Evidence map›Paper›PMID 34376536›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2021

Early Use of High-Dose Glucocorticoid for the Management of irAE Is Associated with Poorer Survival in Patients with Advanced Melanoma Treated with Anti-PD-1 Monotherapy.

Xue Bai, Jiani Hu, Allison Betof Warner, Henry T Quach, Christopher G Cann, Michael Z Zhang, Lu Si, Bixia Tang, Chuanliang Cui, Xiaoling Yang and 23 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 116 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed, 6 pooled it
9.7field-weighted citation impact, top 1% 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

116 citing papers in PubMed, 6 syntheses or guidelines pooled it, 171 citations in OpenAlex.

  1. Clinical Outcomes of Immunosuppressant Drugs in Patients Treated with Immune Checkpoint Inhibitors: A Systematic Review and Meta-Analysis.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2026
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  5. Immune checkpoint inhibitor-related hearing loss: a systematic review and analysis of individual patient data.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2023
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  14. Journal of agricultural and food chemistry · 2026
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56 more citing papers are in PubMed but not listed here.

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

33 authors at 7 institutions in 5 countries.

Xue BaiDepartment of Melanoma and Sarcoma, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and Institute, Beijing, China.
Jiani HuDepartment of Data Sciences (Division of Biostatistics), Dana-Farber Cancer Institute, Boston, Massachusetts.
Allison Betof WarnerMemorial Sloan Kettering Cancer Center, Weill Cornell Medical College, New York, New York.ORCID 0000-0001-6422-2997
Henry T QuachDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.ORCID 0000-0001-9142-6397
Christopher G CannDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Michael Z ZhangDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Lu SiDepartment of Melanoma and Sarcoma, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and Institute, Beijing, China.
Bixia TangDepartment of Melanoma and Sarcoma, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and Institute, Beijing, China.
Chuanliang CuiDepartment of Melanoma and Sarcoma, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and Institute, Beijing, China.
Xiaoling YangDepartment of Melanoma and Sarcoma, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and Institute, Beijing, China.
Xiaoting WeiDepartment of Melanoma and Sarcoma, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and Institute, Beijing, China.
Lalit PallanMelanoma Institute Australia, The University of Sydney, Royal North Shore and Mater Hospitals, Sydney, Australia.
Catriona HarveyMelanoma Institute Australia, The University of Sydney, Royal North Shore and Mater Hospitals, Sydney, Australia.
Michael P ManosCenter for Immune-Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Olivia OuyangCenter for Immune-Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Michelle S Kim
Gyulnara Kasumova
Justine V CohenMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts.
Donald P LawrenceMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts.
Christine FreedmanMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts.
Riley M FaddenMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts.
Krista M RubinMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts.
Tatyana SharovaDepartment of Surgical Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0003-2123-3906
Dennie T FrederickDepartment of Surgical Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
Keith T FlahertyMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts.
Osama E RahmaCenter for Immune-Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Georgina V LongMelanoma Institute Australia, The University of Sydney, Royal North Shore and Mater Hospitals, Sydney, Australia.ORCID 0000-0001-8894-3545
Alexander M MenziesMelanoma Institute Australia, The University of Sydney, Royal North Shore and Mater Hospitals, Sydney, Australia.
Jun GuoDepartment of Melanoma and Sarcoma, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and Institute, Beijing, China.
Alexander N ShoushtariMemorial Sloan Kettering Cancer Center, Weill Cornell Medical College, New York, New York.ORCID 0000-0002-8065-4412
Douglas B JohnsonDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Ryan J SullivanMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0001-5344-6645
Genevieve M BolandDepartment of Surgical Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts. gmboland@partners.org.ORCID 0000-0002-7522-6173
Massachusetts General Hospital · USUnited States Department of the Interior · USMinistry of Education · ETDana-Farber Cancer Institute · USVanderbilt University Medical Center · USMemorial Sloan Kettering Cancer Center · USRoyal North Shore Hospital · AU

Funding

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

Abstract

purposeProgrammed cell death receptor-1 (PD-1) inhibitors are frontline therapy in advanced melanoma. Severe immune-related adverse effects (irAEs) often require immunosuppressive treatment with glucocorticoids (GCCs), but GCC use and its correlation with patient survival outcomes during anti-PD-1 monotherapy remains unclear. EXPERIMENTAL

designIn this multicenter retrospective analysis, patients treated with anti-PD-1 monotherapy between 2009 and 2019 and detailed GCC use, data were identified from five independent cohorts, with median follow-up time of 206 weeks. IrAEs were tracked from the initiation of anti-PD-1 until disease progression, initiation of a new therapy, or last follow-up. Correlations between irAEs, GCC use, and survival outcomes were analyzed.

resultsOf the entire cohort of 947 patients, 509 (54%) developed irAEs. In the MGH cohort [irAE(+)

conclusionsEarly high-dose GCC use was associated with poorer PFS and OS after irAE onset. Judicious use of GCC early during anti-PD-1 monotherapy should be considered. Further prospective randomized control clinical trials designed to explore alternative irAE management options are warranted.

Indexed as

Correlation of DataDrug-Related Side Effects and Adverse ReactionsGlucocorticoidsHumansImmune Checkpoint InhibitorsMelanomaNeoplasm StagingSurvival RateTime FactorsGlucocorticoidsImmune Checkpoint Inhibitors

Identifiers

PMID34376536
PMCPMC9401488
OpenAlexW3192038436

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.