You are now leaving GSK’s website

You are now leaving a GSK Website. By clicking this link, you will be taken to a website that is not owned or controlled by GSK, and GSK is not responsible for the content provided on that site.

Continue

Go back

Image of fictitious patient

Quality of life (QoL) with ZEJULA

Preservation of quality of life icon

QoL preserved
for over 30 cycles of ZEJULA maintenance vs placebo1,2

VIEW QOL

Reduced fatigue icon

Reduced long-term fatigue
in ZEJULA patients vs placebo3,4

Quality of life in the long term

ZEJULA preserved QoL in women with advanced ovarian cancer over 30 cycles of maintenance therapy‡2

Health-related QoL/patient-reported outcomes*‡

A graph showing health-related QoL/patient-reported outcomes A graph showing health-related QoL/patient-reported outcomes

Figure adapted from González-Martín A, et al. 2019

This analysis is exploratory in nature and does not control for Type 1 error; elements more distal to disease and treatment-related symptoms may be influenced by multiple nondrug factors.2

FOSI QoL domains included: mobility, self-care, anxiety/depression, pain/discomfort and usual activities.

*A treatment cycle lasted 28 days
FOSI (Functional Assessment of Cancer Therapy-Ovarian Symptoms Index) is a validated 8-item measure of symptom response to treatment, including lack of energy, vomiting, pain, nausea, stomach swelling, worsening condition, quality of life as assessed by the patient, and cramps in the stomach area.2,5

Discover the efficacy of ZEJULA in PRIMA

Long-term fatigue

ZEJULA reduced the burden of long-term fatigue common among advanced ovarian cancer patients vs placebo3,4

EORTC QLQ-C30 endpoint

A graph showing long-term fatigue in overall population A graph showing long-term fatigue in overall population

Figure adapted from Halla K, et al. 2020

Post-surgical patients reported an improvement in fatigue over more than 15 treatment cycles of ZEJULA vs placebo§3

§The analysis was exploratory in nature and did not control for Type 1 error; elements more distal to disease and treatment-related symptoms may have been influenced. In the PRIMA trial, a treatment cycle lasted 28 days.3

ZEJULA is indicated:6

  • as monotherapy for the maintenance treatment of adult patients with advanced epithelial (FIGO Stages III and IV) high-grade ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy.

Footnotes

EORTC QLQ-C30, European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire; FOSI, Functional Assessment of Cancer Therapy-Ovarian Symptoms Index; MoA, mechanism of action; QoL, quality of life; SE, standard error.

References

  1. González-Martín A, Pothuri B, Vergote I, et al. N Engl J Med. 2019;381(25):2391–2402.
  2. Gonzalez-Martin A, et al. N Engl J Med. 2019; 381: 2391–2402. Supplementary appendix.
  3. Halla K, et al. Presented at the Oncology Nursing Society 45th Annual Congress, April 29–May 3, 2020, San Antonio, Texas. 
  4. Joly F, et al. Study. Annals of Oncology, 2019; DOI: 10.1093/annonc/mdz074.
  5. FACIT.org. Functional Assessment of Cancer Therapy Ovarian Cancer Symptom Index - 8 item version. Available at: https://www.facit.org/measure-english-downloads/fosi-english-downloads. Last accessed: April 2022
  6. ZEJULA Summary of Product Characteristics.

Adverse events should be reported directly to the Health Products Regulatory Authority (HPRA) on their website: www.hpra.ie. Adverse events should also be reported to GlaxoSmithKline on 1800 244 255.

Zejula is a registered trademark of the GlaxoSmithKline group of companies.

December 2023 | PM-IE-NRP-WCNT-220020

February 2022 | PM-GB-NRP-WCNT-210016 v1.0