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Case Rep Oncol. 2010 Sep-Dec; 3(3): 344–348.
Published online 2010 October 1. doi:  10.1159/000321262
PMCID: PMC2988845

Analysis of pO2 in Malignant Ascites of Patients with Peritoneal Dissemination of Gastric Cancer

Abstract

Objective

Oxygen is one of the most important environmental factors for tumor development. In this study, we examined pO2 in malignant ascites in patients with peritoneal carcinomatosis.

Methods

In 21 patients with peritoneal dissemination of gastric cancer, ascitic fluid was collected and its pH, pCO2 and pO2 were determined using a blood gas analyzer.

Results

In 21 patients, pH of malignant ascites was significantly lower than that of arterial blood (7.39 ± 0.07, 7.44 ± 0.02, p < 0.05). Accordingly, pCO2 tended to be higher in ascites than in arterial blood. Unexpectedly, pO2 in malignant ascites showed relatively high values (90.4 ± 27.72 mm Hg), which were mostly the same as those of arterial blood (97.09 ± 10.33 mm Hg, p = 0.858). Even in 19 patients whose samples were collected at bedside in room air, pO2 of malignant ascites was 85.94 ± 23.94 mm Hg, which was patently higher than that in venous blood or in solid tumor tissues.

Conclusion

Since the oxygen level critically affects the sensitivity of tumor cells to chemotherapeutic agents through metabolic transformation, the oxygenic condition in the peritoneal cavity may be beneficial for the progression of peritoneal metastasis, and also clinically important in considering the efficacy of chemotherapy.

Key Words: Malignant ascites, pO2, Gastric cancer, Peritoneal metastasis

Introduction

Peritoneal metastasis with malignant ascites is the most life-threatening mode of metastasis and recurrence in patients with gastric [1] as well as ovarian cancer [2]. Peritoneal metastasis is considered to develop from carcinoma cells detached from the serosal surface of the primary site and dispersed in the peritoneal cavity. In general, the survival of seeded cells is largely dependent on the environment, in other words, the soil [3]. Oxygen supply is one of the most important environmental factors for cancer cell survival [4]. However, the oxygenic condition in the abdominal cavity is largely unknown. In this study, therefore, we collected ascitic fluid from patients with peritoneal dissemination of gastric cancer, and measured pO2 as well as pCO2 and pH.

Patients and Methods

Twenty-one patients with peritoneal dissemination of gastric cancer who were admitted to the University of Tokyo Hospital, Japan, between March and June 2010, were included in this study. All patients had a considerable amount of ascites and had received systemic and/or intraperitoneal chemotherapy. In 19 patients, samples of ascites were collected through a drainage catheter inserted into the abdominal cavity, or through an access port system with the end of the catheter placed in the pelvic cavity and an access port system implanted in the subcutaneous space [5]. In 16 of the 19 patients, arterial blood was obtained by arterial puncture on the same day. In the other 2 cases, an insufficient amount of ascites was collected, and it was thus obtained just after laparotomy under general anesthesia. The samples were kept in a syringe with an airtight seal, and immediately analyzed with a blood gas analyzer, ABL800 (Radiometer, Copenhagen, Denmark). The results were statistically examined by paired Student's t test or simple regression analysis, and differences with p < 0.05 were considered to be significant.

Results

As shown in table table1,1, the pH of malignant ascites was 7.39 ± 0.07, which was slightly but significantly lower than the pH of arterial blood (7.44 ± 0.02, p = 0.033). Consistent with this, ascites showed a slightly higher pCO2 (43.70 ± 5.5 mm Hg) than that of arterial blood (40.72 ± 3.46 mm Hg), although the difference was not statistically significant (p = 0.124). Interestingly, pO2 in malignant ascites showed considerably high levels (90.4 ± 27.72 mm Hg), which were mostly the same as those of arterial blood (97.09 ± 10.33 mm Hg, p = 0.858).

Table 1
pH, pCO2 and pO2 in ascites and arterial blood of the patients with peritoneal metastasis of gastric cancer

In patients 5 and 8, in whom ascites was collected after laparotomy, pO2 was 151 and 133 mm Hg, respectively. Because they were controlled under general anesthesia, they were considered to be subjected to a higher percentage of O2 gas than that in room air. However, even in the other 19 patients, pO2 of ascites was 85.94 ± 23.94 mm Hg, which was not significantly different from that of arterial blood, 97.19 ± 10.40 mm Hg (p = 0.149).

When pO2 in ascites and arterial blood was compared in 16 patients in whom ascites was obtained at bedside in room air, a positive trend was observed, although the correlation was not statistically significant (fig. (fig.11).

Fig. 1
Arterial blood and ascites were collected at bedside at room temperature in 16 patients and immediately measured with a blood gas analyzer.

Discussion

Our data have demonstrated that malignant ascites in gastric cancer patients showed an unexpectedly high oxygen tension, which was almost the same as that of arterial blood. pO2 was sensitive to the change of circumstances, and thus the procedure of sample acquisition and method of measurement are very important in assessment of the data. In our study, however, ascites was directly obtained through an intraperitoneal catheter or a subcutaneously placed port, kept in a syringe with an airtight seal, and immediately analyzed with a blood gas analyzer, just as for analysis of arterial blood. Therefore, it is unlikely that the relatively high pO2 values in malignant ascites are attributable to potential artifact during measurement.

A literature search showed little information on PaO2 in ascites. In 1977, Sheckman et al. [6] reported that the mean pO2 of ascitic fluid from 10 patients with liver cirrhosis was 43 mm Hg. Based on their data, they concluded that this pO2 was so high that anaerobic bacteria cannot survive in it and they are rarely the cause of spontaneous bacterial peritonitis. In 1982, Giltin et al. [7] also examined the ascitic fluid of patients with spontaneous bacterial peritonitis in alcoholic cirrhosis and showed that pO2 of their ascites was 50–82 mm Hg. Although the main aim of their study was to investigate the pH of ascitic fluid and they did not mention pO2 much, their data showed apparently lower values than ours. On the other hand, Simmen et al. [8] reported that pO2 of ascitic fluid with or without infection was 29 (0–160) and 144 (49–174) mm Hg, respectively. This suggests that ascitic fluid may have a higher pO2 in some conditions, although the method and timing of sample collection varied greatly in their study.

More recently, however, Noh et al. [9] have reported that pO2 of ascitic fluid of patients with non-serosal invasive gastric cancer obtained during surgery was 136.49 ± 0.66 mm Hg. This value was considerably higher than that of cirrhotic ascites reported previously and is consistent with our results, or rather higher than our pO2 data. In their study, they collected ascitic fluid during abdominal surgery under general anesthesia. Since the anesthetic gas of operated patients is usually maintained at a relatively higher oxygen supply than that in room air, the high pO2 values were attributable to systemic hyperoxygenation. In fact, pO2 of ascites showed a positive trend with pO2 of arterial blood in our patients; and pO2 of ascites obtained during laparotomy in 2 cases showed the same pO2 values (151 and 133 mm Hg), which were similar to those in the study by Noh et al. Our data, together with those of Noh et al., suggest that pO2 in malignant ascites with peritoneal metastasis may be somehow elevated as compared with that in cirrhotic ascites.

Why is pO2 of malignant ascitic fluid so high? The efficiency of oxygen transfer through the peritoneum is considered to be elevated due to its rich vascular structure. Moreover, in peritoneal metastasis, vascular endothelial growth factor (VEGF) produced from tumor cells may further enhance the vascular permeability through tumor vessels [10]. The hyperpermeability condition may enable efficient oxygen delivery to peritoneal fluid via the microvessels lining the peritoneal cavity. In fact, the level of VEGF has been reported to be markedly high in malignant ascites [11, 12]. The use of bevacizumab, a humanized monoclonal antibody to VEGF, may reduce pO2 as well as the volume of ascites.

In general, the oxygen tension in malignant tumor tissue is considerably decreased, and hypoxia is considered to be related to tumor progression and a poor outcome [13,14,15]. A previous study to measure the oxygen partial pressure in tumors directly using an Eppendorf microelectrode demonstrated that pO2 in human solid tumors was less than 20 mm Hg in most cases. This indicates that malignant ascites contained much more oxygen as compared with the primary tumor, and thus the high oxygen condition is thought to be a rather favorable condition for survival of disseminated tumor cells. This may be an important reason why so many tumor nodules can develop in the abdominal cavity.

In summary, ascites of peritoneal metastasis of gastric cancer shows a notably high level of pO2. Various therapeutic approaches, including systemic chemotherapy, hyperthermia, immune therapy as well as aggressive surgery, have been attempted for peritonitis carcinomatosa. However, none of these has achieved a satisfactory clinical outcome. Recently, however, intraperitoneal chemotherapy has been shown to be effective for peritoneal metastasis in ovarian and gastric cancer [5, 16]. Since the oxygen level critically affects the sensitivity of tumor cells to chemotherapeutic agents through metabolic transformation [17], the relatively high pO2 in malignant ascites is an important issue in considering the effectiveness of chemotherapy, especially intraperitoneal chemotherapy, for peritoneal metastasis.

Acknowledgement

This study was funded by the Ministry of Education, Culture, Sports, Science and Technology of Japan, and the Ministry of Health, Labor and Welfare of Japan.

Footnotes

This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License (www.karger.com/OA-license), applicable to the online version of the article only. Distribution for non-commercial purposes only.

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Articles from Case Reports in Oncology are provided here courtesy of Karger Publishers