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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02428751
Other study ID # 308-2015-005
Secondary ID
Status Recruiting
Phase Phase 3
First received April 17, 2015
Last updated November 17, 2015
Start date September 2015
Est. completion date May 2020

Study information

Verified date November 2015
Source Sun Yat-sen University
Contact Wen-qi Jiang, M.D.
Phone 86-20-87343765
Email wenqi_jiang@163.com
Is FDA regulated No
Health authority China: Health and Family Planning Commission of Guangdong Province
Study type Interventional

Clinical Trial Summary

The combination of rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP regimen) has been the first-line chemotherapy for elderly patients with diffuse large B-cell lymphoma (DLBCL). The treatment-related toxicities, especially the severe cardiac toxicities induced by anthracycline drugs (doxorubicin), have become a major concern among elderly patients. Pegylated liposomal doxorubicin is a formulation of doxorubicin with a prolonged circulation time and unique toxicity profile. Previous single arm studies of elderly patients with lymphoma used pegylated liposomal doxorubicin instead of traditional doxorubicin in combination with rituximab, cyclophosphamide, vincristine, and prednisone (the novel R-CDOP regimen), and demonstrated better safety profile, including less bone marrow suppression and less cardiac toxicities, while maintaining the efficacy. However, the efficacy and safety of these two regimens (R-CHOP and R-CDOP) have not been head-to-head compared in a randomized study. The aim of this study is to compare the efficacy and safety of R-CDOP (rituximab, cyclophosphamide, pegylated liposomal doxorubicin, vincristine, and prednisone) and R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone) in previously untreated elderly patients with DLBCL.


Recruitment information / eligibility

Status Recruiting
Enrollment 216
Est. completion date May 2020
Est. primary completion date March 2020
Accepts healthy volunteers No
Gender Both
Age group 60 Years to 80 Years
Eligibility Inclusion Criteria:

- Pathologically confirmed diagnosis of CD20-positive diffuse large B-cell lymphoma

- 60~80 years old

- Ann Arbor stage I~IV

- ECOG physical score of 0~2

- Have not received previous treatment to lymphoma, including chemotherapy, radiotherapy, or biotherapy

- Have at least one clinically measurable lesion: >= 2cm under physical examination, or >= 1.5cm under computed tomography (CT) or magnetic resonance (MR)

- Life expectancy of >= 3 months

- Serum glutamic oxaloacetic transaminase (SGOT) and serum glutamate pyruvate transaminase and total bilirubin <= 2 × upper limit of normal (ULN)

- Glomerular filtration rate (MDRD method) >= 30ml/min

- No abnormalities in blood coagulative function

- Generally normal bone marrow function: while blood cell >= 3,000/µL, absolute neutrophil count >= 1,500/µL, hemoglobin >= 100g/L, platelet >= 75,000/µL

- No evidence of active hepatitis B or C virus, or human immunodeficiency virus infection

- Left ventricular ejection fraction (LVEF) >= 45% measured by two dimensional echocardiography or multi-gated acquisition (MUGA) scan

- Cardiac function of class I-II in New York Heart Association (NYHA) classification

Exclusion Criteria:

- Patients with indolent lymphoma

- Positive results for in situ hybridization for Epstein-Barr virus encoded RNA (EBER)

- Serum Epstein-Barr virus DNA >= 1,000 copies/ml

- Double-hit lymphoma confirmed by fluorescence in situ hybridization (FISH)

- Primary mediastinal B-cell lymphoma

- Involvement of central nervous system

- Bulky disease (>= 10cm)

- History of cardiac disease, including clinically significant ventricular tachycardia, atrial fibrillation, conduction block, myocardial infarction within 1 year, congestive heart failure, symptomatic coronary heart disease which needs medication

- Known allergic reaction to any component of the agents used in the chemotherapeutic regimens that are used in the study

- Previous exposure to anthracycline drugs, rituximab, or chemotherapy for lymphoma

- History of malignant carcinoma within 5 years (except carcinoma in situ of the skin and uterine cervix, and prostatic carcinoma)

- Currently enrolled in other clinical studies

- Other conditions that the investigators consider as inappropriate for enrolling into this study

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Drug:
Pegylated liposomal doxorubicin
30 mg/m2, IV (in the vein) on day 1 of each 21 day cycle
Doxorubicin
50 mg/m2, IV (in the vein) on day 1 of each 21 day cycle
Rituximab
375 mg/m2, IV (in the vein) on day 0 of each 21 day cycle
Cyclophophamide
750 mg/m2, IV (in the vein) on day 1 of each 21 day cycle
Vincristine
1.4 mg/m2 (2mg in maxium), IV (in the vein) on day 1 of each 21 day cycle
Prednisone
100mg/d, PO on day 1-5 of each 21 day cycle

Locations

Country Name City State
China Guangdong Provincial People's Hospital Guangzhou Guangdong
China Nanfang Hospital of Southern Medical Unversity Guangzhou Guangdong
China Sun Yat-sen University Cancer Center Guangzhou Guangdong
China The First Affiliated Hospital of Guangzhou Medical University Guangzhou Guangdong
China The Second Affiliated Hospital of Sun Yat-sen University Guangzhou Guangdong
China The Third Affiliated Hospital of Sun Yat-sen University Guangzhou Guangdong
China Wujing Zongdui Hospital of Guangdong Province Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Wenqi Jiang

Country where clinical trial is conducted

China, 

References & Publications (16)

Coiffier B, Lepage E, Briere J, Herbrecht R, Tilly H, Bouabdallah R, Morel P, Van Den Neste E, Salles G, Gaulard P, Reyes F, Lederlin P, Gisselbrecht C. CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients with diffuse large-B-cel — View Citation

Coiffier B, Thieblemont C, Van Den Neste E, Lepeu G, Plantier I, Castaigne S, Lefort S, Marit G, Macro M, Sebban C, Belhadj K, Bordessoule D, Fermé C, Tilly H. Long-term outcome of patients in the LNH-98.5 trial, the first randomized study comparing ritux — View Citation

Corazzelli G, Frigeri F, Arcamone M, Lucania A, Rosariavilla M, Morelli E, Amore A, Capobianco G, Caronna A, Becchimanzi C, Volzone F, Marcacci G, Russo F, De Filippi R, Mastrullo L, Pinto A. Biweekly rituximab, cyclophosphamide, vincristine, non-pegylate — View Citation

Feugier P, Van Hoof A, Sebban C, Solal-Celigny P, Bouabdallah R, Fermé C, Christian B, Lepage E, Tilly H, Morschhauser F, Gaulard P, Salles G, Bosly A, Gisselbrecht C, Reyes F, Coiffier B. Long-term results of the R-CHOP study in the treatment of elderly — View Citation

Fisher RI, Gaynor ER, Dahlberg S, Oken MM, Grogan TM, Mize EM, Glick JH, Coltman CA Jr, Miller TP. Comparison of a standard regimen (CHOP) with three intensive chemotherapy regimens for advanced non-Hodgkin's lymphoma. N Engl J Med. 1993 Apr 8;328(14):100 — View Citation

Gimeno E, Sánchez-González B, Alvarez-Larrán A, Pedro C, Abella E, Comín J, Saumell S, García-Pallarols F, Gómez M, Besses C, Salar A. Intermediate dose of nonpegylated liposomal doxorubicin combination (R-CMyOP) as first line chemotherapy for frail elder — View Citation

Gogas H, Papadimitriou C, Kalofonos HP, Bafaloukos D, Fountzilas G, Tsavdaridis D, Anagnostopoulos A, Onyenadum A, Papakostas P, Economopoulos T, Christodoulou C, Kosmidis P, Markopoulos C. Neoadjuvant chemotherapy with a combination of pegylated liposoma — View Citation

Habermann TM, Weller EA, Morrison VA, Gascoyne RD, Cassileth PA, Cohn JB, Dakhil SR, Woda B, Fisher RI, Peterson BA, Horning SJ. Rituximab-CHOP versus CHOP alone or with maintenance rituximab in older patients with diffuse large B-cell lymphoma. J Clin On — View Citation

Heintel D, Skrabs C, Hauswirth A, Eigenberger K, Einberger C, Raderer M, Sperr WR, Knöbl P, Müllauer L, Uffmann M, Dieckmann K, Gaiger A, Jäger U. Nonpegylated liposomal doxorubicin is highly active in patients with B and T/NK cell lymphomas with cardiac — View Citation

Limat S, Daguindau E, Cahn JY, Nerich V, Brion A, Perrin S, Woronoff-Lemsi MC, Deconinck E. Incidence and risk-factors of CHOP/R-CHOP-related cardiotoxicity in patients with aggressive non-Hodgkin's lymphoma. J Clin Pharm Ther. 2014 Apr;39(2):168-74. doi: — View Citation

Luminari S, Montanini A, Caballero D, Bologna S, Notter M, Dyer MJ, Chiappella A, Briones J, Petrini M, Barbato A, Kayitalire L, Federico M. Nonpegylated liposomal doxorubicin (MyocetTM) combination (R-COMP) chemotherapy in elderly patients with diffuse l — View Citation

O'Brien ME, Wigler N, Inbar M, Rosso R, Grischke E, Santoro A, Catane R, Kieback DG, Tomczak P, Ackland SP, Orlandi F, Mellars L, Alland L, Tendler C; CAELYX Breast Cancer Study Group. Reduced cardiotoxicity and comparable efficacy in a phase III trial of — View Citation

Rigacci L, Mappa S, Nassi L, Alterini R, Carrai V, Bernardi F, Bosi A. Liposome-encapsulated doxorubicin in combination with cyclophosphamide, vincristine, prednisone and rituximab in patients with lymphoma and concurrent cardiac diseases or pre-treated w — View Citation

Tulpule A, Espina BM, Berman N, Buchanan LH, Smith DL, Sherrod A, Dharmapala D, Gee C, Boswell WD, Nathwani BN, Welles L, Levine AM. Phase I/II trial of nonpegylated liposomal doxorubicin, cyclophosphamide, vincristine, and prednisone in the treatment of — View Citation

Visani G, Guiducci B, D'Adamo F, Mele A, Nicolini G, Leopardi G, Sparaventi G, Barulli S, Malerba L, Isidori A, Malagola M, Piccaluga PP. Cyclophosphamide, pegylated liposomal doxorubicin, vincristine and prednisone (CDOP) plus rituximab is effective and — View Citation

Zaja F, Tomadini V, Zaccaria A, Lenoci M, Battista M, Molinari AL, Fabbri A, Battista R, Cabras MG, Gallamini A, Fanin R. CHOP-rituximab with pegylated liposomal doxorubicin for the treatment of elderly patients with diffuse large B-cell lymphoma. Leuk Ly — View Citation

* Note: There are 16 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Primary event-free survival (EFS) Defined as time from the date of randomization to the date of disease progression, death due to any cause, termination of treatment, or the most recent follow-up two year No
Secondary overall response rate (ORR) defined as the proportion of patients whose best overall response is either complete remission (CR) or partial remission (PR), which was evaluated in accordance with the International Working Group Recommendations for Response Criteria for non-Hodgkin's lymphoma at week 6, 12, 18, and 24 after randomization No
Secondary complete remission (CR) rate defined as the proportion of patients whose best overall response is complete remission, which was evaluated in accordance with the International Working Group Recommendations for Response Criteria for non-Hodgkin's lymphoma at week 6, 12, 18, and 24 after randomization No
Secondary overall survival (OS) defined as time from the date of randomization to the date of death due to any cause or the most recent follow-up two year No
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