Literature DB >> 36149438

Proton and carbon ion beam treatment with active raster scanning method in 147 patients with skull base chordoma at the Heidelberg Ion Beam Therapy Center-a single-center experience.

Matthias Mattke1,2,3,4, Matteo Ohlinger5,6, Nina Bougatf5,6,7,8, Semi Harrabi5,6, Robert Wolf5,6, Katharina Seidensaal5,6, Thomas Welzel5,6, Falk Röder9, Sabine Gerum9, Malte Ellerbrock6,8, Oliver Jäkel5,6,7,8, Thomas Haberer6,8, Klaus Herfarth5,6,8, Matthias Uhl10, Jürgen Debus5,6,11,7,8,12.   

Abstract

BACKGROUND: This study aimed to compare the results of irradiation with protons versus irradiation with carbon ions in a raster scan technique in patients with skull base chordomas and to identify risk factors that may compromise treatment results.
METHODS: A total of 147 patients (85 men, 62 women) were irradiated with carbon ions (111 patients) or protons (36 patients) with a median dose of 66 Gy (RBE (Relative biological effectiveness); carbon ions) in 4 weeks or 74 Gy (RBE; protons) in 7 weeks at the Heidelberg Ion Beam Therapy Center (HIT) in Heidelberg, Germany. The median follow-up time was 49.3 months. All patients had gross residual disease at the beginning of RT. Compression of the brainstem was present in 38%, contact without compression in 18%, and no contact but less than 3 mm distance in 16%. Local control and overall survival were evaluated using the Kaplan-Meier Method based on scheduled treatment (protons vs. carbon ions) and compared via the log rank test. Subgroup analyses were performed to identify possible prognostic factors.
RESULTS: During the follow-up, 41 patients (27.9%) developed a local recurrence. The median follow-up time was 49.3 months (95% CI: 40.8-53.8; reverse Kaplan-Meier median follow-up time 56.3 months, 95% CI: 51.9-60.7). No significant differences between protons and carbon ions were observed regarding LC, OS, or overall toxicity. The 1‑year, 3‑year, and 5‑year LC rates were 97%, 80%, and 61% (protons) and 96%, 80%, and 65% (carbon ions), respectively. The corresponding OS rates were 100%, 92%, and 92% (protons) and 99%, 91%, and 83% (carbon ions). No significant prognostic factors for LC or OS could be determined regarding the whole cohort; however, a significantly improved LC could be observed if the tumor was > 3 mm distant from the brainstem in patients presenting in a primary situation.
CONCLUSION: Outcomes of proton and carbon ion treatment of skull base chordomas seem similar regarding tumor control, survival, and toxicity. Close proximity to the brainstem might be a negative prognostic factor, at least in patients presenting in a primary situation.
© 2022. The Author(s).

Entities:  

Keywords:  Bragg peak; C12; Heavy ion; High LET; Notochordal sarcoma; Particle therapy

Year:  2022        PMID: 36149438     DOI: 10.1007/s00066-022-02002-4

Source DB:  PubMed          Journal:  Strahlenther Onkol        ISSN: 0179-7158            Impact factor:   4.033


  33 in total

Review 1.  Chordoma: current concepts, management, and future directions.

Authors:  Brian P Walcott; Brian V Nahed; Ahmed Mohyeldin; Jean-Valery Coumans; Kristopher T Kahle; Manuel J Ferreira
Journal:  Lancet Oncol       Date:  2012-02       Impact factor: 41.316

2.  Patient outcome at long-term follow-up after aggressive microsurgical resection of cranial base chordomas.

Authors:  Fortios Tzortzidis; Foad Elahi; Donald Wright; Sabareesh K Natarajan; Laligam N Sekhar
Journal:  Neurosurgery       Date:  2006-08       Impact factor: 4.654

Review 3.  The biology and pathology of selected skull base tumors.

Authors:  L Barnes; S B Kapadia
Journal:  J Neurooncol       Date:  1994       Impact factor: 4.130

4.  Radiotherapeutic factors in the management of cervical-basal chordomas and chondrosarcomas.

Authors:  Georges Noël; Loïc Feuvret; Régis Ferrand; Gilbert Boisserie; Jean-Jacques Mazeron; Jean-Louis Habrand
Journal:  Neurosurgery       Date:  2004-12       Impact factor: 4.654

Review 5.  Adjuvant radiation therapy and chondroid chordoma subtype are associated with a lower tumor recurrence rate of cranial chordoma.

Authors:  Brian J Jian; Orin G Bloch; Isaac Yang; Seunggu J Han; Derick Aranda; Tarik Tihan; Andrew T Parsa
Journal:  J Neurooncol       Date:  2009-12-02       Impact factor: 4.130

6.  Chordoma and chondroid neoplasms of the spheno-occiput. An immunohistochemical study of 41 cases with prognostic and nosologic implications.

Authors:  A Mitchell; B W Scheithauer; K K Unni; P J Forsyth; L E Wold; D J McGivney
Journal:  Cancer       Date:  1993-11-15       Impact factor: 6.860

7.  Three-dimensional reconstruction of human embryonic notochords: clue to the pathogenesis of chordoma.

Authors:  J R Salisbury; M H Deverell; M J Cookson; W F Whimster
Journal:  J Pathol       Date:  1993-09       Impact factor: 7.996

Review 8.  Chordoma. A clinicopathologic study of metastasis.

Authors:  P W Chambers; C P Schwinn
Journal:  Am J Clin Pathol       Date:  1979-11       Impact factor: 2.493

9.  Incidence and relative survival of chordomas: the standardized mortality ratio and the impact of chordomas on a population.

Authors:  Nicolas R Smoll; Oliver P Gautschi; Ivan Radovanovic; Karl Schaller; Damien C Weber
Journal:  Cancer       Date:  2013-03-15       Impact factor: 6.860

10.  Chordoma. A clinicopathologic and prognostic study of a Swedish national series.

Authors:  B Eriksson; B Gunterberg; L G Kindblom
Journal:  Acta Orthop Scand       Date:  1981-02
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