Disease Markers
Volume 2015 (2015), Article ID 786790, 9 pages
http://dx.doi.org/10.1155/2015/786790

Review Article

VEGF Overexpression Is a Valuable Prognostic Factor for Non-Hodgkin’s Lymphoma Evidence from a Systemic Meta-Analysis

Jing Yang,¹ Wenlu Li,² Xin He,¹ Guofei Zhang,³ Lan Yue,⁴ and Ying Chai³

¹Department of Hematology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, China
²College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China
³Department of Thoracic Surgery, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, China
⁴Department of Endocrinology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, China

Received 21 September 2014; Revised 25 January 2015; Accepted 26 January 2015

Academic Editor: Giuseppe Murdaca

Copyright © 2015 Jing Yang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Vascular endothelial growth factor (VEGF) plays a vital role in the progression of Non-Hodgkin’s lymphoma (NHL). Although multiple studies have investigated the relationship between VEGF expression and prognosis of NHL, these studies have yielded conflicting results. Therefore, we performed a meta-analysis to evaluate the role of VEGF in the prognosis of NHL patients. We systematically searched eligible studies from databases and determined that there was a significant correlation between VEGF overexpression and overall survival (HR (hazard ratio) = 1.66, 95% CI: 1.25–2.22, ). Based on subgroup analysis by study location, number of patients, the source of VEGF expression, and study design, we found that VEGF overexpression in surgically resected tissue (HR = 1.95, 95% CI: 1.41–2.69, ), but not in serum (HR = 1.37, 95% CI: 0.96–1.95, ), was associated with poorer prognosis. Additionally, VEGF overexpression did not correlate with performance status, LDH level, IPI score, tumor staging, B symptoms, or NHL relapse. In summary, overexpression of VEGF in lymphoma tissue represents a promising potential prognostic factor in NHL.

1. Introduction

Non-Hodgkin’s lymphoma (NHL) is a highly heterogeneous group of lymphoproliferative malignancies arising from either lymphocytes or natural killer (NK) cells. Based on 2013 estimates from the American Cancer Society, NHL is the fifth most common human malignancy and the sixth highest cause of cancer-related deaths worldwide [1]. Currently, prognostic factors based on clinicopathological characteristics, including Ann Arbor staging and the international prognostic index (IPI), have been widely used in predicting survival of NHL patients [2, 3]. However, patients of similar tumor status and who undergo similar treatments often experience distinct prognoses. Thus, it is urgently necessary to identify individualized biological markers to more accurately predict patient outcomes so as to improve targeted therapies.

Angiogenesis is a crucial process in the growth, development, and metastasis of many tumor types, including NHL [4, 5]. Vascular endothelial growth factor (VEGF) is a prime determinant and regulator of angiogenesis, vasculogenesis, and vascular permeability [6]. VEGF family members, including VEGFA, VEGFB, VEGFC, and VEGFD, are secreted by autocrine stimulation of tumor cells as well as through paracrine influences of the proangiogenic tumour microenvironment [7, 8]. Therefore, VEGF is expected to be a useful biomarker in NHL that is associated with worse prognosis. However, the prognostic and predictive value of VEGF in NHL remains controversial due to the heterogeneity of diseases, different classifications, and methods of analysis (immunohistochemistry, enzyme-linked immunosorbent assay, etc.). Thus, it is necessary to make informed conclusions about the association between VEGF overexpression and prognosis of NHL.

In this study, we performed a meta-analysis to investigate the relationship between VEGF expression and the prognosis of NHL patients to determine whether increased VEGF expression is associated with poor clinical outcome and clinicopathologic characteristics of NHL.

2. Methods

2.1. Literature Search

We performed a systematic electronic search in PubMed and Web of Science databases using the following terms: “VEGF” and “vascular endothelial growth factor,” “Non-Hodgkin’s lymphoma,” “NHL,” “prognosis,” and all possible combinations. For studies containing overlapping patients, we chose the study with the largest number of events to avoid information duplication. We also searched the references of all studies to obtain additional eligible studies.

2.2. Literature Selection Criteria

The inclusion criteria in the meta-analysis were as follows: (1) to provide the histologic diagnosis of NHL; (2) to include the patients untreated; (3) to investigate the relationship between VEGF expression (in serum or surgical tissue) and clinicopathological features or prognosis of NHL; (4) to measure the expression of VEGF via immunohistochemistry (IHC) or enzyme-linked immunosorbent assay (ELISA); (5) to be published in the English language. Articles published in the form of letters, case reports, reviews, and conference abstracts were excluded.

2.3. Data Extraction and Assessment of Study Quality

Two primary investigators (Lan Yue and Wenlu Li) independently reviewed and extracted data from eligible studies; any disagreements were resolved via further review by a third investigator (Ying Chai) until a consensus was reached. The data extracted from each study included first author, publication year, country of origin, total number of patients analyzed (VEGF positive and negative), method of VEGF detection, VEGF cut-off value, source of VEGF, treatment regimen, study design, and clinicopathological and survival data. The quality of each eligible study was assessed using the Newcastle–Ottawa quality assessment scale [9].

2.4. Statistical Analysis

For the pooled analysis of the relationship between VEGF expression and OS, HRs and their 95% CIs (confidence interval) were aggregated to acquire the effective value. Raw data were used if HRs and their 95% CIs were explicitly described in the article. Otherwise, Kaplan-Meier curves of OS were analyzed using Engauge Digitizer version 4.1 (http://digitizer.sourceforge.net/), and the log-rank statistic and number of events were also used to calculate HRs with 95% CIs according to the methods described by Parmar et al. [10]. ORs and their 95% CIs were combined to evaluate the relationship between VEGF expression and clinicopathological characteristics, including performance status (PS), IPI score, stage, B symptoms, LDH levels, and relapse. An observed HR > 1 indicated that patients with VEGF overexpression had worse OS, whereas an observed OR < 1 implied that patients with VEGF overexpression will be more inclined to have unfavorable clinicopathological features. The impact of positive VEGF expression on survival or clinicopathological factors was considered to be statistically significant if the 95% CI did not exceed 1.

Heterogeneity of individual HRs and ORs was assessed using the Chi-square test according to Peto’s method [11]. The inconsistency index statistic (ranging from 0% to 100%) was used to quantify the proportion of the total variation, which is due to interstudy heterogeneity rather than sampling error [12]. A for the -test indicated the existence of heterogeneity among the studies. The pooled ORs and HRs were then calculated by the random-effects model [12]; otherwise, the fixed-effects model was adopted [13]. Begg’s test was used to detect possible publication bias and a value of <0.05 in Begg’s test indicated the existence of publication bias. All calculations were performed using STATA version 12.0 software (Stata Corporation, Collage Station, Texas, USA) and a value < 0.05 was considered statistically significant.

3. Results

3.1. Description of Studies

A total of 143 potentially relevant studies were retrieved by the search strategy described in Figure 1. After scrutinizing the abstracts and full text of these studies, 16 eligible studies were ultimately included in this meta-analysis [5, 14–28]. These studies were published between 2000 and 2013 and included a total of 1518 enrolled patients. Six studies were prospective and 10 were retrospective. Three studies were performed in Turkey, 3 studies in the United States, and 2 studies in Finland. Seven studies tested VEGF level in serum by ELISA, while 9 studies detected VEGF expression in surgical tissue by IHC. According to the disease subtype of NHL, DLBCL was studied in 5 studies, follicular lymphoma (FL) was evaluated in 2 studies, and peripheral T-cell lymphoma (PTL) was studied in 1 study; all others were NHL, including various subtypes such as DLBCL and FL, among others. Of the 16 eligible studies, 13 provided the HR of OS directly or indirectly. We summarized the characteristics of the 16 studies in Table 1.

Table 1: Characteristics of studies included for the meta-analysis.

First author
Year
Country
Patient (P/N)
VEGF source
Method
Disease type
Method to determine the threshold
VEGF positive threshold
HR (95% CI) of OS
Therapy regimen
Quality score
Study type

Riihijärvi [16]
2012
Finland
102 (25/77)
Serum
ELISA
DLBCL
Highest quartile
947 pg/mL
1.096 (0.435–2.762)
R-CHOEP + methotrexate, cytarabine
9
P

Bortolin [15]
2012
Italy
68 (33/35)
Serum
ELISA
NHL
Median value
250 pg/mL
1.21 (0.51–2.89)
ACVBP/CHOP/CHOP like + partial rituximab
6
P

Rujirojindakul [14]
2012
Thailand
79 (NA)
Serum
ELISA
NHL
Median value
516 pg/mL
0.99 (0.51–1.9)
CHOP/R-CHOP
7
P

Labidi [17]
2010
France
60 (NA)
Serum
ELISA
FL
Median value
138 pg/mL
1.002 (0.999–1.005)
CHOP like
5
R

Bono [18]
2003
Finland
143 (46/97)
Serum
ELISA
NHL
Highest tertile
465 pg/mL
1.28 (0.75–2.16)
CHOP/CHOP like
6
P

Niitsu [19]
2002
Japan
149 (73/76)
Serum
ELISA
NHL
Median value
242 pg/mL
8.71 (2.57–29.53)
CHOP/CHOP like
8
P

Salven [20]
2000
America
200 (50/150)
Serum
ELISA
NHL
Highest quartile
462 pg/mL
1.83 (1.1–3.02)
Bleo-CHOP/M-BACOD
6
R

Kim [21]
2011
Korea
51 (30/21)
Surgical tissue
IHC
DLBCL
Percentage of positive cells
Any staining
1.329 (0.695–2.541)
Methotrexate-based chemotherapy + WBRT
6
R

Zhang [22]
2011
China
38 (31/7)
Surgical tissue
IHC
PTL
Intensity score and percentage of positive cells score
Multiplying the intensity core by expressions core >2
7.633 (1.634–35.714)
CHOP/CHOP like
9
P

Paydas [23]
2009
Turkey
177 (108/69)
Surgical tissue
IHC
NHL
Percentage of positive cells
10%
1.578 (1.03–2.418)
Anthracycline containing regimens
7
R

Citak [24]
2008
Turkey
25 (10/15)
Surgical tissue
IHC
NHL
Percentage of positive cells
Any staining
NA
BFM, LMT regimens
7
R

Gratzinger [25]
2008
America
172 (75/97)
Surgical tissue
IHC
DLBCL
Percentage of positive cells
30%
NA
CHOP/CHOP like
8
R

Pazgal [26]
2007
Israel
36 (21/15)
Surgical tissue
IHC
DLBCL
Percentage of positive cells
30%
2.579 (1.007–6.606)
CHOP/CHOP like
6
R

Ganjoo [27]
2008
America
44 (22/22)
Surgical tissue
IHC
DLBCL
Percentage of positive cells
10%
3.421 (0.941–12.447)
CHOP
5
R

Jørgensen [5]
2007
Denmark
103 (64/49)
Surgical tissue
IHC
FL
Staining pattern
Diffuse pattern
2.682 (1.533–4.693)
CHOP like + radiotherapy
7
R

Hazar [28]
2003
Turkey
71 (24/47)
Surgical tissue
IHC
NHL
Percentage of positive cells
Any staining
1.391 (0.745–2.597)
Na
4
R

P/N, the number of positive/negative VEGF expression; VEGF, vascular endothelial growth factor; IHC, immunohistochemistry; ELISA, enzyme linked immunosorbent assay; DLBCL, diffuse large B-cell lymphoma; NHL, Non-Hodgkin lymphoma; FL, follicular lymphoma; NA, not available; HR, hazard ratio; 95% CI, 95% confidence interval; OS, overall survival; P, prospective; R, retrospective.

R-CHOEP, rituximab, cyclophosphamide, doxorubicin, vincristine, etoposide, and prednisone; ACVBP, doxorubicin, cyclophosphamide, vindesine, bleomycin, and prednisone; CHOP, cyclophosphamide, doxorubicin, vincristine, and prednisone; M-BACOD, methotrexate, bleomycin, doxorubicin, cyclophosphamide, vincristine, and dexamethasone; WBRT, whole brain radiation therapy.

Figure 1: Flow diagram of studies selection procedure.

3.2. Methodological Quality of the Studies

The quality of 16 eligible studies included in our meta-analysis was assessed according to the Newcastle-Ottawa Scale (NOS), which is widely used to evaluate the quality of case-control and cohort studies. NOS scores were calculated based on three criteria: selection, comparability, and exposure or outcome. Higher scores signified higher study quality. NOS scores of the 16 eligible studies ranged from 3 to 9. Thirteen studies received a score of greater than 5, which was indicative of a high quality study (Table 1).

3.3. Impact of VEGF Overexpression on OS of NHL

A total of 14 studies in this meta-analysis assessed the impact of VEGF overexpression on OS of NHL. The pooled HR was 1.66 (95% CI: 1.25–2.22) (Figure 2), indicating that VEGF overexpression served as an indicator of poor OS. We also performed subgroup analysis according to study location, number of patients, source of VEGF, and study design. In the subgroup of serum-derived VEGF, the combined HR was 1.37 (95% CI: 0.96–1.95) which did not reach statistical significance () (Table 2, Figure 3), while the combined HR of 1.95 (95% CI: 1.41–2.69) in the subgroup of surgical tissue-derived VEGF was statistically significant () (Table 2, Figure 3). Subgroup analysis on other factors including study location, number of patients, and NOS score did not alter the significance of the prognostic impact of VEGF overexpression.

Table 2: Stratified analysis of pooled hazard ratios of NHL patients with VEGF overexpression.

Stratified analysis
Number of studies
Number of patients
Pooled HR (95% CI)
value
Heterogeneity
Interaction value

(%)
value

Study location

0.512

    Asia
7
798
1.9 (1.21–2.97)
0.005
59.6
0.021

    Europe and America
7
720
1.5 (1.03–2.18)
0.034
72.6
0.001

Number of patients

0.311

    >100
6
874
1.88 (1.29–2.75)
0.001
56.3
0.043

    <100
8
644
1.42 (1-2)
0.047
56.2
0.025

Source of VEGF

0.165

    Serum
7
801
1.37 (0.96–1.95)
0.087
67.7
0.005

    Surgical tissue
7
717
1.95 (1.41–2.69)
0
30.4
0.196

NOS score

0.288

    >5
11
1343
1.75 (1.3–2.36)
0
49.3
0.032

    ≦5
3
175
1.27 (0.78–2.06)
0.333
55.9
0.104

Figure 2: Forrest plot of Hazard ratio (HR) for the association of VEGF overexpression with overall survival (OS). HR > 1 implied worse survival for the group with VEGF overexpression.

Figure 3: Forrest plot of Hazard ratio (HR) for the association of VEGF overexpression with overall survival (OS) according to the source of VEGF expression. Subgroup analysis showed that a significant relation between VEGF overexpression and OS was exhibited in surgical tissue.

3.4. Correlation of VEGF Overexpression with Clinicopathological Parameters of NHL

Four studies investigated the correlation between VEGF overexpression and performance status, LDH level, and IPI score, with pooled ORs of 0.843 (95% CI: 0.39–1.882), 0.981 (95% CI: 0.636–1.51), and 0.452 (95% CI: 0.147–1.389), respectively (Table 3). The associations between VEGF overexpression and tumor staging and B symptoms were also not significant, with aggregated ORs of 0.756 (95% CI: 0.363–1.574) and 0.961 (95% CI: 0.649–1.422) (Table 3). Additionally, we also evaluated the correlation between VEGF overexpression and relapse, in which the combined OR was 0.736 (95% CI: 0.362–1.5) (Table 3). Taken together, there was no significant association between VEGF overexpression and clinicopathological features of NHL.

Table 3: VEGF overexpression and clinicopathological features of NHL.

Clinicopathological features
Number of studies
Number of patients
Analytical model
Pooled OR (95% CI)
value
Heterogeneity

(%)
value

Performance status (ECOG)
(0-1 versus ⩾ 2)
4
502
REM
0.84 (0.39–1.88)
0.64
67.8
0.025

LDH level
(normal versus elevated)
4
502
FEM
0.98 (0.64–1.51)
0.93
5
0.37

IPI score
(0–2 versus 3–5)
4
383
REM
0.45 (0.15–1.39)
0.17
78.3
0.003

Tumor staging
(I II versus III IV)
5
483
REM
0.76 (0.36–1.57)
0.45
62.4
0.03

B symptom
(absent versus present)
5
547
FEM
0.96 (0.65–1.42)
0.84
0
0.61

Relapse
(no versus yes)
3
253
FEM
0.74 (0.36–1.5)
0.4
0
0.72

3.5. Publication Bias

The value of Begg’s test for VEGF overexpression on OS and clinicopathological features of NHL was 0.477, greater than 0.05, indicating the absence of publication bias in these studies (Figure 4).

Figure 4: Begg’s publication bias plot. The value for Begg’s tests is 0.477. It implies publication bias is absent for studies regarding the association of VEGF overexpression with overall survival (OS) in the meta-analysis. Each point represents a separate study for the indicated association.

4. Discussion

VEGF plays a crucial role in the progression of numerous tumor types, including hematopoietic malignancies [29–31]. First, VEGF can stimulate angiogenesis and lymphangiogenesis and increase vascular permeability, which is associated with reduced drug delivery and tumor cell metastasis [14, 32]. Second, VEGF induces activation of antiapoptotic genes, including bcl-2, which protect tumor cells from apoptosis [33]. Third, VEGF works in concert with numerous signaling molecules such as angiopoietins, ephrins, hepatocyte growth factor, hypoxia-inducible factor, IL-6, and endostatin to promote tumor cell survival [34–38]. Third, VEGF impacts hematopoiesis by blocking the differentiation of multiple hematopoietic lineages and inhibits the maturation of dendritic cells by reducing NF-κB activation [32, 39, 40]. It has been also reported that VEGF overexpression is an indicator of poor prognosis in breast carcinoma, lung cancer, and hematopoietic malignancies [41–43]; however, the correlation between VEGF expression in NHL and patient prognosis remains unclear. Thus, we performed a quantitative meta-analysis to determine the association between VEGF expression and the prognosis of NHL.

Our meta-analysis revealed that VEGF overexpression was significantly associated with poorer prognosis of NHL (HR = 1.66, 95% CI: 1.25–2.22, ), but not with clinicopathological features of NHL, such as performance status (OR = 0.843, 95% CI: 0.39–1.882, ), LDH level (OR = 0.981, 95% CI: 0.636–1.51, ), IPI score (OR = 0.452, 95% CI: 0.147–1.389, ), tumor staging (OR = 0.756, 95% CI: 0.363–1.574, ), B symptoms (OR = 0.961, 95% CI: 0.649–1.422, ), or relapse (OR = 0.736, 95% CI: 0.362–1.5, ). The results of our study were in accordance with those of scholars Zhang et al., which even identified VEGF overexpression as an independent prognostic factor through multivariate survival analysis [22]. These results provide rationale to support efforts targeting VEGF in NHL. Bevacizumab is the most effective monoclonal antibody to therapeutically target VEGF [44]. In a phase II trial, 11 of 45 patients with relapsed and aggressive NHL exhibited prolonged stable disease and median time of response after a single treatment with bevacizumab [45]. Furthermore, bevacizumab combined with conventional chemotherapeutics was also shown to be safe and effective in newly diagnosed diffuse large B cell lymphomas [46]. Subgroup analysis further showed that VEGF overexpression in surgical tissue (HR = 1.95, 95% CI: 1.41–2.69, ) but not in serum (HR = 1.37, 95% CI: 0.96–1.95, ) negatively correlated with OS of NHL. It is likely that the VEGF derived from lymphoma tissue only accounts for a minor extent in the serum [16]. In addition, serum VEGF levels in patients with different extents of disease are highly variable, making it difficult to obtain a single cut-off value as a predictor in all NHL patients [14]. Additional clinical trials are warranted to further verify the relationship between the serum VEGF levels in patients with varying degrees of disease in NHL.

We acknowledge several limitations exist in our study. Firstly, there was significant heterogeneity among the 16 studies included in this meta-analysis. Although the random-effects model was used to reduce the influence of heterogeneity, the model did not identify the source of heterogeneity. In order to clarify the source of heterogeneity, differences in study location, number of patients, source of VEGF, and NOS score were analyzed. When the analysis of OS was performed without consideration of these factors, heterogeneity was detected ( 74.3% ); however, when the analysis was limited to studies of surgical tissue, no heterogeneity was found ( 30.4% ). When the analysis of OS was limited to studies of serum VEGF levels, heterogeneity still existed ( 66.7% ), suggesting that the source of VEGF contributes to heterogeneity in our results. In addition, selection bias may be caused by exclusion of non-English articles. Furthermore, although various methods had been used to acquire the primary data we needed, the OS of three studies was still absent; it would inevitably result in evaluability bias. Additionally, univariate prognostic value was included in our analysis due to the limited data provided. Finally, the reliability of the results of prospective cohort studies or retrospective case-control studies selected in our study is lower than that of prospective randomized trials.

In conclusion, this meta-analysis is the first to explore the correlation between VEGF overexpression and survival and clinicopathological features of patients with NHL. VEGF overexpression in surgical tissue rather than in serum significantly correlated with worse overall survival in NHL whereas there was no relationship between VEGF overexpression and clinicopathological characteristics of NHL. Consequently, identify the expression of VEGF in surgical tissue instead of serum may be beneficial for patients before their target therapy. Further adequately designed prospective studies, however, are still necessary to strengthen the results presented here.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Authors’ Contribution

Jing Yang and Wenlu Li contributed equally to this work.

Acknowledgments

This work was supported by the Natural Science Foundation of Zhejiang province (LY13H160016) and Key Projects of Zhejiang Province Science and Technology Plan (2013C03044-7).

References

R. Siegel, D. Naishadham, and A. Jemal, “Cancer statistics, 2013,” CA: Cancer Journal for Clinicians, vol. 63, no. 1, pp. 11–30, 2013.

“A predictive model for aggressive non-Hodgkin's lymphoma. The international Non-Hodgkin's Lymphoma Prognostic Factors Project,” New England Journal of Medicine, vol. 329, no. 14, pp. 987–994, 1993.

T. Sattar, L. K. Griffeth, H. R. Latifi, J. Glass, R. Munker, and D. L. Lilien, “PET imaging today: contribution to the initial staging and prognosis of patients with non-Hodgkin's lymphomas,” The Journal of the Louisiana State Medical Society, vol. 158, no. 4, pp. 193–201, 2006.

D. Hanahan and R. A. Weinberg, “Hallmarks of cancer: the next generation,” Cell, vol. 144, no. 5, pp. 646–674, 2011.

J. M. Jørgensen, F. B. Sørensen, K. Bendix et al., “Angiogenesis in non-Hodgkin's lymphoma: clinico-pathological correlations and prognostic significance in specific subtypes,” Leukemia & Lymphoma, vol. 48, no. 3, pp. 584–595, 2007.

C. K. Poh, Z. Shi, T. Y. Lim, K. G. Neoh, and W. Wang, “The effect of VEGF functionalization of titanium on endothelial cells in vitro,” Biomaterials, vol. 31, no. 7, pp. 1578–1585, 2010.

Q. T. Ho and C. J. Kuo, “Vascular endothelial growth factor: biology and therapeutic applications,” International Journal of Biochemistry and Cell Biology, vol. 39, no. 7-8, pp. 1349–1357, 2007.

D. Ribatti, A. Vacca, B. Nico, M. Fanelli, L. Roncali, and F. Dammacco, “Angiogenesis spectrum in the stroma of B-cell non-Hodgkin's lymphomas. An immunohistochemical and ultrastructural study,” European Journal of Haematology, vol. 56, no. 1-2, pp. 45–53, 1996.

A. Stang, “Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses,” European Journal of Epidemiology, vol. 25, no. 9, pp. 603–605, 2010.

M. K. B. Parmar, V. Torri, and L. Stewart, “Extracting summary statistics to perform meta-analyses of the published literature for survival endpoints,” Statistics in Medicine, vol. 17, no. 24, pp. 2815–2834, 1998.

S. Yusuf, R. Peto, and J. Lewis, “Beta blockade during and after myocardial infarction: an overview of the randomized trials,” Progress in Cardiovascular Diseases, vol. 27, no. 5, pp. 335–371, 1985.

J. P. T. Higgins, S. G. Thompson, J. J. Deeks, and D. G. Altman, “Measuring inconsistency in meta-analyses,” British Medical Journal, vol. 327, no. 7414, pp. 557–560, 2003.

N. Mantel and W. Haenszel, “Statistical aspects of the analysis of data from retrospective studies of disease,” Journal of the National Cancer Institute, vol. 22, no. 4, pp. 719–748, 1959.

P. Rujirojindakul and A. Lekhakula, “Prognostic significance of serum proangiogenic molecules in patients with de novo non-hodgkin lymphomas,” The Scientific World Journal, vol. 2012, Article ID 215231, 5 pages, 2012.

M. T. Bortolin, R. Tedeschi, E. Bidoli et al., “Multiplex analysis of blood cytokines as a prognostic tool in HIV related non-Hodgkin lymphoma patients: a potential role of interleukin-7,” Cytokine, vol. 60, no. 1, pp. 90–95, 2012.

S. Riihijärvi, H. Nurmi, H. Holte et al., “High serum vascular endothelial growth factor level is an adverse prognostic factor for high-risk diffuse large B-cell lymphoma patients treated with dose-dense chemoimmunotherapy,” European Journal of Haematology, vol. 89, no. 5, pp. 395–402, 2012.

S. I. Labidi, C. Ménétrier-Caux, S. Chabaud et al., “Serum cytokines in follicular lymphoma. Correlation of TGF-beta and VEGF with survival,” Annals of Hematology, vol. 89, no. 1, pp. 25–33, 2010.

P. Bono, L. Teerenhovi, and H. Joensuu, “Elevated serum endostatin is associated with poor outcome in patients with non-Hodgkin lymphoma,” Cancer, vol. 97, no. 11, pp. 2767–2775, 2003.

N. Niitsu, M. Okamoto, H. Nakamine et al., “Simultaneous elevation of the serum concentrations of vascular endothelial growth factor and interleukin-6 as independent predictors of prognosis in aggressive non-Hodgkin's lymphoma,” European Journal of Haematology, vol. 68, no. 2, pp. 91–100, 2002.

P. Salven, A. Orpana, L. Teerenhovi, and H. Joensuu, “Simultaneous elevation in the serum concentrations of the angiogenic growth factors VEGF and bFGF is an independent predictor of poor prognosis in non-Hodgkin lymphoma: a single-institution study of 200 patients,” Blood, vol. 96, no. 12, pp. 3712–3718, 2000.

J. A. Kim, S. J. Kim, I.-G. Do et al., “Hypoxia-associated protein expression in primary central nervous system diffuse large B-cell lymphoma: does it predict prognosis?” Leukemia and Lymphoma, vol. 52, no. 2, pp. 205–213, 2011.

W. Zhang, L. Wang, D. Zhou, Q. Cui, D. Zhao, and Y. Wu, “Expression of tumor-associated macrophages and vascular endothelial growth factor correlates with poor prognosis of peripheral T-cell lymphoma, not otherwise specified,” Leukemia and Lymphoma, vol. 52, no. 1, pp. 46–52, 2011.

S. Paydas, G. Seydaoglu, M. Ergin, S. Erdogan, and S. Yavuz, “The prognostic significance of VEGF-C and VEGF-A in non-Hodgkin lymphomas,” Leukemia and Lymphoma, vol. 50, no. 3, pp. 366–373, 2009.

E. C. Citak, A. Oguz, C. Karadeniz, and N. Akyurek, “Role of gelatinases (MMP-2 and MMP-9), TIMP-1, vascular endothelial growth factor (VEGF), and microvessel density on the clinicopathological behavior of childhood non-Hodgkin lymphoma,” Pediatric Hematology and Oncology, vol. 25, no. 1, pp. 55–66, 2008.

D. Gratzinger, S. Zhao, R. J. Tibshirani et al., “Prognostic significance of VEGF, VEGF receptors, and microvessel density in diffuse large B cell lymphoma treated with anthracycline-based chemotherapy,” Laboratory Investigation, vol. 88, no. 1, pp. 38–47, 2008.

I. Pazgal, O. Boycov, O. Shpilberg, E. Okon, and O. Bairey, “Expression of VEGF-C, VEGF-D and their receptor VEGFR-3 in diffuse large B-cell lymphomas,” Leukemia and Lymphoma, vol. 48, no. 11, pp. 2213–2220, 2007.

K. N. Ganjoo, A. M. Moore, A. Orazi, J. A. Sen, C. S. Johnson, and C. S. An, “The importance of angiogenesis markers in the outcome of patients with diffuse large B cell lymphoma: a retrospective study of 97 patients,” Journal of Cancer Research and Clinical Oncology, vol. 134, no. 3, pp. 381–387, 2008.

B. Hazar, S. Paydas, S. Zorludemir, B. Sahin, and I. Tuncer, “Prognostic significance of microvessel density and vascular endothelial growth factor (VEGF) expression in non-Hodgkin's lymphoma,” Leukemia and Lymphoma, vol. 44, no. 12, pp. 2089–2093, 2003.

A. R. Perez-Atayde, S. E. Sallan, U. Tedrow, S. Connors, E. Allred, and J. Folkman, “Spectrum of tumor angiogenesis in the bone marrow of children with acute lymphoblastic leukemia,” The American Journal of Pathology, vol. 150, no. 3, pp. 815–821, 1997.

G. Pruneri, F. Bertolini, D. Soligo et al., “Angiogenesis in myelodysplastic syndromes,” British Journal of Cancer, vol. 81, no. 8, pp. 1398–1401, 1999.

A. Vacca, D. Ribatti, M. Presta et al., “Bone marrow neovascularization, plasma cell angiogenic potential, and matrix metalloproteinase-2 secretion parallel progression of human multiple myeloma,” Blood, vol. 93, no. 9, pp. 3064–3073, 1999.

P. Carmeliet, V. Ferreira, G. Breier et al., “Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele,” Nature, vol. 380, no. 6573, pp. 435–439, 1996.

M. D. Jacobson, J. F. Burne, M. P. King, T. Miyashita, J. C. Reed, and M. C. Raff, “Bcl-2 blocks apoptosis in cells lacking mitochondrial DNA,” Nature, vol. 361, no. 6410, pp. 365–369, 1993.

A. Hajitou, C. Grignet, L. Devy et al., “The antitumoral effect of endostatin and angiostatin is associated with a down-regulation of vascular endothelial growth factor expression in tumor cells,” The FASEB Journal, vol. 16, no. 13, pp. 1802–1804, 2002.

D. Feliers, K. Woodruff, and S. Abboud, “Potential role of insulin-like growth factor binding protein-4 in the uncoupling of bone turnover in multiple myeloma,” British Journal of Haematology, vol. 104, no. 4, pp. 715–722, 1999.

D. Shweiki, A. Itin, D. Soffer, and E. Keshet, “Vascular endothelial growth factor induced by hypoxia may mediate hypoxia-initiated angiogenesis,” Nature, vol. 359, no. 6398, pp. 843–845, 1992.

G. D. Yancopoulos, S. Davis, N. W. Gale, J. S. Rudge, S. J. Wiegand, and J. Holash, “Vascular-specific growth factors and blood vessel formation,” Nature, vol. 407, no. 6801, pp. 242–248, 2000.

W. G. Jiang, T. A. Martin, C. Parr, G. Davies, K. Matsumoto, and T. Nakamura, “Hepatocyte growth factor, its receptor, and their potential value in cancer therapies,” Critical Reviews in Oncology/Hematology, vol. 53, no. 1, pp. 35–69, 2005.

H.-P. Gerber, A. K. Malik, G. P. Solar et al., “VEGF regulates haematopoietic stem cell survival by an internal autocrine loop mechanism,” Nature, vol. 417, no. 6892, pp. 954–958, 2002.

D. I. Gabrilovich, H. L. Chen, K. R. Girgis et al., “Production of vascular endothelial growth factor by human tumors inhibits the functional maturation of dendritic cells,” Nature Medicine, vol. 2, no. 10, pp. 1096–1103, 1996.

B. Linderholm, K. Grankvist, N. Wilking, M. Johansson, B. Tavelin, and R. Henriksson, “Correlation of vascular endothelial growth factor content with recurrences, survival, and first relapse site in primary node-positive breast carcinoma after adjuvant treatment,” Journal of Clinical Oncology, vol. 18, no. 7, pp. 1423–1431, 2000.

A. Yuan, C.-J. Yu, W.-J. Chen et al., “Correlation of total VEGF mRNA and protein expression with histologic type, tumor angiogenesis, patient survival and timing of relapse in non-small-cell lung cancer,” International Journal of Cancer, vol. 89, no. 6, pp. 475–483, 2000.

P. Salven, L. Teerenhovi, and H. Joensuu, “A high pretreatment serum vascular endothelial growth factor concentration is associated with poor outcome in non-Hodgkin's lymphoma,” Blood, vol. 90, no. 8, pp. 3167–3172, 1997.

N. Ferrara, K. J. Hillan, H.-P. Gerber, and W. Novotny, “Discovery and development of bevacizumab, an anti-VEGF antibody for treating cancer,” Nature Reviews Drug Discovery, vol. 3, no. 5, pp. 391–400, 2004.

A. T. Stopeck, J. M. Unger, L. M. Rimsza et al., “A phase II trial of single agent bevacizumab in patients with relapsed, aggressive non-Hodgkin lymphoma: Southwest oncology group study S0108,” Leukemia and Lymphoma, vol. 50, no. 5, pp. 728–735, 2009.

K. N. Ganjoo, C. S. An, M. J. Robertson et al., “Rituximab, bevacizumab and CHOP (RA-CHOP) in untreated diffuse large B-cell lymphoma: safety, biomarker and pharmacokinetic analysis,” Leukemia and Lymphoma, vol. 47, no. 6, pp. 998–1005, 2006.