Minireviews Open Access
Copyright ©The Author(s) 2015. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Oncol. Dec 10, 2015; 6(6): 291-294
Published online Dec 10, 2015. doi: 10.5306/wjco.v6.i6.291
Neoadjuvant chemotherapy followed by surgery in gastric cancer patients with extensive lymph node metastasis
Seiji Ito, Yuichi Ito, Kazunari Misawa, Yasuhiro Shimizu, Taira Kinoshita, Department of Gastroenterological Surgery, Aichi Cancer Center Hospital, Nagoya, Aichi 464-8681, Japan
Author contributions: Ito S wrote the paper; Ito Y, Misawa K, Shimizu Y and Kinoshita T provided critical revision of the article.
Supported by A National Cancer Center Research and Development Fund (23-A-16, 23-A-19, 26-A-4); and a Health and Labour Sciences Research Grant for Clinical Cancer Research (H22-Gan-016) from the Ministry of Health, Labour and Welfare, Japan.
Conflict-of-interest statement: The authors declare no conflict of interest associated with this manuscript.
Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Correspondence to: Seiji Ito, MD, PhD, Department of Gastroenterological Surgery, Aichi Cancer Center Hospital, 1-1 Kanokoden, Chikusa-ku, Nagoya Aichi 464-8681, Japan. seito@aichi-cc.jp
Telephone: +81-52-7626111 Fax: +81-52-7642963
Received: June 10, 2015
Peer-review started: June 11, 2015
First decision: August 4, 2015
Revised: August 26, 2015
Accepted: September 25, 2015
Article in press: September 28, 2015
Published online: December 10, 2015

Abstract

Gastric cancer with extensive lymph node metastasis (ELM) is usually considered unresectable and is associated with poor outcomes. Cases with clinical enlargement of the para-aortic lymph nodes and/or bulky lymph node enlargement around the celiac artery and its branches are generally dealt with as ELM. A standard treatment for gastric cancer with ELM has yet to be determined. Two phase II studies of neoadjuvant chemotherapy followed by surgery showed that neoadjuvant chemotherapy with S-1 plus cisplatin followed by surgical resection with extended lymph node dissection could represent a treatment option for gastric cancer with ELM. However, many clinical questions remain unresolved, including the criteria for diagnosing ELM, optimal regime, number of courses and extent of lymph node dissection.

Key Words: Extended lymph node metastasis, Gastric cancer, Neoadjuvant chemotherapy, Gastrectomy, Lymph node dissection

Core tip: Gastric cancer with extensive lymph node metastasis (ELM) is usually considered unresectable and associated with poor outcomes. Phase II studies of neoadjuvant chemotherapy followed by surgery have shown the efficacy of this multimodal therapy for this pathology, but many clinical questions remain unresolved, including the criteria for diagnosing ELM, optimal regime, number of courses and extent of lymph node dissection.



INTRODUCTION

Surgical resection represents the most important step in the treatment of gastric cancer and is the only approach offering complete cure. Systemic chemotherapy is administered for gastric cancer patients with liver, peritoneal, or other distant metastases, but extensive lymph node metastasis (ELM) stands on the borderline between surgical resection and systemic chemotherapy. The development of treatment for gastric cancer with ELM is a difficult and challenging task. This article reviews previous reports and looks to the future of treatment for gastric cancer with ELM.

ELM IN GASTRIC CANCER

No widely accepted consensus has been reached regarding the definition of ELM. In most reports, cases with clinical enlargement of the para-aortic lymph nodes (PAN) but no other distant metastases have generally been dealt with as ELM[1-3]. The range of PAN that are subject to surgical resection extends from the caudal end of the celiac axis to the cranial side of the inferior mesenteric artery, and is taken to be No. 16a2-b1 in the Japanese classification of gastric cancer[4].

Most reports consider positivity for PAN metastasis with enlargement of ≥ 1 cm in the long axis as ELM[1-3]. In the most recent response evaluation criteria in solid tumors (RECIST)[5], enlargement of ≥ 15 mm in the short axis is considered to represent measurable and assessable lymph nodes. Using multislice computed tomography, Marrelli et al[6] diagnosed clinical metastasis with enlargement of ≥ 8 mm in the short axis of PAN in gastric cancer, and reported positive and negative predictive values of 73% and 97%, respectively, with 93% accuracy.

Indications for surgical intervention do not always need to follow RECIST criteria, as the purpose of these criteria is to objectively evaluate treatment effect. However, further investigation of the criteria for diagnosing ELM is needed in the future.

In a series of Japan Clinical Oncology Group (JCOG) studies by Yoshikawa et al[3] and Tsuburaya et al[1], bulky lymph node enlargement around the celiac artery and its branches (bulky N), in addition to clinical enlargement of PAN, is treated collectively as ELM. The reasons are that patients with such metastases are commonly considered to be inoperable and, similar to PAN-positive patients, prognosis is poor even if curative resection is possible. According to the report by Tsuburaya et al[1], survival outcomes are equivalent in PAN-only patients and bulky N-only patients. Treating PAN metastasis and bulky N as a single disease group has thus been considered reasonable.

STANDARD TREATMENT FOR GASTRIC CANCER WITH ELM

From the 1980s to 1990s, PAN dissection was actively performed at some institutions in Japan. As a result, PAN metastasis was seen in about 20% of patients at maximum, with long-term survival achieved in about 10%-20% of these patients[7,8]. Similar reports have recently been seen from Western countries[9].

On the other hand, JCOG 9501 was conducted to verify the significance of prophylactic PAN dissection, but no meaningful impact was found[10]. As a result, while PAN were categorized as regional lymph nodes in past Japanese classifications[4], the new classifications categorize them as distant lymph nodes[11] that are no longer considered a target of curative resection. PAN are also taken to be distant lymph nodes in Western guidelines[12], and are again not considered a target of curative resection.

However, it must be noted that the results of JCOG 9501 show the ineffectiveness of prophylactic PAN dissection. In that sense, a standard treatment for gastric cancer with clinical PAN metastasis has yet to be determined.

No comprehensive investigations of gastric cancer with bulky N have been reported. In some cases, curative resection may be achieved, but many cases are judged as unresectable because of direct invasion of major blood vessels.

TREATMENT OUTCOMES OF NEOADJUVANT CHEMOTHERAPY FOR GASTRIC CANCER WITH ELM

The JCOG 0001 was a phase II clinical study for gastric cancer patients with ELM[3]. After excluding micrometastases to the liver and peritoneum by staging laparoscopy, irinotecan plus cisplatin combination therapy (IP) was administered as neoadjuvant chemotherapy. This was followed by gastrectomy with extended lymph node dissection including PAN. As a result of three treatment-related deaths, the study was discontinued. However, a subsequent follow-up and survival analysis showed a median survival time (MST) of 14.6 mo and a 3-year survival rate of 27% (95%CI: 15.2%-38.8%), exceeding the 3-year survival rate threshold (15%) established in the initial protocol. Although careful management of adverse events and appropriate patient selection are essential, this treatment could be recommended for gastric cancer patients with ELM.

In the JCOG 0405 study[1], S-1 plus cisplatin combination therapy (SP) was used for neoadjuvant chemotherapy in similar patients, and the primary endpoint was the percentage of complete resections with clear margins in the primary tumor (R0 resection). Fifty-three patients were enrolled, and among the 51 who proved eligible, R0 resection was performed in 42 patients (82.4%). A subsequent survival analysis showed an unexpectedly good 3-year survival rate of 58.5% (95%CI: 44.1%-70.4%).

Some reports have shown better survival results in gastric cancer patients who had only abdominal lymph node metastases. Yoshida et al[13], investigated cases of long-term survival in patients who underwent chemotherapy for advanced gastric cancer, and reported that the 2- and 5-year survival rates of patients with metastasis to the abdominal lymph nodes only were 14.3% and 10.4%, respectively. Park et al[14] reported a 3-year survival rate of 13.1% in gastric cancer patients with isolated involvement of PAN.

In those reports, clinically metastases to the liver and peritoneum that were not obvious may not have been excluded, as such metastases could not be excluded with laparotomy or staging laparoscopy. In addition, the extent of abdominal lymph node involvement in those studies may have partly exceeded that of the two neoadjuvant studies. Accordingly, direct comparison of survival rates between these chemotherapy and neoadjuvant studies is inappropriate. Despite this, the 3-year survival rate seen in the JCOG 0405 study is notably high. Furthermore, Yoshida et al[13] and Park et al[14] reported that some kind of local therapy had been used in many cases of long-term survival in their articles. In view of these results, neoadjuvant chemotherapy followed by surgical resection could represent a useful treatment option for gastric cancer with ELM. However, Tsuburaya et al[1] described a lower 5-year survival rate for patients with both bulky N and PAN. The indication of neoadjuvant chemotherapy followed by surgery for this target is controversial.

OPTIMAL CHEMOTHERAPY REGIME FOR GASTRIC CANCER WITH ELM

From the results of the above-mentioned JCOG 0001 and JCOG 0405 studies, 2 or 3 courses of SP is currently recommended for gastric cancer patients with ELM. For unresectable or recurrent gastric cancer, on the other hand, several triplet regimes such as docetaxel/cisplatin/5-fluorouracil[15] or docetaxel/cisplatin/S-1 combination therapy (DCS)[16-19], have been developed and are reported to provide markedly high response rates. The JCOG 1002 study was therefore undertaken with DCS as neoadjuvant chemotherapy[20], and the results are scheduled to be published soon.

The optimal number of cycles for neoadjuvant chemotherapy has not been established, but 2 or 3 cycles of therapy have been adopted in most neoadjuvant studies. The COMPASS-D trial, a randomized phase II trial with a factorial design comparing 2 and 4 courses of SP and DCS in neoadjuvant chemotherapy, is underway for curable gastric cancer with serosal invasion[21]. Informative results are expected in terms of optimal regime and number of courses of neoadjuvant chemotherapy for gastric cancer from that trial.

No detailed reports have been published regarding the optimal interval between neoadjuvant chemotherapy and surgery, but patients ordinarily receive surgery if they meet adequate organ functions according to laboratory testing within 14 d before surgery[20].

SIGNIFICANCE OF EXTENDED DISSECTION FOR GASTRIC CANCER WITH ELM

In the above-mentioned JCOG 0001 and JCOG 0405 studies, gastrectomy with D2 plus PAN dissection was performed following neoadjuvant chemotherapy. This strategy is based on the high rate of PAN metastasis seen not only in patients with clinical PAN metastasis, but also in patients with bulky N. In addition, complete elimination of cancer cells can hardly be expected with a few courses of neoadjuvant chemotherapy. Inoue et al[22] evaluated the efficacy and feasibility of neoadjuvant chemotherapy with SP in initially unresectable locally advanced gastric cancer, and reported 3-year survival rates of 31.0% and 53.8% in all and curative cases, respectively. However, they also reported that the most common site for initial recurrence after R0 resection was the PAN. Wang et al[2] reported an MST of 29.8 mo after performing gastrectomy with D2 dissection following capecitabine plus oxaliplatin combination therapy in patients with clinical PAN metastasis. Those results should be interpreted with caution, since selection bias for curative cases may have had an effect. The good survival outcomes in the JCOG 0405 and JCOG 0001 studies were obtained with PAN dissection as well as gastrectomy plus D2 lymph node dissection. Given these findings, gastric cancer with ELM should be treated using concurrent PAN dissection not only in patients with PAN metastasis, but also in bulky N-only patients. However, further investigation is needed regarding the optimal extent of lymph node dissection for gastric cancer patients with ELM.

CONCLUSION

A certain level of outcome is expected with multimodal therapy combining neoadjuvant chemotherapy and extended lymph node dissection in gastric cancer patients with ELM. At the same time, many questions remain to be unresolved, including the criteria for diagnosing ELM, optimal regime, number of courses and range of lymph node dissection.

Footnotes

P- Reviewer: Kim KD, Sava G

S- Editor: Ji FF L- Editor: A E- Editor: Li D

References
1.  Tsuburaya A, Mizusawa J, Tanaka Y, Fukushima N, Nashimoto A, Sasako M. Neoadjuvant chemotherapy with S-1 and cisplatin followed by D2 gastrectomy with para-aortic lymph node dissection for gastric cancer with extensive lymph node metastasis. Br J Surg. 2014;101:653-660.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 195]  [Cited by in F6Publishing: 219]  [Article Influence: 21.9]  [Reference Citation Analysis (1)]
2.  Wang Y, Yu YY, Li W, Feng Y, Hou J, Ji Y, Sun YH, Shen KT, Shen ZB, Qin XY. A phase II trial of Xeloda and oxaliplatin (XELOX) neo-adjuvant chemotherapy followed by surgery for advanced gastric cancer patients with para-aortic lymph node metastasis. Cancer Chemother Pharmacol. 2014;73:1155-1161.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 44]  [Cited by in F6Publishing: 41]  [Article Influence: 4.1]  [Reference Citation Analysis (0)]
3.  Yoshikawa T, Sasako M, Yamamoto S, Sano T, Imamura H, Fujitani K, Oshita H, Ito S, Kawashima Y, Fukushima N. Phase II study of neoadjuvant chemotherapy and extended surgery for locally advanced gastric cancer. Br J Surg. 2009;96:1015-1022.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 148]  [Cited by in F6Publishing: 169]  [Article Influence: 11.3]  [Reference Citation Analysis (0)]
4.  Japanese Gastric Cancer Association. Japanese Classification of Gastric Carcinoma - 2nd English Edition -. Gastric Cancer. 1998;1:10-24.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 982]  [Reference Citation Analysis (0)]
5.  Eisenhauer EA, Therasse P, Bogaerts J, Schwartz LH, Sargent D, Ford R, Dancey J, Arbuck S, Gwyther S, Mooney M. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer. 2009;45:228-247.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 15860]  [Cited by in F6Publishing: 19066]  [Article Influence: 1271.1]  [Reference Citation Analysis (1)]
6.  Marrelli D, Mazzei MA, Pedrazzani C, Di Martino M, Vindigni C, Corso G, Morelli E, Volterrani L, Roviello F. High accuracy of multislices computed tomography (MSCT) for para-aortic lymph node metastases from gastric cancer: a prospective single-center study. Ann Surg Oncol. 2011;18:2265-2272.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 30]  [Cited by in F6Publishing: 35]  [Article Influence: 2.7]  [Reference Citation Analysis (0)]
7.  Fujimura T, Nakamura K, Oyama K, Funaki H, Fujita H, Kinami S, Ninomiya I, Fushida S, Nishimura G, Kayahara M. Selective lymphadenectomy of para-aortic lymph nodes for advanced gastric cancer. Oncol Rep. 2009;22:509-514.  [PubMed]  [DOI]  [Cited in This Article: ]
8.  Kunisaki C, Akiyama H, Nomura M, Matsuda G, Otsuka Y, Ono H, Nagahori Y, Hosoi H, Takahashi M, Kito F. Comparison of surgical results of D2 versus D3 gastrectomy (para-aortic lymph node dissection) for advanced gastric carcinoma: a multi-institutional study. Ann Surg Oncol. 2006;13:659-667.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 47]  [Cited by in F6Publishing: 50]  [Article Influence: 2.8]  [Reference Citation Analysis (0)]
9.  Roviello F, Pedrazzani C, Marrelli D, Di Leo A, Caruso S, Giacopuzzi S, Corso G, de Manzoni G. Super-extended (D3) lymphadenectomy in advanced gastric cancer. Eur J Surg Oncol. 2010;36:439-446.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 50]  [Cited by in F6Publishing: 61]  [Article Influence: 4.4]  [Reference Citation Analysis (0)]
10.  Sasako M, Sano T, Yamamoto S, Kurokawa Y, Nashimoto A, Kurita A, Hiratsuka M, Tsujinaka T, Kinoshita T, Arai K. D2 lymphadenectomy alone or with para-aortic nodal dissection for gastric cancer. N Engl J Med. 2008;359:453-462.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 698]  [Cited by in F6Publishing: 720]  [Article Influence: 45.0]  [Reference Citation Analysis (0)]
11.  Japanese Gastric Cancer Association. Japanese classification of gastric carcinoma: 3rd English ed. Gastric Cancer. 2011;14:101-112.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2390]  [Cited by in F6Publishing: 2656]  [Article Influence: 204.3]  [Reference Citation Analysis (0)]
12.  Ajani JA, Bentrem DJ, Besh S, D’Amico TA, Das P, Denlinger C, Fakih MG, Fuchs CS, Gerdes H, Glasgow RE. Gastric cancer, version 2.2013: featured updates to the NCCN Guidelines. J Natl Compr Canc Netw. 2013;11:531-546.  [PubMed]  [DOI]  [Cited in This Article: ]
13.  Yoshida M, Ohtsu A, Boku N, Miyata Y, Shirao K, Shimada Y, Hyodo I, Koizumi W, Kurihara M, Yoshida S. Long-term survival and prognostic factors in patients with metastatic gastric cancers treated with chemotherapy in the Japan Clinical Oncology Group (JCOG) study. Jpn J Clin Oncol. 2004;34:654-659.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 67]  [Cited by in F6Publishing: 74]  [Article Influence: 3.9]  [Reference Citation Analysis (0)]
14.  Park IH, Kim SY, Kim YW, Ryu KW, Lee JH, Lee JS, Park YI, Kim NK, Park SR. Clinical characteristics and treatment outcomes of gastric cancer patients with isolated para-aortic lymph node involvement. Cancer Chemother Pharmacol. 2011;67:127-136.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 22]  [Cited by in F6Publishing: 24]  [Article Influence: 1.7]  [Reference Citation Analysis (0)]
15.  Van Cutsem E, Moiseyenko VM, Tjulandin S, Majlis A, Constenla M, Boni C, Rodrigues A, Fodor M, Chao Y, Voznyi E. Phase III study of docetaxel and cisplatin plus fluorouracil compared with cisplatin and fluorouracil as first-line therapy for advanced gastric cancer: a report of the V325 Study Group. J Clin Oncol. 2006;24:4991-4997.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1331]  [Cited by in F6Publishing: 1405]  [Article Influence: 78.1]  [Reference Citation Analysis (0)]
16.  Fushida S, Fujimura T, Oyama K, Yagi Y, Kinoshita J, Ohta T. Feasibility and efficacy of preoperative chemotherapy with docetaxel, cisplatin and S-1 in gastric cancer patients with para-aortic lymph node metastases. Anticancer Drugs. 2009;20:752-756.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 29]  [Cited by in F6Publishing: 30]  [Article Influence: 2.0]  [Reference Citation Analysis (0)]
17.  Koizumi W, Nakayama N, Tanabe S, Sasaki T, Higuchi K, Nishimura K, Takagi S, Azuma M, Ae T, Ishido K. A multicenter phase II study of combined chemotherapy with docetaxel, cisplatin, and S-1 in patients with unresectable or recurrent gastric cancer (KDOG 0601). Cancer Chemother Pharmacol. 2012;69:407-413.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 57]  [Cited by in F6Publishing: 63]  [Article Influence: 4.8]  [Reference Citation Analysis (0)]
18.  Nakayama N, Koizumi W, Sasaki T, Higuchi K, Tanabe S, Nishimura K, Katada C, Nakatani K, Takagi S, Saigenji K. A multicenter, phase I dose-escalating study of docetaxel, cisplatin and S-1 for advanced gastric cancer (KDOG0601). Oncology. 2008;75:1-7.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 26]  [Cited by in F6Publishing: 28]  [Article Influence: 1.8]  [Reference Citation Analysis (0)]
19.  Sato Y, Takayama T, Sagawa T, Takahashi Y, Ohnuma H, Okubo S, Shintani N, Tanaka S, Kida M, Sato Y. Phase II study of S-1, docetaxel and cisplatin combination chemotherapy in patients with unresectable metastatic gastric cancer. Cancer Chemother Pharmacol. 2010;66:721-728.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 54]  [Cited by in F6Publishing: 57]  [Article Influence: 3.8]  [Reference Citation Analysis (0)]
20.  Katayama H, Ito S, Sano T, Takahari D, Mizusawa J, Boku N, Tsuburaya A, Terashima M, Sasako M. A Phase II study of systemic chemotherapy with docetaxel, cisplatin, and S-1 (DCS) followed by surgery in gastric cancer patients with extensive lymph node metastasis: Japan Clinical Oncology Group study JCOG1002. Jpn J Clin Oncol. 2012;42:556-559.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 18]  [Cited by in F6Publishing: 21]  [Article Influence: 1.8]  [Reference Citation Analysis (0)]
21.  Yoshikawa T, Taguri M, Sakuramoto S, Kunisaki C, Fukunaga T, Ito S, Cho H, Tanabe K, Nishikawa K, Matsui T. A comparison of multimodality treatment: two and four courses of neoadjuvant chemotherapy using S-1/CDDP or S-1/CDDP/docetaxel followed by surgery and S-1 adjuvant chemotherapy for macroscopically resectable serosa-positive gastric cancer: a randomized phase II trial (COMPASS-D trial). Jpn J Clin Oncol. 2012;42:74-77.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 13]  [Cited by in F6Publishing: 15]  [Article Influence: 1.2]  [Reference Citation Analysis (0)]
22.  Inoue K, Nakane Y, Kogire M, Fujitani K, Kimura Y, Imamura H, Tamura S, Okano S, Kwon AH, Kurokawa Y. Phase II trial of preoperative S-1 plus cisplatin followed by surgery for initially unresectable locally advanced gastric cancer. Eur J Surg Oncol. 2012;38:143-149.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 22]  [Cited by in F6Publishing: 30]  [Article Influence: 2.3]  [Reference Citation Analysis (0)]