Evidence map›Paper›PMID 27916626›Full record

Observational studyClinical genitourinary cancer2017

Impact of Sequencing Targeted Therapies With High-dose Interleukin-2 Immunotherapy: An Analysis of Outcome and Survival of Patients With Metastatic Renal Cell Carcinoma From an On-going Observational IL-2 Clinical Trial: PROCLAIM

Joseph I Clark, Michael K K Wong, Howard L Kaufman, Gregory A Daniels, Michael A Morse, David F McDermott, Sanjiv S Agarwala, Lionel D Lewis, John H Stewart, Ulka Vaishampayan and 24 more

Abstract readObservational Study
In one paragraph

Observational study in Clinical genitourinary cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Trial
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  4. Article
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  7. Article
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  9. Review
  10. Long-term progression-free survival of patients with metastatic melanoma or renal cell carcinoma following high-dose interleukin-2.Journal of investigative medicine : the official publication of the American Federation for Clinical Research · 2021
    Article
  11. Article
  12. Landscape of Immunotherapy in Genitourinary Malignancies.Advances in experimental medicine and biology · 2021
    Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Prospects of IL-2 in Cancer Immunotherapy.BioMed research international · 2018
    Review
  20. Review
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

34 authors.

Joseph I ClarkDepartment of Medicine, Loyola University Medical Center, Maywood, IL.
Michael K K WongDepartment of Medicine, University of Southern California, Los Angeles, CA.
Howard L KaufmanDepartment of Surgery, Rutgers Cancer Center Institute of New Jersey, New Brunswick, NJ.
Gregory A DanielsDepartment of Medicine, Moores Cancer Center, University of California San Diego, La Jolla, CA.
Michael A MorseDepartment of Medicine, Duke University Medical Center, Durham, NC.
David F McDermottDepartment of Medicine, Beth Israel Deaconess Medical Center, Boston, MA.
Sanjiv S AgarwalaDepartment of Medicine, St. Luke's University Health Network and Temple University, Easton, PA.
Lionel D LewisDepartment of Medicine, Dartmouth Hitchcock Medical Center, Lebanon, NH.
John H StewartDepartment of Medicine, Duke University Medical Center, Durham, NC.
Ulka VaishampayanDepartment of Medicine, Barbara Ann Karmanos Cancer Institute, Detroit, MI.
Brendan CurtiDepartment of Medicine, Providence Portland Medical Center, Portland, OR.
René GonzalezDepartment of Medicine, University of Colorado Cancer Center, Aurora, CO.
Jose LutzkyDepartment of Medicine, Mount Sinai Medical Center, Miami Beach, FL.
Venkatesh RudraptnaDepartment of Medicine, University of Minnesota Masonic Cancer Center, Minneapolis, MN.
Lee D CranmerDepartment of Medicine, Fred Hutchinson Cancer Research Center, Seattle, WA.
Joanne M JeterDepartment of Medicine, University of Arizona Medical Center, Tucson, AZ.
Ralph J HaukeNebraska Cancer Specialist, Omaha, NE.
Gerald MiletelloHematology/Oncology Clinic, Baton Rouge, LA.
Mohammed M MilhemDepartment of Medicine, University of Iowa Hospital and Clinics, Iowa City, IA.
Asim AminBlumenthal Cancer Center, Charlotte, NC.
John M RichartDivision of Hematology and Oncology, St Louis University Department of Internal Medicine, St Louis, MO.
Mayer FishmanDepartment of Medicine, Moffitt Cancer Center, Tampa, FL.
Sigrun HallmeyerOncology Specialists, Niles, IL.
Sapna P PatelDepartment of Medicine, University of Texas MD Anderson Cancer Center, Houston, TX.
Peter Van VeldhuizenUniversity of Kansas Medical Center, Kansas City, KS.
Neeraj AgarwalDepartment of Medicine, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Bret TabackDepartment of Surgery, Columbia University, New York, NY.
Jonathan S TreismanReiman Cancer Center, Franklin, WI.
Marc S ErnstoffDepartment of Medicine, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH.
Jessica C PerrittPrometheus Laboratories Inc, San Diego, CA.
Hong HuaPrometheus Laboratories Inc, San Diego, CA.
Tharak B RaoPrometheus Laboratories Inc, San Diego, CA.
Janice P DutcherCancer Research Foundation, Chappaqua, NY. Electronic address: jpd4401@aol.com.
Sandra AungPrometheus Laboratories Inc, San Diego, CA.

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI PAUL M STEMMER · 1985 to 2026
$68.4M
NCI NIH HHS P30 CA022453
6 · The paper itself

Abstract

backgroundThis analysis describes the outcome for patients who received targeted therapy (TT) prior to or following high-dose interleukin-2 (HD IL-2). PATIENTS AND

methodsPatients with renal cell carcinoma (n = 352) receiving HD IL-2 were enrolled in Proleukin

resultsOverall, there were 4% complete response (CR), 13% partial response (PR), 39% stable disease (SD), and 43% progressive disease (PD) with HD IL-2. The median overall survival (mOS) was not reached in patients with CR, PR, or SD, and was 15.5 months in patients with PD (median follow-up, 21 months). Sixty-one patients had prior TT before HD IL-2 with an overall response rate (ORR) to HD IL-2 of 19% (1 CR, 9 PR) and an mOS of 22.1 months. One hundred forty-nine patients received TT only after HD IL-2 with an mOS of 35.5 months. One hundred forty-two patients had no TT before or after HD IL-2, and mOS was not reached. The mOS was 8.5 months in PD patients who received HD IL-2 without follow-on TT and 29.7 months in PD patients who received follow-on TT after HD IL-2.

conclusionsHD IL-2 as sole front-line therapy, in the absence of added TT, shows extended clinical benefit (CR, PR, and SD). Patients with PD after HD IL-2 appear to benefit from follow-on TT. Patients who progressed on TT and received follow-on HD IL-2 experienced major clinical benefit. HD IL-2 therapy should be considered in eligible patients.

Indexed as

AdultAgedAged, 80 and overAntineoplastic AgentsCarcinoma, Renal CellDisease-Free SurvivalFemaleHumansImmunotherapyInterleukin-2Kidney NeoplasmsMaleMiddle AgedMolecular Targeted TherapyNeoplasm MetastasisRecombinant ProteinsaldesleukinAntineoplastic AgentsInterleukin-2Recombinant ProteinsAnti-VEGF therapyCytokineKidney cancerTherapy trendsToxicity

Identifiers

PMID27916626
PMCPMC6875755

What OpenQuestion holds

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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.