scholarly journals NIMG-64. IMPACT OF TUMOR LOCATION ON IMAGE-DERIVED VOLUME, PROLIFERATION RATE AND GROWTH VELOCITY IN GLIOBLASTOMA PATIENTS

2019 ◽  
Vol 21 (Supplement_6) ◽  
pp. vi175-vi176
Author(s):  
Julia Lorence ◽  
Kristin Swanson ◽  
Cassandra Rickertsen ◽  
Sara Ranjbar ◽  
Sandra Johnston ◽  
...  

Abstract INTRODUCTION Glioblastoma (GBM) is the most common malignant primary brain tumor in adults with a median overall survival (OS) of 15months. Despite advancements in treatments, prognosis is dismal and the prognostic significance of tumor location is not entirely understood. METHODOLOGY: In our study, we investigated sex-specific volumetric, tumor growth kinetics, and outcome differences among GBMs in various brain locations. Primary GBM patients with pretreatment magnetic resonance imaging (MRI) data (N=289, 173 males, 116 females) were selected from our brain tumor repository. Tumor abnormality was segmented on T1-weighted post-gadolinium contrast agent (T1Gd) MRIs. We utilized the Harvard-Oxford brain atlases to determine the location of GBMs. RESULTS Overall, our study found smaller tumors in the left hemisphere. This may be expected as left-hemispheric GBM symptoms could present earlier, leading to earlier diagnosis and treatment. However, when the cohort was split by sex, we found this observation significant for females only in the parietal lobe (p < 0.0001). Further, female GBMs demonstrated smaller necrotic volume in the left hemisphere (p = 0.030). Sex-specific differences in incidence were noted in the temporal and occipital lobes (2M:1F). Comparing tumor growth kinetics in different brain locations and hemispheres, females had significantly lower tumor proliferation rates in the left hemisphere (p = 0.009) and lower tumor proliferation rates in the left frontal lobe (p = 0.031). Controlling for treatment, patients with frontal lobe tumors had significantly longer OS compared to those with GBMs in the temporal lobe (p = 0.046, 312 days). Differences in growth velocities were noted between frontal and parietal lobe with frontal GBMs having lower velocities in comparison to parietal lobe GBMs. CONCLUSION Together, our results demonstrate that tumor growth and proliferation rates may vary based on location and sex. Additional research is needed to further explore the clinical significance of tumor location.

2004 ◽  
Vol 64 (3) ◽  
pp. 1094-1101 ◽  
Author(s):  
Monica Simeoni ◽  
Paolo Magni ◽  
Cristiano Cammia ◽  
Giuseppe De Nicolao ◽  
Valter Croci ◽  
...  

2015 ◽  
Vol 40 (8) ◽  
pp. 3043-3051 ◽  
Author(s):  
Adeel R. Seyal ◽  
Keyur Parekh ◽  
Atilla Arslanoglu ◽  
Fernanda D. Gonzalez-Guindalini ◽  
Sandra M. Tochetto ◽  
...  

BMC Cancer ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Luis E Bergues Cabrales ◽  
Juan J Godina Nava ◽  
Andrés Ramírez Aguilera ◽  
Javier A González Joa ◽  
Héctor M Camué Ciria ◽  
...  

2009 ◽  
Vol 16 (10) ◽  
pp. 2834-2839 ◽  
Author(s):  
Jonathan H. Lee ◽  
Seza A. Gulec ◽  
Ainura Kyshtoobayeva ◽  
Myung-Shin Sim ◽  
Donald L. Morton

Oncotarget ◽  
2020 ◽  
Vol 11 (18) ◽  
pp. 1618-1628
Author(s):  
Andy Karabajakian ◽  
Thibaut Garrivier ◽  
Carole Crozes ◽  
Nicolas Gadot ◽  
Jean-Yves Blay ◽  
...  

2014 ◽  
Vol 21 (8) ◽  
pp. 950-957 ◽  
Author(s):  
Adeel R. Seyal ◽  
Keyur Parekh ◽  
Yuri S. Velichko ◽  
Riad Salem ◽  
Vahid Yaghmai

1988 ◽  
Vol 74 (3) ◽  
pp. 269-274 ◽  
Author(s):  
Romano Demicheli ◽  
Roberto Foroni ◽  
Fernando C. Giuliani ◽  
Giuseppina Savi

The influence of tumor growth kinetics on response to doxorubicin treatment of C3H mammary carcinoma was investigated. Gompertzian growth curves were obtained for the tumor mass of each mouse by a computerized best fit program. The response was assessed by evaluating: a) the total clonogenic cell reduction as a fraction of the initial tumor volume or the tumor volume that should result at the end of treatment in a free growth condition, and b) the partial clonogenic cell reduction at each drug administration, assuming a first order cell kill hypothesis. Slowly growing tumors at each dose level showed a significantly poorer response than rapidly growing tumors. Each response index exhibited a linear correlation with the specific instantaneous growth rate at the time of treatment. Data also suggested a dose-response dependence.


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