MétaCan
Menu
← Back to cohort

Outcome of 17p Deleted Multiple Myeloma (MM) in the Era of Novel Agents and Tandem Transplantation: A Single Centre Experience

2014· article· en· W2538114067 on OpenAlexaff
Gurdeep Parmar, Esther Masih‐Khan, Eshetu G. Atenafu, Donna Reece, Suzanne Trudel, Rodger E. Tiedemann, Vishal Kukreti, Christine I. Chen

Bibliographic record

VenueBlood · 2014
Typearticle
Languageen
FieldMedicine
TopicMultiple Myeloma Research and Treatments
Canadian institutionsUniversity of TorontoPrincess Margaret Cancer Centre
Fundersnot available
KeywordsMedicineTransplantationMultiple myelomaInternal medicineSurgeryRegimenSingle CenterRetrospective cohort studyOncology

Abstract

fetched live from OpenAlex

Abstract Background: Although overall MM survival has improved in recent years, there is significant heterogeneity, with some patients achieving survival over 10 years, and others succumbing to disease within months of diagnosis. The presence of cytogenetic abnormalities, in particular deletion 17p (del17p), remains a robust and independent prognostic marker. Although novel agents (single or in combinations) and/or tandem transplantation have been studied in myeloma patients with del17p, results are inconsistent and no regimen has clearly emerged as superior. With this background, we report the outcome of MM patients with del17p treated in the era of novel agents and tandem transplantation at our institution. Methods: Using a prospectively maintained MM database, we identified 66 patients with del17p established by non-selective FISH on bone marrow samples, treated at our institution between 2006-2013. Of these, 44/66(66.6%) underwent stem cell transplant. A retrospective chart review of patient, disease, and treatment characteristics, including response and survival outcomes was performed. Prior to 2009, standard therapy at our institution for patients with del17p was a single transplant and tandem transplant was offered only if response rate was less than VGPR. From 2009 on, tandem transplantation was established as our institutional treatment policy for this high-risk subgroup. In this analysis, we aimed to evaluate the outcome of all del17p patients who underwent transplantation and compared single versus tandem transplant outcomes resulting from our policy change. Results: Table 1 shows the patient characteristics and outcomes of the 44 patients with del17p who underwent transplantation at our centre. Patient and disease characteristics: The median age for all patients was 61 (range 31-71 years). High risk features such as elevated LDH, ISS stage II/III and coexistent t(4;14) were seen in 21/44 (48%), 29/42 (69%) and 6/43 (14%) of del17p patients, respectively. Aggressive clinical manifestations such as extra-medullary plasmacytomas and plasma cell leukaemia at diagnosis were seen in 8/44 (18%) and 4/44 (9%) of patients, respectively. Treatment characteristics and response: 34/44 (77%) patients were treated with bortezomib-based and 4/44 (9%) with lenalidomide-based induction therapy. Of the 44 patients, 23/44 underwent single and 21/44 underwent tandem transplant. The response rate (³VGPR) increased from 54% post chemotherapy to 98% post transplant. A total of 35/44 (80%) patients received maintenance therapy with the majority (77%) given lenalidomide. Median duration of maintenance therapy was 7.6 months (range 1- 56.8) Survival outcomes: The median follow-up was 23.6 months (1-95 months). Median overall survival (OS) was not reached but 5 year estimated survival rate for all del17p patients who underwent transplantation was 59% (CI 36-76%) and median progression free survival (PFS) was 29 months (CI 20.2-46.1). In a subgroup analysis, estimated 5 year OS rate in patients who received tandem vs single transplant was 65% and 53% respectively (p=0.3). Similarly, the PFS in patients who underwent tandem vs single transplant was 46 vs 28 months, respectively (p=0.1). Conclusions: 1. The median OS and PFS of del17p myeloma patients treated with novel agents and high dose therapy in our study is comparable to other reported outcomes (e.g., HOVON-65). 2. There was a statistically non-significant trend towards improved OS and PFS in patients receiving tandem transplant when compared to single transplant. Prospective clinical studies are required to clarify this issue. Table 1: Clinical characterstics Median Range Number (%) Male 25/44 (57) Female 19/44 (43) Age (years) 61 31-71 IgG 22/44 (50) IgA 9/44 (20) Light chain only 8/44 (19) Hemoglobin (g/l) 105 60-147 Creatinine(umol/l) 104 42-561 Serum LDH (U/L) 205 92-710 Beta-2 microglobulin 4.4 1.2-44.8 ISS stage I 13/42 (31) ISS stage II 15/42 (35.7) ISS stage III 14/42 (33.3) 13 q deletion 29/43 (67.4) t(4;14) 6/43 (14) BM nucleated cells with 17p deletion (%) 25 10-74 CR 35/44 (80) VGPR 8/44 (18) PR 1/44 (2) Median time to transplant (months) 5.1 2.5-24 Maintainance treatment received 35/44 (80) Disease progressed 22/44 (50) Deaths 11/44 (25) Disclosures Off Label Use: Lenalidomide maintenance therapy after ASCT. Reece:Janssen: Honoraria; Celgene: Honoraria. Trudel:Oncoethix: Research Funding; Glaxo Smith Kline: Honoraria, Research Funding; Novartis: Honoraria; Celgene: Honoraria. Kukreti:Celgene: Honoraria. Chen:Janssen: Honoraria; Celgene: Honoraria.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.002
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.001
Threshold uncertainty score0.006

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0010.000
Open science0.0000.001
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.050
GPT teacher head0.307
Teacher spread0.257 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations2
Published2014
Admission routes1
Has abstractyes

Explore more

Same venueBlood→Same topicMultiple Myeloma Research and Treatments→French-language works237,207→