Durvalumab Plus Olaparib or Cediranib Active and Tolerable in Female Cancers

Share this content:
Durvalumab plus olaparib or intermittent cediranib is clinically active and tolerable in treating female cancers.
Durvalumab plus olaparib or intermittent cediranib is clinically active and tolerable in treating female cancers.

Durvalumab plus olaparib or intermittent cediranib is clinically active and tolerable in treating female cancers, according to results from a phase 1 study published in the Journal of Clinical Oncology.1

Olaparib is a PARP inhibitor and cediranib is a VEGFR 1-3 inhibitor.

“We hypothesized that increased DNA damage by PARP inhibitor and/or reduced VEGF signaling by the VEGFR inhibitor may complement the antitumor activity of immune checkpoint inhibition,” wrote the authors.

This dose-escalation, phase 1 study evaluated the pharmacokinetics, antitumor activity, and safety of durvalumab plus olaparib or cediranib.

The study treated 26 women with recurrent or metastatic solid malignancies who had not received prior immune checkpoint inhibitor therapy. Cancer types included ovarian, triple-negative breast, cervical, and uterine.

All patients received durvalumab 10 mg/kg every 2 weeks or 1500 mg every 4 weeks. Olaparib was administered as 200 or 300 mg twice daily and cediranib was administered as 20 or 30 mg once daily or 20 mg for 5 days then 2 days off.

The recommended phase 2 dosing was 1500 mg every 4 weeks of durvalumab plus 300 mg twice daily of olaparib or 20 mg of intermittent cediranib. There were no dose-limiting toxicities associated with durvalumab plus olaparib.

Treatment-emergent adverse events were hypertension, diarrhea, pulmonary embolism, pulmonary hypertension, and lymphopenia.

Durvalumab plus olaparib resulted in an objective response rate (ORR) of 17% and a disease control rate of 83%. There were 2 partial responses that lasted at least 11 months and 8 patients achieved stable disease for at least 4 months.

The ORR was 50% and the disease control rate was 75% with durvalumab plus cediranib, with 6 partial responses of at least 5 months and 3 achieved stable disease for at least 4 months.

RELATED: Burnout and Productivity Loss Among Gynecologic Oncologists

PD-L1 expression levels did not influence response.

According to the authors, these findings warrant additional studies. Single-arm phase 2 expansion trials are ongoing.

Reference

  1. Lee JM, Cimino-Mathews A, Peer CJ, et al. Safety and clinical activity of the programmed death-ligand 1 inhibitor durvalumab in combination with poly (ADP-ribose) polymerase inhibitor olaparib or vascular endothelial growth factor receptor 1-3 inhibitor cediranib in women's cancers: a dose-escalation, phase I study. J Clin Oncol. 2017 May 4. doi: 10.1200/JCO.2016.72.1340 [Epub ahead of print]

Related Resources

You must be a registered member of Cancer Therapy Advisor to post a comment.

Regimen and Drug Listings

GET FULL LISTINGS OF TREATMENT Regimens and Drug INFORMATION

Bone Cancer Regimens Drugs
Brain Cancer Regimens Drugs
Breast Cancer Regimens Drugs
Endocrine Cancer Regimens Drugs
Gastrointestinal Cancer Regimens Drugs
Gynecologic Cancer Regimens Drugs
Head and Neck Cancer Regimens Drugs
Hematologic Cancer Regimens Drugs
Lung Cancer Regimens Drugs
Other Cancers Regimens
Prostate Cancer Regimens Drugs
Rare Cancers Regimens
Renal Cell Carcinoma Regimens Drugs
Skin Cancer Regimens Drugs
Urologic Cancers Regimens Drugs

Sign Up for Free e-newsletters