M6620 Plus Standard Treatment in Oesophageal and Other Cancer (CHARIOT)

University of Oxford

Status and phase: Completed; Phase 1

Conditions: Solid Tumor; Oesophageal Adenocarcinoma; Squamous Cell Carcinoma

Treatments: Drug: Cisplatin; Radiation: Radiotherapy; Drug: Capecitabine; Drug: M6620

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT03641547

OCTO_072

Details and patient eligibility

About

This Phase I study will test the combination of a novel ATR inhibitor (M6620) with chemoradiotherapy in oesophageal cancer; utilizing three experimental cohorts (Stage A1, A2 and B).

Full description

There is strong scientific rationale for combining ATR inhibitors with DNA damaging agents such as radiation and cisplatin. In particular, ATR inhibition has been shown to be cytotoxic to tumor cells with an impaired DNA damage response, such as those with deficiency in the ATM- or p53 pathway. The high incidence of p53 mutations and the fact that cisplatin and radiation are key therapeutics, makes oesophageal cancer an attractive tumor type to test the activity of an ATR inhibitor. Given the reported synthetic lethal relationship between ATM and ATR, it is likely that ATR inhibition in an ATM- or p53- deficient background will offer a specific and effective way of targeting OAC and SCC of the oesophagus, and enhance the current standard of care.

The trial will be divided into three stages. Stage A1 will explore the combination of M6620 plus radiotherapy in the palliative setting and Stage A2 will explore the combination of M6620 plus chemotherapy in the palliative setting. Stage B, will explore the combination of all 3 (M6620 plus chemoradiotherapy in the radical setting).

In Stage A1 of the study M6620 will be combined with radiotherapy for the first time and the starting dose will be 140mg/m2 M6620, which has been well-tolerated. M6620 will be administered with daily palliative radiotherapy during this stage in order to study the specific interaction of M6620 with radiotherapy (acting as the DNA damaging agent during this trial stage).

In Stage A2 of the study, M6620 will be combined with Cisplatin and Capecitabine combination chemotherapy for the first time; with a starting dose of 90mg/m2 M6620. M6620 will be administered 24 hours post cisplatin infusion, aiming to achieve maximum treatment benefit. Stage A1 and A2 together will help give an indication of a toxicity profile before administration with chemoradiotherapy (Stage B).

Enrollment: 36 patients

Sex: All

Ages: 16+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

For Stage A1:

1. Histologically confirmed adenocarcinoma or squamous cell carcinoma of the oesophagus (not including cervical oesophagus)

2. Tumor length 15cm or less

3. Any stage of disease that is unsuitable for radical CRT or surgery but suitable for palliative RT

4. Baseline investigations available: staging CT scan (within 42 days before first study dose) and endoscopy

5. Previous chemotherapy treatment completed 28 days before first study dose

6. No oesophageal stent in-situ

7. Any gender, aged ≥16 years.

8. Life expectancy of at least 12 weeks

9. ECOG performance score of 0-1

10. Able to comply with protocol fully - absence of any physical, psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial

11. Able to give written (signed and dated) informed consent according to GCP before registration

12. Hematological and biochemical indices within the ranges below:

    • Haemoglobin: ≥8.0g/dL
    • Platelet count : ≥100x10^9/L
    • Absolute neutrophil count: ≥1.5x10^9/L
    • Total bilirubin: ≤1.5 x upper limit of normal unless the subject has known or suspected Gilbert's syndrome
    • AST/ALT: ≤2.5 times the upper limit of normal; ≤5 times if liver metastases
    • Estimated glomerular filtration rate: ≥40ml/min

For Stage A2:

1. Any histologically confirmed advanced solid tumor that is metastatic or unresectable where Investigator considers Cisplatin and Capecitabine based regimen as appropriate.

2. Baseline investigations available: staging CT scan (within 35 days before first study dose)

3. Previous chemotherapy treatment completed 28 days before first study dose

4. Any gender, aged ≥16 years

5. Life expectancy of at least 12 weeks

6. ECOG performance score of 0-1

7. Able to comply with protocol fully - absence of any physical, psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial

8. Able to give written (signed and dated) informed consent according to GCP before registration

9. Hematological and biochemical indices within the ranges below:

   • Haemoglobin: ≥10.0g/dL
   • Platelet count : ≥100x10^9/L
   • Absolute neutrophil count: ≥1.5x10^9/L
   • Total bilirubin: ≤1.5 x upper limit of normal unless the subject has known or suspected Gilbert's syndrome
   • AST/ALT: ≤2.5 times the upper limit of normal; ≤5 times if liver metastases
   • Ca, Mg, Phosphate: within normal limits
   • Estimated glomerular filtration rate: ≥60ml/min

For Stage B:

1. Histologically confirmed adenocarcinoma or squamous cell carcinoma of the oesophagus including Siewert type 1 or 2 tumors with ≤2cm gastric mucosal extension (not including cervical oesophagus)

2. Tumor length 7cm or less

3. Suitable for radical CRT and surgery not an option due to being medically unfit or unsuitable for surgery or patient choice

4. No oesophageal stent in-situ

5. Endoscopically or radiologically documented measurable disease

6. Diagnostic PET CT scan*

7. Staging CT scan*

   *either CT or PET CT scan within 42 days of first study dose

8. Adequate respiratory and cardiac function tests for safe delivery of CRT in the opinion of the Principle Investigator, specifically cardiac ejection fraction ≥60% and lung function FEV1>1 litre or 40% of predicted value or KCO (DLCO/VA) >40% predicted value.

9. Any gender, aged ≥16 years

10. ECOG performance score of 0-1

11. Able to comply with protocol fully - absence of any physical, psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial

12. Able to give written (signed and dated) informed consent according to GCP before registration

13. Haematological and biochemical indices within the ranges below:

    • Haemoglobin: ≥10.0g/dL
    • Platelet count : ≥100x10^9/L
    • Absolute neutrophil count: ≥1.5x10^9/L
    • Total bilirubin: ≤1.5 x upper limit of normal unless the subject has known or suspected Gilbert's syndrome
    • AST/ALT: ≤2.5 times the upper limit of normal; ≤5 times if liver metastases
    • Ca, Mg, Phosphate: within normal limits
    • Estimated glomerular filtration rate: ≥60ml/min

Exclusion criteria

1. Pregnant or breast-feeding women, or women of childbearing potential unless highly effective contraception is used
2. Untreated and multiple brain metastases
3. Clinically significant cardiovascular event within 6 months before study entry to include: a) congestive heart failure requiring therapy, b) unstable angina pectoris, c) myocardial infarction, d) class II/III/IV cardiac disease (New York Heart Association), e) presence of severe valvular heart disease, f) presence of ventricular arrhythmia requiring treatment
4. History of arrhythmia that is symptomatic or requires treatment (CTCAE 3), symptomatic or uncontrolled atrial fibrillation, despite treatment, or asymptomatic sustained ventricular tachycardia. Subjects with atrial fibrillation controlled by medication are permitted.
5. Uncontrolled hypertension (blood pressure ≥160/100 despite optimal therapy)
6. Second or third degree heart block with or without symptoms
7. QTc >450msec in adult male and >470 msec in adult females (by Fridericia's correction) not due to electrolyte abnormality and that does not resolve with correction of electrolytes.
8. History of congenital long QT syndrome
9. History of torsades de pointes (or any concurrent medication with a known risk of inducing torsades de pointes)
10. Trachea-oesophageal fistula or invasion of the tracheo-bronchial tree
11. Treatment with any other investigational agent, or participation in another clinical trial within 28 days prior to the start of treatment
12. Strong CYP3A inhibitors and inducers or haemopoietic growth factors within 14 days before first dose of M6620 (Berzosertib)
13. HER2 gastro-oesophageal positive cancer where anti-Her2 therapies may be more appropriate (however patients who have failed anti-HER2 therapy may be eligible for stage A1 and A2)
14. Unable to have or unwilling to change to low molecular weight heparin instead of Warfarin
15. Other psychological, social or medical condition, physical examination finding or a laboratory abnormality that the Investigator considers would make the patient a poor trial candidate or could interfere with protocol compliance or the interpretation of trial results.
16. Any other active malignancy, with the exception of adequately treated cone-biopsied in situ carcinoma of the cervix uteri and non-melanoma skin lesions.
17. Patients who are known to be serologically positive for Hepatitis B, Hepatitis C or HIV.

Additional Exclusion Criteria for Stage A1 and B:

1. Previous radiotherapy to thorax or upper abdomen

Additional exclusion criteria for Stage A2 and B:

1. History of hand-foot syndrome
2. History of hearing impairment
3. Live vaccine received within 30 days prior to treatment start
4. Complete or Partial DPD deficiency

Additional Exclusion Criteria for Stage B:

1. Previous chemotherapy

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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36 participants in 1 patient group

Stage A1, A2 & B

Experimental group

Description:

The trial is a single arm study. Different populations are recruited to each stage and the stages run independently of each other. Stage A1 \& A2 will commence before Stage B so that safety data can be obtained in the palliative setting prior to Stage B commencing. Stage A1 may be ongoing when Stage B begins. Each Stage has a separate eligibility criteria. Stage A1: M6620 \& palliative radiotherapy Stage A2: M6620 \& palliative chemotherapy (Cisplatin \& Capecitabine) Stage B: M6620 \& definitive chemoradiotherapy

Treatment:

Drug: M6620

Drug: Capecitabine

Radiation: Radiotherapy

Drug: Cisplatin