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Carbonic anhydrase 9 is a predictive marker of survival benefit from lower dose of bevacizumab in patients with previously treated metastatic colorectal cancer
- Yong Sang Hong†1,
- Hyeon Jin Cho†1, 2,
- Sun Young Kim1,
- Kyung Hae Jung1,
- Ji Won Park1,
- Hyo Seong Choi1,
- Jae Hwan Oh1,
- Byung Chang Kim1,
- Dae Kyung Sohn1,
- Dae Yong Kim1 and
- Hee Jin Chang1Email author
© Hong et al; licensee BioMed Central Ltd. 2009
Received: 17 March 2009
Accepted: 21 July 2009
Published: 21 July 2009
Carbonic anhydrase 9 (CA9) is a marker for hypoxia and acidosis, which is linked to a poor prognosis in human tumors. The purpose of this comparative analysis was to evaluate whether CA9 and VEGF expression are associated with survival outcomes in patients with metastatic colorectal cancer (mCRC) after treatment with bevacizumab as second or later line treatment.
Thirty-one mCRC patients who were treated with bevacizumab-containing chemotherapy as second or later line treatment and who had analyzable tumor paraffin blocks were selected for this study. The planned dose of bevacizumab was 5 mg/kg/2-week. Immunohistochemical (IHC) staining of CA9 and VEGF was performed and their expression was scored by the intensity multiplied by percentage of stained area.
The overall response rate was 19.4% and the disease control rate (DCR) was 61.3% with 6 partial responses and 13 cases of stable disease. The DCR was significantly higher in patients with a lower CA9 expression score compared to those with a higher score (80.0% vs. 27.3%, respectively, P = 0.004). The patients with a low CA9 expression score also showed better outcomes with regard to the median progression-free survival (P = 0.028) and overall survival (P = 0.026). However, VEGF expression was not associated with the DCR and survival.
Lower degree of CA9 expression was associated with better clinical outcomes in patients with mCRC treated with lower dose bevacizumab-based chemotherapy. Prospective studies are now needed to determine the correlation between CA9 expression and clinical outcomes after bevacizumab treatment, at different doses and in varied settings.
For the patients with metastatic colorectal cancer (mCRC), 5-fluorouracil (5-FU) based chemotherapy has been the standard regimen [1, 2]. Since the late 1990's, combination chemotherapy with 5-FU/leucovorin (LV) plus oxaliplatin (FOLFOX) or irinotecan (FOLFIRI) has been shown to improve the response rates and survival when used as either first-line or second-line treatment [3–5]. These combination regimens had been the treatment of choice for patients with mCRC before the introduction of bevacizumab.
Bevacizumab, a recombinant humanized monoclonal antibody, targets vascular endothelial growth factor (VEGF), and prevents its interaction with receptors on the vascular endothelial cells that mediate angiogenesis; a process critical for tumor progression [6, 7]. Since the successful results of a landmark study were published in 2004 , bevacizumab has been proven to be effective in several clinical trials when combined with various cytotoxic chemotherapeutic agents in patients with metastatic disease as first-line or neoadjuvant treatment before metastasectomy [9–14]. Thus, bevacizumab plus 5-FU based regimens are highly recommended in previously untreated patients with mCRC. Bevacizumab-containing combination chemotherapy also was proved to be effective as second-line treatment in a phase III trial, E3200 study; however, the approved dose for previously treated patients based on the results from E3200 trial is twice as high as that of first line treatment .
Tumor hypoxia is known to be associated with treatment failure in several malignancies. Carbonic anhydrase 9 (CA9) is one of the representative markers for tumor hypoxia; it is a transmembrane protein that plays a major role in the adaptation and proliferation of cells, in hypoxic and acidic conditions, by regulating the intracellular and extracellular pH [16, 17]. CA9 was initially identified in HeLa cells ; its expression has been found in a variety of tumor types including colorectal cancer . Hypoxia is one of driving forces of tumor angiogenesis; therefore, expression of the hypoxia-inducible enzyme, CA9, might be associated with the outcome of antiangiogenic treatment.
In this study, we aimed to investigate the efficacy of lower dose bevacizumab (5 mg/kg/2-wk), a half of approved dose for second-line setting, for pretreated patients. In addition, clinicopathologic analysis was done to evaluate the correlation between expression of CA9/VEGF and efficacy of bevacizumab-containing regimen.
Patients and tissue samples
From July 2005 to October 2008, 50 patients with previously treated mCRC who received a lower dose of bevacizumab were identified from a prospective medical oncology patient database at the Center for Colorectal Cancer, National Cancer Center, Korea. Among them, study patients were selected according to the following inclusion criteria: 1) patients that were exposed and refractory to previous chemotherapy for metastatic disease prior to treatment with bevacizumab; 2) one or more unidimensionally measurable lesion(s) according to the RECIST (Response Evaluation Criteria in Solid Tumors) criteria  should be present; 3) planned dose of bevacizumab should not be in excess of 5 mg/kg/2-wk; and 4) adequate tumor paraffin blocks for immunohistochemical (IHC) staining should be available. Thirty one patients were finally included in this study.
This study was conducted in accordance with the Helsinki declaration and patients were provided with informed consent prior to receiving the study treatment. Additional informed consents for IHC staining were also obtained where appropriate. The protocol was approved by the Institutional Review Board of the National Cancer Center, Korea (protocol number NCCNCS-08-120).
IHC staining for CA9 and VEGF expression was evaluated by one pathologist (H. J. Chang) without knowledge of the clinical findings. The comparative analysis of the clinical results and CA9 and VEGF expression profiles was performed by medical oncologists (Y.S. Hong and H.J. Cho).
Bevacizumab was administered at a dose of 5 mg/kg every 2 weeks or 7.5 mg/kg every 3 weeks on day 1, according to the schedule of the concomitant chemotherapy regimen. Concomitant cytotoxic chemotherapy regimens were chosen by the attending physicians and included the followings: 2-week scheduled concomitant cytotoxic chemotherapy with LV/5-FU (LV 200 mg/m2 d1, 5-FU 400 mg/m2 d1 and 5-FU 1200 mg/m2/day continuous infusion d1–2), FOLFIRI (irinotecan 180 mg/m2 d1 and LV/5-FU as above) and FOLFOX (oxaliplatin 85 mg/m2 d1 and LV/5-FU as above), and a 3-week scheduled concomitant regimen with oral fluoropyrimidines alone (capecitabine 2500 mg/m2/day or S-1 70 mg/m2/day d1–14). Dose modifications of bevacizumab were not considered, but delays of bevacizumab administration were permitted in synchrony with the schedule of other cytotoxic chemotherapy. Dose modifications of combined cytotoxic drugs were made for hematological or non-hematological toxicity on the basis of the most severe grade of toxicity that occurred during the previous cycle. Patients were treated until disease progression, development of unacceptable toxicity or patient refusal.
Assessments of efficacy and toxicity
Objective tumor responses were assessed every 6 weeks using RECIST criteria; all responses required confirmation at 4 weeks or later. Toxicities were graded according to the National Cancer Institute Common Toxicity Criteria, version 3.0 (NCI-CTC 3.0).
IHC stain for CA9 and VEGF
All patients that showed adequate CA9 and VEGF IHC results and received at least one course of bevacizumab therapy were included in the survival analysis. Descriptive statistics were reported as proportions and medians. The chi-square test and the Fisher's exact test were used to compare proportions. Usually a chi-square test was used, but a Fisher's exact test was used if the expected value of any of the cells of the contingency table was below 5. The Wilcoxon rank-sum test was used to compare medians between the patient groups. The overall survival (OS) and the progression free survival (PFS) were assessed by the Kaplan-Meier method and the 95% confidence interval (95% CI) for the median time to an event was computed. The log-rank test was used to compare survival outcomes of the patient groups and the Cox proportional hazards model was also used to examine the factors associated with survival. The OS was measured from the start of bevacizumab therapy or from the date of first line chemotherapy until death, censoring patients that had not died at the date of the last follow up. The PFS was defined as the time from the date of bevacizumab treatment to the date of disease progression or death by any cause, censoring patients without progression at the date of the last disease assessment. Analyses were performed using Stata version 10.0 (Stata Corp, College Station, Texas, USA).
Patient characteristics and treatment responses
Score of CA 9 expression
Patient characteristics (n = 31)
(n = 20)
(n = 11)
(31.8 – 67.8)
(33.3 – 66.7)
(31.8 – 67.8)
Line of bevacizumab
≥ 3rd line
Site of distant metastasis
Sum of metastatic sites
Disease control rate§
The CA9 expression was negative in 6 patients (19.4%), weakly positive in 1 (3.2%), moderately positive in 11 (35.5%), and strongly positive in 13 patients (41.9%). The mean value for the percent of stained area for the CA9 IHC was 30.1% (range, 0 – 95%) and the mean of expression score was 82.8 (range, 0 – 285). The patient characteristics according to the CA9 expression are shown in Table 1. There was no statistically significant differences in patient characteristics between the groups according to the CA9 expression scores, except for lymph node metastases, which tended to be less frequent in patients with higher CA9 expression (P = 0.081, by chi-square test). The intensity of VEGF expression was negative in 7 (22.6%), weakly positive in 9 (29.0%), moderately positive in 13 (41.9%), and strongly positive in 2 patients (6.5%). The mean percent of stained area for VEGF was 44.5% (range, 0 – 90%) and the mean of expression score was 83.1 (range, 0 – 270). Patient characteristics were also evenly distributed according to VEGF expression, except for more frequent omental metastases in patients with lower VEGF expression (data not shown).
Treatment delivery, toxicity and responses
In total, 200 cycles of lower dose bevacizumab were administered with a median of 4.5 cycles per patient (range 1 – 16 cycles). Fifteen patients (48.4%) received FOLFOX as concomitant cytotoxic chemotherapy, 6 patients (19.3%) received FOLFIRI and 10 patients (32.3%) received fluoropyrimidines alone (5-FU/LV in 7, S-1 in 2 and capecitabine in 1 patient, respectively). These study treatments were the second line treatment in 13 patients (41.9%) and third or later line treatment in 18 patients (58.1%). Combined chemotherapy and the line of bevacizumab were balanced between groups with higher and lower CA9 expression scores, without significant differences. The median delivered dose intensity of bevacizumab was 4.2 mg/kg/2-wk (84.0%). The grade 3 bevacizumab-related toxicities per patient included: thromboembolism (1, 3.2%), bleeding (1, 3.2%) and hypertension (1, 3.2%); grade 2 included proteinuria (5, 16.1%), bleeding (1, 3.2%) and hypertension (2, 6.4%).
The overall response rate was 19.4% (95% CI, 5.5 – 33.3) and the disease control rate was 61.3% (95% CI, 44.2 – 78.4) with 0 complete response, 6 partial responses and 13 stable diseases (Table 1). There were statistically significant differences in the disease control rates; 80.0% (16/20) in patients with a CA9 expression score < 80 and 27.3% (3/11) in those with a CA9 expression score ≥ 80 (P = 0.004). By contrast, the disease control rate was similar in patients with lower VEGF expression compared to those with higher VEGF expression (60.0% vs. 62.5%, respectively. P = 0.919).
In a comparative analysis based on the CA9 expression scores, patients with a lower score (< 80) had improved PFS with bevacizumab when compared to those with a higher score (≥ 80) (4.7 months vs. 2.4 months, respectively; HR 0.42 [95% CI, 0.18–0.94], P = 0.028). A lower CA9 expression score was also associated with a better overall survival compared to higher scores; 24.1 months vs. 10.2 months, respectively (HR 0.35 [95% CI, 0.13–0.92], P = 0.026). However, the PFS and the OS did not differ between the subgroups based on higher or lower VEGF expression scores: the median PFS of patients with VEGF expression scores < 80 was 3.9 months, and those with higher VEGF expression scores had also 3.9 months of PFS (HR 1.54 [95% CI, 0.72–3.30], P = 0.25). The median OS was 9.1 months for patients with VEGF expression scores < 80, whereas it was 11.5 months for those with scores ≥ 80 (HR 1.66 [95% CI, 0.48–5.77], P = 0.68). The median OS from initiation of first-line treatment showed no statistically significant differences based on the CA9 expression scores (P = 0.164) or VEGF expression scores (P = 0.62).
The univariate analysis showed that there were five factors associated with the PFS with a P value < 0.1: the CA9 expression score, gender, the line of treatment with bevacizumab, presence of bony metastases, and number of metastatic sites. Multivariable analysis with the Cox regression hazard model revealed that the CA9 expression score and the number of metastatic sites were significantly associated with the PFS: the risk of progression was significantly increased among patients with higher CA9 scores compared to those with lower CA9 scores (HR = 3.50 [95% CI, 1.39–9.09]; P = 0.007) and for patients with 3 or more metastatic sites compared to those with 1 or 2 metastatic sites (HR = 3.77 [95% CI, 1.27–11.40]; P = 0.016).
In patients with mCRC, bevacizumab has become one of highly recommended agents for first (5 mg/kg/2-wk) and second line (10 mg/kg/2-wk) chemotherapy. There have been many attempts to identify predictive biomarkers to help select those patients that will benefit from targeted agents, such as the association between the KRAS mutation status and survival outcomes in patients with mCRC treated with cetuximab . As for bevacizumab, however, there are no predictive biomarkers identified to be associated with either treatment response or survival in patients with mCRC.
Both VEGF and CA9 are the products of hypoxia-induced pathways. VEGF, a target of bevacizumab, is a critical component of tumor angiogenesis. CA9, a transmembrane protein, converts carbon dioxide to bicarbonate and hydrogen, and thus regulates the microenvironment pH, as well as influences other processes such as cell-cell adhesion, proliferation, and invasion of tumor cells . In this study, we demonstrated that the degree of CA9 expression was associated with a survival benefit after treatment with bevacizumab in previously treated patients with mCRC; however, VEGF expression was not related to the outcome of treatment in these patients. The degree of CA9 expression was divided into high and low using the expression score, which was defined as the intensity multiplied by the percent of stained area; an expression score ≥ 80 was considered to be high. The disease control rates were statistically higher, and the median PFS and OS were statistically lengthened in patients with low CA9 expression scores (< 80). Furthermore, CA9 expression remained significantly associated with the PFS after adjustment for other risk factors in multivariable analysis. The OS from initiation of first-line treatment, however, was not statistically different based on the CA9 expression scores (Figure 3). Thus, CA9 expression could be a predictive marker for a survival benefit, with bevacizumab treatment, rather than a prognostic marker, in patients with mCRC. The mechanism explaining the association of CA9 expression with bevacizumab resistance is unclear. One possible explanation might be suggested by the findings of Selvakumaran et al: where the antitumor effects of bevacizumab were suggested to be dependent on the susceptibility of tumors to hypoxia-induced apoptosis . CA9 accelerates CO2 removal from the intracellular milieu as well as facilitates HCO3 - recycling; thus, it serves to protect the tumor cells from acidosis . Therefore, CA9 might play a role in the metabolic accommodation during hypoxia and may induce resistance to hypoxia-induced apoptosis by bevacizumab, although this hypothesis requires confirmation.
However, in contrast to CA9, VEGF expression was not associated with the clinical outcome of bevacizumab-based therapy. VEGF is a target molecule of bevacizumab and high levels of VEGF expression have been shown to be associated with a poor prognosis in patients with colorectal cancer . In our study, however, there was no clinical significance associated with VEGF expression after bevacizumab treatment. In agreement with the results of the current study, a prior study reported that tumor VEGF expression was not a predictor of responsiveness to bevacizumab therapy .
However, the most frequently reported studies associating CA9 expression with tumor behavior have been in patients with clear cell type renal cell carcinoma (RCC) [31–33]. CA9 is strongly expressed by RCC and it is known to be associated with clinical outcomes. Bui et al reported low CA9 expression (defined as ≤ 85% of tumor cells) was an independent predictor of poor prognosis after nephrectomy  and Atkins et al reported CA9 expression was a predictor of responses to interleukin-2 therapy . Leibovich et al reported CA9 was not an independent predictor of clinical outcomes in patients with RCC after adjusting for the nuclear grade and tumor necrosis ; however, but it seemed to be true that CA9 expression was still one of the factors associated with RCC prognosis. In patients with RCC, a higher expression of CA9 was associated with better survival outcomes.
In terms of prediction of a survival benefit from bevacizumab, it has been reported that low CA9 expression was associated with better survival outcomes in patients with malignant astrocytoma treated with bevacizumab plus irinotecan . From a phase II trial of bevacizumab plus irinotecan in patients with malignant astrocytoma, a comparative analysis was performed with several angiogenic factors including CA9 from tumor specimens by Sathornsumette et al. This phase II trial adopted a high dose regimen of bevacizumab, 10 mg/kg/2-wk . They reported that a higher VEGF expression was associated with radiological responses to bevacizumab, but not with overall survival, and that the CA9 expression was associated with overall survival but not with radiological responses to bevacizumab. To the best of our knowledge, current study firstly suggested the predictive role of CA9 for DCR and PFS in bevacizumab-treated patients.
This study has another advantage showing that lower dose of bevacizumab at 5 mg/kg/2-wk could also result in clinical responses in the second line setting and even in the third or later line. Angiogenesis with VEGF is essential during the early stages of tumor progression; VEGF is expressed throughout the entire tumor life cycle. However, as more time elapses other factors in addition to VEGF itself become important at later stages of progression . Therefore, it can be inferred that bevacizumab is more likely to be effective during the earlier stages of cancer, and that higher doses of bevacizumab may be needed to suppress the already activated VEGF pathways during later stages. Thus, the dose for phase III clinical trials using second-line treatment has been determined to be 10 mg/kg/2-wk, based on several preclinical and clinical studies that showed a dose-dependent effect of bevacizumab [15, 38, 39]. From a phase III trial comparing FOLFOX plus bevacizumab with FOLFOX plus placebo, second-line treatment with bevacizumab was demonstrated to be effective: the median PFS and OS were 7.3 months and 12.9 months with a 22.7% response rate . However, recent clinical data on bevacizumab as first line treatment for non-small cell lung cancer and colorectal cancer demonstrated that there was no significant difference in the response rate and survival between lower dose and higher dose treatment groups[40, 41] Although a phase II trial of lower dose of bevacizumab (5 mg/kg/2-wk) plus 5-FU/LV as a 3rd-line treatment failed to show clinical benefits , the lower dose still remained to be explored in second-line setting. In this study, 13 patients were treated with second line bevacizumab at 5 mg/kg/2-wk; 4 patients (30.8%) had confirmed partial responses and the median PFS was 5.0 months, which was not inferior to previous study. Furthermore, among 18 patients treated with third line or later bevacizumab, at 5 mg/kg/2-wk, 2 confirmed responses were observed (2/18, 11.1%) and the median PFS was lengthened to 4.5 months (95% CI, 1.0 – 8.3) for 11 patients that had a low CA9 expression score.
This study includes several limitations as follow: 1) the line of treatment with bevacizumab and concomitant chemotherapy were not constant, 2) this was a retrospective study with a small sample size, and the analysis had low statistical power, 3) patients without analyzable paraffin blocks were excluded, eliminating some of the patients treated with bevacizumab as second or later line therapy. Further evaluation of CA9 in patients enrolled in randomized prospective trials may confirm the use of CA9 as a marker in patients receiving bevacizumab therapy.
In conclusion, CA9 IHC stain can be easily performed in clinical practice and it can be used to predict survival benefit in patients with previously treated mCRC who are considered to be treated with lower dose of bevacizumab as second or later lines. Further prospective, comparative analysis between the degree of CA9 expression and clinical outcomes in mCRC patients with 1st line or higher dose of bevacizumab will be warranted.
This work was supported by the National Cancer Center Grant (NCC-0910010).
- Brook J: Fluorouracil and low-dose leucovorin versus fluorouracil and high-dose leucovorin: what is the real cost? What is the answer?. J Clin Oncol. 1995, 13 (7): 1830-1831.PubMedGoogle Scholar
- de Gramont A, Bosset JF, Milan C, Rougier P, Bouche O, Etienne PL, Morvan F, Louvet C, Guillot T, Francois E, et al: Randomized trial comparing monthly low-dose leucovorin and fluorouracil bolus with bimonthly high-dose leucovorin and fluorouracil bolus plus continuous infusion for advanced colorectal cancer: a French intergroup study. J Clin Oncol. 1997, 15 (2): 808-815.PubMedGoogle Scholar
- de Gramont A, Figer A, Seymour M, Homerin M, Hmissi A, Cassidy J, Boni C, Cortes-Funes H, Cervantes A, Freyer G, et al: Leucovorin and fluorouracil with or without oxaliplatin as first-line treatment in advanced colorectal cancer. J Clin Oncol. 2000, 18 (16): 2938-2947.PubMedGoogle Scholar
- Douillard JY, Cunningham D, Roth AD, Navarro M, James RD, Karasek P, Jandik P, Iveson T, Carmichael J, Alakl M, et al: Irinotecan combined with fluorouracil compared with fluorouracil alone as first-line treatment for metastatic colorectal cancer: a multicentre randomised trial. Lancet. 2000, 355 (9209): 1041-1047. 10.1016/S0140-6736(00)02034-1.View ArticlePubMedGoogle Scholar
- Tournigand C, Andre T, Achille E, Lledo G, Flesh M, Mery-Mignard D, Quinaux E, Couteau C, Buyse M, Ganem G, et al: FOLFIRI followed by FOLFOX6 or the reverse sequence in advanced colorectal cancer: a randomized GERCOR study. J Clin Oncol. 2004, 22 (2): 229-237. 10.1200/JCO.2004.05.113.View ArticlePubMedGoogle Scholar
- Ferrara N: Molecular and biological properties of vascular endothelial growth factor. J Mol Med. 1999, 77 (7): 527-543. 10.1007/s001099900019.View ArticlePubMedGoogle Scholar
- Presta LG, Chen H, O'Connor SJ, Chisholm V, Meng YG, Krummen L, Winkler M, Ferrara N: Humanization of an anti-vascular endothelial growth factor monoclonal antibody for the therapy of solid tumors and other disorders. Cancer Res. 1997, 57 (20): 4593-4599.PubMedGoogle Scholar
- Hurwitz H, Fehrenbacher L, Novotny W, Cartwright T, Hainsworth J, Heim W, Berlin J, Baron A, Griffing S, Holmgren E, et al: Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer. N Engl J Med. 2004, 350 (23): 2335-2342. 10.1056/NEJMoa032691.View ArticlePubMedGoogle Scholar
- Bir A, Tan W, Wilding GE, Lombardo J, Fakih MG: 5-fluorouracil, leucovorin and oxaliplatin plus bevacizumab in the first-line treatment of metastatic colorectal cancer: a single-institute study. Oncology. 2007, 72 (1–2): 4-9. 10.1159/000110546.View ArticlePubMedGoogle Scholar
- Emmanouilides C, Sfakiotaki G, Androulakis N, Kalbakis K, Christophylakis C, Kalykaki A, Vamvakas L, Kotsakis A, Agelaki S, Diamandidou E, et al: Front-line bevacizumab in combination with oxaliplatin, leucovorin and 5-fluorouracil (FOLFOX) in patients with metastatic colorectal cancer: a multicenter phase II study. BMC Cancer. 2007, 7: 91-10.1186/1471-2407-7-91.View ArticlePubMedPubMed CentralGoogle Scholar
- Giantonio BJ, Levy DE, O'Dwyer PJ, Meropol NJ, Catalano PJ, Benson AB: A phase II study of high-dose bevacizumab in combination with irinotecan, 5-fluorouracil, leucovorin, as initial therapy for advanced colorectal cancer: results from the Eastern Cooperative Oncology Group study E2200. Ann Oncol. 2006, 17 (9): 1399-1403. 10.1093/annonc/mdl161.View ArticlePubMedGoogle Scholar
- Grothey E, Chu E: The clinical efficacy of FOLFIRI and bevacizumab in combination as first-line therapy of metastatic colorectal cancer. Clin Colorectal Cancer. 2007, 6 (9): 621-624.View ArticlePubMedGoogle Scholar
- Gruenberger B, Tamandl D, Schueller J, Scheithauer W, Zielinski C, Herbst F, Gruenberger T: Bevacizumab, capecitabine, and oxaliplatin as neoadjuvant therapy for patients with potentially curable metastatic colorectal cancer. J Clin Oncol. 2008, 26 (11): 1830-1835. 10.1200/JCO.2007.13.7679.View ArticlePubMedGoogle Scholar
- Hurwitz HI, Fehrenbacher L, Hainsworth JD, Heim W, Berlin J, Holmgren E, Hambleton J, Novotny WF, Kabbinavar F: Bevacizumab in combination with fluorouracil and leucovorin: an active regimen for first-line metastatic colorectal cancer. J Clin Oncol. 2005, 23 (15): 3502-3508. 10.1200/JCO.2005.10.017.View ArticlePubMedGoogle Scholar
- Giantonio BJ, Catalano PJ, Meropol NJ, O'Dwyer PJ, Mitchell EP, Alberts SR, Schwartz MA, Benson AB: 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 (12): 1539-1544. 10.1200/JCO.2006.09.6305.View ArticlePubMedGoogle Scholar
- Potter CP, Harris AL: Diagnostic, prognostic and therapeutic implications of carbonic anhydrases in cancer. Br J Cancer. 2003, 89 (1): 2-7. 10.1038/sj.bjc.6600936.View ArticlePubMedPubMed CentralGoogle Scholar
- Robertson N, Potter C, Harris AL: Role of carbonic anhydrase IX in human tumor cell growth, survival, and invasion. Cancer Res. 2004, 64 (17): 6160-6165. 10.1158/0008-5472.CAN-03-2224.View ArticlePubMedGoogle Scholar
- Pastorekova S, Zavadova Z, Kostal M, Babusikova O, Zavada J: A novel quasi-viral agent, MaTu, is a two-component system. Virology. 1992, 187 (2): 620-626. 10.1016/0042-6822(92)90464-Z.View ArticlePubMedGoogle Scholar
- Saarnio J, Parkkila S, Parkkila AK, Haukipuro K, Pastorekova S, Pastorek J, Kairaluoma MI, Karttunen TJ: Immunohistochemical study of colorectal tumors for expression of a novel transmembrane carbonic anhydrase, MN/CA IX, with potential value as a marker of cell proliferation. The American journal of pathology. 1998, 153 (1): 279-285.View ArticlePubMedPubMed CentralGoogle Scholar
- Therasse P, Arbuck SG, Eisenhauer EA, Wanders J, Kaplan RS, Rubinstein L, Verweij J, Van Glabbeke M, van Oosterom AT, Christian MC, et al: New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada. J Natl Cancer Inst. 2000, 92 (3): 205-216. 10.1093/jnci/92.3.205.View ArticlePubMedGoogle Scholar
- Karapetis CS, Khambata-Ford S, Jonker DJ, O'Callaghan CJ, Tu D, Tebbutt NC, Simes RJ, Chalchal H, Shapiro JD, Robitaille S, et al: K-ras mutations and benefit from cetuximab in advanced colorectal cancer. The New England journal of medicine. 2008, 359 (17): 1757-1765. 10.1056/NEJMoa0804385.View ArticlePubMedGoogle Scholar
- Winum JY, Rami M, Scozzafava A, Montero JL, Supuran C: Carbonic anhydrase IX: a new druggable target for the design of antitumor agents. Med Res Rev. 2008, 28 (3): 445-463. 10.1002/med.20112.View ArticlePubMedGoogle Scholar
- Selvakumaran M, Yao KS, Feldman MD, O'Dwyer PJ: Antitumor effect of the angiogenesis inhibitor bevacizumab is dependent on susceptibility of tumors to hypoxia-induced apoptosis. Biochem Pharmacol. 2008, 75 (3): 627-638. 10.1016/j.bcp.2007.09.029.View ArticlePubMedGoogle Scholar
- Swietach P, Vaughan-Jones RD, Harris AL: Regulation of tumor pH and the role of carbonic anhydrase 9. Cancer Metastasis Rev. 2007, 26 (2): 299-310. 10.1007/s10555-007-9064-0.View ArticlePubMedGoogle Scholar
- Lee JC, Chow NH, Wang ST, Huang SM: Prognostic value of vascular endothelial growth factor expression in colorectal cancer patients. Eur J Cancer. 2000, 36 (6): 748-753. 10.1016/S0959-8049(00)00003-4.View ArticlePubMedGoogle Scholar
- Jubb AM, Hurwitz HI, Bai W, Holmgren EB, Tobin P, Guerrero AS, Kabbinavar F, Holden SN, Novotny WF, Frantz GD, et al: Impact of vascular endothelial growth factor-A expression, thrombospondin-2 expression, and microvessel density on the treatment effect of bevacizumab in metastatic colorectal cancer. J Clin Oncol. 2006, 24 (2): 217-227. 10.1200/JCO.2005.01.5388.View ArticlePubMedGoogle Scholar
- Lee S, Shin HJ, Han IO, Hong EK, Park SY, Roh JW, Shin KH, Kim TH, Kim JY: Tumor carbonic anhydrase 9 expression is associated with the presence of lymph node metastases in uterine cervical cancer. Cancer Sci. 2007, 98 (3): 329-333. 10.1111/j.1349-7006.2007.00396.x.View ArticlePubMedGoogle Scholar
- Giatromanolaki A, Koukourakis MI, Sivridis E, Pastorek J, Wykoff CC, Gatter KC, Harris AL: Expression of hypoxia-inducible carbonic anhydrase-9 relates to angiogenic pathways and independently to poor outcome in non-small cell lung cancer. Cancer Res. 2001, 61 (21): 7992-7998.PubMedGoogle Scholar
- Brennan DJ, Jirstrom K, Kronblad A, Millikan RC, Landberg G, Duffy MJ, Ryden L, Gallagher WM, O'Brien SL: CA IX is an independent prognostic marker in premenopausal breast cancer patients with one to three positive lymph nodes and a putative marker of radiation resistance. Clin Cancer Res. 2006, 12 (21): 6421-6431. 10.1158/1078-0432.CCR-06-0480.View ArticlePubMedGoogle Scholar
- Choi SW, Kim JY, Park JY, Cha IH, Kim J, Lee S: Expression of carbonic anhydrase IX is associated with postoperative recurrence and poor prognosis in surgically treated oral squamous cell carcinoma. Hum Pathol. 2008, 39 (9): 1317-1322. 10.1016/j.humpath.2007.10.026.View ArticlePubMedGoogle Scholar
- Atkins M, Regan M, McDermott D, Mier J, Stanbridge E, Youmans A, Febbo P, Upton M, Lechpammer M, Signoretti S: Carbonic anhydrase IX expression predicts outcome of interleukin 2 therapy for renal cancer. Clin Cancer Res. 2005, 11 (10): 3714-3721. 10.1158/1078-0432.CCR-04-2019.View ArticlePubMedGoogle Scholar
- Bui MH, Seligson D, Han KR, Pantuck AJ, Dorey FJ, Huang Y, Horvath S, Leibovich BC, Chopra S, Liao SY, et al: Carbonic anhydrase IX is an independent predictor of survival in advanced renal clear cell carcinoma: implications for prognosis and therapy. Clin Cancer Res. 2003, 9 (2): 802-811.PubMedGoogle Scholar
- Uemura H, Nakagawa Y, Yoshida K, Saga S, Yoshikawa K, Hirao Y, Oosterwijk E: MN/CA IX/G250 as a potential target for immunotherapy of renal cell carcinomas. British journal of cancer. 1999, 81 (4): 741-746. 10.1038/sj.bjc.6690757.View ArticlePubMedPubMed CentralGoogle Scholar
- Leibovich BC, Sheinin Y, Lohse CM, Thompson RH, Cheville JC, Zavada J, Kwon ED: Carbonic anhydrase IX is not an independent predictor of outcome for patients with clear cell renal cell carcinoma. J Clin Oncol. 2007, 25 (30): 4757-4764. 10.1200/JCO.2007.12.1087.View ArticlePubMedGoogle Scholar
- Sathornsumetee S, Cao Y, Marcello JE, Herndon JE, McLendon RE, Desjardins A, Friedman HS, Dewhirst MW, Vredenburgh JJ, Rich JN: Tumor angiogenic and hypoxic profiles predict radiographic response and survival in malignant astrocytoma patients treated with bevacizumab and irinotecan. J Clin Oncol. 2008, 26 (2): 271-278. 10.1200/JCO.2007.13.3652.View ArticlePubMedPubMed CentralGoogle Scholar
- Vredenburgh JJ, Desjardins A, Herndon JE, Dowell JM, Reardon DA, Quinn JA, Rich JN, Sathornsumetee S, Gururangan S, Wagner M, et al: Phase II trial of bevacizumab and irinotecan in recurrent malignant glioma. Clin Cancer Res. 2007, 13 (4): 1253-1259. 10.1158/1078-0432.CCR-06-2309.View ArticlePubMedGoogle Scholar
- Relf M, LeJeune S, Scott PA, Fox S, Smith K, Leek R, Moghaddam A, Whitehouse R, Bicknell R, Harris AL: Expression of the angiogenic factors vascular endothelial cell growth factor, acidic and basic fibroblast growth factor, tumor growth factor beta-1, platelet-derived endothelial cell growth factor, placenta growth factor, and pleiotrophin in human primary breast cancer and its relation to angiogenesis. Cancer Res. 1997, 57 (5): 963-969.PubMedGoogle Scholar
- Johnson DH, Fehrenbacher L, Novotny WF, Herbst RS, Nemunaitis JJ, Jablons DM, Langer CJ, DeVore RF, Gaudreault J, Damico LA, 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 (11): 2184-2191. 10.1200/JCO.2004.11.022.View ArticlePubMedGoogle Scholar
- Yang JC, Haworth L, Sherry RM, Hwu P, Schwartzentruber DJ, Topalian SL, Steinberg SM, Chen HX, Rosenberg SA: A randomized trial of bevacizumab, an anti-vascular endothelial growth factor antibody, for metastatic renal cancer. N Engl J Med. 2003, 349 (5): 427-434. 10.1056/NEJMoa021491.View ArticlePubMedPubMed CentralGoogle Scholar
- Reck M, von Pawel J, Zatloukal P, Ramlau R, Gorbounova V, Hirsh V, Leighl N, Mezger J, Archer V, Moore N, 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 (8): 1227-1234. 10.1200/JCO.2007.14.5466.View ArticlePubMedGoogle Scholar
- Kabbinavar F, Hurwitz HI, Fehrenbacher L, Meropol NJ, Novotny WF, Lieberman G, Griffing S, Bergsland E: 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 (1): 60-65. 10.1200/JCO.2003.10.066.View ArticlePubMedGoogle Scholar
- Chen HX, Mooney M, Boron M, Vena D, Mosby K, Grochow L, Jaffe C, Rubinstein L, Zwiebel J, Kaplan RS: Phase II multicenter trial of bevacizumab plus fluorouracil and leucovorin in patients with advanced refractory colorectal cancer: an NCI Treatment Referral Center Trial TRC-0301. J Clin Oncol. 2006, 24 (21): 3354-3360. 10.1200/JCO.2005.05.1573.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/9/246/prepub
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