Evidence map›Paper›PMID 42142265›Full record

ArticleSupportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer2026

MASCC score and neutropenic complications: what is the likelihood?

Mellar P Davis

Abstract read
PubMed Publisher
In one paragraph

Article in Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

Mellar P DavisOncology Palliative Medicine, Section of Supportive Oncology, Levine Cancer Institute, Charlotte, NC, USA. Mellar.Davis@advocatehealth.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Multinational Association for Supportive Care in Cancer (MASCC) Risk Index is the most widely used tool for stratifying febrile neutropenic cancer patients as low or high risk for serious complications. Studies evaluating its discriminative performance have relied predominantly on sensitivity, specificity, receiver operating characteristic (ROC) curves, and c-statistics-metrics that are mathematically elegant but have limited direct utility in clinical decision-making at the bedside.

methodsSensitivity and specificity data from Rivest et al. [13], the original Klastersky et al. derivation study [3], and the Zheng et al. meta-analysis [10] were used to calculate positive and negative likelihood ratios. Posttest probabilities were derived using Bayesian updating (pretest odds × LR = posttest odds), with a cohort pretest probability of complications of 35%. Likelihood ratios for procalcitonin (Ahn et al.) were applied sequentially to demonstrate the compounding of independent predictors.

resultsApplying Rivest et al. data in the inverted framing (i.e., predicting complication presence), a MASCC score > 21 yields a posttest probability of neutropenic complications of approximately 22%, and MASCC < 21 yields 65%. When procalcitonin ≥ 0.5 ng/mL is added to a high-risk MASCC score, the posttest probability rises to 85%; when procalcitonin is negative in a low-risk patient, it falls to 11%. Likelihood ratios varied meaningfully across Klastersky, Rivest, and Zheng (LR + range: 1.98-4.00; LR - range: 0.29-0.51), reflecting heterogeneity in populations, outcome definitions, and study settings.

conclusionsUnlike sensitivity/specificity and predictive values, LRs are relatively independent of outcome prevalence, making them more transportable across clinical settings, though they are not immune to population and spectrum effects, stopping at sensitivity, specificity, ROC curves, and mathematical completeness but clinical incompleteness. Clinicians, who are the end-users of these tools, deserve the metric that speaks their language: the updated probability that this patient, in front of them, will experience harm.

Indexed as

NeoplasmsNeutropeniaBayes TheoremClinical Decision-MakingHumansLikelihood FunctionsProcalcitoninRisk AssessmentSensitivity and SpecificityProcalcitoninLikelihood ratiosProbabilitySensitivitySpecificity

Identifiers

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.