A PD-L1 score that counts stained tumour cells and immune cells together.
The combined positive score (CPS) is a PD-L1 measure that counts stained tumour cells together with stained lymphocytes and macrophages, divides by the number of viable tumour cells and multiplies by 100, using the 22C3 assay. A CPS of 10 or more defines Pembrolizumab eligibility in Triple-negative breast cancer (TNBC) under KEYNOTE-355, while a CPS of 1 or more is the threshold in head and neck, gastric and cervical cancers. It differs from the Tumour proportion score (TPS), which counts tumour cells only, and from the SP142 immune-cell score used for atezolizumab. The score is attached to the PD-L1 target and is referenced by the Gastric, Oesophageal, Ovarian, Cervical and Head and neck cancer entries and by the KEYNOTE-048, KEYNOTE-689, KEYNOTE-590, KEYNOTE-859 and CheckMate 649 trials.
In plain words · PD-L1 is the tumour's side of the PD-1 brake, and also the biomarker that decides who gets immunotherapy.
Showing the target this term concerns: PD-L1.
The glossary entry explains the word; the readout page carries the scoring rule, the thresholds approvals use, the companion diagnostics and the tests.
The survival gain turns the earlier progression-free survival result into a clear reason to offer pembrolizumab with and after chemoradiotherapy to women with node-positive or stage III-IVA cervical cancer. Because cervical cancer is concentrated in low- and middle-income countries, the benefit reaches most women only if pricing and access follow.
Women with locally advanced cervical cancer that is node-positive or stage III-IVA can be offered pembrolizumab alongside and after chemoradiotherapy to lower the chance of relapse. The result matters most in countries where cervical cancer is common but immunotherapy access is poorest, so its global impact depends on pricing and health-system capacity. It does not apply to early-stage disease treated with surgery or to lower-risk locally advanced disease without nodal involvement.
This is the population-based prevalence for the two label thresholds in early TNBC, and it shows the KEYNOTE-355 CPS 10 gate would admit only about a quarter of unselected patients.
Confirms that the TROP2 antibody-drug conjugates are given without a TROP2 test and that PD-L1 remains the one selection assay in metastatic triple-negative disease, which is why assay harmonisation matters.
For stage II-III triple-negative breast cancer, chemotherapy plus pembrolizumab before surgery and pembrolizumab alone afterwards is now the standard approach worldwide, and the survival gain is real, not just a surrogate. It does not apply to stage I disease or to hormone-receptor-positive or HER2-positive cancers. The price is a year of immunotherapy with a meaningful chance of a permanent endocrine side effect such as hypothyroidism or adrenal insufficiency.
Patients with newly diagnosed advanced stomach or oesophageal adenocarcinoma whose tumour is HER2-negative and PD-L1 positive (CPS 5 or more, or at least 1 in some regions) should receive chemotherapy with nivolumab (or pembrolizumab, from KEYNOTE-859), which adds about three months of median survival and doubles the chance of being alive at three years. The benefit in PD-L1-negative tumours is doubtful, and these patients may be better served by chemotherapy alone or by trials.
The clearest demonstration that PD-L1 positive in triple-negative breast cancer means different things depending on the kit; with atezolizumab withdrawn, pembrolizumab's 22C3 combined positive score of 10 is the surviving standard, and roughly a quarter of patients get a different answer depending on which assay their laboratory runs.
Patients with head and neck squamous cell cancer that has recurred or spread should be treated first with pembrolizumab: alone if their tumour is strongly PD-L1 positive and they can wait for a slower response, or with chemotherapy if the tumour is bulky or PD-L1 low. Cetuximab-based chemotherapy is no longer the default. Long-term follow-up shows a small but real group of patients alive at four to five years, which was almost unheard of before.
Shares PD-L1 assay discordance (SP142, SP263 and 22C3 in breast cancer), IMpassion131, PD-L1 combined positive score 10 in triple-negative breast cancer, Harmonise PD-L1 testing for triple-negative breast cancer around one scored assay, with external quality assurance.
Shares Comparison of SP142 and 22C3 PD-L1 assays in a population-based cohort of triple-negative breast cancer patients in the context of their clinically established scoring algorithms, Harmonise PD-L1 testing for triple-negative breast cancer around one scored assay, with external quality assurance, PD-L1 IHC 22C3 pharmDx, PD-L1 Immunohistochemistry Assay Comparison in Atezolizumab Plus nab-Paclitaxel-Treated Advanced Triple-Negative Breast Cancer.
Shares Harmonise PD-L1 testing for triple-negative breast cancer around one scored assay, with external quality assurance, KEYNOTE-355, PD-L1 CPS (combined positive score), Triple-negative breast cancer roadmap: from a remainder defined by three negative tests to immunotherapy, antibody-drug conjugates and the residual disease problem.
Shares Comparison of SP142 and 22C3 PD-L1 assays in a population-based cohort of triple-negative breast cancer patients in the context of their clinically established scoring algorithms, PD-L1 Immunohistochemistry Assay Comparison in Atezolizumab Plus nab-Paclitaxel-Treated Advanced Triple-Negative Breast Cancer, PD-L1 CPS (combined positive score), PD-L1 expression testing (22C3, SP142, SP263).
Shares Tumour proportion score (TPS), PD-L1 expression testing (22C3, SP142, SP263), Immune checkpoint, Companion diagnostics.
Shares DIAMOND, KEYNOTE-355, Triple-negative breast cancer roadmap: from a remainder defined by three negative tests to immunotherapy, antibody-drug conjugates and the residual disease problem, Metastatic triple-negative breast cancer.
Shares PD-L1 Immunohistochemistry Assay Comparison in Atezolizumab Plus nab-Paclitaxel-Treated Advanced Triple-Negative Breast Cancer, KEYNOTE-522: adding pembrolizumab before and after surgery in early triple-negative breast cancer, Triple-negative breast cancer roadmap: from a remainder defined by three negative tests to immunotherapy, antibody-drug conjugates and the residual disease problem, PD-L1.
Shares KEYNOTE-A18: pembrolizumab with chemoradiotherapy for locally advanced cervical cancer (overall survival), KEYNOTE-A18: pembrolizumab with chemoradiotherapy for locally advanced cervical cancer (progression-free survival), Cervical cancer, Ovarian cancer.