Atezolizumab and pembrolizumab in triple-negative breast cancer: a meta-analysis. Issue 2 (1st February 2022)
- Record Type:
- Journal Article
- Title:
- Atezolizumab and pembrolizumab in triple-negative breast cancer: a meta-analysis. Issue 2 (1st February 2022)
- Main Title:
- Atezolizumab and pembrolizumab in triple-negative breast cancer: a meta-analysis
- Authors:
- Latif, Farah
Bint Abdul Jabbar, Hira
Malik, Hamna
Sadaf, Humaira
Sarfraz, Azza
Sarfraz, Zouina
Cherrez-Ojeda, Ivan - Abstract:
- ABSTRACT: Background: The approval of anti-PD-L1 drugs, including atezolizumab/pembrolizumab in triple-negative breast cancer (TNBC), potentially improveme treatment regimens available for TNBC. Methods: We conducted a meta-analysis to review the efficacy of atezolizumab/pembrolizumab for the treatment of TNBC in both the adjuvant and neoadjuvant settings. We calculated standardized mean difference (SMD) for the associations of progression-free survival (PFS) and overall survival (OS) and odds ratios (ORs) to estimate objective response rate (ORR) and pathological complete response (pCR), using 95% confidence intervals (CIs). Results: Six clinical trials comprising 3612 patients were included. For adjuvant therapies, the ORR (OR = 1.26, P = 0.04) of atezolizumab/pembrolizumab plus chemotherapy was higher in the intention to treat (ITT) arms than the placebo groups in TNBC. A positive effect size was found for PFS in the ITT arms (d = 1.55, P < 0.001). The atezolizumab plus chemotherapy group had a positive effect size for OS compared to control groups (d = 0.52, P < 0.001). In the neoadjuvant setting, patients in ITT arms had higher pCR rates than the control groups (OR = 1.61, P = 0.001). Conclusion: We collate evidence of atezolizumab/pembrolizumab as viable therapeutics among patients with TNBC with PD-L1 subgroups deriving higher benefits. PLAIN LANGUAGE SUMMARY: Immune checkpoint inhibitors (ICI), atezolizumab and pembrolizumab, have received approval for patients withABSTRACT: Background: The approval of anti-PD-L1 drugs, including atezolizumab/pembrolizumab in triple-negative breast cancer (TNBC), potentially improveme treatment regimens available for TNBC. Methods: We conducted a meta-analysis to review the efficacy of atezolizumab/pembrolizumab for the treatment of TNBC in both the adjuvant and neoadjuvant settings. We calculated standardized mean difference (SMD) for the associations of progression-free survival (PFS) and overall survival (OS) and odds ratios (ORs) to estimate objective response rate (ORR) and pathological complete response (pCR), using 95% confidence intervals (CIs). Results: Six clinical trials comprising 3612 patients were included. For adjuvant therapies, the ORR (OR = 1.26, P = 0.04) of atezolizumab/pembrolizumab plus chemotherapy was higher in the intention to treat (ITT) arms than the placebo groups in TNBC. A positive effect size was found for PFS in the ITT arms (d = 1.55, P < 0.001). The atezolizumab plus chemotherapy group had a positive effect size for OS compared to control groups (d = 0.52, P < 0.001). In the neoadjuvant setting, patients in ITT arms had higher pCR rates than the control groups (OR = 1.61, P = 0.001). Conclusion: We collate evidence of atezolizumab/pembrolizumab as viable therapeutics among patients with TNBC with PD-L1 subgroups deriving higher benefits. PLAIN LANGUAGE SUMMARY: Immune checkpoint inhibitors (ICI), atezolizumab and pembrolizumab, have received approval for patients with triple-negative breast cancer (TNBC) expressing PD-L1. Thus far, it has only been approved for patients with unresectable locally advanced or metastatic TNBC. With the IMpassion 130 and KEYNOTE-355 trials introducing the immunotherapy era for TNBC, ongoing trials have started exploring the outcomes of the ICIs in early-stage TNBC in combination. Recently, the ICIs have demonstrated positive efficacy outcomes in neoadjuvant settings. Both the ICIs have shown a safe profile in terms of adverse events. The recent advances made by clinical trials indicate promising results for early-stage and advanced/metastatic TNBC. However, there is a need to harmonize and explore biomarkers and endpoints in the ongoing clinical trials to enhance patient treatment protocols. As TNBC is an aggressive subtype, exploring beyond the PD-L1 positive subgroup is necessary to expand the target population receiving ICIs for TNBC. … (more)
- Is Part Of:
- Expert review of anticancer therapy. Volume 22:Issue 2(2022)
- Journal:
- Expert review of anticancer therapy
- Issue:
- Volume 22:Issue 2(2022)
- Issue Display:
- Volume 22, Issue 2 (2022)
- Year:
- 2022
- Volume:
- 22
- Issue:
- 2
- Issue Sort Value:
- 2022-0022-0002-0000
- Page Start:
- 229
- Page End:
- 235
- Publication Date:
- 2022-02-01
- Subjects:
- Triple-negative breast cancer -- pembrolizumab -- atezolizumab -- chemotherapy -- anti-PD-L1 -- biomarkers -- targeted therapies -- development of novel drugs
Cancer -- Treatment -- Periodicals
616.99406 - Journal URLs:
- http://informahealthcare.com ↗
http://www.future-drugs.com/loi/era ↗ - DOI:
- 10.1080/14737140.2022.2023011 ↗
- Languages:
- English
- ISSNs:
- 1473-7140
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3842.002982
British Library DSC - BLDSS-3PM
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- 20734.xml