Evidence map›Paper›PMID 34478166›Full record

Trial reportCancer2022

JASPER: Phase 2 trial of first-line niraparib plus pembrolizumab in patients with advanced non-small cell lung cancer.

Suresh S Ramalingam, Eddie Thara, Mark M Awad, Afshin Dowlati, Basir Haque, Thomas E Stinchcombe, Grace K Dy, David R Spigel, Sharon Lu, Nithya Iyer Singh and 3 more

Erratum issued 3 registry-linked trialsOpen access · hybridAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to 3 registered trials, which are not on this map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 3% 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.

NCT03308942 phase2completednot on this map

Phase 2, Multi-Arm Study of Niraparib Administered Alone and in Combination With a PD-1 Inhibitor in Patients With Non-Small Cell Lung Cancer

TypeinterventionalSponsorTesaro, Inc.Ran2017 to 2021Enrolled53ConditionsNeoplasmsArmsNiraparib, Pembrolizumab, TSR-042 (Dostarlimab)
NCT04475939 phase3completednot on this map

A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study Comparing Niraparib Plus Pembrolizumab Versus Placebo Plus Pembrolizumab as Maintenance Therapy in Participants Whose Disease Has Remained Stable or Responded to First-Line Platinum -Based Chemotherapy With Pembrolizumab for Stage IIIB/IIIC or IV Non-Small Cell Lung Cancer (ZEAL-1L)

TypeinterventionalSponsorGlaxoSmithKlineRan2020 to 2026Enrolled666ConditionsLung Cancer, Non-Small CellArmsNiraparib, Pembrolizumab, Placebo
NCT07303218 active not recruitingnot on this mapstarted 2025, after this paper: background citation

The HER Project: Homologous Recombination Deficiency in EGFR-Mutated NSCLC, a Retrospective and Prospective Translational Single-center Study

TypeobservationalSponsorIRCCS San RaffaeleRan2025 to 2032Enrolled100ConditionsEGFR, Non Small Cell Lung Cancer, Homologous Recombination Deficiency, PARP InhibitorArmsNo Intervention: Observational Cohort
3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

  1. Pooled it
  2. Cemiplimab in Locally Advanced or Metastatic Secondary Angiosarcomas (CEMangio): A Phase II Clinical Trial and Biomarker Analyses.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Trial
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  19. Next-generation immunotherapy: igniting new hope for lung cancer.Therapeutic advances in medical oncology · 2024
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 10 institutions in 1 country.

Suresh S RamalingamEmory University, Winship Cancer Institute, Atlanta, Georgia.ORCID 0000-0002-0757-3106
Eddie TharaOncology Institute of Hope and Innovation, Los Angeles, California.
Mark M AwadDana-Farber Cancer Institute, Boston, Massachusetts.
Afshin DowlatiUniversity Hospitals Seidman Cancer Center and Case Western Reserve University, Cleveland, Ohio.
Basir HaqueKadlec Clinic Hematology and Oncology, Kennewick, Washington.
Thomas E StinchcombeDuke Cancer Institute, Duke University School of Medicine, Durham, North Carolina.ORCID 0000-0002-3595-8011
Grace K DyRoswell Park Comprehensive Cancer Center, Buffalo, New York.
David R SpigelSarah Cannon Research Institute/Tennessee Oncology, Nashville, Tennessee.
Sharon LuGlaxoSmithKline, Waltham, Massachusetts.
Nithya Iyer SinghGlaxoSmithKline, Waltham, Massachusetts.
Yongqiang TangGlaxoSmithKline, Waltham, Massachusetts.
Iryna TeslenkoGlaxoSmithKline, Waltham, Massachusetts.
Nicholas IannottiHematology Oncology Associates of the Treasure Coast, Port St. Lucie, Florida.
GlaxoSmithKline (United States) · USDana-Farber Cancer Institute · USDuke University · USEmory University · USHematology Oncology Associates · USKadlec Clinic · USOncology Institute of Hope and Innovation · USRoswell Park Comprehensive Cancer Center · USSarah Cannon · USUniversity Hospitals Seidman Cancer Center · US

Funding

GlaxoSmithKline 213352
6 · The paper itself

Abstract

backgroundPoly(ADP-ribose) polymerase (PARP) inhibitors may synergize with programmed cell death receptor-1 (PD-1) inhibitors to enhance adaptive and innate antitumor immune responses. In the phase 2 JASPER study (NCT04475939), the PARP inhibitor niraparib was evaluated in combination with the PD-1 inhibitor pembrolizumab in patients with metastatic and/or locally advanced non-small cell lung cancer (NSCLC).

methodsPatients whose tumors had programmed cell death ligand 1 (PD-L1) tumor proportion scores (TPS) ≥50% (cohort 1) or 1%-49% (cohort 2) received first-line niraparib (200 mg once daily) plus pembrolizumab (200 mg every 3 weeks). The primary end point was investigator-assessed objective response rate (ORR). Secondary end points included duration of response (DoR), progression-free survival (PFS), overall survival (OS), safety, and pharmacokinetics.

resultsThirty-eight patients were enrolled in cohorts 1 and 2. In cohort 1, ORR (95% confidence interval [CI]) was 56.3% (9 of 16 patients; 29.9%-80.2%); 2 of 16 patients had complete responses and 7 of 16 had partial responses (PRs). In cohort 2, ORR was 20.0% (5.7%-43.7%) with 4 of 20 PRs. In cohorts 1 and 2, the median DoR was 19.7 months (95% CI, 4.2 months to not estimable [NE]) and 9.4 months (95% CI, 4.2 months to NE), the median PFS was 8.4 months (95% CI, 3.9-22.1 months) and 4.2 months (95% CI, 2.0-6.2 months), and the median OS was NE (95% CI, 6.0 months to NE) and 7.7 months (95% CI, 4.0-12.5 months), respectively. Grade ≥3 treatment-emergent adverse events occurred in 88.2% and 85.7% of patients in cohorts 1 and 2, respectively. Safety was consistent with known profiles of single-agent niraparib and pembrolizumab.

conclusionsNiraparib plus pembrolizumab showed clinical activity in patients with advanced and/or metastatic NSCLC. LAY SUMMARY: The JASPER clinical trial studied a new combination treatment for advanced or metastatic non-small cell lung cancer (NSCLC). Pembrolizumab, a drug approved for NSCLC, was given with niraparib. Previous research showed that these 2 drugs together might work better than either drug alone. This study found that more than half of patients with high levels of a tumor marker responded to the combination, and one-fifth of patients with lower levels of the marker responded. The types of side effects from the combination were similar to side effects from both drugs alone. These results support more research on this combination.

Indexed as

Antibodies, Monoclonal, HumanizedCarcinoma, Non-Small-Cell LungIndazolesLung NeoplasmsPiperidinesAntineoplastic Combined Chemotherapy ProtocolsHumansPoly(ADP-ribose) Polymerase InhibitorsAntibodies, Monoclonal, HumanizedIndazolesniraparibpembrolizumabPiperidinesPoly(ADP-ribose) Polymerase Inhibitorsclinical studycombination drug therapylung neoplasmsniraparibnon-small cell lung carcinomapembrolizumabpoly(ADP-ribose) polymerase inhibitors

Identifiers

PMID34478166
PMCPMC9293160
OpenAlexW3196318196

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.