Evidence map›Paper›PMID 37667784›Full record

ReviewCureus2023

Programmed Cell Death Protein 1 (PD-1) and Programmed Cell Death Ligand 1 (PD-L1) Immunotherapy: A Promising Breakthrough in Cancer Therapeutics.

Abdelrahman Abaza, Faten Sid Idris, Humna Anis Shaikh, Ilma Vahora, Kiran Prasad Moparthi, Majdah T Al Rushaidi, Meghana Reddy Muddam, Omobolanle A Obajeun, Arturo P Jaramillo, Safeera Khan

Open access · diamondAbstract readReview
In one paragraph

Review in Cureus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 4 pooled it
13.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

44 citing papers in PubMed, 4 syntheses or guidelines pooled it, 58 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 3 countries.

Abdelrahman AbazaPathology, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Faten Sid IdrisPediatrics, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Humna Anis ShaikhPediatrics, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Ilma VahoraGeneral Surgery, Saint George's University School of Medicine, Chicago, USA.
Kiran Prasad MoparthiCollege of Medicine, Sri Venkata Sai (SVS) Medical College, Mahabubnagar, IND.
Majdah T Al RushaidiPsychology, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Meghana Reddy MuddamGeneral Practice, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Omobolanle A ObajeunPaediatrics, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Arturo P JaramilloGeneral Practice, Universidad Estatal de Guayaquil, Machala, ECU.
Safeera KhanInternal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
California Institute of Behavioral Neurosciences and Psychology (United States) · USSVS Medical College · INUniversity of Guayaquil · ECSt. George's School · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The advent of immune checkpoint inhibitors has revolutionized cancer therapy by leveraging the body's immune system to combat malignancies effectively. Among these groundbreaking agents, programmed cell death protein 1 (PD-1) and programmed cell death ligand 1 (PD-L1) inhibitors have emerged as pivotal therapeutic approaches. PD-L1, a key protein expressed on the surface of various cells, including cancer cells, plays a central role in immune regulation by interacting with the programmed cell death protein 1 (PD-1) receptor on T-cells leading to immune suppression. The substantial increase in PD-L1 expression on cancer cell surfaces has driven the exploration of PD-1/PD-L1 inhibitors as potential immunotherapeutic agents. These inhibitors are monoclonal antibodies designed to impede the PD-L1 and PD-1 interaction and disrupt the immunosuppressive signal, thereby reinvigorating the anti-tumor immune response mediated by activated T-cells. Clinical trials investigating PD-1/PD-L1 inhibitors have demonstrated remarkable efficacy in the treatment of diverse advanced or metastatic cancers, including leukemia, non-small cell lung (NSCLC), hepatocellular, melanoma, gastric, colorectal, and breast cancers, among others. Regulatory approvals have been granted for both monotherapy and combination therapy with other cancer treatments, encompassing chemotherapy and additional immune checkpoint inhibitors. While PD-1/PD-L1 inhibitors have exhibited significant success, they are not devoid of challenges. The emergence of intrinsic or acquired resistance, as well as immune-related adverse events, warrants thorough investigation and management. Consequently, researchers have embarked on combination trials to augment the therapeutic potential of PD-1/PD-L1 inhibitors and surmount resistance mechanisms.

Indexed as

cancer therapeuticsclinical trialsimmune check-point inhibitorimmunotherapypathology

Identifiers

PMID37667784
PMCPMC10475160
OpenAlexW4386387979

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.