Literature DB >> 31728884

Treatment-induced lesions in newly diagnosed glioblastoma patients undergoing chemoradiotherapy and heat-shock protein vaccine therapy.

Paula Alcaide-Leon1,2, Tracy L Luks3, Marisa Lafontaine3, Janine M Lupo3, Hideho Okada4, Jennifer L Clarke4, Javier E Villanueva-Meyer3.   

Abstract

OBJECTIVES: Treatment-induced lesions represent a great challenge in neuro-oncology. The aims of this study were (i) to characterize treatment induced lesions in glioblastoma patients treated with chemoradiotherapy and heat-shock protein (HSP) vaccine and (ii) to evaluate the diagnostic accuracy of diffusion weighted imaging for differentiation between treatment-induced lesions and tumor progression.
METHODS: Twenty-seven patients with newly diagnosed glioblastoma treated with HSP vaccine and chemoradiotherapy were included. Serial magnetic resonance imaging evaluation was performed to detect treatment-induced lesions and assess their growth. Quantitative analysis of the apparent diffusion coefficient (ADC) was performed to discriminate treatment-induced lesions from tumor progression. Mann-Whitney U-test and receiver operating characteristic (ROC) curves were used for analysis.
RESULTS: Thirty-three percent of patients developed treatment-induced lesions. Five treatment-related lesions appeared between end of radiotherapy and the first vaccine administration; 4 lesions within the first 4 months from vaccine initiation and 1 at 3.5 years. Three patients with pathology proven treatment-induced lesions showed a biphasic growth pattern progressed shortly after. ADC ratio between the peripheral enhancing rim and central necrosis showed an accuracy of 0.84 (95% CI 0.63-1) for differentiation between progression and treatment-induced lesions.
CONCLUSION: Our findings do not support the iRANO recommendation of a 6-month time window in which progressive disease should not be declared after immunotherapy initiation. A biphasic growth pattern of pathologically proven treatment-induced lesions was associated with a dismal prognosis. The presence of lower ADC values in the central necrotic portion of the lesions compared to the enhancing rim shows high specificity for detection of treatment-induced lesions.

Entities:  

Keywords:  Chemoradiotherapy; Glioblastoma; Heat-shock proteins; Immunotherapy; Magnetic resonance imaging

Mesh:

Substances:

Year:  2019        PMID: 31728884      PMCID: PMC6939141          DOI: 10.1007/s11060-019-03336-3

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  26 in total

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4.  Multimodality image registration by maximization of mutual information.

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5.  Heat shock protein peptide complex-96 (HSPPC-96) vaccination for recurrent glioblastoma: a phase II, single arm trial.

Authors:  Orin Bloch; Andrew T Parsa
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6.  Advanced MRI assessment to predict benefit of anti-programmed cell death 1 protein immunotherapy response in patients with recurrent glioblastoma.

Authors:  Lei Qin; Xiang Li; Amanda Stroiney; Jinrong Qu; Jeffrey Helgager; David A Reardon; Geoffrey S Young
Journal:  Neuroradiology       Date:  2017-01-09       Impact factor: 2.804

Review 7.  Immune infiltration of tumor microenvironment following immunotherapy for glioblastoma multiforme.

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Journal:  Hum Vaccin Immunother       Date:  2017-03-31       Impact factor: 3.452

8.  Immune responses and outcome after vaccination with glioma-associated antigen peptides and poly-ICLC in a pilot study for pediatric recurrent low-grade gliomas.

Authors:  Ian F Pollack; Regina I Jakacki; Lisa H Butterfield; Ronald L Hamilton; Ashok Panigrahy; Daniel P Normolle; Angela K Connelly; Sharon Dibridge; Gary Mason; Theresa L Whiteside; Hideho Okada
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9.  Induction of CD8+ T-cell responses against novel glioma-associated antigen peptides and clinical activity by vaccinations with {alpha}-type 1 polarized dendritic cells and polyinosinic-polycytidylic acid stabilized by lysine and carboxymethylcellulose in patients with recurrent malignant glioma.

Authors:  Hideho Okada; Pawel Kalinski; Ryo Ueda; Aki Hoji; Gary Kohanbash; Teresa E Donegan; Arlan H Mintz; Johnathan A Engh; David L Bartlett; Charles K Brown; Herbert Zeh; Matthew P Holtzman; Todd A Reinhart; Theresa L Whiteside; Lisa H Butterfield; Ronald L Hamilton; Douglas M Potter; Ian F Pollack; Andres M Salazar; Frank S Lieberman
Journal:  J Clin Oncol       Date:  2010-12-13       Impact factor: 44.544

10.  Heat shock protein peptide complex-96 vaccination for newly diagnosed glioblastoma: a phase I, single-arm trial.

Authors:  Nan Ji; Yang Zhang; Yunpeng Liu; Jian Xie; Yi Wang; Shuyu Hao; Zhixian Gao
Journal:  JCI Insight       Date:  2018-05-17
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  2 in total

1.  Centrally Reduced Diffusion Sign for Differentiation between Treatment-Related Lesions and Glioma Progression: A Validation Study.

Authors:  P Alcaide-Leon; J Cluceru; J M Lupo; T J Yu; T L Luks; T Tihan; N A Bush; J E Villanueva-Meyer
Journal:  AJNR Am J Neuroradiol       Date:  2020-10-15       Impact factor: 3.825

2.  Coactosin-Like Protein (COTL1) Promotes Glioblastoma (GBM) Growth in vitro and in vivo.

Authors:  Shike Shao; Yongjun Fan; Chongpei Zhong; Xianlong Zhu; Jiaqiu Zhu
Journal:  Cancer Manag Res       Date:  2020-10-30       Impact factor: 3.989

  2 in total

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