Evidence map›Paper›PMID 35851593›Full record

ArticleBlood advances2023

A phase 1 trial utilizing TMI with fludarabine-melphalan in patients with hematologic malignancies undergoing second allo-SCT.

Misha C Tran, Yasmin Hasan, Amy Wang, Kamil Yenice, Julien Partouche, Wendy Stock, Richard A Larson, Satyajit Kosuri, James L LaBelle, Justin Kline and 6 more

Open access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in Blood advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
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

16 authors at 2 institutions in 1 country.

Misha C TranDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL.ORCID 0000-0001-8412-4470
Yasmin HasanDepartment of Radiation & Cellular Oncology, University of Chicago, Chicago, IL.
Amy WangDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL.
Kamil YeniceDepartment of Radiation & Cellular Oncology, University of Chicago, Chicago, IL.
Julien PartoucheDepartment of Radiation & Cellular Oncology, University of Chicago, Chicago, IL.
Wendy StockDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL.
Richard A LarsonDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL.ORCID 0000-0001-9168-3203
Satyajit KosuriDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL.
James L LaBelleDepartment of Pediatrics, Section of Hematology, University of Chicago, Chicago, IL.
Justin KlineDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL.
Peter A RiedellDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL.ORCID 0000-0003-2719-0580
Andrew S ArtzGehr Family Center for Leukemia Research, City of Hope, Duarte, CA.ORCID 0000-0003-0803-9607
Ralph WeichselbaumDepartment of Radiation & Cellular Oncology, University of Chicago, Chicago, IL.
Michael R BishopDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL.
Bulent AydoganDepartment of Radiation & Cellular Oncology, University of Chicago, Chicago, IL.
Hongtao LiuDepartment of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL.ORCID 0000-0002-3190-7807
University of Chicago · USCity of Hope · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Relapse after allogeneic stem cell transplantation (allo-SCT) remains the primary cause of treatment failure. A second SCT can result in long-term survival in a subset of patients, but the relapse rate remains high. We conducted a single-center, phase 1, modified 3 + 3 dose-escalation study of the feasibility of combining intensity-modulated total marrow irradiation (IM-TMI) with fludarabine and melphalan for conditioning. Between December 2015 and May 2020, 21 patients with relapsed hematologic disease undergoing second or greater allo-SCT were treated with IM-TMI doses of 6 Gy, 9 Gy, or 12 Gy. Dose-limiting toxicity was defined as a grade 3 or higher treatment-related adverse event; mucositis was the primary dose-limiting toxicity. The median times to neutrophil and platelet engraftment were 10 and 18 days, respectively. The 1-year cumulative incidence of graft-versus-host disease was 65% (95% confidence interval CI, 38-83). The nonrelapse mortality at 2 years was 17% (95% CI, 4-39). Cumulative incidence of relapse at 2 years was 35% (95% CI, 13-58). Two-year progression-free survival and overall survival were 48% and 50%. We conclude that combining IM-TMI with fludarabine-melphalan is feasible. We recommend 12 Gy of IM-TMI with fludarabine-melphalan for second SCT, although 9 Gy may be used for older or underweight patients.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsHematologic NeoplasmsHematopoietic Stem Cell TransplantationHumansMelphalanNeoplasm Recurrence, LocalVidarabinefludarabineMelphalanVidarabine

Identifiers

PMID35851593
PMCPMC9898602
OpenAlexW4285803226

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.