Unresectable Advanced Gastric Cancer Effectively Treated by Combined Chemo-Immunotherapy: A Report of Two Cases

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Case Repot Kurume Medical Journal, 47,177-182, 2000 Unresectable Advanced Gastric Cancer Effectively Treated by Combined Chemo-Immunorapy: A Report of Two Cases KEISHIRO AOYAGI, KIKUO KOUFUJI, SHOJIRO YANG, NAOTAKA MURAKAMI, YASUHIRO TERASAKI, YOSHIYA YAMASAKI, JINRYO TAKEDA AND KAZUO SHIROUZU Department of Surgery, Kurume University School of Medicine, Kurume 830-0011, Japan Summary: We have experienced two cases of unresectable advanced gastric cancer effectively treated by chemo-immunorapy. One case of a 68-year-old male patient diagnosed as having inoperable advanced gastric cancer with liver and lung metastasis. This patient treated by combined chemo-immunorapy of MMC 10mg/M, 5'-DFUR 800mg/day and OK-432 5 KE/2W. At 6 months later, a computed tomography (CT) scan and upper gastrointestinal (GI) series revealed that metastatic liver tumors and stomach lesion were remarkably decreased in size, and endoscopic biopsy confirmed no cancer cells in stomach lesion. Moreover, metastatic lung tumor had disappeared on chest X-ray. The or case of a 68-year-old female patient with unresectable advanced gastric cancer treated by combined administration of MMC 10mg/M, 5-FU 200mg/day and OK-432 5 KE/2W. At 2 months treatment, re a reduction in serum carcinoembryonal antigen (CEA) level. At 6 months later, CEA had decreased to normal, primary and metastatic sites had completely disappeared on CT, and endoscopic biopsy confirmed no cancer cells in stomach lesion. This patient has survived to date for 5 years and 6 months treatment. These results suggested that combined chemo-immunorapy of MMC, antimetabolite, and OK-432 an effective treatment for unresectable advanced gastric cancer. Key words gastric cancer, chemorapy, immunorapy INTRODUCTION The prognosis of unresectable advanced gastric cancer has been very poor. The 1-year survival rate of such cases has been only 10% [1]. Moreover, positive-response rate of chemorapy has been very low. However, chemorapy very effective in a few cases. In this paper, we present two cases of unresectable advanced gastric cancer treated effectively by combined chemo-immunorapy. One case an inoperable case with liver and lung metastasis. This case treated by combined rapy of MMC, 5'-DFUR and OK-432, and metastatic liver tumors and stomach lesion were remarkably decreased in size and metastatic lung tumor disappeared. The or case with unresectable advanced gastric cancer treated by combined rapy of MMC, 5-FU and OK-432, and primary and metastatic sites completely disappeared. This patient hass survived to date for 5 years and 6 months treatment. Received for publication January 19, 2000

178 AOYAGI CASE REPORT Case 1 A 68-year-old man visited a private hospital because of diarrhea and weight loss in April 1991. Advanced gastric cancer with metastatic liver tumors diagnosed based on abdominal ultrasonography (US), computed tomography (CT) and upper gastrointestinal endoscopy. The patient referred to Kurume University Hospital for furr examination and treatment for gastric cancer and metastatic liver Fig. 1. a: Before treatment, tric cancer wall of phy. b: At 6 months ment, and upper body type 3 gasfig. 2. a: Before on posterior on tumors on June 17, 1991. Liver, spleen and tumor were not palpable on physical examination on admission. The serum level of carbohydrate antigen 19-9 (CA19-9) normal, and that of carcinoembryonal antigen (CEA) at 16.8ng/ml. Gastrography and upper gastrointestinal endoscopic examination showed gastric cancer type 3, about 10 cm in size, on posterior wall of upper body in stomach (Figs la and 2a). The pathological diagnosis based on a biopsy specimen tubular gastrogra- treatment, a surrounding nized a conversing Borrmann ET AL. surrounding told treat- body, region on ment, disappeared, Kurume Medical Journal Vol. 47, No. 2, 2000 posterior region wall of with recog- upper treat- on endoscopy. b: Eight had an irregular months lesion lesion altered had disappeared. to scar and

EFFICACY adenocarcinoma moderately-differentiated type. CT showed low density masses of 8cm, 2cm and 1.5 cm in size at S8, S3 and S4 respectively in liver suggesting metastatic liver tumors (Fig. 3a). A chest X-ray showed a metastatic tumor in left lung (Fig. 4a). This case concluded to be inoperable. Treatment with combined chemo-immunorapy of MMC 10mg/M, 5'-DFUR 800mg/day and OK-432 5 KE/2W begun from June 25. The patient Fig. 3. a: Before treatment, b: Five months metastatic 179 OF CHEMO-IMMUNOTHERAPY tumor, showed no side effects due to se drugs. The performance status (PS) of patient had been 0 during treatment. At 5 months chemoimmunorapy, CT revealed that metastatic liver tumors at S3, S4 had disappeared, and tumor at S8 remarkably decreased in size from 8cm to 3 cm (Fig. 3b). Moreover, metastatic lung tumor had disappeared on chest X-ray (Fig. 4b). At 6 months rapy, gastrography showed a converging fold on upper body and size in 8cm treatment, metastatic tumor on right reduced lobe of liver on CT. to 3cm. Fig. 4. a: Before treatment, metastatic tumors were in left lung on chest. X-ray (arrow). b: Nine months treatment, metastatic tumors had disappeared. Kurume Medical Journal Vol. 47, No. 2, 2000

180 AOYAGI type 3 tumor had disappeared (Fig. 1b). At 8 months treatment, endoscopic examination showed both and region ET AL. surrounding tumor had altered to a flat lesion (Fig. 2b). Also, endoscopic biopsy confirmed no cancer cells in gastric lesion. At 3 months Fig. 5. a: Before tric treatment, cancer curvature b: Twelve Fig. 6. a: Before treatment, irregular with surround Borrmann of antrum months ment, conversing tumor had disappeared. lesion completely covered 2 type gas- on fold treat-, at antrum endoscopy. b: Twelve epilium months treatment, scar. Kurume Medical Journal Vol. 47, No. 2, 2000 with greater on gastrography. regenerative on but

EFFICACY OF CHEMO-IMMUNOTHERAPY 181 month Fig. 7. Relationship between serum CEA and of treatment. treatment, serum level of CEA decreased to 3.6ng/ml. US showed no metastatic liver tumors in liver, and serum CEA level only slightly at 3.5 ng/ml, in April 1992. However, from July, liver tumor began to metastasize again and patient eventually died of liver metastasis on January 1,1993 Case 2 A 68-year-old woman visited a private hospital because of epigastric pain. The serum level of CEA at 464ng/ml, and advanced gastric cancer diagnosed based on gastrography and endoscopy. The patient referred to Kurume University Hospital for furr examination and treatment for advanced gastric cancer on April 10, 1991. The liver, spleen and tumor were not palpable on physical examination on admission. The serum level of CA 19-9 normal, and that of CEA at 464ng/ml. Gastrography and endoscopic examination showed gastric cancer type 2, 4.5 ~4.0 cm in size on greater curvature of antrum in stomach (Figs 5a and 6a). The pathological diagnosis based on a biopsy specimen moderately-to-poorly differentiated adenocarcinoma. No metastatic liver tumors were, but swellings in No.8 and No.9 lymph nodes were on CT. Surgery performed through a median laparotomy. Several nodules of peritoneal dissemination were on greater omentum, and tumor invaded pancreas head and portal vein on intraoperative US. This tumor concluded to be unresectable, from se intraoperative findings. So, operative procedure exploratory laparotomy. Administration of MMC (18mg iv) given on operative day, and administration of OK-432 (1 KE/day sc) given from second postoperative day to fourth postoperative day. Administration of OK-432 (5 KE sc) every two days begun from sixth postoperative day. Administration of 5-FU (200mg/day po) begun from 14th postoperative day, and patient left hospital on 17th postoperative day. After that, patient treated by combined administration of MMC (10mg/month), 5-FU (200mg/day) and OK-432 (5 KE/2 weeks). At 2 months operation, re a decrease in serum CEA level (175ng/ml). At 6 months operation, serum CEA level had decreased to normal (2.9 ng/ml). An endoscopic examination showed tumor decreased in size, and region changed to a flat lesion. The central lesion reduced, and. changed to a flat lesion covered with regenerative epilium. Moreover, endoscopic biopsy confirmed no gastric cancer cells. At 12 months operation, an scar on gastrography (Fig. 5b), and tumor completely disappeared with an scar on endoscopic examination (Fig. 6b). Swellings in lymph nodes completely disappeared on CT. The side-effect of treatment only slight leukopenia, grade 2. The PS of patient had been 0 during treatment. The patient had survived for 5 years and 6 months from treatment (Fig. 7). DISCUSSION Generally, various combined chemorapy of 5- FU, MMC and CDDP have been administered for unresectable gastric cancer, but a positive-response rate has been only about 20-30% [2]. Here, we present two cases with a good response to chemorapy consisting of MMC (10mg/month) intravenous administration, and 5'-DFUR (800 mg/day) or 5-FU (200mg/day) per oral administration, and immunorapy of OK-432 (5 KE/2 weeks) intrasubcutaneus administration. Kurihara et al. [3] reported features of cases with good response to chemorapy were Borrmann 2 macroscopic type, differentiated histological type, without metastatic lesions, and with good PS. The features of macroscopical improvement in gastric cancer by chemorapy alteration in tumor to a flat lesion [3]. Both our two cases were differentiated histological type with good PS, and macroscopic type (case 2) Borrmann 2 type. The tumors were altered to a flat lesion by chemorapy. Cases that have responded well to chemorapy were clinically Kurume Medical Journal Vol. 47, No. 2, 2000

182 AOYAGI ET AL. improved a short period [4-6], and at about 6 months treatment, no cancer cells were confirmed by endoscopic biopsy in se cases [6,7]. In our two cases, at 2 or 3 months treatment, re a decrease in serum CEA level, and at 6 or 8 months treatment, no cancer cells were confirmed by endoscopic biopsy. Some reports have said that administration of 5'-DFUR effective for a metastatic lesion from gastroenterological cancer [8-11], and that combined chemorapy of MMC and 5'-DFUR effective for both primary and metastatic lesion in gastroenterological cancer [12-14]. There have been many cases on efficacy of combined chemorapy of MMC and antimetabolite [2]. Arinaga et al. [15] have reported efficacy of combined chemo-immunorapy of MMC and OK-432. Both our two cases had no severe side effect, and PS in se cases good during treatment. Combined chemoimmunorapy of MMC, antimetabolite and OK-432 is thought to be an effective treatment for unresectable gastric cancer and is useful for an improved quality of life of patient. REFERENCES 1. Kurihara M, and Nakaj ima S. Actual medical treatment. In: Chemorapy of Gastric Cancer, Shinkoigaku, Tokyo, pp 85-158,1981. (in Japanese) 2. Kodama I, Aoyagi K, Tanaka T, Kumegawa H, Ohta J et al. A case of advanced gastric cancer with liver and lung metastasis effectively treated by combined chemoimmunorapy of MMC, 5'-DFUR, OK-432. Jpn J Cancer Chemor (Gann to Kagakuryoho) 1993; 20:1237-1240. (in Japanese) 3. Kurihara M, Shirakabe H, and Izumi T. Cytotoxic chemorapy for advanced gastric cancer -from viewpoint of macroscopic improvement on x-ray and gastroscopic views. Stomach and Intestine (I to Cho) 1979;14:1623-1637. (in Japanese) 4. Fukuyama E, Koizumi K, and Kurihara M. Unresectable advanced gastric cancer treated by combined chemorapy of 5'--DFUR, CDDP, MMC. Oncologia 1993; 26:345-350. (in Japanese) 5. Sasaki Y, Sasaki A, Itoh T, and Nehashi Y. Complete response in a case of unresectable gastric cancer with a combination of tegafur, 5-fluorouracil and mitomycin C. Jpn J Cancer Chemor (Gann to Kagakuryoho) 1988; 15:2793-2795. (in Japanese) 6. Fujita K, and Matsue H. Improvement of radiologic and endoscopic appearances of gastric cancer (Borrmann's type 2) by anti-cancer chemorapy. Stomach and Intestine (I to Cho) 1979; 14:1675-1678. (in Japanese) 7. Futatsuki K, Kanda Y, Shimada S, Ishibashi I, Takemori Y et al. A case of advanced gastric cancer showing complete cure by immunochemorapy with FT-207 and OK-432 confirmed by thorough histologic examination of total gastrectomy materials. Jpn J Cancer Clin (Gann no Rinsho) 1985; 31:870-876. (in Japanese) 8. Taguchi T, Sakai K, Terasawa T, Irie K, Okajima K et al. Phase II study of 5'-DFUR (5'-deoxy-5-fluorouridine) by cooperative study group. Jpn J Cancer Chemor (Gann to Kagakuryoho) 1985; 12:2179-2184. (in Japanese) 9. Kimura K, and Suga S. Pharmacological and pharmacodynamic aspects cancer chemorapy with special reference to 5-fluorouracil and its derivatives. Jpn J Cancer Chemor (Gain to Kagakuryoho) 1982; 9:1321-1326. (in Japanese) 10. Nakaguchi K, Nakano Y, Kitahara T, Onoe K, Nagamine H et al. A resected case of gastric carcinoma with complete remission of Virchow's node metastasis by 5'- DFUR administration. Jpn J Cancer Chemor (Gann to Kagakuryoho) 1990; 17:2101-2104. (in Japanese) 11. Matsuda M, Nagao K, Baba K, Nishimura R, Matsuoka Y et al. A case of multiple pulmonary metastases from rectal cancer which responded completely to combination chemorapy using 5'-DFUR and MMC. Jpn J Cancer Chemor (Gann to Kagakuryoho) 1989; 16:2659-2662. (in Japanese) 12. Watanabe S, Mayama M, Oguro M, Wakatsuki S, and Majima H. A case of advanced gastric cancer in which a combination rapy of 5'-DFUR and MMC markedly effective. Jpn J Cancer Chemor (Gann to Kagakuryoho) 1990; 17:2105-2108. (in Japanese) 13. Fujita F, Fujita M, Shimozuma K, and Taguchi T. Combination chemorapy of human gastrointestinal and breast cancer xenografts in nude mice with 5'-deoxy- 5-fluorouridine and mitomycin C. J Jpn Soc Cancer Ther 1986; 21:1386-1396. (in Japanese) 14. Nagamachi Y, Nakano G, Sakamoto K, Takenoshita S, Matsuzawa T et al. Combination chemorapy, 5'-DFUR and MMC on patients with advanced or recurrent stomach and colorectal cancer. J New Remedies Clinics (Shinyaku to Rinsho) 1990; 39:1384-1389. (in Japanese) 15. Arinaga S, Adachi M, and Karimine S. A case of advanced gastric cancer with liver metastasis effectively treated by combined chemoimmunorapy MMC and OK-432. Oncologia 1993; 26:379-382. (in Japanese) Kurume Medical Journal Vol. 47, No. 2, 2000