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POLIVY in combination with rituximab, cyclophosphamide, doxorubicin, and prednisone (R-CHP) is indicated for the treatment of adult patients with previously untreated diffuse large B-cell lymphoma (DLBCL).1

 

POLIVY in combination with bendamustine and rituximab is indicated for the treatment of adult patients with relapsed/refractory (R/R) DLBCL who are not candidates for haematopoietic stem cell transplant.1

nil

Prescribing Information

NICE recommends and SMC accepts POLIVY+R-CHP for untreated diffuse large B-cell lymphoma (DLBCL) 2,3

Polivy in combination with rituximab, cyclophosphamide, doxorubicin, and prednisone (R-CHP) can be used as an option to treat previously untreated DLBCL in adults when:

  • they have an International Prognostic Index (IPI) score of 2 to 5

In the UK, approximately 5,500 patients are diagnosed with DLBCL per year.4 Effective treatment at first line (1L) is the best opportunity to achieve a successful outcome in DLBCL.5,6

 

POLIVY+R-CHP was the first treatment in over 20 years showing superiority over
R-CHOP, offering longer progression-free survival (PFS) and a generally comparable safety profile.7

 

POLARIX was the first phase III study in 20 years with a significant improvement in PFS and EFSeff over R-CHOP in previously untreated DLBCL.7

Expert perspectives on the POLARIX trial data

 

Watch the videos below to hear the views of Professor Graham Collins, Consultant Haematologist, The Churchill Hospital, Oxford, on the POLARIX trial data and its implications for UK clinical practice.

 

For UK prescribing information, please click here or scan the QR code in the videos.

We are dedicated to supporting HCPs to achieve optimal patient outcomes, If you have any questions about our products, from practical matters to understanding the data, please do not hesitate to contact us.

 

Contact our team to discuss POLIVY

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Abbreviations:

1L, first-line; DLBCL, diffuse large B-cell lymphoma; EFSeff, event-free survival for efficacy causes; HCP, healthcare professional; NICE, National Institute for Health and Care Excellence; PFS, progression free survival; R-CHP, rituximab, cyclophosphamide, doxorubicin, prednisone; R-CHOP, rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone; R/R, relapsed/refractory; SMC, Scottish Medicines Consortium.

References:

  1. POLIVY Summary of Product Characteristics.
  2. NICE Technology appraisal gudiance TA874. Published: 01 March 2023. Available at https://www.nice.org.uk/guidance/ta874. Accessed: March 2026.
  3. SMC2525. Published 05 May 2023. Available at: https://scottishmedicines.org.uk/media/7614/polatuzumab-vedotin-polivy-final-may-2023-for-website.pdf. Accessed: March 2026.
  4. Cancer Research UK. Diffuse Large B-Cell Lymphoma. Available at: https://www.cancerresearchuk.org/about-cancer/non-hodgkin-lymphoma/types/diffuse-large-B-cell-lymphoma. Accessed: March 2026.
  5. Maurer MJ, Ghesquières H, et al. J Clin Oncol. 2014;32(10):1066–1073.
  6. Nowakowski GS. Clin Adv Hematol Oncol. 2021;19(5):284–287.
  7. Tilly H, et al. N Engl J Med. 2022;386(4):351–363.
▼ This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions. Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. You can also report via the free Yellow Card app available from the Apple App Store or Google Play Store. Adverse events should also be reported to Roche Products Ltd. Please contact Roche Drug Safety Centre by emailing welwyn.uk_dsc@roche.com or calling +44 (0)1707 367554. Adverse reactions should be reported by brand name and batch number.
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