Inclusion Criteria:

1. Previously untreated and histologically confirmed diffuse large B-cell lymphoma
according to REAL/WHO classification.

2. Stage II, III or IV disease

3. CD20+

4. Age ≥ 18 years

5. ECOG performance status ≤ 2

6. At least one objectively bidimensionally measurable lesion as demonstrated by CT,
spiral CT, or MRI that can be followed for response as target lesion. Patients with
the following sites of disease are NOT eligible:

- Patients with only skin lesions or only palpable lymph nodes.

- Patients with spleen or bone marrow as only site of disease.

7. Life expectancy ≥ 3 months

8. Serum bilirubin ≤ 1.5 x the institution's upper limit normal (ULN) and creatinine ≤
2.0 ULN and AST or ALT ≤ 2.0 x the institution's ULN. If hepatic involvement by
lymphoma is present, AST or ALT may be ≤ 5.0 x the institution's ULN.

9. LVEF ≥ 50% determined by MUGA scan.

10. Ability to comply with the visit schedule and assessments required by the protocol.

11. Signed approved informed consent, with understanding of study procedures.

Exclusion Criteria:

1. Any prior chemotherapy (except intrathecal chemotherapy at diagnosis and pretreatment
corticosteroid therapy) or radiotherapy: Patients may receive corticosteroid
pretreatment therapy for up to 7 days after randomization, pending Investigator's
decision to reduce tumor burden.

2. Histological diagnosis of T-cell lymphoma or any B-cell lymphoma other than diffuse
large B-cell.

3. History of indolent lymphoma

4. Active CNS involvement based on clinical evaluation .

5. HIV-related lymphoma.

6. Major thoracic and/or abdominal surgery within the 4 weeks before randomization from
which the patient has not fully recovered except for diagnosis of NHL. Patients who
have had minor surgery may be enrolled after a ≥ 1 week recovery period except for
diagnosis of NHL.

7. Clinically significant cardiovascular abnormalities

8. Serious (NCI CTCAE grade 3-4) intercurrent infection at randomization or deep seated
or systemic mycotic infections.

9. Clinical symptoms suggesting unresolved HIV, HBV or HCV infection. Patients with
seropositivity presumed to be due to prior vaccination against Hepatitis B virus or
resolved infection will not be excluded.

10. Active or history of another malignancy except cured basal cell carcinoma of skin or
carcinoma in situ of uterine cervix. Patients who have been in remission from another
previous malignancy for >5 years will be considered eligible.

11. Known hypersensitivity to the excipients or the study drugs that the patient will
receive.

12. Any contraindications to the study drugs as described in the Summary of Product
Characteristics or package inserts. 13. Neurological contraindication to vincristine
(e.g. peripheral neuropathy).

14. Any condition which, in the judgment of the Investigator, would place the subject at
undue risk, interfere with the results of the study, or make the subject otherwise
unsuitable. 15. General status that, in the opinion of the Investigator does not permit
the administration of eight courses of CHOP-R/CPOP-R. 16. Treatment with any other
investigational study drug within 30 days before randomization. Patient must have
recovered from all side effects of other investigational therapy. 17. Potentially fertile
men and women and their sexual partners not willing to use adequate contraception as
defined by the Investigator during the study and for 6 months after the last day of study
drug administration.

18. Any circumstance at the time of study entry that would preclude completion of the
study or the required follow-up.