Combination chemoradiotherapy with temozolomide, vincristine, and interferon-β might improve outcomes regardless of O6-methyl-guanine-DNA-methyltransferase (MGMT) promoter methylation status in newly glioblastoma

被引:3
作者
Asano, Kenichiro [1 ]
Fumoto, Toshio [1 ]
Matsuzaka, Masashi [2 ,3 ]
Hasegawa, Seiko [4 ]
Suzuki, Naoya [5 ]
Akasaka, Kenichi [5 ]
Katayama, Kosuke [1 ]
Kamataki, Akihisa [6 ]
Kurose, Akira [6 ]
Ohkuma, Hiroki [1 ]
机构
[1] Hirosaki Univ, Dept Neurosurg, Grad Sch Med, 5 Zaifu Cho, Hirosaki, Aomori 0368562, Japan
[2] Hirosaki Univ Hosp, Clin Res Support Ctr, 53 Hon Cho, Hirosaki, Aomori 0368563, Japan
[3] Hirosaki Univ Hosp, Dept Med Informat, 53 Hon Cho, Hirosaki, Aomori 0368563, Japan
[4] Kuroishi Gen Hosp, Dept Neurosurg, 1-70 Kitami Cho, Kuroishi, Aomori 0360541, Japan
[5] Towada City Hosp, Dept Neurosurg, 8-14 Nishi Jyuniban Cho, Towada, Aomori 0340093, Japan
[6] Hirosaki Univ, Dept Anat Pathol, Grad Sch Med, 53 Honcho, Hirosaki, Aomori 0368563, Japan
关键词
Newly glioblastoma; Combination therapy; Temozolomide; Interferon-beta; MGMT; NEWLY-DIAGNOSED GLIOBLASTOMA; RANDOMIZED PHASE-III; ADJUVANT TEMOZOLOMIDE; MAINTENANCE TEMOZOLOMIDE; RADIATION-THERAPY; PROGNOSTIC VALUE; ADULT PATIENTS; RADIOTHERAPY; SURVIVAL; METHYLTRANSFERASE;
D O I
10.1186/s12885-021-08592-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundThis investigator-initiated, open-label, single-arm, single-institute study was conducted to investigate the effectiveness of induction combination chemoradiotherapy and long-term maintenance therapy with temozolomide (TMZ) plus interferon (IFN)-beta for glioblastoma.MethodsThe initial induction combination chemoradiotherapy comprised radiotherapy plus TMZ plus vincristine plus IFN-beta. Maintenance chemotherapy comprised monthly TMZ, continued for 24-50cycles, plus weekly IFN-beta continued for as long as possible. The primary endpoint was 2-year overall survival (2y-OS). The study protocol was to be considered valid if the expected 2y-OS was over 38% and the lower limit of the 95% confidence interval (CI) was no less than 31.7% compared with historical controls, using Kaplan-Meier methods. Secondary endpoints were median progression-free survival (mPFS), median OS (mOS), 5-year OS rate (5y-OS), and mPFS and mOS classified according to MGMT promoter methylation status.ResultsForty-seven patients were analyzed. The 2y-OS was 40.7% (95%CI, 27.5-55.4%). The mPFS and mOS were 11.0months and 18.0months, respectively, and 5y-OS was 20.3% (95%CI, 10.9-34.6%). The mPFS in groups with and without MGMT promoter methylation in the tumor was 10.0months and 11.0months (p=0.59), respectively, and mOS was 24.0months and 18.0months (p=0.88), respectively. The frequency of grade 3/4 neutropenia was 19.1%.ConclusionsThe 2y-OS with induction multidrug combination chemoradiotherapy and long-term maintenance therapy comprising TMZ plus IFN-beta tended to exceed that of historical controls, but the lower limit of the 95%CI was below 31.7%. Although the number of cases was small, this protocol may rule out MGMT promoter methylation status as a prognostic factor.Trial registrationUniversity Hospital Medical Information Network (number UMIN000040599).
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相关论文
共 53 条
[1]  
[Anonymous], 2017, Neurol Med Chir (Tokyo), V57, P9, DOI 10.2176/nmc.sup.2017-0001
[2]  
Aoki T, 2006, J NEUROSURG, V105, P385, DOI 10.3171/jns.2006.105.3.385
[3]  
Aydin B, 2010, ANTICANCER RES, V30, P2303
[4]   A phase II randomized, multicenter, open-label trial of continuing adjuvant temozolomide beyond 6 cycles in patients with glioblastoma (GEINO 14-01) [J].
Balana, Carmen ;
Angeles Vaz, Maria ;
Manuel Sepulveda, Juan ;
Mesia, Carlos ;
del Barco, Sonia ;
Pineda, Estela ;
Munoz-Langa, Jose ;
Estival, Anna ;
de las Penas, Ramon ;
Fuster, Jose ;
Girones, Regina ;
Miguel Navarro, Luis ;
Gil-Gil, Miguel ;
Alonso, Miriam ;
Herrero, Ana ;
Peralta, Sergio ;
Olier, Clara ;
Perez-Segura, Pedro ;
Covela, Maria ;
Martinez-Garcia, Maria ;
Berrocal, Alfonso ;
Gallego, Oscar ;
Luque, Raquel ;
Javier Perez-Martin, Franciso ;
Esteve, Anna ;
Munne, Nuria ;
Domenech, Marta ;
Villa, Salvador ;
Sanz, Carolina ;
Carrato, Cristina .
NEURO-ONCOLOGY, 2020, 22 (12) :1851-1861
[5]   Long-term therapy with temozolomide is a feasible option for newly diagnosed glioblastoma: a single-institution experience with as many as 101 temozolomide cycles [J].
Barbagallo, Giuseppe M. V. ;
Paratore, Sabrina ;
Caltabiano, Rosario ;
Palmucci, Stefano ;
Parra, Hector Soto ;
Privitera, Giuseppe ;
Motta, Fabio ;
Lanzafame, Salvatore ;
Scaglione, Giorgio ;
Longo, Antonio ;
Albanese, Vincenzo ;
Certo, Francesco .
NEUROSURGICAL FOCUS, 2014, 37 (06)
[6]   The prognostic value of MGMT promoter methylation in glioblastoma: A meta-analysis of clinical trials [J].
Binabaj, Maryam Moradi ;
Bahrami, Afsane ;
ShahidSales, Soodabeh ;
Joodi, Marjan ;
Mashhad, Mona Joudi ;
Hassanian, Seyed Mahdi ;
Anvari, Kazem ;
Avan, Amir .
JOURNAL OF CELLULAR PHYSIOLOGY, 2018, 233 (01) :378-386
[7]   Is more better? The impact of extended adjuvant temozolomide in newly diagnosed glioblastoma: a secondary analysis of EORTC and NRG Oncology/RTOG [J].
Blumenthal, Deborah T. ;
Gorlia, Thierry ;
Gilbert, Mark R. ;
Kim, Michelle M. ;
Nabors, L. Burt ;
Mason, Warren P. ;
Hegi, Monika E. ;
Zhang, Peixin ;
Golfinopoulos, Vassilis ;
Perry, James R. ;
Nam, Do Hyun ;
Erridge, Sara C. ;
Corn, Benjamin W. ;
Mirimanoff, Rene O. ;
Brown, Paul D. ;
Baumert, Brigitta G. ;
Mehta, Minesh P. ;
van den Bent, Martin J. ;
Reardon, David A. ;
Weller, Michael ;
Stupp, Roger .
NEURO-ONCOLOGY, 2017, 19 (08) :1119-1126
[8]  
Darlix A, 2013, ANTICANCER RES, V33, P3467
[9]   Methylation of MGMT promoter does not predict response to temozolomide in patients with glioblastoma in Donostia Hospital [J].
Egana, Larraitz ;
Auzmendi-Iriarte, Jaione ;
Andermatten, Joaquin ;
Villanua, Jorge ;
Ruiz, Irune ;
Elua-Pinin, Alejandro ;
Aldaz, Paula ;
Querejeta, Arrate ;
Sarasqueta, Cristina ;
Zubia, Felix ;
Matheu, Ander ;
Sampron, Nicolas .
SCIENTIFIC REPORTS, 2020, 10 (01)
[10]  
Esteller M, 1999, CANCER RES, V59, P793