Retrospective analyses of cisplatin-based doublet combination chemotherapy in patients with advanced gastric cancer
© Lim et al; licensee BioMed Central Ltd. 2010
Received: 3 March 2010
Accepted: 26 October 2010
Published: 26 October 2010
Cisplatin-based chemotherapy, in combination with fluoropyrimidines or taxanes, have demonstrated efficacy against advanced gastric cancer (AGC). This retrospective study was performed with the data obtained from our cancer chemotherapy registry and eight another cancer centers.
In 2008, a total of 283 AGC patients were treated with cisplatin-based doublet chemotherapy in the first-line setting: capecitabine plus cisplatin (XP, n = 77), S-1 plus cisplatin (SP, n = 97), taxanes (docetaxel, paclitaxel) plus cisplatin (TP, n = 72), and 5-fluorouracil plus platinum (FP, n = 37). The primary endpoint of this study was overall survival (OS) and the secondary endpoints were safety, response rate and progression-free survival (PFS).
The median age was 54 years with a range of 28-78 years and median delivered number of chemotherapy cycles were XP: 4, SP: 5, TP: 5 and FP: 5, respectively. Objective tumor responses (38%; 95% CI, 32-43%) were 40% for XP, 42% for SP, 36% for DP, and 24% for FP. The estimated median PFS was 4.5 months (95% CI, 3.6-5.4 months) and the median OS was 12.3 months (95% CI, 10.8-13.7 months). No statistically significant difference was found between each regimen used as first-line chemotherapy. At multivariate analysis, independent prognostic parameters for OS were prior gastrectomy, peritoneal dissemination, performance status and hemoglobin level
All of the cisplatin-based doublet chemotherapy regimens appear to be active as first-line chemotherapy for AGC. With better patient selection according to clinical parameters and molecular markers, clinical outcomes of AGC patients in first-line setting can be improved.
Gastric cancer is the most frequently occurring malignancy in Korea, and is one of the main causes of cancer death . For patients with recurrent, metastatic, or advanced gastric cancer (AGC), chemotherapy can improve survival, and possibly, provide significant palliation of symptoms [2, 3]. Several randomized trials have demonstrated that 5-fluorouracil (5-FU)-based chemotherapy is superior to best supportive care in terms of survival and preservation of quality of life (QOL) [2, 3]. While the treatment options for AGC have expanded in recent years to include newer agents such as taxanes (paclitaxel and docetaxel), irinotecan and oxaliplatin, the prognosis of AGC patients remains poor.
Multi-drug combination chemotherapy regimens have generally provided significantly higher response rates, but no better overall survival . Despite the lack of evidence for benefit associated with cisplatin-based combination chemotherapy, it is a common practice to offer cisplatin-based doublet or triplet chemotherapy for AGC patients in the first-line setting, because 5-FU monotherapy has only limited activity. Recently, oral fluoropyrimidines, including capecitabine and S-1, are replacing infusional 5-FU. Both capecitabine and S-1 are considered to be more tolerable than 5-FU, and has been shown to exhibit antitumor activity against AGC [5–7]. Administration of docetaxel, as a component of cisplatin-based doublet or triplet, has also produced significant benefit for AGC patients [8–10]. Although it is currently unclear whether combination of 3 active drugs is superior to doublet combination, our recent randomized study suggested that cisplatin-based doublet and triplet chemotherapy showed similar outcomes .
A decision of chemotherapy regimens for an individual patient may be a common clinical situation. Factors considered include the extent of disease, the potential toxicity, especially for those with impaired swallowing or with low performance status, as well as the activity of chemotherapy. Because well-designed, randomized, controlled clinical trials are sparse in AGC, an exploratory, or retrospective analysis seems to be an important source of data to allow the definition of optimal treatment, enhance patient counseling, and generate hypotheses for future studies. We therefore decided to evaluate cisplatin-based combination regimens as first-line chemotherapy for AGC. The present evaluation was also done with the intent to plan and develop improved therapeutic strategies for chemotherapy-naïve AGC patients.
This is a multicenter, retrospective study. Between January and December 2008, 283 patients were treated with first-line cisplatin-based doublet combination regimens at 9 tertiary centers in Korea. The criteria for case inclusion were as follows: (1) histologically confirmed diagnosis of gastric adenocarcinoma, (2) no prior chemotherapy or radiotherapy except for adjuvant treatments, (3) presence of metastatic disease, (4) availability of clinical data at the beginning of therapy and follow-up. All patients had been treated with taxane/cisplatin or fluoropyrimidine/cisplatin doublet combination regimens as their first-line therapy for advanced disease. We excluded patients who were enrolled in clinical trials to ensure the choice of chemotherapy regimen was at the discretion of the treating physician. We collected follow-up patient data from the cancer registry. All the data was prospectively recorded and only the survival data was updated at the time of analyses. Written informed consent was given by all patients prior to receiving chemotherapy, according to institutional guidelines. Approval of the study was obtained from the institutional review board or ethics committee.
All patients received cisplatin-based first-line chemotherapy for AGC. Cisplatin was, in all cases, given at a dose of 60-100 mg/m2 infusion on day 1 in combination with capecitabine (1000 mg/m2 bid po on days 1-14, XP; n = 77), S-1 (40 mg/m2 bid po on days 1-21, SP; n = 97), docetaxel (75 mg/m2 iv on day 1, DP; n = 72), or 5-FU (800-1000 mg/m 2 iv on days 1-5 as a protracted continuous infusion, FP; n = 37). Chemotherapy was repeated every 3 weeks (XP, DP and FP) or every 5 weeks (SP) according to the regimen. The treating physician determined chemotherapy regimen, as well as the initial dose of cisplatin, for each patient. Treatment was continued until disease progression or lack of clinical benefit, withdrawal of consent, justifiable withdrawal at the investigator's discretion, or toxicity. Toxicities were graded according the National Cancer Institute (NCI) criteria (CTCAE v3). The dosage of the subsequent cycles was adjusted according to the toxic effects that developed during the preceding cycle. All patients received standard supportive regimen consisting of hydration and antiemetics. The prophylactic use of hematopoietic growth factors was not allowed during treatment, except for patients with febrile neutropenia or grade 4 myelosuppression at the treating physician's discretion. After this combination chemotherapy had failed, second-line chemotherapy was recommended to all the patients if their performance status was preserved. According to the guidelines and department policies, all tumor measurements were assessed after every 2 courses of chemotherapy, by using spiral abdominopelvic computed tomography (CT) scan and other tests that were used initially to stage the tumor. Tumor response was evaluated according to the Response Evaluation Criteria for Solid Tumors (RECIST) . As a general principle for determining clinical response, a confirmatory CT scan was recommended at least 4 weeks apart.
The primary endpoint of this study was overall survival (OS). The starting point of OS and progression-free survival (PFS) was the first day of chemotherapy. The date of disease progression or death from causes other than AGC was used in calculating PFS. Time to death, whatever the cause, was used to calculate OS. PFS and OS were estimated according to the Kaplan-Meier method and the statistical significance of survival curves between groups was tested with a log-rank test. To examine the impact of clinical and treatment variables on the outcomes of chemotherapy, multivariate Cox regression models were used. Covariates included were age (below vs. ≥ median), gender, previous gastrectomy, an Eastern Cooperative Oncology Group (ECOG) performance status (0-1 vs. ≥2), weight loss (>5%) before treatment, number of involved sites (one vs. ≥2), metastases (liver, bone, and bone marrow), presence of ascites, baseline chemistry profiles (serum albumin, alkaline phosphatase, and bilirubin), and chemotherapy regimens. Laboratory parameters were initially recorded as continuous variables and later dichotomized according to the median value of each variable (below vs. ≥ median). All P values were two-sided, with P < 0.05 indicating statistical significance.
XP (n = 77)
SP (n = 97)
DP (n = 72)
FP (n = 37)
ECOG performance status
Abdominal lymph nodes
Chemotherapy compliance and toxicity
XP (n = 77)
SP (n = 97)
DP (n = 72)
FP (n = 37)
Reasons for discontinuation
Overall grade 3 or 4 toxicity
Of a total of 283 patients, 22 could not be evaluated for responses because of the absence of any measurable lesions or early discontinuation of therapy. Objective responses to cisplatin-based chemotherapy were noted in 107 patients (response rate, 38%; 95% confidence interval [CI], 32-43%), including two complete responses seen in XP patients; 40% for XP, 42% for SP, 36% for DP, and 24% for FP. Patients who had a poor performance status (≥2 in ECOG scale) were significantly less likely to respond to first-line chemotherapy (24% vs. 40%; p < 0.001) compared to those with an ECOG performance status of 0 or 1. Other factor associated with lack of optimal response was the presence of peritoneal dissemination (31% vs. 45%; p = 0.047). Response rate was not significantly influenced by age, gender, weight loss, baseline laboratory parameters, metastasis, or chemotherapy regimen.
Univariate analysis according to baseline clinical parameters
10.3 - 13.4
11.3 - 15.4
0 or 1
11.9 - 14.6
1.0 - 10.8
6.0 - 9.8
10.3 - 16.4
No. of involved site(s)
11.4 - 14.3
6.7 - 10.3
10.4 - 14.1
9.5 - 14.8
10.7 - 14.2
6.5 - 9.5
12.4 - 15.4
8.4 - 12.7
10.8 - 14.4
9.6 - 14.3
6.7 - 15.7
11.7 - 14.8
8.6 - 15.4
7.1 - 15.5
Multivariate analysis according to baseline clinical parameters
No prior gastrectomy
Two or more metastatic sites
Poor performance status
After first-line failure, second-line chemotherapy was administered for more than half of patients (n = 162). Specifically, 34 (44%) XP patients received second-line chemotherapy, and 55 (57%) SP patients, 49 (68%) DP patients and 24 (65%) FP patients were treated with second-line therapy. OS was longer in the group able to receive second-line chemotherapy (13.9 vs. 10.1 months, p = 0.024) than in those without further treatment.
Despite recent advances in the treatment of AGC , AGC patients treated with first-line chemotherapy have median OS rarely exceeding 12 months. In the current multicenter, retrospective analysis, outcomes for AGC are comparable to those in the published trials of combination chemotherapy. Although this study is retrospective in nature, the results provide a piece of evidence that patients with AGC may derive an indisputable benefit from cisplatin-based doublet chemotherapy.
AGC is an incurable condition where the aim of treatment is to improve survival and to palliate symptoms. Disease may respond to several types of chemotherapy initially, and these treatments have been shown to provide palliation as indicated by improvement in duration and/or quality of survival [2, 3]. The best choice of chemotherapy regimen for patients with AGC is still a matter of controversy and requires further investigation . Currently, fluoropyrimidine and cisplatin combination chemotherapy is accepted as a standard regimen by many oncologists. It is presently unclear whether the triplet combination is superior to cisplatin-based doublets for patients with AGC. A meta-analysis showed a difference in OS of approximately 2 months in favor of the anthracycline-containing triplets versus doublets . However, our recently published, randomized phase II study comparing epirubicin, cisplatin plus capecitabine combination with cisplatin plus capecitabine doublet showed similar efficacy outcomes . Among other 3-drug combination regimens, docetaxel-containing triplet chemotherapy (docetaxel, cisplatin and 5-FU) showed superior time-to-progression (5.6 months vs. 3.7 months) to doublet (cisplatin and 5-FU) . However, the observed OS benefit of triplet was less than one month (9.2 months vs. 8.6 months), and there was substantial grade 3 or 4 toxicity.
In our analysis, there appears to be no advantage of one cisplatin-based doublet over the others. While there was no relevant difference is OS between treatment groups, it is worth considering the possible role that second-line therapy could have had on survival. More than half of patients received second-line chemotherapy. Furthermore, our observation that PFS was shorter with DP or FP than XP or SP is likely related to negative prognostic factors influencing the choice of intravenous chemotherapeutic agents instead of oral ones. AGC patients who already had peritoneal dissemination, with or without ascites, could not tolerate oral agents. Similarly, we cannot rule out a possibility that the choice of a chemotherapeutic agent depends on previous ones. Although we could not assess time to recurrence after the completion of adjuvant therapy, some AGC patients have received adjuvant chemotherapy with 5-FU, so it seems more prudent to avoid fluoropyrimidines in the first-line regimen for reasons of efficacy. Patients with rapidly progressing disease are an unfavorable setting of patients unlikely to benefit from first-line chemotherapy. For the present, the decision to use specific drug(s) in patients with AGC should be determined by their relative merits on a case-by-case basis.
It is also necessary to better define the sub-population of patients who truly benefit from combination chemotherapy because there is potential for toxicity from the treatment. Therefore, the identification of factors allowing the selection of patients who are likely to benefit from chemotherapy is an important challenge. In a pooled analysis of 3 randomized trials, Chau et al.  investigated the prognostic significance of the baseline factors in 1080 chemotherapy-naïve patients with esophagogastric cancer. They found that poor performance status, metastases to liver and peritoneum, and alkaline phosphatase significantly predicted poor survival. Our previous retrospective study in 1455 AGC patients have revealed that poor prognostic factors were no previous gastrectomy, low albumin, high alkaline phosphatase, bone metastasis, the presence of ascites, and a poor performance status . In the current study, hemoglobin level, along with prior gastrectomy, peritoneal dissemination of disease and performance status, emerged as the significant survival predictor. When interpreting the results, it is of note that this analysis represents only a small sample of patients, and we cannot completely exclude the possibility that lower levels of performance status may be reflective of other occult predictors for a poor prognosis.
Although it is conceived that the rationale for offering palliative gastrectomy to patients with unresectable or metastatic gastric cancer is to avoid tumor bleeding, perforation, obstruction, or to improve the outcome by reducing tumor burden, the role of palliative gastrectomy in AGC patients with metastatic disease needs clarification. A randomized trial (reductive gastrectomy for advanced tumor in two Asian countries, REGATTA, KGCA01/JCOG0705) is underway. Besides clinical parameters, appropriate patient selection based on molecular markers is one of the most extensively studied areas in clinical research. While it is still at an early stage and it would take years before we can see clinical application, extensive work is ongoing to identify possible molecular markers, including epidermal growth factor receptor (EGFR) or vascular endothelial growth factor (VEGF) expression [16, 17], Her2/neu amplification , and excision repair cross-complementing gene 1 (ERCC1) , that could be linked to sensitivity or resistance to specific agents, as well as specific genotype variations harbored in different ethnicities. The predictive value of KRAS mutation in metastatic colorectal cancer patients treated with anti-EGFR monoclonal antibodies, cetuximab or panitumumab, has recently been suggested . While gastric cancer is sharing many phenotypic and molecular genetic changes with colorectal cancer, recent molecular studies in gastric cancer have mostly found a lower incidence of KRAS mutation than in colorectal cancer [21, 22].
Although cisplatin is often used in combination with other agents, it is well known that cisplatin is associated with significant toxicity and usually requires a high level of clinical monitoring and supportive care including intensive intravenous hydration. Oxaliplatin-based regimens have been actively investigated to improve the efficacy and tolerability of combination chemotherapy for AGC patients[5, 23]. Oxaliplatin has significant activity against some cisplatin-resistant tumors and a favorable safety profile over cisplatin.
The comparison of the regimens that were the focus of this analysis suggests that cisplatin-based combination chemotherapy may represent a therapeutic ceiling as far as cytotoxic agents are concerned. As seen in a recent phase III study , there is clearly interest in exploring molecular markers, and it may be that further advances in the treatment of AGC will only be achieved with development of novel targeted agents. Also, with better patient selection, clinical outcomes of AGC patients in first-line setting can be improved. Emerging science and the knowledge of disease may further guide us to develop individualized treatment for AGC patients.
This study was supported in part by a grant of the Korea Health 21 R&D Project, Ministry of Health & Welfare, Republic of Korea (0412-CR01-0704-0001).
- Won YJ, Sung J, Jung KW, Kong HJ, Park S, Shin HR, Park EC, Ahn YO, Hwang IK, Lee DH, et al: Nationwide Cancer Incidence in Korea, 2003-2005. Cancer Res Treat. 2009, 41 (3): 122-131. 10.4143/crt.2009.41.3.122.View ArticlePubMedPubMed CentralGoogle Scholar
- Pyrhonen S, Kuitunen T, Nyandoto P, Kouri M: Randomised comparison of fluorouracil, epidoxorubicin and methotrexate (FEMTX) plus supportive care with supportive care alone in patients with non-resectable gastric cancer. Br J Cancer. 1995, 71 (3): 587-591.View ArticlePubMedPubMed CentralGoogle Scholar
- Glimelius B, Ekstrom K, Hoffman K, Graf W, Sjoden PO, Haglund U, Svensson C, Enander LK, Linne T, Sellstrom H, et al: Randomized comparison between chemotherapy plus best supportive care with best supportive care in advanced gastric cancer. Ann Oncol. 1997, 8 (2): 163-168. 10.1023/A:1008243606668.View ArticlePubMedGoogle Scholar
- Ohtsu A, Yoshida S, Saijo N: Disparities in gastric cancer chemotherapy between the East and West. J Clin Oncol. 2006, 24 (14): 2188-2196. 10.1200/JCO.2006.05.9758.View ArticlePubMedGoogle Scholar
- Cunningham D, Starling N, Rao S, Iveson T, Nicolson M, Coxon F, Middleton G, Daniel F, Oates J, Norman AR: Capecitabine and oxaliplatin for advanced esophagogastric cancer. N Engl J Med. 2008, 358 (1): 36-46. 10.1056/NEJMoa073149.View ArticlePubMedGoogle Scholar
- Kang YK, Kang WK, Shin DB, Chen J, Xiong J, Wang J, Lichinitser M, Guan Z, Khasanov R, Zheng L, et al: Capecitabine/cisplatin versus 5-fluorouracil/cisplatin as first-line therapy in patients with advanced gastric cancer: a randomised phase III noninferiority trial. Ann Oncol. 2009, 20 (4): 666-673. 10.1093/annonc/mdn717.View ArticlePubMedGoogle Scholar
- Koizumi W, Narahara H, Hara T, Takagane A, Akiya T, Takagi M, Miyashita K, Nishizaki T, Kobayashi O, Takiyama W, et al: S-1 plus cisplatin versus S-1 alone for first-line treatment of advanced gastric cancer (SPIRITS trial): a phase III trial. Lancet Oncol. 2008, 9 (3): 215-221. 10.1016/S1470-2045(08)70035-4.View ArticlePubMedGoogle Scholar
- Park SH, Kang WK, Lee HR, Park J, Lee KE, Lee SH, Park JO, Kim K, Kim WS, Chung CW, et al: Docetaxel plus cisplatin as second-line therapy in metastatic or recurrent advanced gastric cancer progressing on 5-fluorouracil-based regimen. Am J Clin Oncol. 2004, 27 (5): 477-480. 10.1097/01.coc.0000136018.81814.79.View ArticlePubMedGoogle Scholar
- Park KW, Ahn JS, Park YS, Lee J, Kang JH, Park JO, Lim HY, Im YH, Kang WK, Park K, et al: Phase II study of docetaxel and cisplatin combination chemotherapy in metastatic gastric cancer. Cancer Chemother Pharmacol. 2007, 59 (1): 17-21. 10.1007/s00280-006-0253-2.View ArticlePubMedGoogle Scholar
- Van Cutsem E, Moiseyenko VM, Tjulandin S, Majlis A, Constenla M, Boni C, Rodrigues A, Fodor M, Chao Y, Voznyi E, et al: 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 (31): 4991-4997. 10.1200/JCO.2006.06.8429.View ArticlePubMedGoogle Scholar
- Yun J, Lee J, Park SH, Park JO, Park YS, Lim HY, Kang WK: A randomised phase II study of combination chemotherapy with epirubicin, cisplatin and capecitabine (ECX) or cisplatin and capecitabine (CX) in advanced gastric cancer. Eur J Cancer. 2010, 46 (5): 885-891. 10.1016/j.ejca.2009.12.015.View ArticlePubMedGoogle 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
- Wagner AD, Grothe W, Haerting J, Kleber G, Grothey A, Fleig WE: Chemotherapy in advanced gastric cancer: a systematic review and meta-analysis based on aggregate data. J Clin Oncol. 2006, 24 (18): 2903-2909. 10.1200/JCO.2005.05.0245.View ArticlePubMedGoogle Scholar
- Chau I, Norman AR, Cunningham D, Waters JS, Oates J, Ross PJ: Multivariate prognostic factor analysis in locally advanced and metastatic esophago-gastric cancer--pooled analysis from three multicenter, randomized, controlled trials using individual patient data. J Clin Oncol. 2004, 22 (12): 2395-2403. 10.1200/JCO.2004.08.154.View ArticlePubMedGoogle Scholar
- Lee J, Lim T, Uhm J, Park K, Park S, Lee S, Park J, Park Y, Lim H, Sohn T, et al: Prognostic model to predict survival following first-line chemotherapy in patients with metastatic gastric adenocarcinoma. Ann Oncol. 2007, 18 (5): 886-891. 10.1093/annonc/mdl501.View ArticlePubMedGoogle Scholar
- Galizia G, Lieto E, Orditura M, Castellano P, Mura AL, Imperatore V, Pinto M, Zamboli A, De Vita F, Ferraraccio F: Epidermal growth factor receptor (EGFR) expression is associated with a worse prognosis in gastric cancer patients undergoing curative surgery. World J Surg. 2007, 31 (7): 1458-1468. 10.1007/s00268-007-9016-4.View ArticlePubMedGoogle Scholar
- Lieto E, Ferraraccio F, Orditura M, Castellano P, Mura AL, Pinto M, Zamboli A, De Vita F, Galizia G: Expression of vascular endothelial growth factor (VEGF) and epidermal growth factor receptor (EGFR) is an independent prognostic indicator of worse outcome in gastric cancer patients. Ann Surg Oncol. 2008, 15 (1): 69-79. 10.1245/s10434-007-9596-0.View ArticlePubMedGoogle Scholar
- Park DI, Yun JW, Park JH, Oh SJ, Kim HJ, Cho YK, Sohn CI, Jeon WK, Kim BI, Yoo CH, et al: HER-2/neu amplification is an independent prognostic factor in gastric cancer. Dig Dis Sci. 2006, 51 (8): 1371-1379. 10.1007/s10620-005-9057-1.View ArticlePubMedGoogle Scholar
- Matsubara J, Nishina T, Yamada Y, Moriwaki T, Shimoda T, Kajiwara T, Nakajima TE, Kato K, Hamaguchi T, Shimada Y, et al: Impacts of excision repair cross-complementing gene 1 (ERCC1), dihydropyrimidine dehydrogenase, and epidermal growth factor receptor on the outcomes of patients with advanced gastric cancer. Br J Cancer. 2008, 98 (4): 832-839. 10.1038/sj.bjc.6604211.View ArticlePubMedPubMed CentralGoogle Scholar
- Lievre A, Bachet JB, Boige V, Cayre A, Le Corre D, Buc E, Ychou M, Bouche O, Landi B, Louvet C, et al: KRAS mutations as an independent prognostic factor in patients with advanced colorectal cancer treated with cetuximab. J Clin Oncol. 2008, 26 (3): 374-379. 10.1200/JCO.2007.12.5906.View ArticlePubMedGoogle Scholar
- Lee KH, Lee JS, Suh C, Kim SW, Kim SB, Lee JH, Lee MS, Park MY, Sun HS, Kim SH: Clinicopathologic significance of the K-ras gene codon 12 point mutation in stomach cancer. An analysis of 140 cases. Cancer. 1995, 75 (12): 2794-2801. 10.1002/1097-0142(19950615)75:12<2794::AID-CNCR2820751203>3.0.CO;2-F.View ArticlePubMedGoogle Scholar
- Hongyo T, Buzard GS, Palli D, Weghorst CM, Amorosi A, Galli M, Caporaso NE, Fraumeni JF, Rice JM: Mutations of the K-ras and p53 genes in gastric adenocarcinomas from a high-incidence region around Florence, Italy. Cancer Res. 1995, 55 (12): 2665-2672.PubMedGoogle Scholar
- Al-Batran SE, Hartmann JT, Probst S, Schmalenberg H, Hollerbach S, Hofheinz R, Rethwisch V, Seipelt G, Homann N, Wilhelm G, et al: Phase III trial in metastatic gastroesophageal adenocarcinoma with fluorouracil, leucovorin plus either oxaliplatin or cisplatin: a study of the Arbeitsgemeinschaft Internistische Onkologie. J Clin Oncol. 2008, 26 (9): 1435-1442. 10.1200/JCO.2007.13.9378.View ArticlePubMedGoogle Scholar
- Cvitkovic E: Ongoing and unsaid on oxaliplatin: the hope. Br J Cancer. 1998, 77 (Suppl 4): 8-11.View ArticlePubMedPubMed CentralGoogle Scholar
- Van Cutsem E, Kang Y, Chung H, Shen L, Sawaki A, Lordick F, Hill J, Lehle M, Feyereislova A, Bang Y: Efficacy results from the ToGA trial: A phase III study of trastuzumab added to standard chemotherapy (CT) in first-line human epidermal growth factor receptor 2 (HER2)-positive advanced gastric cancer (GC). J Clin Oncol. 2009, 27 (18s): abstr LBA4509Google Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/10/583/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.