Evidence map›Paper›PMID 29367713›Full record

ArticleBone marrow transplantation2018

Secondary malignancies after high-dose chemotherapy in germ cell tumor patients: a 34-year retrospective study of the European Society for Blood and Marrow Transplantation (EBMT).

Andrea Necchi, Salvatore Lo Vullo, Simona Secondino, Giovanni Rosti, Manuela Badoglio, Patrizia Giannatempo, Daniele Raggi, Francesco Lanza, Christian Chabannon, Chiara Bonini and 3 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Autologous Hematopoietic Stem Cell Transplantation for Male Germ Cell Tumors: Improved Outcomes Over 3 Decades.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2019
    Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 2 countries.

Andrea NecchiFondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy. andrea.necchi@istitutotumori.mi.it.
Salvatore Lo VulloFondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.ORCID http://orcid.org/0000-0002-4444-9526
Simona SecondinoFondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Giovanni RostiFondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Manuela BadoglioEBMT Study Office, EBMT, Paris, France.ORCID http://orcid.org/0000-0003-3226-2024
Patrizia GiannatempoFondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Daniele RaggiFondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Francesco LanzaHospital of Ravenna, Ravenna, Italy.
Christian ChabannonInstitut Paoli-Calmettes, Marseille, France.ORCID http://orcid.org/0000-0002-3755-4889
Chiara BoniniUniversità Vita-Salute San Raffaele and IRCCS San Raffaele Hospital, Milano, Italy.
Luigi MarianiFondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Paolo PedrazzoliFondazione IRCCS Policlinico San Matteo, Pavia, Italy.
European Society for Blood and Marrow Transplantation, Cellular Therapy & Immunobiology Working Party – Solid Tumor sub-committee
Fondazione IRCCS Istituto Nazionale dei Tumori · ITPoliclinico San Matteo Fondazione · ITEuropean Society for Blood and Marrow Transplantation · FRInstitut Paoli-Calmettes · FROspedale "Santa Maria delle Croci" di Ravenna · ITVita-Salute San Raffaele University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to assess the incidence and risk factors of secondary malignancy (SM) in the young adult patients who received high-dose chemotherapy (HDCT) for germ cell tumors (GCT). The EBMT database was interrogated. Criteria for patient selection included adult male GCT and HDCT administered in any line of therapy. Cumulative incidence methods were used to estimate the time-to-SM diagnosis. Univariable Fine and Gray proportional hazard regression evaluated risk factors of SM occurrence. From 1981 to 2015, 9153 autografts were identified. Among 5295 patients, 59 cases of SM, developed after a median follow-up of 3.8 years, were registered. Of these patients, 23 (39%) developed hematologic SM, 34 (57.6%) solid SM (two patients had uncoded SM). Twenty-year cumulative incidence of solid versus hematologic SM was 4.17% (95% CI: 1.78-6.57) versus 1.37% (95% CI: 0.47-2.27). Median overall survival after SM was significantly shorter for patients who developed hematologic SM versus solid SM (8.6 versus 34.4 months, p = 0.003). Age older than 40 years at the time of HDCT was significantly associated with hematologic, but not solid, SM development (p = 0.004 versus p = 0.234). SM occurrence post-HDCT showed different patterns of incidence and mortality in GCT. These data may be important to optimize patient selection, counseling and follow-up after HDCT.

Indexed as

AdultEuropeFemaleHumansMaleNeoplasms, Germ Cell and EmbryonalNeoplasms, Second PrimaryRetrospective StudiesTime Factors

Identifiers

PMID29367713
OpenAlexW2789662153

What OpenQuestion holds

Textmetadata
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.