dd-MVAC as neoadjuvant chemotherapy for muscle-invasive bladder cancer: a single-center study
- Authors: Tikhomirova T.E.1, Anokhin A.Y.1,2, Israelyan E.R.1, Lud A.N.1, Gutorov S.L.1, Vashakmadze N.L.1, Arakelyan G.A.1, Klimov A.V.1,3, Rumyantsev A.A.1, Matveev V.B.1,2
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Affiliations:
- N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
- Sechenov First Moscow State Medical University (Sechenovskiy University)
- N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia
- Issue: Vol 21, No 4 (2025)
- Pages: 88-96
- Section: DIAGNOSIS AND TREATMENT OF URINARY SYSTEM TUMORS. URINARY BLADDER CANCER
- Published: 27.02.2026
- URL: https://oncourology.abvpress.ru/oncur/article/view/1978
- DOI: https://doi.org/10.17650/1726-9776-2025-21-4-88-96
- ID: 1978
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Full Text
Abstract
Aim. To evaluate the efficacy, safety, and feasibility of dd-MVAC (methotrexate, vinblastine, doxorubicin, cyclophosphamide) chemotherapy in real-world clinical practice.
Materials and methods. Patients were enrolled between September 2022 and May 2025. They were scheduled to receive six cycles of neoadjuvant dd-MVAC chemotherapy, supported by granulocyte colony-stimulating factor from day 4 to day 9 of each cycle, repeated every two weeks. Eligible patients had urothelial bladder cancer staged as cT2–4a, N0–3, M0, with creatinine clearance of ≥50 mL/min. The primary endpoint was the pathological complete response (pCR) rate. Secondary endpoints included toxicity, the number of treatment cycles completed, and pathological response.
Results. The study included 40 patients. Of these, 87 % (n = 35) completed six cycles of dd-MVAC, while 8 % (n = 3) and 5 % (n = 2) completed five and four cycles, respectively. Full protocol drug doses were administered to 57 % of patients (n = 23), while a 15 % dose reduction was required in 43 % (n = 17). The majority of these dose reductions (59 %, n = 10) were implemented after the fifth cycle. The most frequent grade 3 adverse events (per Common Terminology Criteria for Adverse Events (CTCAE) v.5.0) were hematological: neutropenia in 40 % (n = 16), anemia in 10 % (n = 4), and thrombocytopenia in 10 % (n = 4). One fatal case of febrile neutropenia occurred. The most common grade 1–2 adverse event was asthenia reported in 80 % (n = 32) of patients. Surgical treatment was performed in 80 % (n = 32) of the cohort. Cystectomy was conducted in 91 % (n = 29) of these surgical patients, while organ-preserving surgery was performed in 9 % (n = 3). A complete pathological response (ypT0pN0) was achieved in 53 % (n = 17) of surgically treated patients, and downstaging to
Conclusion. The dd-MVAC regimen is an effective and feasible neoadjuvant therapy for muscle-invasive bladder cancer, enabling the majority of patients to complete the full preoperative course of chemotherapy.
Keywords
About the authors
Tatiana E. Tikhomirova
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Author for correspondence.
Email: tikhomirova777@mail.ru
ORCID iD: 0000-0002-7313-4013
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522
A. Yu. Anokhin
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia; Sechenov First Moscow State Medical University (Sechenovskiy University)
Email: tikhomirova777@mail.ru
ORCID iD: 0000-0001-8981-5748
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522; Build. 2, 8 Trubetskaya St., Moscow 119048
E. R. Israelyan
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: tikhomirova777@mail.ru
ORCID iD: 0000-0002-6666-549X
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522
A. N. Lud
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: tikhomirova777@mail.ru
ORCID iD: 0000-0002-2624-3030
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522
S. L. Gutorov
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: tikhomirova777@mail.ru
ORCID iD: 0000-0001-5912-1155
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522
N. L. Vashakmadze
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: tikhomirova777@mail.ru
ORCID iD: 0000-0002-9029-2590
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522
G. A. Arakelyan
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: tikhomirova777@mail.ru
ORCID iD: 0000-0003-3528-1466
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522
A. V. Klimov
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia; N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia
Email: tikhomirova777@mail.ru
ORCID iD: 0000-0003-0727-2976
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522; 1 Ostrovityanova St., Moscow 117513
A. A. Rumyantsev
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: tikhomirova777@mail.ru
ORCID iD: 0000-0003-4443-9974
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522
V. B. Matveev
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia; Sechenov First Moscow State Medical University (Sechenovskiy University)
Email: tikhomirova777@mail.ru
ORCID iD: 0000-0001-7748-9527
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522; Build. 2, 8 Trubetskaya St., Moscow 119048
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