Evidence map›Paper›PMID 29848457›Full record

ArticleJournal of geriatric oncology2018

Do older patients with non-small cell lung cancer also benefit from first-line platinum-based doublet chemotherapy? Observations from a pooled analysis of 730 prospectively-treated patients (Alliance Study A151622).

Josephine L Feliciano, Jennifer G Le-Rademacher, Ajeet Gajra, Martin J Edelman, Tyler Zemla, Ryan McMurray, Hongbin Chen, Arti Hurria, Hyman Muss, Harvey J Cohen and 2 more

Abstract read
In one paragraph

Article in Journal of geriatric oncology, 2018. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Population-Based Outcomes in NSCLC.JNCI cancer spectrum · 2019
    Article
  4. 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

12 authors.

Josephine L FelicianoThe Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, 401 N Broadway, Baltimore, MD 21287, United States.
Jennifer G Le-RademacherDepartment of Health Sciences Research, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, United States; Department of Oncology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, United States.
Ajeet GajraState University of New York Upstate, 766 Irving Ave., Syracuse, NY 13210, United States.
Martin J EdelmanFox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA 19111, United States.
Tyler ZemlaDepartment of Health Sciences Research, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, United States.
Ryan McMurrayDepartment of Health Sciences Research, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, United States.
Hongbin ChenRoswell Park Cancer Institute, Elm & Carlton Streets, Buffalo, NY 14263, United States.
Arti HurriaCity of Hope Comprehensive Cancer Center, 1500 E. Duarte Rd., Duarte, CA 91010, United States.
Hyman MussUniversity of North Carolina, Chapel, Hill, 143 W. Franklin St., Chapel Hill, NC 27514, United States.
Harvey J CohenCenter for the Study of Aging and Human Development and Cancer Institute, Duke University, Duke Cancer Institute, 201 Trent Dr., Durham, NC 27110, United States.
Rogerio LilenbaumYale Cancer Center, Yale School of Medicine, 333 Cedar St., New Haven, CT 06510, United States.
Aminah JatoiDepartment of Oncology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, United States. Electronic address: jatoi.aminah@mayo.edu.

Funding

Collaborations and NCORP Collective ManagementUG1CA189823 · NCI · MAYO CLINIC ROCHESTER · PI Evanthia Galanis, Olwen Hahn · 2014 to 2026
$120.6M
TRANSLATIONAL RESEARCHU10CA025224 · NCI · MAYO CLINIC ROCHESTER · PI BUCKNER, JAN C · 1985 to 2013
$85.0M
NCI, National Clinical Trials Network Lead Academic Participating Site (LAPS) UG1 (funded extension)UG1CA232760 · NCI · MAYO CLINIC ROCHESTER · PI Judy Caroline Boughey, Aaron Scott Mansfield · 2019 to 2026
$8.5M
Naional Cancer Institute, Naitonal Clinical Trials Network U10 Lead Academic SiteU10CA180790 · NCI · MAYO CLINIC ROCHESTER · PI ALBERTS, STEVEN R, BOUGHEY, JUDY CAROLINE · 2014 to 2018
$6.6M
Network Lead Academic Participating Site Grant from the Roswell Cancer Inst.U10CA180866 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI ERNSTOFF, MARC S, LELE, SHASHIKANT · 2014 to 2018
$2.9M
NCTN Lead Academic Participating Sites ApplicationU10CA180838 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CAREY, LISA A · 2014 to 2018
$2.8M
NCI National Clinical Trials Network U10U10CA180857 · NCI · DUKE UNIVERSITY · PI BARBORIAK, DANIEL P, BRIZEL, DAVID M · 2014 to 2018
$2.0M
NCI NIH HHS U10 CA025224NCI NIH HHS U10 CA180790NCI NIH HHS U10 CA180838NCI NIH HHS U10 CA180857NCI NIH HHS U10 CA180866NCI NIH HHS UG1 CA189823NCI NIH HHS UG1 CA232760
6 · The paper itself

Abstract

objectiveThis study sought to define the role of first-line platinum-based doublet chemotherapy in older patients with non-small cell lung cancer (NSCLC). MATERIALS AND

methodsWe analyzed three first-line NSCLC trials: CALGB 9730, CALGB 30203, and CALGB 30801, which tested carboplatin and paclitaxel; carboplatin and gemcitabine; and carboplatin with either pemetrexed or gemcitabine, respectively. Overall survival was the primary endpoint. Age-based comparisons with a cutpoint of 65 years were performed with Cox proportional hazards models with adjustments for sex, tumor histology, cancer stage, chemotherapy, and smoking history and after stratifying by performance score. Secondary endpoints were grade 3-5 adverse events, chemotherapy cycles completed, and whether toxicity prompted chemotherapy discontinuation.

results730 patients were included; 337 (46%) were 65+ years of age. No statistically significant difference in survival was observed for older (≥65) versus younger patients (HR = 1.096; 95% CI = (0.94, 1.28); p = 0.25). A trend emerged with increased odds of a grade 3-5 adverse event for patients ≥65 years versus <65 years (OR = 1.52; 95% CI = (0.99, 2.31); p = 0.05). The proportion of completed chemotherapy cycles was marginally lower in older patients (difference = -5%; 95% CI = (-9, 0.2); p = 0.06) for those ≥65 years versus <65 years, but no statistically significant difference occurred in the rate of chemotherapy discontinuation for toxicity (OR = 1.4; 95% CI = (0.85, 2.19); p = 0.21) for patients ≥65 years versus <65 years. A cutpoint of 70 years yielded similar results.

conclusionThese findings support carboplatin doublet-based chemotherapy in select older patients with advanced NSCLC.

Indexed as

AgedAge FactorsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsCarboplatinCarcinoma, Non-Small-Cell LungDeoxycytidineFemaleGemcitabineHumansLung NeoplasmsMaleNeoplasm StagingPaclitaxelPemetrexedProspective StudiesAntineoplastic AgentsCarboplatinDeoxycytidineGemcitabinePaclitaxelPemetrexedCarboplatinChemotherapyGeriatric oncologyLung cancerOlder patients

Identifiers

PMID29848457
PMCPMC6233872

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Registered trials

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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.