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Status unknownNCT03071822Updated Jun 11, 2018

Combination Chemotherapy Including Cisplatin, Ifosfamide, Gemcitabine, L-asparaginase, Etoposide and Dexamethasone as Treatment of Newly Diagnosed and Relapsed/Refractory Peripheral T Cell Lymphomas

A Phase 4 interventional study of cisplatin and ifosfamide in Peripheral T Cell Lymphoma, sponsored by The University of Hong Kong. Status unknown at 1 site in Hong Kong. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2018-06-11.

Sponsored by The University of Hong Kong · Phase 4, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jun 2018), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 4
Study type
Interventional
Enrollment
50
Allocation
Not applicable
Ages
18 Years to 80 Years
Sex
All
01

Study summary

The PIGLETS regimen was devised to replace the conventional SMILE regimen in management of extranodal NK/T cell lymphoma in our institution. It had been three years since the introduction of PIGLETS regimen in treatment of NK malignancies. The response rate is encouraging, with an overall response rate (ORR) of 90% in NK malignancies. Side effects are generally tolerable. The investigator therefore propose the use of PIGLETS on newly diagnosed or relapsed/refractory PTCLs.

Read the detailed description

Peripheral T cell lymphomas (PTCLs) are a group of heterogenous lymphoid malignancies derived from post-thymic mature T-lymphocytes. They are further classified according to their putative origin, immunophenotype, sites of involvement and clinical behaviour. Common subtypes include PTCL-not otherwise specified (PTCL-NOS), angioimmunoblastic T cell lymphoma (AITL) and anaplastic large cell lymphoma (ALCL). With the exception of ALCL, PTCLs behave aggressively and their response to chemotherapy is typically poor. CHOP regimen (cyclophosphamide, doxorubicin, vincristine, prednisolone) borrowed from treatment of B-cell lymphoma is commonly used. However, there is no randomized controlled trial evaluating its efficacy. Moreover, despite the initial response of 40-70%, most patients suffer from disease relapse, giving rise to disappointing five year disease free survival (DFS) and overall survival (OS), typically in the range of 30% and 20%, respectively. As a result, there is not yet a standard agreed-on regimen for treatment of PTCLs in an upfront setting.

One of the possible mechanisms behind the intrinsic resistance to chemotherapy in PTCLs is the overexpression of multi-drug resistance (MDR) gene/P-glycoprotein (P-gp), which mediates active efflux of chemotherapeutic medications out of intracellular compartment. Regimens combining drugs which are independent of the P-gp pathway were proven to be successful in the management of PTCL, extranodal NK/T cell lymphoma, a lymphoma also expressing high level of MDR gene/P-glycoprotein. The PIGLETS regimen was devised to replace the conventional SMILE regimen in management of extranodal NK/T cell lymphoma in our institution. It had been three years since the introduction of PIGLETS regimen in treatment of NK malignancies. The response rate is encouraging, with an overall response rate (ORR) of 90% in NK malignancies. Side effects are generally tolerable. The investigator therefore propose the use of PIGLETS on newly diagnosed or relapsed/refractory PTCLs.

Expected toxicity:

  1. The PIGLETS regimen had been in used since 2013, with the toxicities well known to the investigators
  2. Typical side effects of chemotherapy would be anticipated, including cytopenia, alopecia, mucositis and emesis. These can all be managed with supportive therapy
  3. Anaphylactic reaction to L-asparaginase may occur, but a small test dose will be given before formal administration to ensure the absence of allergy. Prophylactic antihistamine and glucocorticoids will also be given.
02

Conditions studied

  • Peripheral T Cell Lymphoma

Keywords

  • PTCLs
03

In context

Lymphoma

5,578 studies on the registry are indexed under Lymphoma; 825 are open to participants now.

This study's planned enrollment of 50 is above the median of 40 across 4,509 interventional studies indexed under Lymphoma.

Browse Lymphoma studies →

Lead sponsor

The University of Hong Kong is the lead sponsor of 1,262 studies on the registry; 340 are open to participants now.

Of its 8 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Patients between the age of 18 - 80 years, with confirmed PTCLs
  2. Adequate organ functions
  3. ECOG performance status of \<=2
  4. No history of hypersensitivity to any of the components of the PIGLETS regimen
  5. Informed consent obtained

Exclusion criteria

Exclusion Criteria:

  1. Inadequate organ functions
  2. ECOG performance status of >=3
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
50 participants (estimated)

Study arms

  • Experimental
    PIGLETs

    Patient will be given this combination of chemotherapy (cisplatin, ifosfamide, gemcitabine, L-asparaginase, etoposide and dexamethasone) for a total of 6 courses

    Drug: cisplatin · Drug: ifosfamide · Drug: gemcitabine · Drug: L-asparaginase · Drug: etoposide · Drug: dexamethasone

Interventions

  • Drugcisplatin

    PIGLETs

  • Drugifosfamide

    PIGLETs

  • Druggemcitabine

    PIGLETs

  • DrugL-asparaginase

    PIGLETs

  • Drugetoposide

    PIGLETs

  • Drugdexamethasone

    PIGLETs

06

What researchers measure

Primary outcomes

  1. Adverse events and severe adverse events

    Incidence of AE and SAE by severity grading as assessed according to CTCAE v4.03 Incidence of AE and SAE by severity grading as assessed according to CTCAE v4.03

    Time frame: 1 year

  2. Overall response rate (ORR)

    proportion of patients achieving CR or CRi or partial remission (PR)

    Time frame: 3 months

  3. Overall response rate (ORR)

    proportion of patients achieving CR or CRi or partial remission (PR)

    Time frame: 6 months

07

Study locations

1 of 1 sites recruiting
  • The University of Hong Kong
    Hong Kong, Hong Kong
    • King Hei Lu, MMedSc · Contact · khlu@hku.hk · 852-22554361
    • Zoe Chan, BNs · Contact · zoechan1@hku.hk · 852-22551654
    • Yok Lam Kwong, MD(HK) · Principal investigator
    • Thomas Chan, MBBS(HK) · Sub investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 11, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03071822
Lead sponsor
The University of Hong Kong
Responsible party
Professor Yok-lam Kwong (Chair Professor, The University of Hong Kong) — Principal investigator
First posted
Mar 7, 2017
Start date
Feb 24, 2017
Primary completion
Jul 31, 2021 (estimated)
Completion
Feb 28, 2022 (estimated)
Last update
Jun 11, 2018

Study contacts

Sau Yan Thomas Chan, MBBS
Contact
thomas28@netvigator.com
852-22554361
Crosby Lu, BN
Contact
khlu@hku.hk
852-22555161
Yok Lam Kwong, MBBS
principal investigator · The University of Hong Kong

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Jun 2018. You cannot join it, but the record below documents what was studied.

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