Evidence map›Paper›PMID 32337489›Full record

ArticleJNCI cancer spectrum2019

Survival in Early Phase Immuno-Oncology Trials: Development and Validation of a Prognostic Index.

Daphne Day, Christina Guo, Yada Kanjanapan, Ben Tran, Anna Spreafico, Anthony M Joshua, Lisa Wang, Albiruni R Abdul Razak, Natasha B Leighl, Aaron R Hansen and 4 more

Abstract read
In one paragraph

Article in JNCI cancer spectrum, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Use of supportive care services and advance care planning among early phase oncology clinical trial participants.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Article
  2. Article
  3. 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

14 authors.

Daphne DayDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Canada.ORCID 0000-0001-8262-2441
Christina GuoDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Parkville, Melbourne, Australia.
Yada KanjanapanDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Canada.ORCID 0000-0002-9807-8695
Ben TranDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Parkville, Melbourne, Australia.
Anna SpreaficoDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Canada.
Anthony M JoshuaDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Canada.
Lisa WangDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Canada.
Albiruni R Abdul RazakDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Canada.
Natasha B LeighlDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Canada.
Aaron R HansenDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Canada.
Marcus O ButlerDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Canada.
Lillian L SiuDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Canada.ORCID 0000-0002-3500-0540
Jayesh DesaiDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Parkville, Melbourne, Australia.
Philippe L BedardDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmuno-oncology (IO) is rapidly evolving in early drug development. We aimed to develop and prospectively validate a prognostic index for patients treated in IO phase I trials to assist with patient selection.

methodsThe development cohort included 192 advanced solid tumor patients treated in 13 IO phase I trials, targeting immune checkpoint and/or co-stimulatory molecules. A prognostic scoring system was developed from multivariate survival analysis of 10 clinical factors, and subsequently validated in two independent validation cohorts (n = 152 and n = 80).

resultsIn the development cohort, median age was 57.5 years (range = 20.4-84.8 years). Median progression-free survival and overall survival (OS) were 13.4 and 73.6 weeks, respectively, 90-day mortality was 16%, and overall response rate was 20%. In multivariate analysis, Eastern Cooperative Oncology Group performance status greater than or equal to 1 (hazard ratio [HR] = 3.2, 95% confidence interval [CI] = 1.8 to 5.7;

conclusionsThe PM-IPI is a validated prognostic score for patients treated in phase I IO trials and may aid in improving patient selection.

Identifiers

PMID32337489
PMCPMC7050022

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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.