Evidence map›Paper›PMID 33849927›Full record

ArticleJournal for immunotherapy of cancer2021

Prognostic impact of early tumor shrinkage and depth of response in patients with microsatellite instability-high metastatic colorectal cancer receiving immune checkpoint inhibitors.

Giovanni Fucà, Francesca Corti, Margherita Ambrosini, Rossana Intini, Massimiliano Salati, Elisabetta Fenocchio, Paolo Manca, Chiara Manai, Francesca Daniel, Alessandra Raimondi and 14 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Journal for immunotherapy of cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Deciphering radiological stable disease to immune checkpoint inhibitors.Annals of oncology : official journal of the European Society for Medical Oncology · 2022
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  19. Letter to the Editor from ColleJournal for immunotherapy of cancer · 2021
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  20. Author response to ColleJournal for immunotherapy of cancer · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 7 institutions in 1 country.

Giovanni FucàDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0002-1560-2253
Francesca CortiDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Margherita AmbrosiniDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Rossana IntiniDepartment of Oncology, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Massimiliano SalatiDepartment of Oncology and Hematology, University Hospital Modena, Modena, Italy.
Elisabetta FenocchioDepartment of Medical Oncology, Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy.
Paolo MancaDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Chiara ManaiDepartment of Oncology, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Francesca DanielDepartment of Oncology, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Alessandra RaimondiDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Federica MoranoDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Salvatore CoralloDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Michele PrisciandaroDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Andrea SpallanzaniDepartment of Oncology and Hematology, University Hospital Modena, Modena, Italy.
Virginia QuaràDepartment of Medical Oncology, Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy.
Carmen BelliDivision of Early Drug Development, European Institute of Oncology IRCCS, Milan, Italy.
Marta VaianiRadiology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Giuseppe CuriglianoDivision of Early Drug Development, European Institute of Oncology IRCCS, Milan, Italy.
Chiara CremoliniDepartment of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.
Filippo De BraudDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Maria Di BartolomeoDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Vittorina ZagonelDepartment of Oncology, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Sara LonardiDepartment of Oncology, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Filippo PietrantonioDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy filippo.pietrantonio@istitutotumori.mi.it.ORCID 0000-0002-8530-8420
Fondazione IRCCS Istituto Nazionale dei Tumori · ITIstituto Oncologico Veneto · ITCandiolo Cancer Institute · ITUniversity of Milan · ITUniversity of Modena and Reggio Emilia · ITEuropean Institute of Oncology · ITUniversity of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs) are the new standard of care in microsatellite instability-high (MSI-H)/deficient mismatch repair (dMMR) metastatic colorectal cancer (mCRC). Since tumor response dynamic parameters already shown a strong association with survival outcomes in patients with mCRC treated with first-line therapy, we investigated the association of early tumor shrinkage (ETS) and depth of response (DoR) in patients with MSI-H/dMMR mCRC treated with ICIs.

methodsThis is a retrospective, multicenter, cohort study in patients with dMMR and/or MSI-high mCRC treated with ICIs (anti-PD-1/PD-L1 with or without anti-CTLA-4 agents) with measurable disease and at least one post-baseline radiological disease reassessment. The Kaplan-Meier method and Cox proportional-hazards regression models were used for survival analyses. A maximally selected statistics method in a Cox regression model for progression-free survival (PFS) was used to determine the optimal cut-offs for ETS and DoR.

resultsWe included a total of 169 patients: 116 (68.6%) were treated with anti-PD-1 monotherapy, whereas 53 (31.4%) with anti-PD-1 plus anti-CTLA-4 agents. Patients with primary progressive disease (N=37, 21.9%), experienced an extremely poor overall survival (OS) and were evaluated separately. In patients with clinical benefit, we observed a significant association between ETS and DoR with both OS and PFS, and we identified a relative reduction of at least 1% as the optimal cut-off for ETS and a relative reduction of at least 50% as the optimal cut-off for DoR.

conclusionsETS and DoR are important prognostic factors in patients with MSI-high mCRC treated with ICIs that might be useful to design treatment intensification/deintensification strategies. A prospective validation of both is warranted.

Indexed as

Microsatellite InstabilityAgedColorectal NeoplasmsDisease ProgressionFemaleHumansImmune Checkpoint InhibitorsItalyMaleNeoplasm MetastasisProgression-Free SurvivalRetrospective StudiesRisk AssessmentRisk FactorsTime FactorsTumor BurdenImmune Checkpoint Inhibitorsgastrointestinal neoplasmsimmunotherapytumor biomarkers

Identifiers

PMID33849927
PMCPMC8051394
OpenAlexW3156872567

What OpenQuestion holds

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LicenceCC BY-NC
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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.