Evidence map›Paper›PMID 28960862›Full record

ArticleAsia-Pacific journal of clinical oncology2018

Correlating Ki67 and other prognostic markers with Oncotype DX recurrence score in early estrogen receptor-positive breast cancer.

Aaron C Tan, Bob T Li, Kazi Nahar, Suzanne Danieletto, Eva S Fong, Trevor Currer, Andrew Parasyn, Philip Middleton, Heidi Wong, Denis Smart and 4 more

Open access · greenAbstract read
In one paragraph

Article in Asia-Pacific journal of clinical oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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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

14 authors at 3 institutions in 2 countries.

Aaron C TanSAN Integrated Cancer Centre, Sydney Adventist Hospital, Wahroonga, Australia.ORCID http://orcid.org/0000-0001-7292-1114
Bob T LiDivision of Solid Tumor Oncology, Department of Medicine, Memorial Sloan Kettering Cancer Center, and Weill Cornell Medical College, New York, NY, USA.
Kazi NaharSAN Integrated Cancer Centre, Sydney Adventist Hospital, Wahroonga, Australia.
Suzanne DanielettoSAN Integrated Cancer Centre, Sydney Adventist Hospital, Wahroonga, Australia.
Eva S FongSAN Integrated Cancer Centre, Sydney Adventist Hospital, Wahroonga, Australia.
Trevor CurrerSAN Integrated Cancer Centre, Sydney Adventist Hospital, Wahroonga, Australia.
Andrew ParasynSAN Integrated Cancer Centre, Sydney Adventist Hospital, Wahroonga, Australia.
Philip MiddletonSAN Integrated Cancer Centre, Sydney Adventist Hospital, Wahroonga, Australia.
Heidi WongSAN Integrated Cancer Centre, Sydney Adventist Hospital, Wahroonga, Australia.
Denis SmartSAN Integrated Cancer Centre, Sydney Adventist Hospital, Wahroonga, Australia.
Josie J RutovitzSAN Integrated Cancer Centre, Sydney Adventist Hospital, Wahroonga, Australia.
Philip McCloudMcCloud Consulting Group, Australia.
T Michael HughesSAN Integrated Cancer Centre, Sydney Adventist Hospital, Wahroonga, Australia.
Gavin M MarxSAN Integrated Cancer Centre, Sydney Adventist Hospital, Wahroonga, Australia.
Sydney Adventist Hospital · AUThe University of Sydney · AUFishwell Consulting (Australia) · AU

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

aimDecisions regarding adjuvant chemotherapy for early breast cancer are complex. Ki67 is increasingly used, in conjunction with conventional prognostic markers, to help decide the use of adjuvant chemotherapy for early breast cancer. Ki67 has been proposed as an economical alternative to Oncotype DX recurrence score (RS), which is a validated prognostic marker for disease recurrence and predictive marker for benefit from chemotherapy. This study aimed to determine in patients where conventional prognostic markers did not provide a clear recommendation for adjuvant chemotherapy, whether Ki67 could be a substitute for RS.

methodsWe reviewed all cases of luminal-type node-negative early breast cancer (T1-2, N0-1mi, M0, estrogen receptor positive, HER2 negative) referred for Oncotype DX testing by the multidisciplinary team at an Australian tertiary private hospital from 14th December 2006 to 31st December 2013, when conventional prognostic markers did not provide a clear recommendation for adjuvant chemotherapy. RS was correlated with Ki67, along with other conventional prognostic markers including tumor size, grade, mitotic rate and lymphovascular invasion. Spearman's rank order correlation coefficient and Pearson product-moment correlation coefficient (r) were used for ordinal and continuous variables, respectively.

resultsA total of 58 patients were analyzed, median Ki67 was 15% (range 2-50%) and the median RS was 16 (range 3-65). There was no positive correlation between Ki67 and RS (r = 0.01, P = 0.93). No single conventional prognostic marker was shown to significantly correlate with RS, including tumor size (r = -0.02, P = 0.88), grade (r = 0.10, P = 0.44), mitotic rate (r = -0.07, P = 0.69) and lymphovascular invasion (r = -0.12, P = 0.39).

conclusionKi67 and conventional prognostic markers do not correlate with Oncotype DX RS. In the setting where conventional prognostic markers do not show a clear indication for or against adjuvant chemotherapy as determined by consensus in a multidisciplinary team, Ki67 is not a substitute for Oncotype DX testing. RS may provide additional information to aid decision making for adjuvant chemotherapy.

Indexed as

AgedBreast NeoplasmsFemaleHumansKi-67 AntigenMiddle AgedNeoplasm Recurrence, LocalPrognosisReceptors, EstrogenRetrospective StudiesKi-67 AntigenReceptors, Estrogenearly breast cancerKi67Oncotype DX

Identifiers

PMID28960862
PMCPMC8075631
OpenAlexW2760808322

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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.