Evidence map›Paper›PMID 33627685›Full record

ArticleScientific reports2021

A phase I dose-finding, pharmacokinetics and genotyping study of olaparib and lurbinectedin in patients with advanced solid tumors.

Andres Poveda, Ana Oaknin, Ignacio Romero, Angel Guerrero-Zotano, Lorena Fariñas-Madrid, Victor Rodriguez-Freixinos, Pedro Mallol, Raquel Lopez-Reig, Jose Antonio Lopez-Guerrero

Open access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in Scientific reports, 2021. 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
1.4field-weighted citation impact, top 16% 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, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. PARP inhibitors in non-ovarian gynecologic cancers.Therapeutic advances in medical oncology · 2024
    Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Exceptional response to lurbinectedin and irinotecan inTherapeutic advances in chronic disease · 2022
    Article
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

9 authors at 7 institutions in 2 countries.

Andres PovedaOncogynecologic Department, Initia Oncology, Hospital Quironsalud Valencia, Avda Blasco Ibañez, 14, 46 010, Valencia, Spain. apoveda@initiaoncologia.com.
Ana OakninMedical Oncology Department, Vall D'Hebron University Hospital, Vall D'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
Ignacio RomeroDepartment of Medical Oncology, Fundación Instituto Valenciano de Oncología (IVO), Valencia, Spain.
Angel Guerrero-ZotanoDepartment of Medical Oncology, Fundación Instituto Valenciano de Oncología (IVO), Valencia, Spain.
Lorena Fariñas-MadridMedical Oncology Department, Vall D'Hebron University Hospital, Vall D'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
Victor Rodriguez-FreixinosDepartment of Medical Oncology and Hematology, Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Canada.
Pedro MallolClinical Trials Department, FINCIVO (Fundación de Investigación Clínica del IVO), Valencia, Spain.
Raquel Lopez-ReigLaboratory of Molecular Biology, Fundación Instituto Valenciano de Oncología, Valencia, Spain.
Jose Antonio Lopez-GuerreroLaboratory of Molecular Biology, Fundación Instituto Valenciano de Oncología, Valencia, Spain.
Fundación Instituto Valenciano de Oncología · ESCentro de Investigacion Principe Felipe · ESHospital Quirónsalud Barcelona · ESSunnybrook Health Science Centre · CAUniversitat de València · ESVall d'Hebron Hospital Universitari · ESVall d'Hebron Institute of Oncology

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The poly (ADP-Ribose) polymerase (PARP) inhibitor olaparib has shown antitumor activity in patients with ovarian or breast cancer with or without BRCA1/2 mutations. Lurbinectedin is an ecteinascidin that generates DNA double-strand breaks. We hypothesized that the combination of olaparib and lurbinectedin maximizes the DNA damage increasing the efficacy. A 3 + 3 dose-escalation study examined olaparib tablets with lurbinectedin every 21 days. The purpose of this phase I study is to determine the dose-limiting toxicities (DLTs) of the combination, to investigate the maximum tolerated dose (MTD), the recommended phase II dose (RP2D), efficacy, pharmacokinetics, in addition to genotyping and translational studies. In total, 20 patients with ovarian and endometrial cancers were included. The most common adverse events were asthenia, nausea, vomiting, constipation, abdominal pain, neutropenia, anemia. DLT grade 4 neutropenia was observed in two patients in dose level (DL) 5, DL4 was defined as the MTD, and the RP2D was lurbinectedin 1.5 mg/m

Indexed as

AgedCarbolinesGenotypeHeterocyclic Compounds, 4 or More RingsHumansMaximum Tolerated DoseMiddle AgedNeoplasmsPhthalazinesPiperazinesPoly(ADP-ribose) Polymerase InhibitorsCarbolinesHeterocyclic Compounds, 4 or More RingsolaparibPhthalazinesPiperazinesPM 01183Poly(ADP-ribose) Polymerase Inhibitors

Identifiers

PMID33627685
PMCPMC7904806
OpenAlexW3131966309

What OpenQuestion holds

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LicenceCC BY
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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.