Purpose: Patients with central nervous system (CNS) metastases were excluded from bevacizumab trials following a case of fatal cerebral hemorrhage in a patient with hepatocellular carcinoma in 1997. Safety information for bevacizumab-treated patients with CNS metastases was reviewed to determine whether general exclusion of these patients from bevacizumab treatment is still justified.

Experimental Design: A retrospective exploratory analysis was conducted using datasets from 13 randomized controlled phase II/III trials (dataset A), two open-label single-arm safety trials (dataset B), and two prospective studies including patients with treated CNS metastases (dataset C). In datasets A and B, known CNS metastasis was an exclusion criterion; patients with CNS metastasis had unrecognized CNS metastases at study entry or developed them during the trial. All reported cerebral hemorrhage grades in patients with CNS metastases were quantified.

Results: In dataset A, occult brain metastases were identified in 187 of 8,443 patients (91 in bevacizumab arms and 96 in non-bevacizumab arms). Three bevacizumab-treated patients (3.3%) developed grade 4 cerebral hemorrhage, whereas one control-arm patient (1.0%) developed grade 5 cerebral hemorrhage. In dataset B, 321 of 4,382 patients had initially occult CNS metastases, in whom two grade 1 and one grade 3 cerebral hemorrhage (0.9%) were reported. In 131 patients with treated CNS metastases in dataset C, one bevacizumab-treated patient (0.8%) developed grade 2 cerebral hemorrhage.

Conclusions: In this selected population, patients with CNS metastases are at similar risk of developing cerebral hemorrhage, independent of bevacizumab therapy. Consequently, such patients with CNS metastases from advanced/metastatic breast cancer, non–small cell lung carcinoma, and renal and colorectal cancer should not be generally excluded from bevacizumab therapy or clinical trials. Clin Cancer Res; 16(1); 269–78

Since the occurrence of fatal intracranial bleeding in a patient with hepatocellular carcinoma and a previously undiagnosed brain metastasis, bevacizumab has been contraindicated in Europe for use in patients with central nervous system (CNS) metastases. The results of the present retrospective analysis of >12,000 patients have shown that the risk of cerebral hemorrhage is not disproportionately higher in these patients, suggesting that administration of bevacizumab should no longer be contraindicated based solely on the presence of CNS metastasis. On the basis of the information in this report, the European Medicines Authority has recently decided that this contraindication is no longer justified. The translational relevance of these findings is stated in the conclusion of this article: Selected patients with CNS metastases should not be excluded from bevacizumab therapy in advanced/metastatic breast cancer, non–small cell lung carcinoma, and renal and colorectal cancer. Treatment decisions should be driven by the benefit/risk assessment made by physicians for individual patients.

Bevacizumab is a recombinant humanized monoclonal antibody that selectively binds to and neutralizes the biological activity of human vascular endothelial growth factor (VEGF; refs. 1, 2), thus reducing tumor vascularization and inhibiting tumor growth (3). Bevacizumab has shown efficacy in combination with chemotherapy in metastatic breast, colorectal, and non–small cell lung carcinoma (NSCLC), and in combination with interferon in renal cell carcinoma (48).

Patients with central nervous system (CNS) metastases have until recently been routinely excluded from bevacizumab trials, following a single case in 1997 of a 29-year-old patient with hepatocellular carcinoma (HCC) who experienced a fatal cerebral hemorrhage from a previously undiagnosed brain metastasis in a phase I study of bevacizumab (9). However, CNS metastases from HCC have an inherent tendency to bleed because patients with HCC are likely to have coagulopathy due to impaired liver function, resulting in cerebral hemorrhage incidences of up to 87.5%, independent of the type of therapy received (1013).

Since the single case of CNS hemorrhage in 1997 through to February 2009, >577,000 patients have been exposed to bevacizumab. More safety data have thus become available, particularly in patients with occult CNS metastases at study entry and in those developing CNS metastases due to disease progression. Independent reports have concluded that there is no increased risk of cerebral hemorrhage in bevacizumab-treated patients with CNS metastases (1417). In patients with NSCLC and CNS metastases who were treated with bevacizumab, the risk of tumor-associated CNS hemorrhage was reported to be similar to rates in control patients with metastases who did not receive bevacizumab (1417). Furthermore, recent phase II data supporting the use of bevacizumab in the treatment of high-grade gliomas (1820) have called into question the exclusion of patients with CNS metastases from bevacizumab clinical trials.

To assess the risk of cerebral hemorrhage in patients with CNS metastases treated with bevacizumab and to revisit the exclusion of these patients from trials, we conducted a retrospective exploratory analysis of safety data from 13 phase II/III randomized controlled trials (RCTs; refs. 48, 2128), two open-label single-arm safety studies (29, 30), and two recent prospective studies that included patients with treated CNS metastases (14, 31).

Three datasets were analyzed for the purpose of this safety review using the National Cancer Institute Common Terminology Criteria for Adverse Events; all reported adverse events of cerebral hemorrhage in patients with CNS metastases were included. The datasets were as follows: 13 RCTs (48, 2128); 2 open-label single-arm safety studies: SAiL (Safety of Avastin in Lung; MO19390) and ATHENA (Avastin Therapy for Advanced Breast Cancer; MO19391; refs. 29, 30); and 2 prospective studies including patients with treated CNS metastases: ATLAS (AVF3671g) and PASSPORT (AVF3752g; refs. 14, 31).

Randomized controlled trials

The analysis was based on safety data from 13 completed bevacizumab RCTs conducted by the Eastern Cooperative Oncology Group (ECOG), Roche, and Genentech, which included a total of 8,443 patients (Table 1). The cutoff date for the analysis was March 31, 2008. Patients in the Roche and Genentech studies were included in the analysis if they had received at least one dose of study drug (chemotherapy, bevacizumab, or placebo). Patients who were randomized to the control arm of a study but received at least one dose of bevacizumab during the study treatment phase were also included in the bevacizumab-treated population. For ECOG trials, the safety population as defined in the study protocol was used.

Table 1.

Randomized controlled trials (dataset A)

StudyTreatmentIndicationTotal (N)Patients with CNS metastasis (n)
BevNon-Bev
Roche 
    BO17704, AVAiL (21) Bev + cisplatin + gemcitabine vs placebo + cisplatin + gemcitabine Nonsquamous NSCLC 986 18 20 
    BO17705, AVOREN (4) Bev + IFN alfa-2a vs placebo + IFN alfa-2a Metastatic renal cell carcinoma 641 10 13 
    BO17706, AViTA (22) Bev + gemcitabine + erlotinib vs placebo + gemcitabine + erlotinib Pancreatic cancer 583 
    BO17708, AVADO (23) Bev + docetaxel vs placebo + docetaxel Metastatic breast cancer 730 18 11 
    NO16966 (24) XELOX or FOLFOX4 + Bev vs XELOX or FOLFOX4 + placebo Metastatic CRC 1369 
Genentech 
    AVF2107 (5) Bev + IFL vs placebo + IFL Metastatic CRC 901 
    AVF2192 (25) Bev + 5-FU/FA vs placebo + 5-FU/FA Metastatic CRC 204 
    AVF0780 (26) 2 doses of Bev + 5-FU/FA vs 5-FU/FA Metastatic CRC 102 
    AVF0757 (6) 2 doses of Bev + carboplatin + paclitaxel vs carboplatin + paclitaxel Nonsquamous NSCLC 98 
    AVF2119 (27) Bev + capecitabine vs capecitabine Metastatic breast cancer 444 
ECOG 
    E2100 (7) Bev + paclitaxel vs paclitaxel Metastatic breast cancer 711 10 
    E3200 (28) Bev + FOLFOX4 vs FOLFOX4 Metastatic CRC 806 
    E4599 (8) Bev + paclitaxel + carboplatin vs paclitaxel + carboplatin Nonsquamous NSCLC 868 16 21 
Total number of patients 8,443 91 96 
StudyTreatmentIndicationTotal (N)Patients with CNS metastasis (n)
BevNon-Bev
Roche 
    BO17704, AVAiL (21) Bev + cisplatin + gemcitabine vs placebo + cisplatin + gemcitabine Nonsquamous NSCLC 986 18 20 
    BO17705, AVOREN (4) Bev + IFN alfa-2a vs placebo + IFN alfa-2a Metastatic renal cell carcinoma 641 10 13 
    BO17706, AViTA (22) Bev + gemcitabine + erlotinib vs placebo + gemcitabine + erlotinib Pancreatic cancer 583 
    BO17708, AVADO (23) Bev + docetaxel vs placebo + docetaxel Metastatic breast cancer 730 18 11 
    NO16966 (24) XELOX or FOLFOX4 + Bev vs XELOX or FOLFOX4 + placebo Metastatic CRC 1369 
Genentech 
    AVF2107 (5) Bev + IFL vs placebo + IFL Metastatic CRC 901 
    AVF2192 (25) Bev + 5-FU/FA vs placebo + 5-FU/FA Metastatic CRC 204 
    AVF0780 (26) 2 doses of Bev + 5-FU/FA vs 5-FU/FA Metastatic CRC 102 
    AVF0757 (6) 2 doses of Bev + carboplatin + paclitaxel vs carboplatin + paclitaxel Nonsquamous NSCLC 98 
    AVF2119 (27) Bev + capecitabine vs capecitabine Metastatic breast cancer 444 
ECOG 
    E2100 (7) Bev + paclitaxel vs paclitaxel Metastatic breast cancer 711 10 
    E3200 (28) Bev + FOLFOX4 vs FOLFOX4 Metastatic CRC 806 
    E4599 (8) Bev + paclitaxel + carboplatin vs paclitaxel + carboplatin Nonsquamous NSCLC 868 16 21 
Total number of patients 8,443 91 96 

Abbreviations: 5-FU/FA, 5-fluorouracil/folinic acid; Bev, bevacizumab; CRC, colorectal cancer; FOLFOX4, 5-FU/FA plus oxaliplatin; IFL, irinotecan plus 5-FU/FA; XELOX, capecitabine and oxaliplatin.

Initially, the patient database was searched for patients with CNS metastases using the following search terms: brain; malignant neoplasm of spinal cord; central nervous system, neoplasm; cerebellar tumor; meningeal neoplasm; nervous system, neoplasm; spinal cord neoplasm; neoplasm of uncertain behavior of meninges; and neoplasm of uncertain behavior of brain and spinal cord. With the primary aim of identifying cases of cerebral hemorrhage, the following two-step analysis was done. First, experienced medical professionals (medical doctors and oncologists employed by Roche) identified CNS metastases through a detailed review of individual patient files. As the presence of CNS metastases at enrollment was an exclusion criterion for all RCTs, patients identified during this medical review either had occult (undiagnosed/unrecognized) CNS metastases at baseline or developed CNS metastases during the trials. Second, the patients with CNS metastases identified by this procedure were analyzed for reports of cerebral hemorrhage (all grades were included), applying the Medical Dictionary for Regulatory Activities (version 10.1) term “intracranial hemorrhage.”

In 10 of the 13 studies, related hemorrhage events were collected until at least 21 d after the last study drug administration. In AVF2119g, hemorrhage events were collected up to 7 d after the last study dose in the control arm and 21 d in the bevacizumab arm. In AVF2107g and AVF2192g, bleeding events were collected for 14 d after the last dose.

In 11 of the 13 studies, chronic daily treatment with aspirin >325 mg/d was an exclusion criterion. Use of aspirin was not allowed in studies AVF0780g and AVF0757g. BO17708 was the only study not to have therapeutic oral or parenteral anticoagulation as an exclusion criterion. In all studies except BO17705 and BO17708, corticosteroid use was generally permitted.

Large open-label single-arm safety studies

The occurrence of cerebral hemorrhage in patients with CNS metastases was analyzed in two ongoing, fully recruited, single-arm, open-label studies (data cutoff date March 10, 2009, for SAiL and March 16, 2009, for ATHENA; refs. 29, 30). The analysis included a total of 4,382 patients (2,166 in SAiL; 2,216 in ATHENA).

SAiL is an open-label study of bevacizumab in combination with platinum-containing chemotherapy as first-line treatment for patients with advanced or recurrent nonsquamous NSCLC. Similarly, ATHENA is an open-label study of bevacizumab plus taxane–based therapy for the first-line treatment of patients with locally recurrent or metastatic breast cancer. The primary objective of both studies was to assess the safety profile of bevacizumab when used as first-line treatment in a broader population. Evidence of CNS metastases at study commencement (even if previously treated) was an exclusion criterion for both studies, hence the specific safety of bevacizumab was assessed in patients who either developed CNS metastases during treatment or had occult CNS metastases at study entry.

In ATHENA and SAiL, bleeding events had to be reported up to 6 mo after the last bevacizumab infusion, irrespective of severity and causal relationship. Prophylactic anticoagulation was allowed, but aspirin (>325 mg/d) or therapeutic anticoagulation (oral or parenteral) within 10 d of the first bevacizumab dose was an exclusion criterion. Concomitant use of steroids was allowed during the trials at the physicians' discretion.

Prospective studies including patients with treated CNS metastases

Patients with a history of treated CNS metastases were included in these two prospective trials that combined bevacizumab with chemotherapy in patients with NSCLC (14, 31). The fully recruited PASSPORT study specifically included patients with treated CNS metastases; 115 patients were analyzed (data cutoff date was June 23, 2008). ATLAS included 26 patients with CNS metastases out of a total of 730 enrolled (data cutoff date was October 12, 2007).

PASSPORT is an open-label single-arm phase II trial of bevacizumab in combination with first- or second-line therapy in patients with treated CNS metastases from nonsquamous NSCLC. First- and second-line therapy consisted of either chemotherapy or erlotinib with bevacizumab, according to institutional standards. The primary objective was to assess the rate of symptomatic CNS hemorrhage grade ≥2 during bevacizumab therapy. Patients with CNS metastases were allowed to enter the trial after previous treatment with whole CNS radiation therapy and/or neurosurgery. After treatment of CNS metastases, the absence of progression or CNS hemorrhage had to be confirmed clinically and by magnetic resonance imaging or computed tomography.

ATLAS is a randomized, double-blind, placebo-controlled phase IIIb trial comparing bevacizumab therapy with or without erlotinib after completion of chemotherapy with bevacizumab for the first-line treatment of locally advanced, recurrent, or metastatic NSCLC. Patients were initially treated with four cycles of bevacizumab in combination with the investigators' choice of platinum-based chemotherapy regimens. Patients who did not experience disease progression and did not have significant toxicity were randomized to receive maintenance therapy with bevacizumab plus erlotinib or bevacizumab plus placebo until disease progression. Patients with a history of CNS metastases were eligible for enrollment if they had received treatment with whole brain radiation therapy and/or neurosurgery.

In ATLAS and PASSPORT, patients were followed for adverse events for 30 and 60 d, respectively, after discontinuation of study treatment.

PASSPORT permitted concomitant treatment including low-dose aspirin, therapeutic heparin/warfarin, and corticosteroids. ATLAS excluded patients with an ongoing requirement at screening for dexamethasone treatment or chronic therapeutic warfarin. Low-dose aspirin and therapeutic heparin were allowed.

Randomized controlled clinical trials

Thirteen RCTs across various indications (locally advanced, unresectable, or metastatic NSCLC; renal, pancreatic, breast, and colorectal cancer) were included in the analysis (Table 1). Overall, 8,443 patients were enrolled, of whom 4,760 received bevacizumab. A total of 187 patients (2.2%) were identified as having CNS metastases: 91 (1.9%) in the bevacizumab-treated group and 96 (2.6%) in the control group (i.e., non–bevacizumab-treated patients). Demographic characteristics, performance status (ECOG, Karnofsky), and study indications were similar in both groups (Table 2).

Table 2.

Demographic characteristics of patients identified with CNS metastasis in each dataset

Patients with CNS metastasesRandomized controlled trialsLarge open-label single-arm safety studiesStudies including patients with treated CNS metastases
Bev (n = 91)Non-Bev (n = 96)ATHENA (n = 140)SAiL (n = 181)ATLAS (n = 26)PASSPORT (n = 115)
Sex, n (%) 
    Male 34 (37.4) 44 (45.8) 0 (0) 100 (55.2) 17 (65.4) 62 (53.9) 
    Female 57 (62.6) 52 (54.2) 140 (100) 81 (44.8) 9 (34.6) 53 (46.1) 
Age, y 
    Median (range) 58 (23-81) 58 (33-81) 52 (26-81) 56 (29-78) 61 (39-75) 60 (23-90) 
ECOG PS at baseline, n (%) 
    0 30 (42.9)* 29 (39.7) 74 (52.9) 81 (44.8) 8 (30.8) 44 (38.3) 
    1 40 (57.1)* 44 (60.3) 57 (40.7) 86 (47.5) 17 (65.4) 71 (61.7) 
    2 — — 9 (6.4) 14 (7.7) 1 (3.8) — 
Karnofsky score at baseline, n (%) 
    100-91% 4 (36.4) 6 (46.2)§     
    90-81% 2 (18.2) 7 (53.8)§     
    80-71% 5 (45.5) —     
Study indication, n (%) 
    CRC 16 (17.6) 18 (18.8) — — — — 
    NSCLC 36 (39.6) 43 (44.8) — 181 (100) 26 (100) 115 (100) 
    Breast 28 (30.8) 22 (22.9) 140 (100) — — — 
    Other 11 (12.1) 13 (13.5) — — — — 
Patients with CNS metastasesRandomized controlled trialsLarge open-label single-arm safety studiesStudies including patients with treated CNS metastases
Bev (n = 91)Non-Bev (n = 96)ATHENA (n = 140)SAiL (n = 181)ATLAS (n = 26)PASSPORT (n = 115)
Sex, n (%) 
    Male 34 (37.4) 44 (45.8) 0 (0) 100 (55.2) 17 (65.4) 62 (53.9) 
    Female 57 (62.6) 52 (54.2) 140 (100) 81 (44.8) 9 (34.6) 53 (46.1) 
Age, y 
    Median (range) 58 (23-81) 58 (33-81) 52 (26-81) 56 (29-78) 61 (39-75) 60 (23-90) 
ECOG PS at baseline, n (%) 
    0 30 (42.9)* 29 (39.7) 74 (52.9) 81 (44.8) 8 (30.8) 44 (38.3) 
    1 40 (57.1)* 44 (60.3) 57 (40.7) 86 (47.5) 17 (65.4) 71 (61.7) 
    2 — — 9 (6.4) 14 (7.7) 1 (3.8) — 
Karnofsky score at baseline, n (%) 
    100-91% 4 (36.4) 6 (46.2)§     
    90-81% 2 (18.2) 7 (53.8)§     
    80-71% 5 (45.5) —     
Study indication, n (%) 
    CRC 16 (17.6) 18 (18.8) — — — — 
    NSCLC 36 (39.6) 43 (44.8) — 181 (100) 26 (100) 115 (100) 
    Breast 28 (30.8) 22 (22.9) 140 (100) — — — 
    Other 11 (12.1) 13 (13.5) — — — — 

NOTE: Karnofsky score was only collected in the AVOREN and AViTA studies; all other studies reported ECOG PS.

Abbreviation: ECOG PS, Eastern Cooperative Oncology Group performance status.

*n = 70.

n = 73.

n = 11.

§n = 13.

Median duration of study treatment in patients with CNS metastases was longer in the bevacizumab-treated group compared with the control group: 168 days (range, 1-658 days) versus 106 days (range, 1-493 days). Median time from first treatment to diagnosis of CNS metastases was 190 days [range, −23 (i.e., 23 days before treatment started) to 676 days] and 149 days (range, −49 to 543 days) in the bevacizumab and control groups, respectively.

In the bevacizumab-treated group, 14 of 91 patients (15.4%) were on study treatment at diagnosis or after being diagnosed with CNS metastases compared with 16 of 96 patients (16.7%) in the control arm. The median number of days between the end of treatment and diagnosis of CNS metastases was 18 days [range, −450 (i.e., diagnosis of CNS metastases was 450 days before the last bevacizumab dose) to 183 days] and 18 days (range, -541 to 216 days) in the bevacizumab-treated and control groups, respectively. The median time between the end of bevacizumab treatment and diagnosis of CNS metastases was shorter than the half-life of bevacizumab (approximately 20 days; ref. 32), reflecting the time-related exposure of bevacizumab to the CNS metastases.

Of the 91 patients treated with bevacizumab who experienced CNS metastases, 3 (3.3%) developed grade 4 cerebral hemorrhage compared with 1 of 96 control patients (1.0%) who developed grade 5 cerebral hemorrhage (Table 3). Possible confounding factors, concomitant medications, and relevant history were collected where possible (Table 4). In the bevacizumab-treated patients, the cause of death was progressive disease for two patients (cause of death was not stated for the other patient who died 6 months after the occurrence of cerebral hemorrhage), whereas the cause of death was cerebral hemorrhage in the control patient (Table 4).

Table 3.

Incidences of cerebral hemorrhage in patients with CNS metastases in the safety datasets analyzed

DatasetCerebral hemorrhage
BevacizumabNon-bevacizumab
Randomized controlled trials* (n = 91) (n = 96) 
All, n (%) 3 (3.3) 1 (1.0) 
    Grade 4 
    Grade 5 
Large open-label single-arm safety studies* (n = 321) No control 
All, n (%) 3 (0.9) — 
    Grade 1 — 
    Grade 3 — 
Studies including patients with treated CNS metastases (n = 131)§ No control 
All, n (%) 1 (0.8) — 
    Grade 2 — 
DatasetCerebral hemorrhage
BevacizumabNon-bevacizumab
Randomized controlled trials* (n = 91) (n = 96) 
All, n (%) 3 (3.3) 1 (1.0) 
    Grade 4 
    Grade 5 
Large open-label single-arm safety studies* (n = 321) No control 
All, n (%) 3 (0.9) — 
    Grade 1 — 
    Grade 3 — 
Studies including patients with treated CNS metastases (n = 131)§ No control 
All, n (%) 1 (0.8) — 
    Grade 2 — 

*CNS metastasis was an exclusion criterion.

SAiL, n = 181; ATHENA, n = 140.

Inclusion of patients with CNS metastasis was allowed when adequately treated.

§ATLAS, n = 26; PASSPORT, n = 115.

Table 4.

Details of patients who experienced cerebral hemorrhage

Treatment groupStudy, indicationDemographicsTotal treatment cyclesLast treatment dayDay of CNS metastasis diagnosisDay of cerebral hemorrhageDay of deathAdditional information from case narratives (excluding cerebral hemorrhage)
Randomized controlled trials 
    Bev ECOG 3200, CRC 59 y, male 59 83 71 268 Severe AEs during study: grade 4 hypertension; grade 3 seizure on day of cerebral hemorrhage 
Cause of death: not stated 
    Bev ECOG 3200, CRC 75 y, male 29 39 39 114 Severe AE during study: grade 3 seizure on day of cerebral hemorrhage 
Cause of death: CRC progression 
    Bev ECOG 4599, NSCLC 68 y, male 13 267 289 288 306 Severe AE during study: grade 3 pancreatitis with INR of 1.6 one day before diagnosis of cerebral hemorrhage 
Cause of death: NSCLC progression 
    Non-Bev BO17705, RCC 66 y, female NA 405 407 407 409 Patient collapsed on day 407 and was diagnosed with BM and cerebral hemorrhage 
Cause of death: cerebral hemorrhage 
Large open-label single-arm safety studies 
    Bev SAiL, NSCLC 44 y, male 168 319 319 450 Newly diagnosed CTC grade 1 hypertension 7 mo before diagnosis of CNS metastasis 
No concomitant anticoagulant treatment at diagnosis of CNS metastasis 
Cause of death: unknown 
    Bev SAiL, NSCLC 59 y, female 13 265 273 273 313 Heparin treatment started for PE 7 mo before diagnosis of CNS metastasis 
During study: newly diagnosed PE 7 mo before diagnosis of CNS metastasis 
Cause of death: progression of disease 
    Bev SAiL, NSCLC 56 y, male 147 167 162 173 Grade 1 hemoptysis 4 mo before diagnosis of cerebral hemorrhage 
No concomitant anticoagulant treatment at diagnosis of cerebral hemorrhage 
Cause of death: progression of disease 
Studies including patients with treated CNS metastases 
    Bev ATLAS, NSCLC 60 y, male 14 287 Present at baseline 286 343 Concomitant treatment at diagnosis of cerebral hemorrhage: NSAID 
Cause of death: progression of disease 
Treatment groupStudy, indicationDemographicsTotal treatment cyclesLast treatment dayDay of CNS metastasis diagnosisDay of cerebral hemorrhageDay of deathAdditional information from case narratives (excluding cerebral hemorrhage)
Randomized controlled trials 
    Bev ECOG 3200, CRC 59 y, male 59 83 71 268 Severe AEs during study: grade 4 hypertension; grade 3 seizure on day of cerebral hemorrhage 
Cause of death: not stated 
    Bev ECOG 3200, CRC 75 y, male 29 39 39 114 Severe AE during study: grade 3 seizure on day of cerebral hemorrhage 
Cause of death: CRC progression 
    Bev ECOG 4599, NSCLC 68 y, male 13 267 289 288 306 Severe AE during study: grade 3 pancreatitis with INR of 1.6 one day before diagnosis of cerebral hemorrhage 
Cause of death: NSCLC progression 
    Non-Bev BO17705, RCC 66 y, female NA 405 407 407 409 Patient collapsed on day 407 and was diagnosed with BM and cerebral hemorrhage 
Cause of death: cerebral hemorrhage 
Large open-label single-arm safety studies 
    Bev SAiL, NSCLC 44 y, male 168 319 319 450 Newly diagnosed CTC grade 1 hypertension 7 mo before diagnosis of CNS metastasis 
No concomitant anticoagulant treatment at diagnosis of CNS metastasis 
Cause of death: unknown 
    Bev SAiL, NSCLC 59 y, female 13 265 273 273 313 Heparin treatment started for PE 7 mo before diagnosis of CNS metastasis 
During study: newly diagnosed PE 7 mo before diagnosis of CNS metastasis 
Cause of death: progression of disease 
    Bev SAiL, NSCLC 56 y, male 147 167 162 173 Grade 1 hemoptysis 4 mo before diagnosis of cerebral hemorrhage 
No concomitant anticoagulant treatment at diagnosis of cerebral hemorrhage 
Cause of death: progression of disease 
Studies including patients with treated CNS metastases 
    Bev ATLAS, NSCLC 60 y, male 14 287 Present at baseline 286 343 Concomitant treatment at diagnosis of cerebral hemorrhage: NSAID 
Cause of death: progression of disease 

Abbreviations: AE, adverse event; BM, brain metastases; CTC, Common Toxicity Criteria; INR, international normalized ratio; NA, not available; NSAID, nonsteroidal anti-inflammatory drug; PE, pulmonary embolism; RCC, renal cell carcinoma.

Mortality rates in patients with CNS metastases were calculated from the date of randomization to death across the RCTs. The 30-, 60-, and 90-day mortality rates were 0%, 1%, and 3% in the bevacizumab group compared with 1%, 3%, and 5% in the control group, respectively (Fig. 1A). Mortality rate analyses were also conducted from the date of CNS metastasis diagnosis to death. The rates for 30-, 60-, and 90-day mortality were 16%, 33%, and 55% in the bevacizumab group compared with 19%, 31%, and 51% in the control group, respectively (Fig. 1B).

Fig. 1.

Mortality rates in the population of patients identified from the randomized controlled trials as having brain metastases. A, 30-, 60-, and 90-d mortality from time of randomization to death. B, 30-, 60-, and 90-d mortality from time of diagnosis of central nervous system metastasis to death.

Fig. 1.

Mortality rates in the population of patients identified from the randomized controlled trials as having brain metastases. A, 30-, 60-, and 90-d mortality from time of randomization to death. B, 30-, 60-, and 90-d mortality from time of diagnosis of central nervous system metastasis to death.

Close modal

Open-label single-arm safety studies

This analysis was based on the 4,382 patients in the safety populations of the two studies; 181 of 2,166 patients in SAiL (8.4%) and 140 of 2,216 in ATHENA (6.3%) developed CNS metastases (Table 2). The median time from first treatment to CNS metastasis diagnosis was 237 days [range, –6 (i.e., 6 days before treatment started) to 787 days] and 267 days (range, 1-662 days) in SAiL and ATHENA, respectively. In the 321 patients with CNS metastases, six were treated with bevacizumab after diagnosis of CNS metastasis, none of whom developed cerebral hemorrhage. The median time between the end of bevacizumab treatment and diagnosis of CNS metastasis was 61 days [range, −162 (i.e., diagnosis of CNS metastases was 162 days before the last dose of bevacizumab) to 448 days] and 83 days (range, −236 to 437 days) in SAiL and ATHENA, respectively.

A search through all reported adverse events identified three cases (0.9%) of cerebral hemorrhage up to 183 days after the last bevacizumab dose (Table 3) in the 321 patients with CNS metastases. Of the three patients from the SAiL trial, two developed a grade 1 cerebral hemorrhage 15 and 151 days after the last dose of bevacizumab, and the third had a grade 3 cerebral hemorrhage 8 days after the last bevacizumab dose while receiving concomitant anticoagulation therapy. The cause of death was progressive disease for two patients and unknown for one patient who died 131 days after the occurrence of cerebral hemorrhage (Table 4).

Prospective studies including patients with treated CNS metastases: ATLAS and PASSPORT

This analysis included 131 patients from these studies. The fully recruited PASSPORT phase II trial enrolled 115 patients with NSCLC and treated CNS metastases; 106 were evaluable for safety. In the ongoing ATLAS study, 26 of 730 enrolled patients (3.6%) had treated CNS metastases, of whom 25 were evaluable for safety (Table 2).

The median number of bevacizumab cycles was 5 in PASSPORT and 4 in ATLAS (range, 1-17 cycles for both). Median treatment duration was 85 days (range, 1-379 days) for PASSPORT and 70 days (range, 1-366 days) for ATLAS.

In the 131 safety-evaluable patients with treated CNS metastases, one patient (0.8%) from the ATLAS trial developed a grade 2 cerebral hemorrhage after disease progression (Table 3). The cause of death was progressive disease; the patient died 93 days after the occurrence of cerebral hemorrhage (Table 4).

This analysis addressed whether patients with CNS metastases are at increased risk of cerebral hemorrhage when treated with bevacizumab. The retrospective exploratory safety review of RCTs identified that 2.2% of patients had CNS metastases. The rate of cerebral hemorrhage in the bevacizumab-treated group was 3.3%, compared with 1.0% in the non-bevacizumab group. This difference in rates in the few patients with CNS metastases and cerebral hemorrhage does not seem disproportionately high. Mortality rates were similar between the bevacizumab and control arms.

In SAiL and ATHENA, 3 cases of cerebral hemorrhage in 321 patients (0.9%) with occult CNS metastases were reported, whereas in two prospective NSCLC trials including patients with treated CNS metastases, a single patient developed a grade 2 cerebral hemorrhage (0.8%). Consequently, there seemed to be no difference in the rate of cerebral hemorrhage in patients with treated and untreated CNS metastases. The reported incidences of cerebral hemorrhage in retrospective studies of patients with CNS metastases from peripheral tumors not exposed to bevacizumab range from 5% to 29% (3337). Comparing these background rates with those presented here, there is no apparent increased risk of cerebral hemorrhage in bevacizumab-treated patients with CNS metastases. A potential reason for the lower rates of cerebral hemorrhage in this analysis might be the selected patient population included in the trials (e.g., most had an ECOG performance status of 0 or 1), which potentially does not reflect the real-life cancer population with clinically symptomatic CNS metastases.

Several investigators have independently provided arguments for including patients with CNS metastases in clinical trials of VEGF inhibitors (17, 38). A database search of clinical trials examined the cerebral hemorrhage risk with anti-VEGF therapy, such as bevacizumab, sorafenib, and sunitinib, in the presence or absence of CNS metastases. Fifty-seven studies were identified, totaling 10,598 patients, and a low rate of <1% was reported for cerebral hemorrhage. Four trials specifically examined anti-VEGF therapy in patients with CNS metastases—each reported no cases of cerebral hemorrhage (38). The authors concluded that there was no evidence that anti-VEGF therapy confers an increased risk of cerebral hemorrhage, regardless of the presence of CNS metastases.

Recent case reports addressing treatment of CNS metastases with bevacizumab include four cases of patients with treated CNS metastases from breast cancer (39) and a treatment-naive patient with CNS metastases from colorectal cancer (40). None of these cases reported tumor-associated cerebral hemorrhage. Similarly, preliminary data of bevacizumab use in patients with CNS metastases from malignant melanoma do not suggest an increased risk of cerebral hemorrhage (41).

Data are available from bevacizumab trials in primary malignant brain tumors. Although these tumors are different from CNS metastases of primary tumors, highly vascularized high-grade malignant gliomas are interesting in this context, as any potential propensity of bevacizumab to precipitate cerebral hemorrhage might be evident in these patients. Bevacizumab, as a single agent and in combination with irinotecan, has been shown to be well tolerated and to induce significant responses in patients with recurrent malignant glioblastoma multiforme. In a phase II trial of bevacizumab alone and in combination with irinotecan that was done in 167 highly pretreated patients with recurrent glioblastoma multiforme, two patients in the bevacizumab arm (2.4%) experienced grade 1 cerebral hemorrhage, whereas three patients in the bevacizumab/irinotecan arm (3.8%) experienced grade 1, 2, and 4 cerebral hemorrhage (42). Another phase II trial using bevacizumab and irinotecan in 33 patients with recurrent malignant glioma reported one patient with cerebral hemorrhage, which occurred after the ninth cycle; the patient made a full recovery (19). A comparison of these data with retrospective data from patients with primary brain tumors, of whom 5% to 10% experienced cerebral hemorrhage without bevacizumab treatment, does not indicate an apparent increase in the risk of cerebral hemorrhage with bevacizumab (43).

The limitations of this analysis are self-evident: Retrospective exploratory analyses cannot serve as a replacement for prospective trials. Furthermore, this analysis compares selected patient populations across trials and indications with different pretreatments/treatments and follow-up times. Unreported or missing data might have biased results. Only a randomized prospective study for each tumor type could systematically address this question, and although such trials are difficult to conduct, an ongoing trial is evaluating the efficacy and safety of bevacizumab in NSCLC patients with untreated and asymptomatic CNS metastases (NCT00800202). Another limitation is that computed tomography scans were not routinely performed and therefore only symptomatic cerebral hemorrhages were identified.

Despite these limitations, the available data indicate that the risk of cerebral hemorrhage in bevacizumab-treated patients with CNS metastases does not seem disproportionately high compared with those who did not receive bevacizumab. Moreover, exclusion of patients with CNS metastases from bevacizumab treatment was based on a single patient with occult CNS metastasis from HCC, a cancer that has a high incidence of cerebral hemorrhage, independent of the treatment received. Consequently, patients with CNS metastases in advanced/metastatic breast cancer, NSCLC, and renal and colorectal cancer should not be generally excluded from bevacizumab therapy or from trials. For other indications, no data thus far exist regarding the effect of bevacizumab on patients with brain metastases and further studies are warranted. The findings presented in this article are limited to bevacizumab and cannot be extrapolated to other inhibitors of VEGF signaling.

In conclusion, in this selected patient population, patients with CNS metastases are at a similar risk of developing a cerebral hemorrhage, independent of bevacizumab therapy. Results from ongoing studies will provide further guidance regarding the use of bevacizumab in patients with brain metastases. Final results from the ATLAS study, which included patients with brain metastases, will be of particular interest. Treatment decisions should be driven by the benefit/risk assessment made by physicians for individual patients.

B. Besse received an honorarium in 2007 for speaking on behalf of Roche; U.-P. Rohr, S.F. Lasserre, and S. Augustus are employed by Roche; P. Compton and J. Huang are employed by Genentech.

We thank Martina Makrutzki (Roche) and Korinna Pilz (Roche) for reviewing patient files and identifying patients with brain metastases, Patricia Werner and Petra van Wetten for reviewing the manuscript, and Vanessa Gray-Schopfer, HPM (Geneva) SA, for providing part of the medical writing services.

Grant Support: Roche.

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

1
Ferrara
N
,
Gerber
HP
,
LeCouter
J
. 
The biology of VEGF and its receptors
.
Nat Med
2003
;
9
:
669
6
.
2
Ferrara
N
,
Hillan
KJ
,
Novotny
W
. 
Bevacizumab (Avastin), a humanized anti-VEGF monoclonal antibody for cancer therapy
.
Biochem Biophys Res Commun
2005
;
333
:
328
5
.
3
Rosen
LS
. 
VEGF-targeted therapy: therapeutic potential and recent advances
.
Oncologist
2005
;
10
:
382
91
.
4
Escudier
B
,
Pluzanska
A
,
Koralewski
P
, et al
. 
Bevacizumab plus interferon alfa-2a for treatment of metastatic renal cell carcinoma: a randomised, double-blind phase III trial
.
Lancet
2007
;
370
:
2103
11
.
5
Hurwitz
H
,
Fehrenbacher
L
,
Novotny
W
, et al
. 
Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer
.
N Engl J Med
2004
;
350
:
2335
42
.
6
Johnson
DH
,
Fehrenbacher
L
,
Novotny
WF
, et al
. 
Randomized phase II trial comparing bevacizumab plus carboplatin and paclitaxel with carboplatin and paclitaxel alone in previously untreated locally advanced or metastatic non-small-cell lung cancer
.
J Clin Oncol
2004
;
22
:
2184
91
.
7
Miller
K
,
Wang
M
,
Gralow
J
, et al
. 
Paclitaxel plus bevacizumab versus paclitaxel alone for metastatic breast cancer
.
N Engl J Med
2007
;
357
:
2666
76
.
8
Sandler
A
,
Gray
R
,
Perry
MC
, et al
. 
Paclitaxel-carboplatin alone or with bevacizumab for non-small-cell lung cancer
.
N Engl J Med
2006
;
355
:
2542
50
.
9
Gordon
MS
,
Margolin
K
,
Talpaz
M
, et al
. 
Phase I safety and pharmacokinetic study of recombinant human anti-vascular endothelial growth factor in patients with advanced cancer
.
J Clin Oncol
2001
;
19
:
843
50
.
10
Choi
HJ
,
Cho
BC
,
Sohn
JH
, et al
. 
Brain metastases from hepatocellular carcinoma: prognostic factors and outcome: brain metastasis from HCC
.
J Neurooncol
2009
;
91
:
307
13
.
11
Chang
L
,
Chen
YL
,
Kao
MC
. 
Intracranial metastasis of hepatocellular carcinoma: review of 45 cases
.
Surg Neurol
2004
;
62
:
172
7
.
12
Murakami
K
,
Nawano
S
,
Moriyama
N
, et al
. 
Intracranial metastases of hepatocellular carcinoma: CT and MRI
.
Neuroradiology
1996
;
38
Suppl 1
:
S31
5
.
13
Seinfeld
J
,
Wagner
AS
,
Kleinschmidt-DeMasters
BK
. 
Brain metastases from hepatocellular carcinoma in US patients
.
J Neurooncol
2006
;
76
:
93
8
.
14
Socinski
MA
,
Langer
CJ
,
Huang
JE
, et al
. 
Safety of bevacizumab in patients with non-small-cell lung cancer and brain metastases
.
J Clin Oncol
2009
;
27
:
5255
61
.
15
Archer
V
,
Reck
M
,
Sandler
AB
, et al
. 
Risk of symptomatic central nervous system (CNS) progression and secondary hemorrhage in patients with non-squamous non-small cell lung cancer (NSCLC) receiving bevacizumab (BV)-based first-line therapy
.
J Clin Oncol
2008
;
26
:
15s
.
abstr 8114
.
16
Morgensztern
D
,
Govindan
R
. 
Treatment of patients excluded from Eastern Cooperative Oncology Group 4599 and AVAiL studies: focus on brain metastasis and squamous histology
.
Clin Lung Cancer
2008
;
9
Suppl 2
:
S57
61
.
17
Oh
Y
,
Stewart
DJ
. 
Systemic therapy for lung cancer brain metastases: a rationale for clinical trials
.
Oncology (Williston Park)
2008
;
22
:
168
178
;
discussion 178, 183, 188 passim
.
18
Bokstein
F
,
Shpigel
S
,
Blumenthal
DT
. 
Treatment with bevacizumab and irinotecan for recurrent high-grade glial tumors
.
Cancer
2008
;
112
:
2267
73
.
19
Desjardins
A
,
Reardon
DA
,
Herndon
JE
 II
, et al
. 
Bevacizumab plus irinotecan in recurrent WHO grade 3 malignant gliomas
.
Clin Cancer Res
2008
;
14
:
7068
73
.
20
Lai
A
,
Filka
E
,
McGibbon
B
, et al
. 
Phase II pilot study of bevacizumab in combination with temozolomide and regional radiation therapy for up-front treatment of patients with newly diagnosed glioblastoma multiforme: interim analysis of safety and tolerability
.
Int J Radiat Oncol Biol Phys
2008
;
71
:
1372
80
.
21
Reck
M
,
von Pawel
J
,
Zatloukal
P
, et al
. 
Phase III trial of cisplatin plus gemcitabine with either placebo or bevacizumab as first-line therapy for nonsquamous non-small-cell lung cancer: AVAiL
.
J Clin Oncol
2009
;
27
:
1227
34
.
22
Van Cutsem
E
,
Vervenne
WL
,
Bennouna
J
, et al
. 
Phase III trial of bevacizumab in combination with gemcitabine and erlotinib in patients with metastatic pancreatic cancer
.
J Clin Oncol
2009
;
27
:
2231
7
.
23
Miles
D
,
Chan
A
,
Romieu
G
, et al
. 
Randomized, double-blind, placebo-controlled, phase III study of bevacizumab with docetaxel or docetaxel with placebo as first-line therapy for patients with locally recurrent or metastatic breast cancer (mBC): AVADO
.
J Clin Oncol
2008
;
26
:
15s
.
abstr LBA1011
.
24
Saltz
LB
,
Clarke
S
,
Díaz-Rubio
E
, et al
. 
Bevacizumab in combination with oxaliplatin-based chemotherapy as first-line therapy in metastatic colorectal cancer: a randomized phase III study
.
J Clin Oncol
2008
;
26
:
2013
9
.
25
Kabbinavar
FF
,
Schulz
J
,
McCleod
M
, et al
. 
Addition of bevacizumab to bolus fluorouracil and leucovorin in first-line metastatic colorectal cancer: results of a randomized phase II trial
.
J Clin Oncol
2005
;
23
:
3697
705
.
26
Kabbinavar
F
,
Hurwitz
HI
,
Fehrenbacher
L
, et al
. 
Phase II, randomized trial comparing bevacizumab plus fluorouracil (FU)/leucovorin (LV) with FU/LV alone in patients with metastatic colorectal cancer
.
J Clin Oncol
2003
;
21
:
60
5
.
27
Miller
KD
,
Chap
LI
,
Holmes
FA
, et al
. 
Randomized phase III trial of capecitabine compared with bevacizumab plus capecitabine in patients with previously treated metastatic breast cancer
.
J Clin Oncol
2005
;
23
:
792
9
.
28
Giantonio
BJ
,
Catalano
PJ
,
Meropol
NJ
, et al
,
for the Eastern Cooperative Oncology Group Study E3200
. 
Bevacizumab in combination with oxaliplatin, fluorouracil, and leucovorin (FOLFOX4) for previously treated metastatic colorectal cancer: results from the Eastern Cooperative Oncology Group Study E3200
.
J Clin Oncol
2007
;
25
:
1539
44
.
29
Dansin
E
,
Mezger
J
,
Isla
D
, et al
. 
Safety of bevacizumab-based therapy as first-line treatment of patients with advanced or recurrent non-squamous non-small cell lung cancer (NSCLC): MO19390 (SAiL)
.
J Clin Oncol
2008
;
26
:
15s
.
abstr 8085
.
30
Pierga
J
,
Pritchard
KI
,
Cortes-Funes
H
, et al
. 
MO19391: An open-label safety study of bevacizumab plus taxane-based therapy as first-line treatment of patients with locally recurrent (LR) or metastatic breast cancer (MBC)
.
J Clin Oncol
2008
;
26
:
15s
.
abstr 1140
.
31
Polikoff
J
,
Hainsworth
JD
,
Fehrenbacher
L
, et al
. 
Safety of bevacizumab (Bv) therapy in combination with chemotherapy in subjects with non-small cell lung cancer (NSCLC) treated on ATLAS
.
J Clin Oncol
2008
;
26
:
15s
.
abstr 8079
.
32
Yoo
H
,
Nam
BH
,
Yang
HS
,
Shin
SH
,
Lee
JS
,
Lee
SH
. 
Growth rates of metastatic brain tumors in nonsmall cell lung cancer
.
Cancer
2008
;
113
:
1043
7
.
33
Byrne
TN
,
Cascino
TL
,
Posner
JB
. 
Brain metastasis from melanoma
.
J Neurooncol
1983
;
1
:
313
7
.
34
Lieu
AS
,
Hwang
SL
,
Howng
SL
,
Chai
CY
. 
Brain tumors with hemorrhage
.
J Formos Med Assoc
1999
;
98
:
365
7
.
35
Maiuri
F
,
D'Andrea
F
,
Gallicchio
B
,
Carandente
M
. 
Intracranial hemorrhages in metastatic brain tumors
.
J Neurosurg Sci
1985
;
29
:
37
41
.
36
Mandybur
TI
. 
Intracranial hemorrhage caused by metastatic tumors
.
Neurology
1977
;
27
:
650
5
.
37
Mathieu
D
,
Kondziolka
D
,
Cooper
PB
, et al
. 
Gamma knife radiosurgery in the management of malignant melanoma brain metastases
.
Neurosurgery
2007
;
60
:
471
82
.
38
Carden
CP
,
Larkin
JM
,
Rosenthal
MA
. 
What is the risk of intracranial bleeding during anti-VEGF therapy?
Neuro Oncol
2008
;
10
:
624
30
.
39
Labidi
S
,
Bachelot
T
,
Ray Coquard
IL
, et al
. 
Bevacizumab and paclitaxel for breast cancer patients with central nervous system metastases: a case series
.
Clin Breast Cancer
2009
;
9
:
118
21
.
40
Bhaskara
A
,
Eng
C
. 
Bevacizumab in the treatment of a patient with metastatic colorectal carcinoma with brain metastases
.
Clin Colorectal Cancer
2008
;
7
:
65
8
.
41
Gonzalez-Cao
M
,
Viteri
S
,
Diaz-Lagares
A
, et al
. 
Preliminary results of the combination of bevacizumab and weekly paclitaxel in advanced melanoma
.
Oncology
2008
;
74
:
12
6
.
42
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
.
43
Nutt
SH
,
Patchell
RA
. 
Intracranial hemorrhage associated with primary and secondary tumors
.
Neurosurg Clin N Am
1992
;
3
:
591
9
.