Predicting the response of patients with advanced urothelial cancer to methotrexate, vinblastine, Adriamycin, and cisplatin (MVAC) after the failure of gemcitabine and platinum (GP)
Platinum-based systemic chemotherapy is the treatment of choice for patients with advanced urothelial carcinoma (UC). Although no chemotherapeutic regimen is established as a second-line therapy, recent studies reported that methotrexate, vinblastine, Adriamycin and cisplatin (MVAC) elicited a significant response in patients who failed gemcitabine and platinum (GP) chemotherapy. We investigated the clinical factors useful for predicting a favourable response to MVAC in UC patients who failed GP.
Methods
Forty-five patients with advanced UC who received second-line MVAC chemotherapy after failure with first-line GP chemotherapy were enrolled in this study. Univariate and multivariate analyses based on Cox’s regression were performed to identify independent prognostic factors for progression-free survival (PFS) after second-line MVAC chemotherapy.
Results
The median follow-up period after the first MVAC administration was 10.0 months. The median PFS and overall survival (OS) were 6.5 months (95 % confidence interval [CI]: 5.1–7.9) and 14.5 months (95 % CI, 7.4–21.4), respectively. The overall response rate was 57.8 %. The response to first-line GP chemotherapy (hazard ratio [HR], 2.500; p = 0.012) and patient age (HR, 1.047; p = 0.033) were predictors of PFS after MVAC chemotherapy.
Conclusions
The response to first-line GP chemotherapy and age were independent predictors of PFS in patients who received second-line MVAC chemotherapy. This report is the first to describe independent predictors of PFS after MVAC chemotherapy.
Systemic chemotherapy is the treatment of choice for metastatic, recurrent or inoperable urothelial carcinoma (UC). Methotrexate, vinblastine, Adriamycin and cisplatin (MVAC) chemotherapy was used worldwide as the standard treatment since the first report of its efficacy in 1985 [1]. However, since gemcitabine and cisplatin (GC) chemotherapy showed similar efficacy as MVAC but with less toxicity in a large, randomized, multinational and multicentre phase III study of GC combination chemotherapy, [2] GC regimens are now used mostly as the initial systemic chemotherapy for UC.
GC chemotherapy has an excellent response rate in patients with advanced UC, and up to 20 % of individuals have achieved a complete response of long-term, disease-free survival [3]. However, most patients eventually experience disease progression or relapse after GC. Several regimens have been investigated in the second-line setting after the failure of GC, including taxanes, vinflunine, ifosfamide, ixabepilone and pemetrexed; [4–9] however, no regimen has yet achieved a competent survival benefit in the second-line setting.
Recently, a small number of clinical trials proposed that platinum-based regimens are effective in a significant portion of patients in whom platinum-based chemotherapy initially failed when the regimen was based on cisplatin but using different agents in the second-line setting. The efficacy and safety of MVAC chemotherapy as a second-line treatment after the failure of gemcitabine and platinum (GP) chemotherapy has been reported in several small-scale studies [10–13]. However, there is a lack of predictive factors available for the personalized selection of chemotherapeutic regimens in patients with UC. Therefore, we investigated the factors predictive of a favourable response to second-line MVAC chemotherapy after GP in patients with advanced UC to facilitate the development of a tailored second-line treatment strategy. Here, we investigated the predictive value of the response to first-line GP chemotherapy for selecting suitable candidates for the MVAC regimen as the second-line chemotherapy in patients with advanced UC.
Methods
Study population
The medical ethics committee of Severance Hospital, Yonsei University Health Care System (Seoul, Korea) approved this retrospective study. Our medical ethics committee allows exempt of informed consent if the research uses the collection or study of existing data, documents and records and these sources are publicly available and the information is recorded by the investigator in such a manner that subjects cannot be identified. From these regulations, our study was classified as exempt from the informed consent requirement because this study was based on the collection of existing publicly available data, documents and records, and we recorded all data in a manner that subjects cannot be identified. Between July 2004 and August 2014, 64 consecutive patients who received MVAC chemotherapy as the second-line treatment due to the relapse or disease progression of UC after first-line GP chemotherapy in the only metastatic setting were included in this study. Nineteen of the 64 patients were excluded because of incomplete medical records (seven patients), another synchronous metastatic malignancy (five patients), an atypical carcinoma (four patients) or a history of neoadjuvant chemotherapy (three patients). Forty-five patients were included in the final analysis.
Treatment
Before starting chemotherapy, all patients were required to have an Eastern Cooperative Oncology Group (ECOG) performance status (PS) ≤ 2, adequate hematologic parameters (absolute granulocyte count ≥ 1,500/dL, haemoglobin ≥ 8.5 g/dL and a platelet count ≥ 100,000/dL) and sufficient hepatic (serum bilirubin ≤ 1.5 mg/dL) and renal (estimated glomerular filtration rate ≥ 50 mL/min) function. Methotrexate was given at a dose of 30 mg/m2 on days 1, 15 and 22, vinblastin was given at a dose of 3 mg/m2 on days 2, 15 and 22, Adriamycin was given at a dose of 30 mg/m2 on day 2 and cisplatin was given at a dose of 70 mg/m2 on day 2. The cycles were repeated every 28 days, and treatment continued until the disease regressed or the toxicity was intolerable.
Response and toxicity assessment and dose modification
Basically, after the completion of three cycles, imaging tools (computed tomography scans, radionuclide bone scans or positron emission tomography) were used to evaluate the treatment response after three cycles, except for cases with symptomatic progression. Performance status, haematological parameters and liver and kidney function were measured weekly in each patient to assess for potential toxicity. The response was evaluated according to the Response Evaluation Criteria for Solid Tumours, [14] and toxicity was determined using the National Cancer Institute Common Toxicity Criteria (ver. 4.0). The platinum dose was reduced by 20–30 % in patients who experienced grade 4 haematological toxicity or grade 3/4 non-haematological toxicity.
Outcomes
The end point of the study was PFS in patients who received MVAC chemotherapy. The PFS of patients who received MVAC chemotherapy was defined as the time from the date of the beginning of the first MVAC cycle to the date that progression was identified, death, or loss to follow-up. Progression was defined as a ≥ 20 % increase in the overall sum of the diameter of the target lesions on radiological assessments.
Clinical data and statistical analysis
All included patients were divided into good or poor response groups based on the response to the first-line GP chemotherapy. The good response group included the complete response (CR) and partial response (PR) groups to first-line GP chemotherapy, while the poor response group included the stable disease (SD) and progression disease (PD) groups [15]. The baseline characteristics of the two groups were then compared using Chi-squared tests. PFS after MVAC chemotherapy was calculated using the Kaplan-Meier method, and statistical significance was determined using log rank tests. Age, haematological parameters, liver and kidney function, serum albumin concentration at the beginning of the first MVAC and time to progression (TTP) after first-line GP chemotherapy were included in the analysis as continuous variables. Clinical nodal status, distant metastatic status, ECOG PS at the beginning of the first MVAC and response to previous GP chemotherapy were analysed as categorical variables. Statistical analyses to identify independent predictors of progression after MVAC chemotherapy were performed using univariate and multivariate Cox’s proportional hazard regression analyses. Variables that were significant in the univariate analysis (p < 0.05) were entered into the multivariate model. All statistical analyses were performed using SPSS Statistics version 20.0.0 (IBM Corp., Armonk, NY, USA). For all analyses, a two-sided p-value <0.05 was considered to indicate statistical significance.
Results
Patients
The median follow-up period after the first MVAC administration was 10.0 months. The median PFS and overall survival (OS) were 6.5 months (95 % confidence interval [CI] 5.1–7.9) and 14.5 months (95 % CI 7.4–21.4), respectively. The overall response rate was 57.8 %. A CR was achieved in two patients (4.4 %) and a PR in twenty-four (53.3 %). The baseline characteristics of the study population, including the response to first-line GP chemotherapy, are presented in Table 1.
Table 1
Patient characteristics
Sex
Patients (%)
Female
0 (0.0 %)
Male
45 (100 %)
Age, median (year, range)
65 (60–72)
Primary tumor site
Bladder
30 (66.7 %)
Ureter or renal pelvic
6 (13.3 %)
Ureter or renal pelvic with bladder
9 (20.0 %)
Nodal status
N0
6 (13.3 %)
N1
8 (17.8 %)
N2
19 (42.2 %)
N3
12 (26.7 %)
Distant metastatic site at the time of MVAC administration
Lung
21 (46.7 %)
Bone
16 (35.6 %)
Liver
9 (20.0 %)
Other
4 (8.9 %)
Absence
16 (35.6 %)
Single
13 (28.9 %)
Multiple
16 (35.6 %)
ECOG performance status (PS)
PS 0
20 (44.4 %)
PS 1
23 (51.1 %)
PS 2
2 (4.4 %)
MVAC methotrexate vinblastine Adriamycin cisplatin, ECOG Easton Cooperative Oncologic Group
Characteristics of good and poor responses to previous GC chemotherapy
All included patients were divided into two groups: a good response group and a poor response group, according to the response to first-line GP chemotherapy. The characteristics of the two groups are presented in Table 2. The median treatment-free intervals (TFI) between GP and MVAC chemotherapies for the good and poor response groups were 2.5 and 1.7 months, respectively. There were significant differences in haemoglobin and serum bilirubin levels between the two groups, but not in the variable related to the response to first-line GP chemotherapy (TTP and the number of cycles of first-line GP chemotherapy). The PFS of patients in each of the two groups was calculated using the Kaplan-Meier method. The median PFS after second-line MVAC chemotherapy was 8.0 months (95 % CI 5.4–10.7) in the good response group and 3.7 months (95 % CI 2.6–4.8) in the poor response group. The results of the log rank test indicated a statistically significant difference (p = 0.008) in PFS between the two groups (Fig. 1).
Table 2
Comparison of several factors for patients who were divided by the response to first-line GP chemotherapy
Good (n = 30)
Poor (n = 15)
P
Age, median (year, range)
64.0 (58.5–73.0)
66.0 (64.0–71.0)
0.289
Type of platinum compound used as the first-line
0.695
Cisplatin
23 (76.7 %)
13 (86.7 %)
Carboplatin
7 (23.3 %)
2 (13.3 %)
Response to the first-line GP chemotherapy
-
CR
11 (36.7 %)
-
PR
19 (63.3 %)
-
SD
-
5 (33.3 %)
PD
-
10 (66.6 %)
TTP of the first-line GP chemotherapy, median (months, range)
11.6 (7.8–14.2)
3.13 (2.2–5.0)
<0.001
Cycles of the first-line GP chemotherapy, median (range)
6.0 (6.0–7.3)
4.0 (3.0–4.0)
<0.001
TFI between GP and MVAC, median (months, range)
2.5 (0.7–9.9)
1.7 (0.6–3.4)
0.202
Primary tumor site
>0.999
Bladder
20 (66.7 %)
10 (66.7 %)
Ureter or renal pelvic
4 (13.3 %)
2 (13.3 %)
Ureter or renal pelvic with bladder
6 (20.0 %)
3 (20.0 %)
Clinical N stage
0.453
N0
4 (13.3 %)
2 (13.3 %)
N1
5 (16.7 %)
3 (20.0 %)
N2
11 (36.7 %)
8 (53.3 %)
N3
10 (33.3 %)
2 (13.3 %)
Distant metastatic site at the time of MVAC administration
Kaplan-Meier curve for progression-free survival (%) in the good response and poor response groups. The good response group included patients who achieved a complete or partial response to first-line GP chemotherapy, whereas the poor response group included individuals with stable or progressive disease after first-line GP chemotherapy
Prognostic predictors of PFS after MVAC chemotherapy
Univariate and multivariate Cox’s regression analyses were performed to identify the independent predictive factors of PFS after MVAC chemotherapy. The results of the univariate and multivariate analyses demonstrated that age (hazard ratio [HR] = 1.047, p = 0.033) and response to first-line GC chemotherapy (HR = 2.500, p = 0.012) were predictors of PFS after MVAC chemotherapy (Table 3).
Table 3
Predictors of progression-free survival
Variables
HR
95 % CI
P
Univariate analysis
Age
1.046
1.004–1.089
0.031
Type of platinum compound used as the first-line (cisplatin vs carboplatin)
1.670
0.750–3.718
0.209
TTP of the first-line GP chemotherapy
0.951
0.885–1.022
0.175
Cycles of the first-line GP chemotherapy
0.947
0.834–1.076
0.404
TFI between GP and MVAC
0.991
0.943–1.042
0.735
Primary tumor site
Bladder vs ureter or renal pelvis/ ureter or renal pelvis with bladder
1.525
0.782–2.975
0.216
Bladder/ ureter or renal pelvis vs ureter or renal pelvis with bladder
1.735
0.806–3.733
0.159
Nodal status
N (0 vs 1,2,3)
1.074
0.413–2.789
1.074
N (0,1 vs 2,3)
0.712
0.354–1.431
0.340
N (0,1,2 vs 3)
0.541
0.246–1.193
0.128
Metastatic site
M0 vs M1
1.335
0.670–2.658
0.411
Lung
1.502
0.798–2.872
0.207
Bone
1.207
0.631–2.310
0.569
Liver
1.854
0.862–3.987
0.114
Others
1.056
0.371–3.007
0.919
Multi-organ metastasis (absence vs presence)
1.696
0.874–3.294
0.118
Hemoglobin
0.846
0.661–1.082
0.182
Absolute neutrophil count
1.000
1.000–1.000
0.823
Platelet count
1.001
0.997–1.004
1.001
eGFR
1.000
0.979–1.021
0.989
Serum bilirubin
0.529
0.077–3.630
0.517
Serum albumin
0.417
0.161–1.078
0.071
ECOG performance status (0 vs 1,2)
1.333
0.699–2.543
0.382
Response to first-line GP
2.520
1.245–5.015
0.010
Multivariate
Age
1.047
1.004–1.093
0.033
Response to first-line GP
2.500
1.228–5.098
0.012
HR hazard ratio, CI confidence interval, TTP time to progression, GP gemcitabine platinum, TFI treatment free interval, MVAC methotrexate vinblastine Adriamycin cisplatin, eGFR estimated glomerular filtration rate, ECOG Easton Cooperative Oncologic Group, Boldface significant 2-tailed
Toxicity
Anaemia, neutropenia, and thrombocytopenia ≥ grade 3 developed in 25, 29, and 20 patients, respectively. A blood transfusion or granulocyte colony-stimulating factor was administered to patients who experienced severe haematological complications. Alopecia was the most common non-haematological toxicity. Most of the non-haematological toxicities were not life threatening and were tolerated by the patients. The toxicities experienced by the patients are presented in Table 4.
Table 4
Toxicities
Toxicity
All grade (%)
Grade ≥3 (%)
Hematologic
Anemia
34 (66.7 %)
25 (49.0 %)
Neutropenia
40 (78.4 %)
29 (56.9 %)
Thrombocytopenia
31 (60.8 %)
20 (39.2 %)
Non-hematologic
Mucositis
7 (13.7 %)
4 (7.8 %)
Alopecia
44 (86.3 %)
-
Nausea/vomiting
35 (68.6 %)
3 (5.9 %)
Anorexia
28 (56.9 %)
2 (3.9 %)
Diarrhea/constipation
5 (9.8 %)
-
Fatigue
10 (19.6 %)
-
Infection
10 (19.6 %)
8 (15.7 %)
Discussion
MVAC elicited a significant response rate in GP-failed patients with advanced urothelial cancer in the current study, which is consistent with the results reported in previous studies using MVAC in the second-line setting. Since Han et al. reported the efficacy and toxicity of MVAC as a second-line chemotherapy, [13] several additional studies have assessed the efficacy of this second-line treatment regimen [10–12]. The current study demonstrated that MVAC resulted in a significantly higher response rate and longer PFS after the failure of GP in patients with advanced UC who responded to GP as the first-line chemotherapy compared with non-responders. The response rate and median PFS of patients administered second-line MVAC after GP was 77 % and 8.0 months in responders compared with 40 % and 3.7 months in non-responders, respectively. This suggests that re-challenge using a platinum-based regimen could induce a high response rate and durable PFS after the initial failure of first-line platinum-based chemotherapy in patients with advanced UC. In addition, a higher response rate and longer PFS could be achieved by patient selection.
Several studies have reported efforts to find an effective chemotherapeutic regimen after the failure of platinum-based chemotherapy for patients with metastatic, recurrent and inoperable UC [16]. Among the non-platinum-based combination regimens, paclitaxel and gemcitabine have achieved the greatest response rate and PFS of the regimens tested to date in a phase 2 study [17]. Paclitaxel and gemcitabine chemotherapy yielded a 60 % response rate and a 14.4-month median OS. However, 25 of the 41 patients had been treated using first-line platinum-based chemotherapy in a neo-adjuvant or adjuvant setting, and the response rate was only 27 % in the metastatic setting. Bellmunt et al., reported that Vinflunine improved median PFS and OS in a phase 3 study [18]. However, Vinflunine yield only and 8.6 % response rate, and did not demonstrate fully satisfactory survival benefits. Consequently, no satisfactory standard therapy has been found in a second-line setting [19].
Several investigators have questioned whether failure of one platinum-based chemotherapy means true resistance to another platinum-based chemotherapy in UC patients, because different combinations of chemotherapeutic agents exert different synergistic effects on cancer cells, even if they are all based on platinum [10–13, 20]. Edeline et al. and Karadimou et al. suggested that patients with a history of first-line GP chemotherapy in an adjuvant setting and a relatively better ECOG performance status had a more favourable response after second-line MVAC chemotherapy [11, 12]. In addition, Han et al. suggested that patients with a complete or partial response to first-line platinum-based chemotherapy were more likely to show a favourable response to a second-line platinum-based chemotherapy [13]. Gondo et al. also supported a relationship between the responses to first-line and second-line platinum-based chemotherapy in their study on the efficacy and safety of GC as second-line chemotherapy after the failure of first-line MVAC [20]. However, all these studies were limited by a small sample size. The current study is the first to report that the response to first-line GP is a statistically significant predictive marker for response rate and PFS after second-line MVAC, and it also demonstrates that proper patient selection could achieve a higher response rate and longer PFS in patients with advanced UC.
There are several possible explanations for the re-response phenomenon to platinum-based chemotherapy in patients who failed a first platinum-based chemotherapy. Even after UC cells acquire platinum resistance and the disease progresses, the cells might acquire total resistance to gemcitabine but have incomplete resistance to platinum. Several authors suggested that the synergic effects of combination chemotherapy appear to be able to overcome the resistance of first-line platinum-based chemotherapy in ovarian and lung cancer [21–23]. Combination therapy using more than two agents induces synergistic anti-cancer effects, and different combinations of chemotherapeutic agents can induce different synergies. The MVAC regimen might induce different synergistic effects from those of the GP regimen in UC. Methotrexate, vinblastine and Adriamycin might support the anti-cancer activity of cisplatin differently from that of gemcitabine; therefore, these different effects can affect the response of GP-failed patients to MVAC.
One of the problems with second-line treatment of advanced UC patients is that performance generally deteriorates after the failure of first-line chemotherapy due to cancer progression, delayed recovery of marrow function or decreased organ function. This limits the choice of chemotherapeutic agents in the second-line setting, because the lack of response to second-line treatment can be fatal if it results in further progression of metastases and deterioration of general performance and organ function. Therefore, the appropriate selection of a second-line therapeutic regimen is critical in patients with advanced UC. Additionally, patients receiving MVAC chemotherapy could experience a variety of complications. Several studies have reported MVAC chemotherapy-based toxicities [24–28]. Haematological toxicities developed in ~70 % of the patients in the current study, and many different non-haematological toxicities also occurred. Because these complications can be life threatening, the use of second-line MVAC chemotherapy should be considered carefully and used only in patients who can benefit from this approach. Therefore, accurately predicting patients who will have a favourable response to second-line MVAC chemotherapy is critical.
The main strength of the current study was the identification of independent predictors of PFS in patients who received second-line MVAC chemotherapy, even though the results might have been affected by the retrospective nature of the study and the small number of patients included in the analysis. These results need to be confirmed and validated by analysing data from a larger prospective study.
Conclusions
The response to first-line GP is an important predictive and prognostic factor for second-line MVAC in patients with advanced UC. MVAC chemotherapy should be considered as second-line treatment for advanced UC patients who originally responded to GP.
Abbreviations
UC:
Urothelial carcinoma
GP:
Gemcitabine and platinum
GC:
Gemcitabine and cisplatin
MVAC:
Methotrexate, vinblastine, Adriamycin and cisplatin
ECOG PS:
Eastern Cooperative Oncology Group performance status
eGFR:
Estimated glomerular filtration rate
PFS:
Progression-free survival
OS:
Overall survival
TTP:
Time to progression
TFI:
Treatment-free interval
CR:
Complete response
PR:
Partial response
SD:
Stable disease
PD:
Progression disease
Declarations
Acknowledgements
This work was partly supported by Amanda Hendrix in BioScience. She is a language editor and has made significant revision of the manuscript.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Authors’ Affiliations
(1)
Department of Urology and Urological Science Institute, Yonsei University College of Medicine
References
Sternberg CN, Yagoda A, Scher HI, Watson RC, Ahmed T, Weiselberg LR, et al. Preliminary results of M-VAC (methotrexate, vinblastine, doxorubicin and cisplatin) for transitional cell carcinoma of the urothelium. J Urol. 1985;133(3):403–7.PubMedGoogle Scholar
von der Maase H, Hansen SW, Roberts JT, Dogliotti L, Oliver T, Moore MJ, et al. Gemcitabine and cisplatin versus methotrexate, vinblastine, doxorubicin, and cisplatin in advanced or metastatic bladder cancer: results of a large, randomized, multinational, multicenter, phase III study. J Clin Oncol. 2000;18(17):3068–77.PubMedGoogle Scholar
Stenzl A, Cowan NC, De Santis M, Jakse G, Kuczyk MA, Merseburger AS, et al. The updated EAU guidelines on muscle-invasive and metastatic bladder cancer. Eur Urol. 2009;55(4):815–25.View ArticlePubMedGoogle Scholar
Vaughn DJ, Srinivas S, Stadler WM, Pili R, Petrylak D, Sternberg CN, et al. Vinflunine in platinum-pretreated patients with locally advanced or metastatic urothelial carcinoma: results of a large phase 2 study. Cancer. 2009;115(18):4110–7.View ArticlePubMedGoogle Scholar
Dreicer R, Li S, Manola J, Haas NB, Roth BJ, Wilding G. Phase 2 trial of epothilone B analog BMS-247550 (ixabepilone) in advanced carcinoma of the urothelium (E3800): a trial of the Eastern Cooperative Oncology Group. Cancer. 2007;110(4):759–63.View ArticlePubMedGoogle Scholar
Sweeney CJ, Roth BJ, Kabbinavar FF, Vaughn DJ, Arning M, Curiel RE, et al. Phase II study of pemetrexed for second-line treatment of transitional cell cancer of the urothelium. J Clin Oncol. 2006;24(21):3451–7.View ArticlePubMedGoogle Scholar
von der Maase H. Gemcitabine in transitional cell carcinoma of the urothelium. Expert Rev Anticancer Ther. 2003;3(1):11–9.View ArticlePubMedGoogle Scholar
Vaughn DJ, Broome CM, Hussain M, Gutheil JC, Markowitz AB. Phase II trial of weekly paclitaxel in patients with previously treated advanced urothelial cancer. J Clin Oncol. 2002;20(4):937–40.View ArticlePubMedGoogle Scholar
Witte RS, Elson P, Bono B, Knop R, Richardson RR, Dreicer R, et al. Eastern Cooperative Oncology Group phase II trial of ifosfamide in the treatment of previously treated advanced urothelial carcinoma. J Clin Oncol. 1997;15(2):589–93.PubMedGoogle Scholar
Lee JH, Kang SG, Kim ST, Kang SH, Choi IK, Park YJ, et al. Modified MVAC as a Second-Line Treatment for Patients with Metastatic Urothelial Carcinoma after Failure of Gemcitabine and Cisplatin Treatment. Cancer Res Treat. 2014;46(2):172–7.View ArticlePubMedPubMed CentralGoogle Scholar
Edeline J, Loriot Y, Culine S, Massard C, Albiges L, Blesius A, et al. Accelerated MVAC chemotherapy in patients with advanced bladder cancer previously treated with a platinum-gemcitabine regimen. Eur J Cancer. 2012;48(8):1141–6.View ArticlePubMedGoogle Scholar
Karadimou A, Lianos E, Pectasides D, Dimopoulos MA, Bamias A. Efficacy of methotrexate/vinblastine/doxorubicin cisplatin combination in gemcitabine-pretreated patients with advanced urothelial cancer: a retrospective analysis. Open access journal of urology. 2010;2:193–9.PubMedPubMed CentralGoogle Scholar
Han KS, Joung JY, Kim TS, Jeong IG, Seo HK, Chung J, et al. Methotrexate, vinblastine, doxorubicin and cisplatin combination regimen as salvage chemotherapy for patients with advanced or metastatic transitional cell carcinoma after failure of gemcitabine and cisplatin chemotherapy. Br J Cancer. 2008;98(1):86–90.View ArticlePubMedGoogle Scholar
Eisenhauer EA, Therasse P, Bogaerts J, Schwartz LH, Sargent D, Ford R, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer. 2009;45(2):228–47.View ArticlePubMedGoogle Scholar
Pond GR, Bellmunt J, Fougeray R, Choueiri TK, Qu AQ, Niegisch G, et al. Impact of response to prior chemotherapy in patients with advanced urothelial carcinoma receiving second-line therapy: implications for trial design. Clin Genitourin Cancer. 2013;11(4):495–500.View ArticlePubMedGoogle Scholar
Sonpavde G, Sternberg CN, Rosenberg JE, Hahn NM, Galsky MD, Vogelzang NJ. Second-line systemic therapy and emerging drugs for metastatic transitional-cell carcinoma of the urothelium. Lancet Oncol. 2010;11(9):861–70.View ArticlePubMedGoogle Scholar
Sternberg CN, Calabro F, Pizzocaro G, Marini L, Schnetzer S, Sella A. Chemotherapy with an every-2-week regimen of gemcitabine and paclitaxel in patients with transitional cell carcinoma who have received prior cisplatin-based therapy. Cancer. 2001;92(12):2993–8.View ArticlePubMedGoogle Scholar
Bellmunt J, Theodore C, Demkov T, Komyakov B, Sengelov L, Daugaard G, et al. Phase III trial of vinflunine plus best supportive care compared with best supportive care alone after a platinum-containing regimen in patients with advanced transitional cell carcinoma of the urothelial tract. J Clin Oncol. 2009;27(27):4454–61.View ArticlePubMedGoogle Scholar
Network NCC. NCCN clinical practice guidelines in Oncology. Bladder cancer version 2 2014. National Comprehensive Cancer Network, 2014. In.; 2014.Google Scholar
Gondo T, Ohori M, Hamada R, Tanaka A, Satake N, Takeuchi H, et al. The efficacy and safety of gemcitabine plus cisplatin regimen for patients with advanced urothelial carcinoma after failure of M-VAC regimen. Int J Clin Oncol. 2011;16(4):345–51.View ArticlePubMedGoogle Scholar
Sekine I, Nokihara H, Horiike A, Yamamoto N, Kunitoh H, Ohe Y, et al. Phase I study of cisplatin analogue nedaplatin (254-S) and paclitaxel in patients with unresectable squamous cell carcinoma. Br J Cancer. 2004;90(6):1125–8.View ArticlePubMedPubMed CentralGoogle Scholar
Yamada H, Uchida N, Maekawa R, Yoshioka T. Sequence-dependent antitumor efficacy of combination chemotherapy with nedaplatin, a newly developed platinum, and paclitaxel. Cancer Lett. 2001;172(1):17–25.View ArticlePubMedGoogle Scholar
Reed E, Kohn EC, Sarosy G, Dabholkar M, Davis P, Jacob J, et al. Paclitaxel, cisplatin, and cyclophosphamide in human ovarian cancer: molecular rationale and early clinical results. Semin Oncol. 1995;22(3 Suppl 6):90–6.PubMedGoogle Scholar
Necchi A, Mariani L, Giannatempo P, Raggi D, Fare E, Nicolai N, et al. Long-term efficacy and safety outcomes of modified (simplified) MVAC (methotrexate/vinblastine/doxorubicin/cisplatin) as frontline therapy for unresectable or metastatic urothelial cancer. Clin Genitourin Cancer. 2014;12(3):203–209.e201.View ArticlePubMedGoogle Scholar
Witjes JA, Wullink M, Oosterhof GO, de Mulder P. Toxicity and results of MVAC (methotrexate, vinblastine, adriamycin and cisplatin) chemotherapy in advanced urothelial carcinoma. Eur Urol. 1997;31(4):414–9.PubMedGoogle Scholar
Viens P, Gravis G, Bladou F, Lechevallier E, Baume D, Camerlo J, et al. Impact of recombinant human granulocyte colony stimulating factor on dose intensity and toxicity of three cycles of methotrexate, vinblastine, doxorubicin and cisplatin in patients with previously untreated urothelial bladder carcinoma. Eur Cytokine Netw. 1996;7(3):395–9.PubMedGoogle Scholar
Igawa M, Kadena H, Ueda M, Usui T. Association between patient characteristics and treatment history, and toxicity associated with methotrexate, vinblastine, adriamycin and cisplatin (M-VAC) for advanced urothelial cancer. Br J Urol. 1994;73(3):263–7.View ArticlePubMedGoogle Scholar
Bahnson RR, Ernstoff MS, Miller RJ, O'Donnell WF. Toxicity comparison of neoadjuvant versus adjuvant methotrexate, vinblastine, doxorubicin, and cisplatin (M-VAC) in radical cystectomy patients. J Surg Oncol. 1990;45(3):143–5.View ArticlePubMedGoogle Scholar
