOM-RT was available. All patients were treated with PBS. To evaluate the dosimetric impact of PBS, we compared delivered PBS plans with VMAT butterfly photon plans optimized to have the same target volume coverage, when feasible. Between 2016 and 2021, twelve patients (median 26 years) received PBS ETRT (median 30.6 Gy (RBE)). Despite the large superior/inferior (SI, median 22.2 cm) and left/right (LR, median 22.8 cm) extent of the ETRT targets, all patients were treated with one isocenter except for two patients (both with SI and LR > 30 cm). Most commonly, anterior beams, with or without posterior beams, were used. Compared to photons, PBS had greater target coverage, better conformity, and lower dose heterogeneity while achieving lower doses to the lungs and heart, but not to the breast. No acute grade 3+ toxicities were reported, including pneumonitis. Proton ETRT in this small cohort was safely delivered with PBS and was associated with an improved sparing of the heart and lungs compared to VMAT.
Impact of proton PBS machine operating parameters on the effectiveness of layer rescanning for interplay effect mitigation in lung SBRT treatment
Liang, Xiaoying , Flampouri, Stella , Park, Justin C., Yaddanapudi, Sridhar , Tan, Jun , Beltran, Chris , Tan, Jun , Shen, Jiajian , Yaddanapudi, Sridhar , Beltran, Chris J , Liang, Xiaoying , Liu, Chunbo , Shen, Jiajian , Lu, Bo, Furutani, Keith M. , Tan, Jun

Journal of Applied Clinical Medical Physics | April 9, 2024 | Volume: 25 | Issue: 7 | Pages: No page available

10.1002/acm2.14342 Get It

Abstract Background Rescanning is a common technique used in proton pencil beam scanning to mitigate the interplay effect. Advances in machine operating parameters across different generations of particle therapy systems have led to improvements in beam delivery time (BDT). However, the potential impact of these improvements on the effectiveness of rescanning remains an underexplored area in the existing research. Methods We systematically investigated the impact of proton machine operating parameters on the effectiveness of layer rescanning in mitigating interplay effect during lung SBRT treatment, using the CIRS phantom. Focused on the Hitachi synchrotron particle therapy system, we explored machine operating parameters from our institution's current (2015) and upcoming systems (2025A and 2025B). Accumulated dynamic 4D dose were reconstructed to assess the interplay effect and layer rescanning effectiveness. Results Achieving target coverage and dose homogeneity within 2% deviation required 6, 6, and 20 times layer rescanning for the 2015, 2025A, and 2025B machine parameters, respectively. Beyond this point, further increasing the number of layer rescanning did not further improve the dose distribution. BDTs without rescanning were 50.4, 24.4, and 11.4 s for 2015, 2025A, and 2025B, respectively. However, after incorporating proper number of layer rescanning (six for 2015 and 2025A, 20 for 2025B), BDTs increased to 67.0, 39.6, and 42.3 s for 2015, 2025A, and 2025B machine parameters. Our data also demonstrated the potential problem of false negative and false positive if the randomness of the respiratory phase at which the beam is initiated is not considered in the evaluation of interplay effect. Conclusion The effectiveness of layer rescanning for mitigating interplay effect is affected by machine operating parameters. Therefore, past clinical experiences may not be applicable to modern machines.
AAPM Task Group Report 290: Respiratory motion management for particle therapy
Li, Heng , Flampouri, Stella , Jee, Kyung‐Wook , Lin, Liyong , Moyers, Michael F. , Rottmann, J, Tryggestad, E., Vedam, Sastry, Tryggestad, Erik, Lin, Liyong , Dong, Lei , Bert, Christoph , Chang, Joe Y. , Mori, Shinichiro

Medical Physics | January 23, 2022 | Volume: 49 | Issue: 4 | Pages: No page available

10.1002/mp.15470 Get It

Abstract Dose uncertainty induced by respiratory motion remains a major concern for treating thoracic and abdominal lesions using particle beams. This Task Group report reviews the impact of tumor motion and dosimetric considerations in particle radiotherapy, current motion‐management techniques, and limitations for different particle‐beam delivery modes (i.e., passive scattering, uniform scanning, and pencil‐beam scanning). Furthermore, the report provides guidance and risk analysis for quality assurance of the motion‐management procedures to ensure consistency and accuracy, and discusses future development and emerging motion‐management strategies. This report supplements previously published AAPM report TG76, and considers aspects of motion management that are crucial to the accurate and safe delivery of particle‐beam therapy. To that end, this report produces general recommendations for commissioning and facility‐specific dosimetric characterization, motion assessment, treatment planning, active and passive motion‐management techniques, image guidance and related decision‐making, monitoring throughout therapy, and recommendations for vendors. Key among these recommendations are that: (1) facilities should perform thorough planning studies (using retrospective data) and develop standard operating procedures that address all aspects of therapy for any treatment site involving respiratory motion; (2) a risk‐based methodology should be adopted for quality management and ongoing process improvement.
Selection of Mediastinal Lymphoma Patients for Proton Therapy Within the Proton Collaborative Group Registry
Pankuch, Mark , McGee, L.A. , Rossi, Carl J., Flampouri, Stella , Hajj, Carla , Molitoris, Jason K. , Chang, John, Stevens, Craig , Rosen, L, Vargas, Carlos , Hartsell, William F. , McGee, Lisa, Tseng, Yolanda D. , Mohindra, Pranshu , Tsai, Henry K.

American Journal of Clinical Oncology | April 16, 2021 | Volume: 44 | Issue: 6 | Pages: 269-274

10.1097/coc.0000000000000819 Get It

Purpose: As patients with mediastinal lymphoma are typically young with curable disease, advanced radiation techniques such as proton therapy are often considered to minimize subacute and late toxicity. However, it is unclear which mediastinal lymphoma patients are treated with proton therapy. Within a prospective, multi-institutional proton registry, we characterized mediastinal lymphoma patients treated with proton therapy and assessed concordance with consensus recommendations published in 2018 by the International Lymphoma Radiation Oncology Group (ILROG). Methods: Eligible patients included those with lymphoma of the mediastinum treated exclusively with proton therapy for whom digital imaging and communications in medicine (DICOM) treatment data were available for review. Given the challenge with reliably visualizing the left mainstem coronary artery, the inferior-most aspect of the left pulmonary artery (PA) was used as a surrogate. Extent of disease was characterized as upper mediastinum (above level of left PA), middle mediastinum (below left PA but at or above level of T8), or low mediastinum (below T8). Results: Between November 2012 and April 2019, 56 patients were treated and met inclusion criteria. Patients treated with proton therapy were young (median, 24 y; range: 12 to 88), with over half being female (55%). Patients were most commonly treated at initial diagnosis (86%) and had Hodgkin lymphoma (79%). Most patients (96%) had mediastinal disease that extended down to the level of the heart: 48% had middle and 48% had low mediastinal involvement. Nearly all patients (96%) met the ILROG consensus recommendations: 95% had lower mediastinal disease, 46% were young females, and 9% were heavily pretreated. Heart (mean) and lung dose (mean, V5, V20) were significantly associated with lowest extent of mediastinal disease. Conclusions: Mediastinal lymphoma patients treated with proton therapy are typically young with lower mediastinal involvement. Within a prospective, multi-institutional proton registry, nearly all treated patients fit the ILROG consensus recommendations regarding which mediastinal lymphoma patients may most benefit from proton therapy.
Impact of unfavorable factors on outcomes among inoperable stage II-IV Nonsmall cell lung cancer patients treated with proton therapy
Zhu, He J., Nichols, R.C., Morris, Christopher G. , Flampouri, Stella , Pham, Dat C. , Klassen, Christopher, Seeram, Vandana , Cury, James, Jones, Lisa, McGee, L.A. , Hoppe, Bradford S. , McGee, Lisa, Hoppe, Bradford S , Henderson, Randal H.

Acta Oncologica | January 18, 2019 | Volume: 58 | Issue: 3 | Pages: 313-319

10.1080/0284186x.2018.1546060 Get It