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Torunn I. Yock

Researcher at Harvard University

Publications -  217
Citations -  7231

Torunn I. Yock is an academic researcher from Harvard University. The author has contributed to research in topics: Radiation therapy & Proton therapy. The author has an hindex of 46, co-authored 196 publications receiving 5874 citations. Previous affiliations of Torunn I. Yock include Hampton University & Emory University.

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Incidence of second malignancies among patients treated with proton versus photon radiation.

TL;DR: The use of proton radiation therapy was not associated with a significantly increased risk of secondary malignancies compared with photon therapy and longer follow-up of these patients is needed to determine if there is a significant decrease in second malignancy.
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Long-term toxic effects of proton radiotherapy for paediatric medulloblastoma: a phase 2 single-arm study

TL;DR: Proton radiotherapy resulted in acceptable toxicity and had similar survival outcomes to those noted with conventional radiotherapy, suggesting that the use of the treatment may be an alternative to photon-based treatments.
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An evidence based review of proton beam therapy: the report of ASTRO's emerging technology committee.

TL;DR: Current data do not provide sufficient evidence to recommend PBT in lung cancer, head and neck cancer, GI malignancies, and pediatric non-CNS malignancy, but there is evidence for the efficacy of PBT but no suggestion that it is superior to photon based approaches.
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Proton radiotherapy for childhood ependymoma: initial clinical outcomes and dose comparisons.

TL;DR: Preliminary disease control with proton therapy compares favorably with the literature and Dosimetric comparisons show the advantage of proton radiation compared with IMRT in the treatment of ependymoma.
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Ultrasensitive Measurement of Hotspot Mutations in Tumor DNA in Blood Using Error-Suppressed Multiplexed Deep Sequencing

TL;DR: An approach that uses next-generation sequencing to quantify the small fraction of DNA molecules that contain tumor-specific mutations within a background of normal DNA in plasma and shows the successful use of this method to follow treatment-associated changes in circulating tumor DNA levels in patients with non-small cell lung cancer.