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Clinical Trials/NCT03810872
NCT03810872
Unknown
Phase 2

An Open Explorative Phase II, Open Label Study of Afatinib in the Treatment of Advanced Cancer Carrying an EGFR, a HER2 or a HER3 Mutation

AZ-VUB5 sites in 1 country87 target enrollmentJune 21, 2017

Overview

Phase
Phase 2
Intervention
Afatinib
Conditions
Cancers Harbouring an EGFR Mutation, (Excluding Non-squamous Non- Small Cell Lung Cancer, a Registered Indication), a HER2 Mutation or a HER3 Mutation
Sponsor
AZ-VUB
Enrollment
87
Locations
5
Primary Endpoint
Response rate
Last Updated
7 years ago

Overview

Brief Summary

Objective(s):To investigate the efficacy and safety of afatinib in EGFR, HER 2 and HER3 mutated cancers, regardless of cancer type, excluding EGFR mutated non-small cell lung cancer.

Methodology:Open label, genomic driven trial (basket trial)

No. of patients total entered:Optimal Simon two stage design for the three genetic driven cohorts: 10 patients will be enrolled per cancer type in the first stage and an additional 19 in the second stage (maximum total 87 patients)

Indication : cancers harbouring an EGFR mutation(excluding non-squamous non- small cell lung cancer, a registered indication), a HER2 mutation or a HER3 mutation

Test product(s) : Afatinib At progression paclitaxel will be added for those patients that have no contra-indications

dose: Starting dose of afatinib at 40 mg/day. Dose increase to 50 mg in the absence of adverse events. Stepwise dose reduction to 30,20, 10 mg/day according to drug-related adverse events.

At progression, addition of paclitaxel 80 mg/m2 weekly 3w/4 to afatinib 40 mg/day .

mode of admin. : Oral for afatinib Intravenous for paclitaxel

Duration of treatment: Continuous treatment until progression or unacceptable adverse events or withdrawal of consent.

At disease progression, add paclitaxel until progression or unacceptable adverse event or withdrawal of consent if no contra-indications.

Criteria for efficacy: Primary Endpoint:

• Response rate (CR+ PR) via RECIST v1.1

Secondary Endpoints:

  • Disease control rate (CR+PR+SD)
  • Progression free survival
  • Overall survival
  • To correlate tumor response with findings on tumor biopsies
  • To investigate resistance mechanisms
  • response rate (CR+ PR) determined by RECIST and progression free survival on the combination therapy of afatinib and paclitaxel

Criteria for safety: Incidence and intensity of adverse events according CTCAE v4.0

Registry
clinicaltrials.gov
Start Date
June 21, 2017
End Date
December 2022
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
AZ-VUB
Responsible Party
Principal Investigator
Principal Investigator

Dr. Lore Decoster

Coordinator Investigator

AZ-VUB

Eligibility Criteria

Inclusion Criteria

  • Women and men with locally advanced or metastatic cancers harboring either an activating EGFR mutation or a HER2 mutation or a HER3 mutation
  • Failure of at least one line of standard systemic therapy
  • No eligibility for other open genomic driven phase I, II or III trial available for these tumor genotypes
  • ECOG performance status ≤2
  • Patient with a life expectancy \>3 months
  • Patients able to provide written informed consent prior to enrollment into the clinical trial.
  • Adequate organ function

Exclusion Criteria

  • Non squamous non-small cell lung cancer harbouring an EGFR mutation (registered indication)
  • Chemotherapy, biological therapy or investigational agents within four weeks prior to the start of study treatment
  • Known hypersensitivity to afatinib or the excipients of any of the trial drugs
  • Prior treatment with afatinib

Arms & Interventions

Open label

Afatinib 40 mg/day during Period 1 Afatinib 40 mg/day + Paclitaxel 80mg/kg/3w during Period 2

Intervention: Afatinib

Open label

Afatinib 40 mg/day during Period 1 Afatinib 40 mg/day + Paclitaxel 80mg/kg/3w during Period 2

Intervention: Paclitaxel

Outcomes

Primary Outcomes

Response rate

Time Frame: 6 weeks

Incidence and intensity of adverse events

Time Frame: 4 weeks

Secondary Outcomes

  • Disease control rate(6 weeks)
  • Progression free survival(6 weeks)
  • Overall survival(6 weeks)

Study Sites (5)

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