Evidence map›Paper›PMID 32606174›Full record

ArticleIn vivo (Athens, Greece)

High-dose Radiotherapy for Oligo-progressive NSCLC Receiving EGFR Tyrosine Kinase Inhibitors: Real World Data.

Mariacarmela Santarpia, Giuseppe Altavilla, Nicolo Borsellino, Andrea Girlando, Gianfranco Mancuso, Stefano Pergolizzi, Dario Piazza, Antonio Pontoriero, Maria Rosaria Valerio, Vittorio Gebbia

Open access · diamondAbstract read
In one paragraph

Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
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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 5 institutions in 1 country.

Mariacarmela SantarpiaMedical Oncology Unit, Depart. of Human Pathology "G. Barresi", University of Messina, Messina, Italy.
Giuseppe AltavillaMedical Oncology Unit, Depart. of Human Pathology "G. Barresi", University of Messina, Messina, Italy.
Nicolo BorsellinoMedical Oncology Unit, Ospedale Buccheri La Ferla, Palermo, Italy.
Andrea GirlandoRadiotherapy Unit, Istituto Clinico Humanitas, Catania, Italy.
Gianfranco MancusoMedical Oncology and Supportive Care Unit, La Maddalena Cancer Center, Palermo, Italy.
Stefano PergolizziUnit of Radiation Oncology, Department of Biomedical, Dental Science and Morphological and Functional Images, University of Messina, Messina, Italy.
Dario PiazzaGSTU Foundation for Cancer Research, Palermo, Italy.
Antonio PontorieroUnit of Radiation Oncology, Department of Biomedical, Dental Science and Morphological and Functional Images, University of Messina, Messina, Italy.
Maria Rosaria ValerioMedical Oncology Unit, Department of Oncology, University of Palermo, Palermo, Italy.
Vittorio GebbiaMedical Oncology and Supportive Care Unit, La Maddalena Cancer Center, Palermo, Italy vittorio.gebbia@gmail.com.
University of Messina · ITLa Maddalena · ITFondazione Humanitas per la Ricerca · ITOspedale Buccheri la Ferla Fatebenefratelli · ITUniversity of Palermo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimLocal ablative treatments for oligo-progressive, EGFR mutated non-small cell lung cancer (mut-NCSLC) may improve long-term disease control and survival. We analyzed the efficacy of hypo-fractionated, high-dose radiation therapy (HDRT), in association with prolonged EGFR tyrosine kinase inhibitors (TKI) in oligo-progressive, EGFR mutant-NSCLC. PATIENTS AND

methodsProgression-free survival-1 (PFS-1, date from initiation of TKI therapy until oligo-progression or death), and progression-free survival-2 (PFS-2, date of focal progression until further progression or death) were evaluated.

resultsThirty-six patients were analyzed. The median PFS 1 was 12.5 months. HDHRT consisted of intensity-modulated RT and stereotactic RT in 23 (64%) and 13 (36%) patients respectively. The median PFS 2 was 6.3 months. Overall survival was 38.7 months.

conclusionHypo-fractionated HDRT plus TKI therapy, is associated with a significant prolongation of disease control (overall PFS: 18.8 months), with manageable side effects. These real-world data support the use of local ablative approaches in oligo-progressive EGFR mut-NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsErbB ReceptorsHumansMutationProgression-Free SurvivalProtein Kinase InhibitorsRetrospective StudiesEGFR protein, humanErbB ReceptorsProtein Kinase InhibitorsEGFRhigh-dose radiotherapyNon-small cell lung canceroligo-progression

Identifiers

PMID32606174
PMCPMC7439904
OpenAlexW3039619179

What OpenQuestion holds

Textmetadata
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.