The Effect of Timing of Radiotherapy in Patients with Newly-Diagnosed Glioblastoma Multiforme Receiving Temozolomide: An Analysis Based on the University of California, San Francisco Experience.
This study suggests that starting radiation 30-34 days after surgery may be better than starting sooner - or later than 35 days.. However, they did not correlate it with WHY some patients waited 30-34 days, others waited over 34 days and yet others had radiation sooner. That might account for the differences. To test this correctly, patients should be randomized to start radiation at the standard time or at 32 days and see if there is a difference.
Posted on: 08/17/2014
. Neurosurgery. 2014 Aug;61 Suppl 1:193.
Journal of Neuro-Oncology Award 105 The Effect of Timing of Radiotherapy in Patients with Newly-Diagnosed Glioblastoma Multiforme Receiving Temozolomide: An Analysis Based on the University of California, San Francisco Experience.
Han SJ, Rutledge WC, Molinaro A, Chang S, Clarke JL, Prados M, Berger MS, Butowski N.
The effect of timing of initiation of radiotherapy (RT) after surgery on the outcome of patients with glioblastoma multiforme (GBM) remains controversial. Reports suggested that delayed RT may be positively associated with survival for GBM patients. To further explore this issue, we analyzed 3 clinical trials for newly diagnosed GBM patients receiving Temozolomide (TMZ) conducted at The University of California, San Francisco.
From 2004 through 2010, 207 adult patients with supratentorial GBM were enrolled into 3 clinical trials that consisted of RT plus TMZ and an experimental agent. Timing of RT was defined as the time interval between definitive surgery and commencement of RT, which was intended to be within 6 weeks per protocol eligibility. Overall survival (OS) and progression-free survival (PFS), measured from study registration, were estimated using the Kaplan-Meier method. Analysis by classification and regression trees was used to determine the cut-off values for timing of RT at which there was a significant difference in OS and PFS. Cox proportional hazards model was used to assess the effect of RT timing (in days) on clinical outcomes, adjusting for treatment protocol, age, Karnofsky Performance Scale, and extent of resection.
The median wait time between surgery and RT was 29.5 days (range: 7-89 days). There was no significant difference in timing of RT with respect to baseline variables, except for resection extent: patients who were given RT earlier were more likely to have undergone a biopsy than more extensive surgery. Unexpectedly, a short delay in RT administration (at 30-34 days) was predictive of prolonged OS (HR = 0.58, P < .02) as well as prolonged PFS (HR = 0.55, P < .001), compared to early initiation of RT (<29 days), after adjusting for protocol and baseline prognostic variables, including extent of resection. Interestingly, a longer delay of RT initiation past 34 days was not associated with improved OS or PFS compared to early initiation (HR = 0.89, P = .54, HR = 0.76, P = .14, respectively).
There may be an optimal window in which a short delay in start of RT may be associated with prolonged OS and PFS.
PMID: 25032556 [PubMed - as supplied by publisher]
Click HERE to return to brain tumor news headlines