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Retrospective analysis to evaluate the efficacy and the safety of Bevacizumab in the treatment of recurrent malignant gliomas



There is no consensus therapy recommended for recurrent malignant gliomas (MGs). In 2009, Bevacizumab (BEV) was approved by the FDA as single-agent for recurrent glioblastoma (GBM). The aim of this retrospective study was to evaluate the efficacy and the safety of BEV alone or in combination with Fotemustine (FTM) in recurrent MGs. This represents an interim analysis of a larger study on BEV in MGs patients.


We analyzed 17 recurrent MGs patients, 12 GBM (70.6%) and 5 anaplastic gliomas (29.4%), underwent first-line therapy with Stupp regimen. BEV was administered as off-label therapy, at a dose of 10 mg/kg every 14 days, in 13 patients as third-line therapy and in 4 patients as second-line therapy associated with FTM. The assessment of MGMT methylation and IDH1 mutation was conducted.


One complete response (5.9%), 7 partial responses (41.2%), 3 stable diseases (17.6%) and 6 progression diseases (35.3%) were assessed using RANO criteria. Median PFS (mPFS) and OS (mOS) were 5 and 8.3 months respectively, with a 6 months-PFS of 41.2%. Methylated patients and wild-type IDH1 patients showed longer mPFS and mOS without statistical significance. Six patients (35.3%) experienced long response with high number of cycles (11-40), long PFS (11-40 months) and OS (12-42 months). BEV was well-tolerated with grade 1-2 proteinuria and hypertension in 53% and 47.1% of patients respectively. Only one patient developed grade 3 proteinuria after 30 cycles and another one developed pulmonary embolism. No other grade 3-4 toxicities were observed.


This retrospective study showed the efficacy and the safety of BEV alone or in association with FTM in the treatment of MGs.

The protocol (No: Beva-Glio/Sep 2016).


Malignant gliomas (MGs) are the most common primary malignant brain tumors in adults and include anaplastic gliomas (AG) and glioblastoma multiforme (GBM), which account for 6% and 54% of all gliomas respectively. GBM is the most common MG characterised by a high recurrence and mortality rate and low response rate to treatment [1]. The standard first-line treatment of GBM includes maximal safe surgical resection followed by radiotherapy plus concomitant and adjuvant temozolomide (TMZ), as defined in the EORTC phase III trial [2, 3]. However, despite the optimal standard therapy, recurrence rates remain high (~ 90%) with median survival ranges from 15 to 18 months for GBM [4] and from 2 to 5 years for AG [5]. Nowadays, there is no consensus therapy recommended for recurrent MGs and different treatment options are under investigation, such as second-line chemotherapy, immunotherapy, target therapy, radiotherapy and additional surgery. MGs are characterised by an intense vascular proliferation with an elevated expression of vascular endothelial growth factor (VEGF): for these biological characteristics MGs are, therefore, suitable targets of anti-angiogenic therapies [6]. Vessel density degree and VEGF level expression have been shown to directly correlate with the biologic aggressiveness of MGs and a worse prognosis [7,8,9,10].

It has been demonstrated that VEGF inhibition leads to a decreased growth of glioma cells and to reduce both peritumoral edema and, therefore, the need for corticosteroid therapy [9, 11]. This decrease of steroids use for prolonged periods reduce long-term adverse effects improving quality of life of patients.

In 2009, Bevacizumab (BEV), a humanized monoclonal antibody against VEGF-A, was approved by the United States Food and Drug Administration (FDA) [12] as a single-agent for the treatment of recurrent GBM. The approval was based on two phase 2 studies of BEV both alone and in combination with irinotecan (IRI) which demonstrated improvements in response rate (RR) and 6-month PFS (PFS-6) [8, 13]. In Europe, BEV was not approved by the European Medical Agency (EMA) due to the uncertain impact on overall survival (OS) and the lack of non-BEV control arm. Many other prospective or retrospective studies evaluated the efficacy of BEV as single-agent both in recurrent GBM and AG [13,14,15,16,17], or in combination with IRI [18], TMZ, carmustine, lomustine, carboplatin, etoposide and target therapies such as cetuximab, erlotinib, sorafenib [19]. In these clinical trials, single-agent BEV reached PFS-6 rates from 18 to 42.6%, a median PFS from 2.8 to 4.2 months and a median OS from 6.5 to 10.5 months [19]. There is little data available on the combination of BEV with Fotemustine (FTM), the nitrosourea mostly used for recurrent MGs in Europe [20,21,22,23]. The combination of BEV plus FTM has been suggested as active and safe in untreated metastatic melanoma patients [24]. The aim of this retrospective study was to evaluate the efficacy and the safety of BEV alone or in combination with FTM in the treatment of recurrent MGs patients.


Study population

This retrospective study was approved by the ethics committee of S.M.Goretti Hospital of Latina, Sapienza University of Rome. From August 2011 through July 2016 we performed a retrospective analysis of recurrent MGs patients treated with BEV (off-label use) at Policlinico Umberto I of Rome and S.M.Goretti Hospital of Latina, both Sapienza University of Rome. This represents an interim analysis of a larger study on BEV in MGs patients.

BEV was administered as third-line therapy after second-line therapy with FTM or as second-line therapy in combination with FTM. All patients underwent first-line therapy with maximum safe resection and radiotherapy plus concomitant/adjuvant TMZ as Stupp schedule [3]. We excluded those patients treated with other adjuvant TMZ therapy, second and third-line therapies. Stupp schedule consists of radiotherapy (60 Gy/30 fractions) plus concomitant daily TMZ (75 mg/mq/die), followed by 6 cycles of adjuvant TMZ (50-200 mg/mq/die for 5 days every 28 days) for maintenance [2, 3]. FTM treatment, according to the Addeo schedule [25], consists of an induction phase dose of 80 mg/mq every 2 weeks for 5 consecutive weeks followed by a 4-week rest period and a maintenance phase dose of 80 mg/mq every 4 weeks. For all patients, the initial diagnosis was established by magnetic resonance imaging (MRI) and histologically using WHO criteria [26]. The progression after first-line and second-line therapy was assessed by MRI and histological examination when a surgery at recurrence was performed.

Clinical data included patients characteristics (gender, age and Karnofsky-Performance-Status (KPS) at recurrence pre-BEV), tumor characteristics (laterality and lobe, histotype, molecular markers at diagnosis) and treatment information (first-line and second-line therapy, surgery at recurrence, BEV as monotherapy or in combination, median cycles of BEV, corticosteroids use).

Treatment plan

All patients included in the analysis underwent treatment with BEV (off-label use) administered intravenously at a dose of 10 mg/kg every 14 days until disease progression or unacceptable toxicity. In patients having undergone re-resection, BEV was commenced 4-6 weeks after surgery and establishment of normal craniotomy wound healing. Blood pressure and proteinuria were monitored prior each administration of BEV.

Response and toxicity evaluation

All patients were followed clinically by a multidisciplinary team and radiologically by 3 Tesla MRI scans (contrast-enhanced T1-weighted, T2/FLAIR-weighted, perfusion-weighted and diffusion-weighted scans and MR spectroscopy). A baseline MRI scan, acquired prior to initiation of BEV treatment, was performed. The first MRI evaluation was made after 2 cycles of BEV or after the induction phase of FTM and then every two cycles of BEV or FTM in the maintenance phase, or whenever progression disease was clinically suspected.

Evaluation response was assessed according to RANO criteria [27] as complete (CR) and partial (PR) response, stable (SD) and progression (PD) disease. Overall response rate (ORR) was defined as the sum of CR and PR and disease control (DC) was defined as the sum of CR, PR and SD. Diagnosis of recurrence was determined by MRI in all patients and by histological examination when a second surgical resection was made. Subgroup analysis according to the response to BEV in correlation to patients characteristics and biomarkers was performed using χ2 test. Responder patients were defined as patients with SD, PR and CR.

We also evaluate the clinical benefit measuring change in corticosteroid use, functional status and neurologic symptoms. All adverse events, as worsening of previous symptoms or development of new symptoms during treatment, were graded according to the Common Terminology Criteria for Adverse Events (CTCAE) of the National Cancer Institute, version 4.03 [28]. Toxicity assessment was performed at each cycle or, if clinically indicated, at weekly intervals.

Statistical analysis

Survival analysis was conducted on the efficacy of BEV in recurrent MGs in terms of 6 months and 12 months PFS (PFS-6, PFS-1y) and OS (OS-6, OS-1y), median PFS (mPFS) and OS (mOS) from BEV treatment. Safety analysis evaluated the toxicity profile of BEV treatment. PFS was measured from the start of BEV therapy to diagnosis of PD evidenced by MRI or to death from any cause or to last follow-up assessment. OS was measured from the start of treatment with BEV to death from any cause or last follow-up. Median PFS and OS were estimated with their 95% confidence interval. Survival curves of PFS and OS were generated using the Kaplan–Meier method. Differences in PFS and OS were evaluated using the log-rank test (Mantel-Cox) for statistical significance, which was defined at the p < 0.05 level [29].


Patients’ characteristics

Between August 2011 and May 2016, 17 patients with recurrent MGs receiving BEV as second-line or third line treatment were included in the analysis. Of 17 patients, 15 patients were treated at Policlinico Umberto I of Rome and 2 patients at S.M.Goretti Hospital of Latina. Patient, tumor and treatment characteristics are summarized in Table 1.

Table 1 Patients’ characteristics at recurrence

Most patients were male (58.8%), the median age was 50 years (range 26-66 years) and median KPS was 80 (range 60-100). All patients had an histological diagnosis of MGs: GBM was the predominant histotype (70.6%), while grade III gliomas represented the 29.4% of the total. Fifteen patients (88.2%) presented a monolobar localization and 2 patients (11.8%) presented the involvement of two or more lobes.

The assessment of the O6-Methylguanine-DNA methyltransferase (MGMT) promoter methylation status was conducted in 12 patients (70.6%). MGMT promoter was methylated in 9 patients (52.9%) and unmethylated in 3 patients (17.5%). The assessment of the isocitrate dehydrogenase 1 (IDH1) mutation status was conducted in 8 patients (47%). IDH1 was mutated in 5 patients and wild-type in 3 patients.

All patients underwent surgery at diagnosis but only 2 patients underwent surgery at recurrence before BEV treatment. All patients underwent first-line therapy with maximum safe resection and Stupp treatment with a mPFS of 12.9 months (range 2-129.6). BEV was administered (off-label use) in 13 patients (76.5%) in third line therapy after a second-line therapy with FTM and in 4 patients (23.5%) as a second-line therapy in association with FTM. Patients treated with second-line FTM had a mPFS of 2.2 months (range 1.3-6.9).

All patients received at least two administrations of BEV and the median number of cycles administered was 8 (range 2-40). First response assessment using RANO criteria was performed after about 5 weeks after initiation of treatment (mean 35 ± 12 days). At the start of treatment 13 patients (76.5%) were on corticosteroid treatment.

Activity evaluation

All patients included in the study were assessable for response analysis. Among the 17 patients, one complete response (5.9%), 7 partial responses (41.2%), 3 stable diseases (17.6%) and 6 progression diseases (35.3%) were observed. ORR and DCR were of 47.1% and 64.7% respectively.

The mPFS was 5 months (95% CI 2-8 months) with a PFS-6 of 41.2% and a PFS-1y of 29.4%. The mOS was 8.3 months (95% CI 3.9-12.7 months) with an OS-6 of 58.8% and a OS-1y of 35.3%. In grade III gliomas patients, mPFS and mOS were higher than GBM patients without statistical significance (7 vs 5 months p = 0.5, and 8.3 vs 6 months, p = 0.6 respectively).

Six patients (35.3%) experienced a long response characterized by a high number of administered cycles (range 11-40), long PFS (range 11-40 months) and OS (range 12-45 months). Results are summarized in Table 2. Figure 1 shows the curves of PFS and OS from the start of BEV.

Table 2 Results obtained by using BEV in MGs
Fig. 1

Kaplan-Meier survival curves of PFS (a) and OS (b) from start of BEV treatment of the patients analysed in the study

Activity according to MGMT methylation and IDH1 mutation

Methylated patients appeared to experience both longer mPFS (5 versus 2 months) and mOS (9.5 versus 2.5 months) than unmethylated patients, but this did not reach statistical significance (p = 0.43 and 0.24, respectively).

Wild-type IDH1 patients showed both longer mPFS (12 versus 2 months) and mOS (13 versus 9.5 months) than mutated IDH1 patients, but this did not reach statistical significance (p = 0.82 and 0.59 respectively).

Correlations between response and patient’s characteristics/biomarkers

Subgroup analysis was performed to identify correlations between responder/non-responder patients and clinical characteristics or tumor biomarkers such as sex, histology, tumor side, MGMT methylation, IDH1 mutation and OS. The results showed a significant correlation between the response to BEV and OS (p < 0.001) and between the response to BEV and MGMT methylation (p < 0.05). We didn’t find any other significant relationship among the other subgroup analysis.

Clinical benefit

Patients had an important clinical benefit from BEV treatment in terms of improvement of performance status, improvement of neurological symptoms and decrease of steroid use.

An improvement in neurological symptoms was observed in 8 patients (47.1%). Of them, 4 patients (50%) had a discontinuation of corticosteroid use and 1 patient had a reduction of corticosteroid dose (12.5%) at the time of response. KPS improved in 64.7% of patients.

In the 13 patients treated with corticosteroids, a discontinuation of dexamethasone was observed in 4 patients (30.8%) and a reduction of dexamethasone dosage was shown in 5 patients (38.5%). Of the 4 patients who were not receiving dexamethasone before BEV, all of them remained without corticosteroids.

Of the 11 responding patients, 4 patients discontinued steroids (36.4%), 3 patients reduced steroid dosage (27.3%) and 4 patients, who were not on corticosteroids, remained without steroid therapy (36.4%).

Toxicity evaluation

All 17 patients were evaluated for safety (Table 3). BEV was generally well-tolerated with grade 1-2 hypertension observed in 6 (35.3%) and 2 (11.8%) patients respectively. Grade 1-2 proteinuria was observed in 7 (41.2%) and 2 (11.8%) patients respectively. Only one patient developed grade 3 proteinuria after 30 cycles of treatment and another patient developed an uncomplicated pulmonary embolism (grade 3 thromboembolic event). We observed grade 1 skin toxicities in 17.6% of patients, as acneiform rash, eritema and skin ulcer. We observed grade 1 anemia in 17.6% of patients, grade 1 leucopenia in 11.8% of patients, grade 2 leucopenia in 23.5% of patients and grade 1-2 thrombocytopenia in 11.8% of patients. Grade 4 toxicities, hemorrhagic events, treatment interruption or death related to BEV were not documented.

Table 3 Toxicities by grade of severity, according to the CTCAE (version 4.03)


For newly diagnosed MGs, radiotherapy plus concomitant and adjuvant TMZ after maximal safe surgical resection has become the standard therapy [4, 30]. However, there is not yet consensus on the treatment of recurrent MGs and treatment recommendations are still based on non-controlled phase II trials. In the United States, BEV as a single-agent is a valuable and active treatment option for recurrent GBM and AG [30]. It was approved in 2009 for the treatment of recurrent GBM by the FDA [12] based on the results of two uncontrolled phase II trials [8, 13] which have shown improvements in RR and PFS both as single-agent and combination therapy. In Europe, BEV was not approved as a treatment option of GBM due to the lack of phase III studies and of an evident clinical benefit in terms of OS.

Several single-arm monotherapy trials, randomized trials and single-arm combination therapy studies containing BEV were developed [19]. Phase II clinical trials on BEV as monotherapy (Table 4) reported similar results with mPFS of 1-4.2 months, PFS-6 of 18–42.6%, mOS of 6.4–12 months and RR of 28-43% [19, 31, 32]. Furthermore, a recent meta-analysis conducted by Wang et al. in 2014 [33] on the use of single angiogenesis inhibitors in the treatment of recurrent GBM, demonstrated a mPFS of 3 months and a mOS of 8.5 months in the group of clinical trials evaluating BEV. The combination therapy studies of BEV reported survival results and response rates similar to those reported by BEV monotherapy studies [19, 31, 34]. Some retrospective and prospective trials (Table 4) evaluated the efficacy of the combination of BEV with FTM [20,21,22,23]. The choice of this association was based on the rational that BEV could improve the activity of cytotoxic molecules without worsening primary toxicities of each agent [21, 22]. Soffietti et al. [21] showed that the association of BEV with FTM at first recurrence in GBM patients achieved RR of 52% and DCR of 89% and observed a mPFS of 5.2 months and a mOS of 9.1 months. Similar results were reported by a retrospective analysis conducted by Liu et al. [22] with RR of 46.5%, DCR of 90.9%, a mPFS of 5 months and a mOS of 8 months.

Table 4 Survival results of the main clinical trials evaluating Bevacizumab as single-agent or in combination with FTM

Soffietti et al. [23] in 2012, with the association of FTM and BEV in the treatment of first-relapsed grade III gliomas, reported response rates and survival results similar to those observed in the treatment of GBM.

BEV is a treatment generally well tolerated and the most common adverse events are hypertension, proteinuria, hemorrhage and thromboembolic complications, which are present in similar rates in the different clinical studies [32, 34, 35].

In our study, we observed a RR of 47.1%, mPSF of 5 months, PFS-6 of 41.2% and mOS of 8.3 months. These results were comparable with other retrospective and phase II trials on single-agent BEV or BEV associated with FTM reported in the literature (Table 4). Six patients experienced long response with a high number of administered cycles (range 11-40), long PFS ranged 11-40 months and OS ranged 12-45 months.

From our subgroup analysis, responder patients are statistically significantly correlated with a longer OS (p < 0.001) and the MGMT methylation (p < 0.05). Other clinical characteristics or tumor biomarkers seemed not to be correlated with the response to BEV.

In our retrospective analysis, methylated MGMT patients compared to unmethylated MGMT patients showed a longer mPFS (5 months vs 2 months, respectively) and a longer mOS (9.5 months vs 2.5 months, respectively) but without statistical significance (p = 0.44 and p = 0.24, respectively). Moreover, wild-type IDH patients compared to mutated IDH1 patients experienced longer mPFS (12 months vs 5 months, respectively) and mOS (13 vs 9.5 months, respectively) but without statistical significance (p = 0.82 and p = 0.59, respectively).

The prognostic significance of MGMT promoter methylation in the treatment of MGs remains controversial.

A meta-analysis conducted by Zhang et al. [36] in 2013 showed that methylated MGMT status in GBM patients was associated with better PFS and OS regardless of therapeutic intervention and associated with longer OS with alkylating agents. However, in the setting of BEV treatment, MGMT and IDH seemed not to be good prognostic factors [37].

In our retrospective analysis, we observed that the clinical benefit with BEV was not defined only in terms of tumor response but also in terms of improvement of performance status, decreased dependency on corticosteroids and improvement in symptoms of disease.

In our study, BEV was generally well tolerated and the most common adverse events include hypertension and proteinuria of grade 1-2. No grade 3-4 were observed, except for only one patient who developed grade 3 proteinuria after 30 administrations of BEV and one grade 3 thromboembolic event (uncomplicated pulmonary embolism).

Moreover, the combination of BEV plus FTM was well tolerated. In the BEV + FTM group of patients, the rate of BEV related toxicities was consistent with those reported in other similar trials [20,21,22,23].

This study has limitations related to the retrospective design, the low sample size and the unselection of the population analysed. In addition, the population is heterogeneous for histology, time of recurrence and type of treatment (monotherapy or combination BEV). Despite these limitations, it’s important to underline that survival results and response rate of BEV in previous prospective and retrospective studies are similar regardless of the specific histotype of MGs [16, 20], time of recurrence [8, 38, 39] and the use of BEV in monotherapy or in combination with other therapeutic agents [19, 31, 34]. Another limitation is that molecular markers, such as IDH1 mutation and MGMT status, were not available for all patients, even though their prognostic and/or predictive significance in the treatment with BEV are still not understood [37].

Future phase III studies are needed to establish if combination therapy with BEV is superior to single-agent therapy for recurrent MGs and the optimal therapeutic agent for the combination treatment with BEV. Further studies are needed also to investigate biomarkers and genetic patterns which may help to identify patients who may benefit from treatment with BEV reaching long-term responses.


In conclusion, our retrospective study showed that BEV as single-agent and in combination therapy, in off-label use, is a valid treatment option also in unselected recurrent MGs patients which provides significant survival benefits with acceptable toxicity profile. However, further phase III clinical trials are needed.



Anaplastic gliomas




Complete response


Common Terminology Criteria for Adverse Events


Disease control


European Medical Agency


Food and Drug Administration






Isocitrate dehydrogenase 1


Institutional Review Board






O6-Methylguanine-DNA methyltransferase


Malignant gliomas


Median overall survival


Median progression free survival


Magnetic resonance imaging


Overall response rate


12 months overall survival


Progression disease


12 months progression free survival


6 months progression free survival


Partial response


Response rate


Stable disease




Vascular endothelial growth factor


  1. 1.

    Ostrom QT, Gittleman H, Farah P, et al. CBTRUS statistical report: primary brain and central nervous system tumors diagnosed in the United States in 2006–2010. Neuro-Oncology. 2013;15(sup 6):ii1–56.

  2. 2.

    Stupp R, Mason WP, Van den Bent MJ, et al. Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. N Engl J Med. 2005;352:987–96.

  3. 3.

    Stupp R, Hegi ME, Mason WP, et al. Effects of radiotherapy with concomitant and adjuvant temozolomide versus radiotherapy alone on survival in glioblastoma in a randomised phase III study: 5-year analysis of the EORTC-NCIC trial. Lancet Oncol. 2009;10:459–66.

  4. 4.

    Weller M, Cloughesy T, Perry JR, et al. Standards of care for treatment of recurrent glioblastoma-are we there yet? Neuro-Oncology. 2013;215:4–27.

  5. 5.

    Fabi A, Metro G, Vidiri A, et al. Low-dose fotemustine for recurrent malignant glioma: a multicenter phase II study. J Neuro-Oncol. 2010;100:209–15.

  6. 6.

    Jo J, Schiff D, Purow B. Angiogenic inhibition in high-grade gliomas: past, present and future. Expert Rev Neurother. 2012;12:733–47.

  7. 7.

    Desjardins A, Reardon DA, Herndon IIJE, et al. Bevacizumab plus irinotecan in recurrent WHO grade 3 malignant gliomas. Clin Cancer Res. 2008;14(21):7068–73.

  8. 8.

    Friedman HS, Prados MD, Wen PY, et al. Bevacizumab alone and in combination with irinotecan in recurrent glioblastoma. J Clin Oncol. 2009;27:4733–40.

  9. 9.

    Birk HS, Han SJ, Butowski NA. Treatment options for recurrent high-grade gliomas. CNS Oncol. 2017;6(1):61–70.

  10. 10.

    Chamberlain MC. Bevacizumab for the treatment of recurrent glioblastoma. Clin Med Insights. 2011;5:117–29.

  11. 11.

    Chamberlain MC. Bevacizumab for recurrent malignant gliomas: efficacy, toxicity, and patterns of recurrence. Neurology. 2009;72(8):772–4.

  12. 12.

    Cohen MH, Shen YL, Keegan P, Pazdur R. FDA drug approval summary: Bevacizumab (Avastin) as treatment of recurrent glioblastoma multiforme. Oncologist. 2009;14:11311138.

  13. 13.

    Kreisl TN, Kim L, Moore K, et al. Phase II trial of single-agent Bevacizumab followed by Bevacizumab plus irinotecan at tumor progression in recurrent glioblastoma. J Clin Oncol. 2009;27:740–5.

  14. 14.

    Chamberlain MC, Johnston SK. Salvage therapy with single agent Bevacizumab for recurrent glioblastoma. J Neuro-Oncol. 2010;96:259–69.

  15. 15.

    Raizer JJ, Grimm S, Chamberlain MC, et al. A phase 2 trial of singleagent Bevacizumab given in an every-3-week schedule for patients with recurrent high-grade gliomas. Cancer. 2010;116(22):5297–305.

  16. 16.

    Kreisl TN, Zhang W, Odia Y, et al. A phase II trial of single-agent Bevacizumab in patients with recurrent anaplastic glioma. Neuro-Oncology. 2011;13:1143–50.

  17. 17.

    Nagane M, Nishikawa R, Narita Y, et al. Phase II study of single-agent Bevacizumab in Japanese patients with recurrent malignant glioma. Jpn J Clin Oncol. 2012;42:887–95.

  18. 18.

    Zhang G, Huang S, Wang Z. A meta-analysis of Bevacizumab alone and in combination with irinotecan in the treatment of patients with recurrent glioblastoma multiforme. J Clin Neurosci. 2012;19(12):1636–40.

  19. 19.

    Seystahl K, Wick W, Weller M. Therapeutic options in recurrent glioblastoma-an update. Crit Rev Oncol Hematol. 2016;99:389–408.

  20. 20.

    Vaccaro V, Fabi A, Vidiri A, et al. Activity and safety of Bevacizumab plus fotemustine for recurrent malignant gliomas. Biomed Res Int. 2014;2014:351252.

  21. 21.

    Soffietti R, Trevisan E, Bertero L, et al. Bevacizumab and fotemustine for recurrent glioblastoma: a phase II study of AINO (Italian Association of Neuro-Oncology). J Neuro-Oncol. 2014;116(3):533–41.

  22. 22.

    Liu Z, Zhang G, Zhu L, et al. Retrospective analysis of Bevacizumab in combination with fotemustine in Cinese patients with recurrent glioblastoma multiforme. BioMed Res Inter. 2015;2015:723612.

  23. 23.

    Soffietti R, Trevisan E, Bosa C, et al. Phase II trial of Bevacizumab and fotemustine in recurrent grade III gliomas. J Clin Oncol. 2012;30:Abstract 2075.

  24. 24.

    Del Vecchio M, Mortarini R, Canova S, et al. Bevacizumab plus fotemustine as first-line treatment in metastatic melanoma patients: clinical activity and modulation of angiogenesis and lymphangiogenesis factors. Clin Cancer Res. 2010;16:5862–72.

  25. 25.

    Addeo R, Caraglia M, De Santi MS, et al. A new schedule of fotemustine in temozolomide-pretreated patients with relapsing glioblastoma. J Neuro-Oncol. 2011;102(3):417–24.

  26. 26.

    Louis DN, Perry A, Reifenberger G, et al. The 2016 World Health Organization classification of tumors of the central nervous system: a summary. Acta Neuropathol. 2016;131:803–20.

  27. 27.

    Wen PY, Macdonald DR, Reardon DA, et al. Updated response assessment criteria for high-grade gliomas: response assessment in neuro-oncology working group. J Clin Oncol. 2010;28:1963–72.

  28. 28.

    Common Terminology Criteria for Adverse Events v4.03 (CTCAE). Available at: Last Accessed 22 July 2016.

  29. 29.

    Kaplan E, Meier P. Nonparametric estimation from incomplete observations. J Am Stat Assoc. 1958;53:457–81.

  30. 30.

    National Comprehensive Cancer Network. NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines ®): Central Nervous System Cancers. Version 1.2015. Available at: Accessed July 20 2016.

  31. 31.

    Narita Y. Drug review: safety and efficacy of Bevacizumab for glioblastoma and other brain tumors. Jpn J Clin Oncol. 2013;43:587–95.

  32. 32.

    Narita Y. Bevacizumab for glioblastoma. Ther Clin Risk Manag. 2015;11:1759–65.

  33. 33.

    Wang Y, Xing D, Zhao M, et al. The role of a single angiogenesis inhibitor in the treatment of recurrent glioblastoma multiforme: a meta-analysis and systematic review. PLoS One. 2016;11(3):e0152170.

  34. 34.

    Gil-Gil MJ, Mesia C, Rey M, et al. Bevacizumab for the treatment of glioblastoma. Clin Med Insights Oncol. 2013;7:123–35.

  35. 35.

    Brandes AA, Bartolotti M, Tosoni A, et al. Practical management of Bevacizumab-related toxicities in glioblastoma. Oncologist. 2015;20(2):166–75.

  36. 36.

    Zhang K, Wang XQ, Zhou B, et al. The prognostic value of MGMT promoter methylation in glioblastoma multiforme: a meta-analysis. Familial Cancer. 2013;12(3):449–58.

  37. 37.

    Schaub C, Tichy J, Schäfer N, et al. Prognostic factors in recurrent glioblastoma patients treated with Bevacizumab. J Neuro-Oncol. 2016;

  38. 38.

    Piccioni DE, Selfridge J, Mody RR, et al. Deferred use of Bevacizumab for recurrent glioblastoma is not associated with diminished efficacy. Neuro-Oncology. 2014;16(6):815–22.

  39. 39.

    Hamza MA, Mandel JJ, Conrad CA, et al. Survival outcome of early versus delayed Bevacizumab treatment in patients with recurrent glioblastoma. J Neuro-Oncol. 2014;119(1):135–40.

  40. 40.

    Taal W, Oesterkamp HM, Walenkamp AM, et al. Single-agent Bevacizumab or lomustine versus a combination of Bevacizumab plus lomustine in patients with recurrent glioblastoma (BELOB trial): a randomised controlled phase 2 trial. Lancet Oncol. 2014;15:943–53.

  41. 41.

    Field KM, Simes J, Nowak AK, et al. Randomized phase 2 study of carboplatin and Bevacizumab in recurrent glioblastoma. Neuro-Oncology. 2015;17:1504–13.

  42. 42.

    Puduvalli V, Wu J, Yuan Y, et al. Brain tumor trials collaborative Bayesian adaptive randomized phase II trial of Bevacizumab plus vorinostat versus Bevacizumab alone in adults with recurrent glioblastoma (BTTC-1102). J Clin Oncol. 2015;33:abstr 2012.

  43. 43.

    Hacibekiroglu I, Kodaz H, Erdogan B, et al. Single-agent Bevacizumab is an effective treatment in recurrent glioblastoma. Med Oncol. 2015;32(2):460.

  44. 44.

    Brandes AA, Finocchiaro G, Zagonel V, et al. AVAREG: a phase II, randomized, noncomparative study of fotemustine or Bevacizumab for patients with recurrent glioblastoma. Neuro-Oncology. 2016;18(9):1304–12.

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We thank the research nurses and the patients at Policlinico Umberto I of Rome and S.M.Goretti Hospital of Latina for taking patient samples and for participating in this study, respectively.

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The data and materials can be found from the first author and corresponding author.

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AP and SER contributed equally to this work. AP, SER, VB ad ST, designed the study. AP, SP, CF1, CP selected patients, obtained informed consent and collected clinical data. AP, SER, and CF4 performed the experiments and performed statistical analyses. AP, SER and SM wrote the manuscript. All authors participated to interpret data as well as corrected and approved of the final manuscript. All authors read and approved the final manuscript.

Correspondence to Arsela Prelaj.

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Ethics approval and consent to participate

The protocol (No: Beva-Glio/Sep 2016) was retrospectively approved by the ethics committee of S.M.Goretti Hospital of Latina, Sapienza University of Rome. Consent for publication not applicable.

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The authors declare that they have no competing interests.

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Prelaj, A., Rebuzzi, S., Salvati, M. et al. Retrospective analysis to evaluate the efficacy and the safety of Bevacizumab in the treatment of recurrent malignant gliomas. transl med commun 3, 6 (2018).

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  • Bevacizumab
  • Recurrent glioblastoma
  • Recurrent malignant glioma
  • Fotemustine
  • Retrospective study