Evidence map›Paper›PMID 37095004›Full record

ReviewThoracic cancer2023

Correlations between pathogenic variants in DNA repair genes and anticancer treatment efficacy in stage IV non-small cell lung cancer: A large real-world cohort and review of the literature.

Itamar Averbuch, Roi Tschernichovsky, Oded Icht, Daniel A Goldstein, Raz Mutai, Elizabeth Dudnik, Ofer Rotem, Nir Peled, Aaron M Allen, Smadar Laufer-Geva and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in Thoracic cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
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

12 authors at 5 institutions in 1 country.

Itamar AverbuchDavidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.ORCID 0000-0003-1784-4528
Roi TschernichovskyDavidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.
Oded IchtDavidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.
Daniel A GoldsteinDavidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.
Raz MutaiDavidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.
Elizabeth DudnikOncology Division, Assuta Medical Center, Tel Aviv, Israel.
Ofer RotemDavidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.
Nir PeledOncology Division, Shaare Zedek Medical Center, Jerusalem, Israel.
Aaron M AllenOncology Division, Shaare Zedek Medical Center, Jerusalem, Israel.
Smadar Laufer-GevaDavidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.
Yael GoldbergThe Raphael Recanati Genetic Institute, Rabin Medical Center, Petah Tikva, Israel.
Alona ZerFishman Oncology Institute, Rambam Health Care Campus, Haifa, Israel.
Rabin Medical Center · ILShaare Zedek Medical Center · ILAssuta Medical Center · ILRafael Advanced Defense Systems (Israel) · ILRambam Health Care Campus · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMutations in genes involved in DNA damage repair (DDR), a hallmark of cancer, are associated with increased cancer cell sensitivity to certain therapies. This study sought to evaluate the association of DDR pathogenic variants with treatment efficacy in patients with advanced non-small cell lung cancer (NSCLC).

methodsA retrospective cohort of consecutive patients with advanced NSCLC attending a tertiary medical center who underwent next-generation sequencing in 01/2015-8/2020 were clustered according to DDR gene status and compared for overall response rate (ORR), progression-free survival (PFS) (patients receiving systemic therapy), local PFS (patients receiving definitive radiotherapy), and overall survival (OS) using log-rank and Cox regression analyses.

resultsOf 225 patients with a clear tumor status, 42 had a pathogenic/likely pathogenic DDR variant (pDDR), and 183 had no DDR variant (wtDDR). Overall survival was similar in the two groups (24.2 vs. 23.1 months, p = 0.63). The pDDR group had a higher median local PFS after radiotherapy (median 45 months vs. 9.9 months, respectively; p = 0.044), a higher ORR (88.9% vs. 36.2%, p = 0.04), and a longer median PFS (not reached vs. 6.0 months, p = 0.01) in patients treated with immune checkpoint blockade. There was no difference in ORR, median PFS, and median OS in patients treated with platinum-based chemotherapy.

conclusionOur retrospective data suggest that in patients with stage 4 NSCLC, pathogenic variants in DDR pathway genes may be associated with higher efficacy of radiotherapy and immune checkpoint inhibitors (ICIs). This should be further explored prospectively.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsDNA RepairHumansImmune Checkpoint InhibitorsRetrospective StudiesTreatment OutcomeImmune Checkpoint InhibitorsDNA damage repair mutationsimmunotherapynon-small cell lung cancerplatinum-based chemotherapyradiotherapy

Identifiers

PMID37095004
PMCPMC10260479
OpenAlexW4366814156

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.