Postoperative NEOadjuvant TEMozolomide followed by chemoradiotherapy versus upfront chemoradiotherapy for glioblastoma multiforme (NEOTEM) trial: Interim results

被引:2
作者
Sharifian, Azadeh [1 ]
Kazemian, Ali [1 ,2 ]
Farzin, Mostafa [1 ,3 ]
Amirkhani, Nikan [4 ]
Farazmand, Borna [2 ]
Naderi, Soheil [5 ]
Khalilian, Alireza [1 ,2 ]
Pourrashidi, Ahmad [6 ]
Amjad, Ghazaleh [7 ]
Kolahdouzan, Kasra [1 ,2 ]
Abyaneh, Romina [2 ]
Jablonska, Paola Anna [8 ]
Ghalehtaki, Reza [1 ,2 ]
机构
[1] Univ Tehran Med Sci, Canc Inst, Sch Med, Dept Radiat Oncol,IKHC, Tehran, Iran
[2] Univ Tehran Med Sci, Canc Res Inst, Radiat Oncol Res Ctr, IKHC, Tehran, Iran
[3] Univ Tehran Med Sci, Neurosci Inst, Brain & Spinal Cord Injury Res Ctr, Tehran, Iran
[4] Univ Tehran Med Sci, Sch Med, Tehran, Iran
[5] Iran Univ Med Sci, Dept Neurosurg, Tehran, Iran
[6] Univ Tehran Med Sci, Sina Hosp, Dept Neurosurg, Tehran, Iran
[7] Univ Pittsburgh, UPMC Hillman Canc Ctr, Radiol Dept, Pittsburgh, PA USA
[8] Hosp Univ Navarra, Radiat Oncol Dept, Pamplona, Spain
关键词
chemoradiotherapy; glioblastoma; MGMT methylation; neoadjuvant temozolomide; progression-free survival; NEWLY-DIAGNOSED GLIOBLASTOMA; PHASE-II; OPEN-LABEL; ADJUVANT TEMOZOLOMIDE; RADIATION-THERAPY; MALIGNANT GLIOMA; PLUS CONCOMITANT; RADIOTHERAPY; MULTICENTER; SURVIVAL;
D O I
10.1093/noajnl/vdae195
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Glioblastoma multiforme (GBM) is an aggressive brain tumor with poor survival rates despite current treatments. The standard of care (SOC) includes surgery, followed by radiotherapy plus concurrent and adjuvant chemotherapy with temozolomide (TMZ). This phase II trial assessed the safety and efficacy of neoadjuvant TMZ (nTMZ) before and during chemoradiotherapy in newly diagnosed GBM patients.Methods Newly diagnosed GBM patients who underwent maximal safe resection were randomized into 2 groups. One received nTMZ before standard chemoradiotherapy and adjuvant TMZ (intervention). The other received standard chemoradiotherapy followed by adjuvant TMZ (control). Primary endpoints were progression-free survival (PFS) at 6 and 12 months. Secondary endpoints included overall survival, radiological and clinical responses, and adverse events.Results Of 35 patients, 16 were in the intervention group and 19 in the control group. Median PFS was 9 months (95% CI: 3.93-14.06) versus 3 months (95% confidence interval [CI]: 1.98-4.01) in the control and intervention groups (P = .737), with a high progression rate (73.4%) during nTMZ treatment. The 6-month PFS rates were 58% versus 25% (P = .042), and 12-month PFS rates were 26% versus 25% (P = .390) in the control and intervention groups, respectively. Patients with unmethylated O6-methylguanine-DNA methyltransferase (MGMT) and those with good performance status (PS) had significantly worse PFS with nTMZ. However, those who underwent larger extent of resection exhibited significantly better PFS with nTMZ. Adverse events were similar between groups.Conclusions Neoadjuvant TMZ before SOC chemoradiotherapy did not improve outcomes for newly diagnosed GBM patients and is unsuitable for those with unmethylated MGMT and good PS. However, It may benefit patients with near or gross total resection. Further research is needed to refine GBM treatment strategies. Glioblastoma is an aggressive brain cancer with limited treatment options. Standard treatment involves surgery, followed by radiation and chemotherapy with a drug called temozolomide (TMZ). The authors of this study wanted to determine whether giving even more TMZ chemotherapy before radiation would help patients live longer. To do this they conducted a clinical trial where 35 patients were randomly assigned to receive additional early chemotherapy or standard treatment. Their results showed that giving additional early chemotherapy did not change how long patients lived. Side effects were similar between groups.
引用
收藏
页数:12
相关论文
共 39 条
[1]   Neoadjuvant phase II multicentre study of new agents in patients with malignant glioma after minimal surgery. Report of a cohort of 187 patients treated with temozolomide [J].
Brada, M ;
Ashley, S ;
Dowe, A ;
Gonsalves, A ;
Huchet, A ;
Pesce, G ;
Reni, M ;
Saran, F ;
Wharram, B ;
Wilkins, M ;
Wilkins, P .
ANNALS OF ONCOLOGY, 2005, 16 (06) :942-949
[2]   Optimal Timing of Radiotherapy Following Gross Total or Subtotal Resection of Glioblastoma: A Real-World Assessment using the National Cancer Database [J].
Buszek, Samantha M. ;
Al Feghali, Karine A. ;
Elhalawani, Hesham ;
Chevli, Neil ;
Allen, Pamela K. ;
Chung, Caroline .
SCIENTIFIC REPORTS, 2020, 10 (01)
[3]  
Chevli N, 2017, NEURO-ONCOLOGY, V19, P219
[4]   Correlation between O6-methylguanine-DNA methyltransferase and survival in inoperable newly diagnosed glioblastoma patients treated with neoadjuvant temozolomide [J].
Chinot, Olivier L. ;
Barrie, Maryline ;
Fuentes, Stephane ;
Eudes, Nathalie ;
Lancelot, Sophie ;
Metellus, Philippe ;
Muracciole, Xavier ;
Braguer, Diane ;
Ouafik, L'Houcine ;
Martin, Pierre-Marie ;
Dufour, Henry ;
Figarella-Branger, Dominique .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (12) :1470-1475
[5]   Commentary: Lomustine-temozolomide combination therapy versus standard temozolomide therapy in patients with newly diagnosed glioblastoma with methylated MGMT promoter (CeTeG/NOA-09): a randomised, open-label, phase 3 trial [J].
Das, Sunit ;
Sahgal, Arjun ;
Perry, James R. .
FRONTIERS IN ONCOLOGY, 2020, 10
[6]   Advancements in Glioma Care: Focus on Emerging Neurosurgical Techniques [J].
De Simone, Matteo ;
Conti, Valeria ;
Palermo, Giuseppina ;
De Maria, Lucio ;
Iaconetta, Giorgio .
BIOMEDICINES, 2024, 12 (01)
[7]   MINI-MENTAL STATE - PRACTICAL METHOD FOR GRADING COGNITIVE STATE OF PATIENTS FOR CLINICIAN [J].
FOLSTEIN, MF ;
FOLSTEIN, SE ;
MCHUGH, PR .
JOURNAL OF PSYCHIATRIC RESEARCH, 1975, 12 (03) :189-198
[8]   Salvage temozolomide for prior temozolomide responders [J].
Franceschi, E ;
Omuro, AMP ;
Lassman, AB ;
Demopoulos, A ;
Nolan, C ;
Abrey, LE .
CANCER, 2005, 104 (11) :2473-2476
[9]  
Friedman HS, 2000, CLIN CANCER RES, V6, P2585
[10]   Optimal Sequence for Total Neoadjuvant Therapy in Locally Advanced Rectal Cancer: An Evidence-Based Review [J].
Ghalehtaki, Reza ;
Nourbakhsh, Forouzan ;
Abyaneh, Romina ;
Sharifian, Azadeh ;
Pashapour-Khoyi, Sheyda ;
Aghili, Mahdi ;
Gambacorta, Maria Antonietta ;
Counago, Felipe .
CANCER MEDICINE, 2024, 13 (19)