Clinical Outcomes of Carbon Ion Radiation Therapy for Malignant Peripheral Nerve Sheath Tumors

被引:0
|
作者
Fiore, Maria Rosaria [1 ]
Chalaszczyk, Agnieszka [1 ]
Barcellini, Amelia [1 ,2 ]
Vitolo, Viviana [1 ]
Fontana, Giulia [1 ]
Russo, Stefania [3 ]
Rotondi, Marco [1 ]
Molinelli, Silvia [3 ]
Mirandola, Alfredo [3 ]
Bazani, Alessia [3 ]
Orlandi, Ester [1 ,4 ]
机构
[1] CNAO Natl Ctr Oncol Hadrontherapy, Clin Dept, Radiat Oncol Unit, Pavia, Italy
[2] Univ Pavia, Dept Internal Med & Med Therapy, Pavia, Italy
[3] CNAO Natl Ctr Oncol Hadrontherapy, Phys Dept, Radiat Oncol Unit, Pavia, Italy
[4] Univ Pavia, Dept Clin Surg Diagnost & Pediat Sci, Pavia, Italy
关键词
RADIOTHERAPY; MANAGEMENT; SURVIVAL; EXPERIENCE; SARCOMA; MPNST;
D O I
10.1016/j.adro.2024.101619
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To investigate the outcome and toxicity of patients affected by malignant peripheral nerve sheath tumors (MPNSTs) treated with high-dose carbon ion radiation therapy (CIRT). Methods and Materials: We retrospectively analyzed the outcome of 23 patients with MPNSTs treated between July 2013 and December 2020. Out of these, 13 patients (56.5%) had incompletely resected tumors, 8 patients (34.7%) experienced recurrence after surgery, and 2 patients (8.7%) had unresectable tumors. Before CIRT treatment, 4 patients underwent a second surgery after the first local recurrence (LR), and 1 patient underwent a third surgery for the second local relapse of the disease. Six (26%) patients received neoadjuvant chemotherapy. The most frequent tumor site was the brachial plexus (n = 9; 39.1%). In 5 patients (21.7%), neurofibromatosis type 1 disorder was found, while 4 patients (17, 4%) had radiation-induced MPNSTs. The median CIRT prescribed total dose was 69.8 Gy (relative biological effectiveness; range, 54-76.8) delivered in a median of 16 fractions (range, 15-22). Eleven patients (47.82%) were treated according to a sequential boost protocol with a median prescribed dose to clinical target volume LR of Results: After a median follow-up time of 23 months (range, 3-100 months), the overall survival rates at 1 and 2 years were 82.38% and 61.51%, respectively. The 1-year and 2-year local relapse-free survival rates were 65.07% and 48.80%, respectively, and the 1-year and 2-year progression-free survival rates were 56.37% and 40.99%, respectively. No patients showed acute or late grade 4 toxicity or any treatment-related deaths. Ten patients (43.48%) reported acute toxicities of grade >= 2, which included dermatitis in 6 patients, mucositis in 2 patients, and peripheral neuropathy in 4 patients. Eight patients (34.78%) reported late toxicities of grade >= 2, mainly Conclusions: High-dose CIRT shows favorable local effects with acceptable toxicities in patients with gross residual and LR after surgery or unresectable malignant peripheral nerve sheath tumors. Advanced treatment modalities such as particle therapy should be (c) 2024 The Authors. Published by Elsevier Inc. on behalf of American Society for Radiation Oncology. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页数:9
相关论文
共 50 条
  • [21] Treatment and survival differences across tumor sites in malignant peripheral nerve sheath tumors: a SEER database analysis and review of the literature
    Martin, Enrico
    Muskens, Ivo S.
    Coert, J. H.
    Smith, Timothy R.
    Broekman, Marike L. D.
    NEURO-ONCOLOGY PRACTICE, 2019, 6 (02) : 134 - 143
  • [22] Clinical Signs of Neurofibromatosis Impact on the Outcome of Malignant Peripheral Nerve Sheath Tumors
    Lamm, W.
    Schur, S.
    Koestler, W. J.
    Funovics, P.
    Windhager, R.
    Amann, G.
    Panotopoulos, J.
    Pokrajac, B.
    Brodowicz, T.
    ONCOLOGY, 2014, 86 (02) : 122 - 126
  • [23] A-Z of malignant peripheral nerve sheath tumors
    Kamran, S. C.
    Shinagare, A. B.
    Howard, S. A.
    Hornick, J. L.
    Ramaiya, N. H.
    CANCER IMAGING, 2012, 12 (03): : 475 - 483
  • [24] Intracranial Malignant Peripheral Nerve Sheath Tumors Not Associated with a Cranial Nerve: Systematic Review and Illustrative Case
    Mackel, Charles E.
    Medeiros, Isabela
    Moore, Brian E.
    Zhao, Qing
    Jha, Ribhu
    WORLD NEUROSURGERY, 2021, 156 : 76 - 91
  • [25] Treatment of malignant peripheral nerve sheath tumors in pediatric NF1 disease
    Martin, Enrico
    Flucke, Uta E.
    Coert, J. Henk
    van Noesel, Max M.
    CHILDS NERVOUS SYSTEM, 2020, 36 (10) : 2453 - 2462
  • [26] Malignant peripheral nerve sheath tumors of the spine: A SEER database analysis
    Stadler, James A., III
    Qadri, Usama
    Tang, Jessica A.
    Scheer, Justin K.
    Melkonian, Stephanie C.
    Smith, Zachary A.
    Lam, Sandi K.
    JOURNAL OF CLINICAL NEUROSCIENCE, 2014, 21 (07) : 1106 - 1111
  • [27] Survival outcomes of malignant peripheral nerve sheath tumors (MPNSTs) with and without neurofibromatosis type I (NF1): a meta-analysis
    Lim, Zhixue
    Gu, Tian Yuan
    Tai, Bee Choo
    Puhaindran, Mark Edward
    WORLD JOURNAL OF SURGICAL ONCOLOGY, 2024, 22 (01)
  • [28] Malignant Peripheral Nerve Sheath Tumors in Childhood: 13 Cases From a Single Center
    Demir, Haci Ahmet
    Varan, Ali
    Yalcin, Bilgehan
    Akyuz, Canan
    Kutluk, Tezer
    Buyukpamukcu, Munevver
    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2012, 34 (03) : 204 - 207
  • [29] Analysis of treatment sequence and outcomes in patients with relapsed malignant peripheral nerve sheath tumors
    Zhang, Lindy
    Lemberg, Kathryn M.
    Calizo, Ana
    Varadhan, Ravi
    Siegel, Alan H.
    Meyer, Christian F.
    Blakeley, Jaishri O.
    Pratilas, Christine A.
    NEURO-ONCOLOGY ADVANCES, 2023, 5 (01)
  • [30] Malignant nerve sheath tumors Response
    Dunn, Gavin P.
    Spiliopoulos, Konstantinos
    Plotkin, Scott R.
    Hornicek, Francis J.
    Harmon, David C.
    Delaney, Thomas F.
    Williams, Ziv
    JOURNAL OF NEUROSURGERY, 2013, 118 (01) : 141 - 141