Literature DB >> 19636016

Phase I dose escalation, pharmacokinetic and pharmacodynamic study of naptumomab estafenatox alone in patients with advanced cancer and with docetaxel in patients with advanced non-small-cell lung cancer.

Hossein Borghaei1, Katherine Alpaugh, Gunnar Hedlund, Göran Forsberg, Corey Langer, Andre Rogatko, Robert Hawkins, Svein Dueland, Ulrik Lassen, Roger B Cohen.   

Abstract

PURPOSE: Two phase I studies were conducted of ABR-217620 alone or in combination with docetaxel. This is a recombinant fusion protein consisting of a mutated variant of the superantigen staphylococcal enterotoxin E (SEA/E-120) linked to fragment antigen binding moiety of a monoclonal antibody recognizing the tumor-associated antigen 5T4. PATIENTS AND METHODS: Patients with non-small-cell lung cancer (NSCLC), pancreatic cancer (PC), and renal cell cancer (RCC) received 5 daily boluses of ABR-217620 (3-month cycles) in escalating doses to determine the maximum-tolerated dose (MTD; ABR-217620 dose escalation monotherapy [MONO] study). Doses were selected based on individual patient anti-SEA/E-120 titers pretreatment. Patients with NSCLC received 4 daily, escalating doses of ABR-217620 followed by docetaxel in 21-day cycles (ABR-217620 dose escalation combination with docetaxel [COMBO] study).
RESULTS: Thirty-nine patients were enrolled in the MONO study and 13 were enrolled in the COMBO study. The monotherapy MTD was 26 microg/kg (NSCLC and PC) and 15 microg/kg (RCC). Dose-limiting toxicities (DLTs) in the MONO study were fever, hypotension, acute liver toxicity, and vascular leak syndrome. In the COMBO study, the MTD was 22 microg/kg (neutropenic sepsis). Adverse events included grade 1 to 2 fever, hypotension, nausea, and chills. Treatment caused a systemic increase of inflammatory cytokines and selective expansion of SEA/E-120 reactive T-cells. Tumor biopsies demonstrated T-cell infiltration after therapy. Fourteen patients (36%) had stable disease (SD) on day 56 of the MONO study. Two patients (15%) in the COMBO study had partial responses, one in a patient with progressive disease on prior docetaxel, and five patients (38%) had SD on day 56.
CONCLUSION: ABR-217620 was well tolerated with evidence of immunological activity and antitumor activity.

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Year:  2009        PMID: 19636016      PMCID: PMC2734423          DOI: 10.1200/JCO.2008.20.2515

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  21 in total

1.  Selective ablation of acute myeloid leukemia using antibody-targeted chemotherapy: a phase I study of an anti-CD33 calicheamicin immunoconjugate.

Authors:  E L Sievers; F R Appelbaum; R T Spielberger; S J Forman; D Flowers; F O Smith; K Shannon-Dorcy; M S Berger; I D Bernstein
Journal:  Blood       Date:  1999-06-01       Impact factor: 22.113

2.  Enterotoxin residues determining T-cell receptor V beta binding specificity.

Authors:  M J Irwin; K R Hudson; J D Fraser; N R Gascoigne
Journal:  Nature       Date:  1992-10-29       Impact factor: 49.962

3.  Immune response during tumor therapy with antibody-superantigen fusion proteins.

Authors:  A Rosendahl; J Hansson; A Sundstedt; T Kalland; M Dohlsten
Journal:  Int J Cancer       Date:  1996-09-27       Impact factor: 7.396

4.  Superantigens interact with MHC class II molecules outside of the antigen groove.

Authors:  P Dellabona; J Peccoud; J Kappler; P Marrack; C Benoist; D Mathis
Journal:  Cell       Date:  1990-09-21       Impact factor: 41.582

5.  Superantigen-based immunotherapy: a phase I trial of PNU-214565, a monoclonal antibody-staphylococcal enterotoxin A recombinant fusion protein, in advanced pancreatic and colorectal cancer.

Authors:  B J Giantonio; R K Alpaugh; J Schultz; C McAleer; D W Newton; B Shannon; Y Guedez; M Kotb; L Vitek; R Persson; P O Gunnarsson; T Kalland; M Dohlsten; B Persson; L M Weiner
Journal:  J Clin Oncol       Date:  1997-05       Impact factor: 44.544

6.  Repeated treatment with antibody-targeted superantigens strongly inhibits tumor growth.

Authors:  A Rosendahl; K Kristensson; J Hansson; L Ohlsson; T Kalland; M Dohlsten
Journal:  Int J Cancer       Date:  1998-04-13       Impact factor: 7.396

7.  Phase I trial of recombinant immunotoxin RFB4(dsFv)-PE38 (BL22) in patients with B-cell malignancies.

Authors:  Robert J Kreitman; David R Squires; Maryalice Stetler-Stevenson; Pierre Noel; David J P FitzGerald; Wyndham H Wilson; Ira Pastan
Journal:  J Clin Oncol       Date:  2005-08-01       Impact factor: 44.544

8.  Monoclonal antibody-superantigen fusion proteins: tumor-specific agents for T-cell-based tumor therapy.

Authors:  M Dohlsten; L Abrahmsén; P Björk; P A Lando; G Hedlund; G Forsberg; T Brodin; N R Gascoigne; C Förberg; P Lind
Journal:  Proc Natl Acad Sci U S A       Date:  1994-09-13       Impact factor: 11.205

9.  Complete regression of human B-cell lymphoma xenografts in mice treated with recombinant anti-CD22 immunotoxin RFB4(dsFv)-PE38 at doses tolerated by cynomolgus monkeys.

Authors:  R J Kreitman; Q C Wang; D J FitzGerald; I Pastan
Journal:  Int J Cancer       Date:  1999-03-31       Impact factor: 7.316

10.  A phase II study of a 5T4 oncofoetal antigen tumour-targeted superantigen (ABR-214936) therapy in patients with advanced renal cell carcinoma.

Authors:  D M Shaw; N B Connolly; P M Patel; S Kilany; G Hedlund; O Nordle; G Forsberg; J Zweit; P L Stern; R E Hawkins
Journal:  Br J Cancer       Date:  2007-02-06       Impact factor: 7.640

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  23 in total

Review 1.  Have we overestimated the benefit of human(ized) antibodies?

Authors:  Daniel R Getts; Meghann T Getts; Derrick P McCarthy; Emily M L Chastain; Stephen D Miller
Journal:  MAbs       Date:  2010-11-01       Impact factor: 5.857

2.  Antibodies to watch in 2010.

Authors:  Janice M Reichert
Journal:  MAbs       Date:  2010-01-16       Impact factor: 5.857

Review 3.  Adaptive dose-finding studies: a review of model-guided phase I clinical trials.

Authors:  Alexia Iasonos; John O'Quigley
Journal:  J Clin Oncol       Date:  2014-06-30       Impact factor: 44.544

4.  Outcomes of patients with advanced non-small cell lung cancer treated in a phase I clinic.

Authors:  Filip Janku; Apostolia M Tsimberidou; Xuemei Wang; David S Hong; Aung Naing; Jing Gong; Ignacio Garrido-Laguna; Henrique A Parsons; Ralph G Zinner; Razelle Kurzrock
Journal:  Oncologist       Date:  2011-02-21

5.  Two-stage design for phase I-II cancer clinical trials using continuous dose combinations of cytotoxic agents.

Authors:  Mourad Tighiouart
Journal:  J R Stat Soc Ser C Appl Stat       Date:  2018-06-22       Impact factor: 1.680

6.  Dose escalation with overdose control using a quasi-continuous toxicity score in cancer Phase I clinical trials.

Authors:  Zhengjia Chen; Mourad Tighiouart; Jeanne Kowalski
Journal:  Contemp Clin Trials       Date:  2012-04-25       Impact factor: 2.226

7.  Escalation with overdose control using all toxicities and time to event toxicity data in cancer Phase I clinical trials.

Authors:  Zhengjia Chen; Ye Cui; Taofeek K Owonikoko; Zhibo Wang; Zheng Li; Ruiyan Luo; Michael Kutner; Fadlo R Khuri; Jeanne Kowalski
Journal:  Contemp Clin Trials       Date:  2014-02-12       Impact factor: 2.226

Review 8.  A comprehensive overview of targeted therapy in metastatic renal cell carcinoma.

Authors:  Z Mihaly; Z Sztupinszki; P Surowiak; B Gyorffy
Journal:  Curr Cancer Drug Targets       Date:  2012-09       Impact factor: 3.428

9.  5T4 oncofetal antigen is expressed in high risk of relapse childhood pre-B acute lymphoblastic leukemia and is associated with a more invasive and chemotactic phenotype.

Authors:  F V Castro; O J McGinn; S Krishnan; G Marinov; J Li; A J Rutkowski; E Elkord; D J Burt; M Holland; R Vaghjiani; A Gallego; V Saha; P L Stern
Journal:  Leukemia       Date:  2012-01-23       Impact factor: 11.528

10.  Is more better? An analysis of toxicity and response outcomes from dose-finding clinical trials in cancer.

Authors:  Kristian Brock; Victoria Homer; Gurjinder Soul; Claire Potter; Cody Chiuzan; Shing Lee
Journal:  BMC Cancer       Date:  2021-07-05       Impact factor: 4.430

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