Evidence map›Paper›PMID 26216417›Full record

ArticleCancer immunology research2015

Intrathecal Administration of Tumor-Infiltrating Lymphocytes Is Well Tolerated in a Patient with Leptomeningeal Disease from Metastatic Melanoma: A Case Report.

Isabella C Glitza, Cara Haymaker, Chantale Bernatchez, Luis Vence, Michelle Rohlfs, Jessie Richard, Carol Lacey, Rahmatu Mansaray, Orenthial J Fulbright, Renjith Ramachandran and 9 more

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Cancer immunology research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.1field-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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Leptomeningeal Metastases: New Opportunities in the Modern Era.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Cellular immunotherapy for malignant gliomas.Expert opinion on biological therapy · 2016
    Review
  18. Review
  19. 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

19 authors at 1 institution in 1 country.

Isabella C GlitzaMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas. icglitza@mdanderson.org.
Cara HaymakerMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Chantale BernatchezMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Luis VenceImmunology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Michelle RohlfsMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Jessie RichardMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Carol LaceyMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Rahmatu MansarayStem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Orenthial J FulbrightStem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Renjith RamachandranStem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Christopher TothStem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Seth WardellStem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Sapna P PatelMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Scott E WoodmanMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Wen-Jen HwuMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Laszlo G RadvanyiMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Michael A DaviesMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Nicholas E PapadopoulosMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Patrick HwuMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
TRAINING FOR ACADEMIC ONCOLOGY/HEMATOLOGYT32CA009666 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Michael Davies, Courtney DiNardo · 1994 to 2026
$9.8M
NCI NIH HHS CA16672NCI NIH HHS P30 CA016672NCI NIH HHS T32 CA009666
6 · The paper itself

Abstract

unlabelledPatients with leptomeningeal disease (LMD) from melanoma have very poor outcomes and few treatment options. We present a case of intrathecal (i.t.) administration of autologous tumor-infiltrating lymphocytes (TIL) in a patient with LMD from metastatic melanoma. The patient developed LMD after previous treatments with surgery, high-dose bolus interleukin-2 (HD IL2), and systemic TIL infusion and experienced radiographic progression after intrathecal IL2 (i.t. IL2) therapy. The patient received weekly treatment with increasing numbers of i.t. TIL followed by twice-weekly i.t. IL2. The patient received three i.t. TIL infusions and did not experience any toxicities beyond those expected with i.t. IL2 therapy. Analysis of cerebrospinal fluid demonstrated increased inflammatory cytokines following the i.t. TREATMENTS: Subsequent imaging demonstrated disease stabilization, and neurological deficits also remained stable. The patient expired 5 months after the initiation of i.t. TIL therapy with disease progression in the brain, liver, lung, and peritoneal and retroperitoneal lymph nodes, but without LMD progression. These results demonstrate the safety of i.t. administration of TIL in melanoma patients with LMD and support the feasibility of conducting a prospective clinical trial to determine this therapy's clinical benefit among these patients.

Indexed as

CytokinesDisease ProgressionFatal OutcomeHumansInjections, SpinalLymphocytes, Tumor-InfiltratingMaleMelanomaMeningeal CarcinomatosisMiddle AgedCytokines

Identifiers

PMID26216417
PMCPMC4861225
OpenAlexW2145776171

What OpenQuestion holds

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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.