Overview

Savolitinib Plus Docetaxel as 2L in EGFR/ALK/ROS1/MET ex14m-wildtype NSCLC With MET Overexpression

Status:
Not yet recruiting
Trial end date:
2027-08-31
Target enrollment:
0
Participant gender:
All
Summary
This is a prospective, pilot, single-arm, single-center study exploring the efficacy and safety of savolitinib plus docetaxel as second-line therapy in patients with MET overexpressed, EGFR/ALK/ROS1/MET ex14m-wildtype advanced NSCLC. Participants will receive treatment of docetaxel (60 mg/m2, ivgtt, q3w) in combination with savolitinib (300mg or 200mg according to safety run-in recommendation, p.o., BID) after informed consent signed. Treatment will continue until either objective disease progression, unacceptable toxicity occurs, consent is withdrawn, other discontinuation criterion is met, or study completion.
Phase:
Phase 1/Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
The First Affiliated Hospital of Guangzhou Medical University
Treatments:
Docetaxel
Criteria
Inclusion Criteria:

1. Capable of giving signed informed consent which includes compliance with the
requirements and restrictions listed in the informed consent form (ICF) and in this
protocol.

2. Provision of signed and dated, written ICF prior to any mandatory study specific
procedures, sampling, and analyses.

3. Female or males age ≥18 years at the time of signing the ICF.

4. Histologically or cytologically confirmed locally advanced or metastatic
EGFR/ALK/ROS1/MET ex14m-wildtype NSCLC.

5. Has only received first line systemic treatment of non-targeted advanced NSCLC.

- Prior MET inhibitor therapy is not allowed.

- At least 28 days since last treatment.

6. MET overexpression as determined IHC on tumor tissue.

- MET overexpression by IHC, 3+ in ≥50% of tumor cells

- Local IHC results are acceptable.

7. WHO or Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 with no
deterioration over the previous 2 weeks prior to baseline or day of first dosing and a
minimum life expectancy of 12 weeks.

8. At least 1 lesion that can be accurately measured at baseline as ≥10 mm in the longest
diameter (except lymph nodes, which must have short axis ≥15 mm) with computed
tomography (CT) or magnetic resonance imaging (MRI) and is suitable for accurate
repeated measurements.

9. Adequate haematological function defined as:

- Haemoglobin ≥9 g/dL (no transfusion in the past 2 weeks).

- Absolute neutrophil count ≥1.5×10^9/L.

- Platelet count ≥100,000/μL (no transfusion in the past 10 days)

10. Adequate liver function defined as:

- Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤2.5 x the
upper limit of normal (ULN) with total bilirubin (TBL) ≤ ULN

- OR TBL >ULN to ≤1.5x ULN with ALT and AST ≤ ULN, alkaline phosphatase (ALP) ≤
2.5x ULN

11. Adequate renal function defined as a serum creatinine <1.5 times the institutional ULN
OR a glomerular filtration rate ≥50 mL/min, as assessed using the standard methodology
at the investigating centre (eg, Cockcroft-Gault, Modification of Diet in Renal
Disease or Chronic Kidney Disease Epidemiology Collaboration formulae,
ethylenediaminetetraacetic acid clearance or 24-hour urine collection). Confirmation
of creatinine clearance is only required when creatinine is >1.5 times ULN.

12. Adequate coagulation parameters, defined as:

-International Normalisation Ratio (INR) <1.5 and activated partial thromboplastin
time <1.5 x ULN unless patients are receiving therapeutic anti coagulation which
affects these parameters.

13. Patients with known tumor thrombus or deep vein thrombosis are eligible if clinically
stable on low molecular weight heparin (LMWH) for ≥2 weeks.

14. Ability to swallow and retain oral medications.

15. Willingness and ability to comply with study and follow-up procedures.

16. Females of childbearing potential should be willing to use highly effective
contraceptive measures, should not be breast feeding, and must have a negative
pregnancy test if of childbearing potential or must have evidence of non-childbearing
potential by fulfilling one of the following criteria at screening:

Post-menopausal is defined as aged more than 50 years and amenorrhoeic for at least 12
months following cessation of all exogenous hormonal treatments; women under the age
of 50 years would be considered postmenopausal if they have been amenorrhoeic for 12
months or more following cessation of exogenous hormonal treatments and with LH and
FSH levels in the post-menopausal range for the institution; or women with
documentation of irreversible surgical sterilisation by hysterectomy, bilateral
oophorectomy or bilateral salpingectomy.

17. Male patients with a female partner of childbearing potential should be willing to use
barrier contraception during the study and for 6 months following discontinuation of
study drug. Patients should refrain from donating sperm from the start of dosing until
6 months after discontinuing study treatment.

Exclusion Criteria:

1. As judged by the investigator, active gastrointestinal disease or other condition that
will interfere significantly with the absorption, distribution, metabolism, or
excretion of oral therapy (eg, ulcerative disease, uncontrolled nausea, vomiting,
diarrhoea Grade ≥2, and malabsorption syndrome).

2. Any of the following cardiac diseases currently or within the last 6 months:

- Unstable angina pectoris

- Congestive heart failure (New York Heart Association [NYHA] ≥Grade 2)

- Acute myocardial infarction

- Stroke or transient ischemic attack

3. Uncontrolled hypertension (BP ≥150/95 mmHg despite medical therapy).

4. Mean resting correct QT interval (QTcF) >470 msec for women and >450 msec for men on
screening obtained from 3 electrocardiograms (ECGs) or factors that may increase the
risk of QTcF prolongation such as chronic hypokalaemia not correctable with
supplements, congenital or familial long QT syndrome, or family history of unexplained
sudden death under 40 years of age in first-degree relatives or any concomitant
medication known to prolong the QT interval and cause Torsade de Pointes.

5. Any clinically important abnormalities in rhythm, conduction or morphology of resting
electrocardiograms (ECGs), e.g. complete left bundle branch block, third degree heart
block, second degree heart block, PR interval >250 msec.

6. Serious underlying medical condition at the time of treatment that would impair the
ability of the patient to receive protocol treatment.

7. Wide field radiotherapy (including therapeutic radioisotopes such as strontium 89)
administered ≤28 days or limited field radiation for palliation ≤7 days prior to
starting study drug or has not recovered from side effects of such therapy.

8. Major surgical procedures ≤28 days of beginning study drug or minor surgical
procedures ≤7 days. No waiting is required following port-a-cath placement.

9. As judged by the investigator, any evidence of severe or uncontrolled systemic
diseases, including renal transplant, active bleeding diatheses or uncontrolled
hypertension, which in the investigator's opinion makes it undesirable for the patient
to participate in the trial or which would jeopardise compliance with the protocol.

10. Active hepatitis B (HBV) (positive HBV surface antigen [HBsAg] result) or hepatitis C
(HCV). Patients with a past or resolved HBV or HCV infection are eligible if:

- Negative for HBsAg and positive for hepatitis B core antibody [anti-HBc] or

- Positive for HBsAg, but for >6 months have had normal transaminases and HBV DNA
levels between 0 to 2000 IU/mL (inactive carrier state) and willing to start and
maintain antiviral treatment for at least the duration of the study.

- Patients with a past or resolved HBV infection must have monthly monitoring of
ALT and HBV DNA

- HBV DNA levels >2000 IU/mL but on prophylactic antiviral treatment for the past 3
months and will maintain the antiviral treatment during the study.

- Patients with positive HCV antibody are eligible only if the polymerase chain
reaction is negative for HCV ribonucleic acid.

11. Presence of other active cancers, or history of treatment for invasive cancer, within
the last 5 years. Patients with Stage I cancer who have received definitive local
treatment at least 3 years previously and are considered unlikely to recur are
eligible. All patients with previously treated in situ carcinoma (ie, non-invasive)
are eligible, as are patients with history of non-melanoma skin cancer.

12. Unresolved toxicities from any prior therapy greater than Common Terminology Criteria
for Adverse Events (CTCAE) Grade 1 at the time of starting study
treatment/randomization with the exception of alopecia.

13. Spinal cord compression or brain metastases unless asymptomatic, stable, and not
requiring steroids for at least 2 weeks prior to start of study intervention. Subjects
with leptomeningeal metastases are ineligible.

14. Past medical history of ILD/pneumonitis, drug-induced ILD, radiation pneumonitis which
required steroid treatment, or any evidence of clinically active ILD.

15. Known serious active infection including, but not limited to, tuberculosis, or human
immunodeficiency virus (positive human immunodeficiency virus 1/2 antibodies).

16. History of liver cirrhosis of any origin and clinical stage; or history of other
serious liver disease or chronic disease with relevant liver involvement, with or
without normal LFTs, such as

- Hemochromatosis

- Alpha-1 Antitrypsin deficiency

- Autoimmune hepatitis (AIH)

- Primary sclerosing cholangitis (PSC)

- Primary biliary cirrhosis (PBC)

- Biopsy-confirmed Non-Alcoholic Steatohepatitis (NASH) with advanced fibrosis

- Biopsy- confirmed Alcoholic Steatohepatitis with advanced fibrosis

- Wilson's disease

- Hepatocellular carcinoma

17. Known contraindications to docetaxel administration.

18. Known hypersensitivity to the active or inactive excipients of docetaxel or
savolitinib or drugs with a similar chemical structure or class.

19. Women who are either pregnant or breast-feeding.

20. Patients with previous medical history of Stevens Johnson syndrome (SJS) and serious
cutaneous toxicity.

21. Prior exposure to HGF/MET inhibitors, e.g., foretinib, crizotinib, cabozantinib,
merestinib, onartuzumab, capmatinib, tepotinib, etc.

22. Patients currently receiving (or unable to stop use prior to receiving the first dose
of study treatment) medications or herbal supplements known to be strong inducers of
CYP3A4, strong inhibitors of CYP1A2, within 2 weeks of the first dose of study
treatment will be excluded. Herbal preparations/medications are not allowed throughout
the study. These herbal medications include, but are not limited to: St. John's wort,
kava, ephedra (ma huang), gingko biloba, dehydroepiandrosterone (DHEA), yohimbe, saw
palmetto, and ginseng. Patients should stop using these herbal medications 7 days
prior to first dose of study drug (three weeks for St John's wort). All patients must
try to avoid concomitant use of any medications, herbal supplements and/or ingestion
of foods with known inducer effects on CYP3A4 during the study and for 3 months later
the last dose intake (detailed description in Appendix G).

23. Participation in another clinical study with a study interventional medication
administered within five half-lives of the compound or 3 months, whichever is greater
or investigational medicinal device administered in the last 30 days prior to
randomisation/first dose of study intervention or concurrent enrolment in another
clinical study, unless it is an observational (non-interventional) clinical study or
during the follow-up period of an interventional study.

24. Involvement in the planning and/or conduct of the study (applies to both AstraZeneca
staff and/or staff at the study site).

25. Judgment by the investigator that the participant should not participate in the study
if the participant is unlikely to comply with study procedures, restrictions and
requirements.

26. For women only-Currently breastfeeding.

27. Previous enrolments in the present study.

28. Without civil capacity or with restricted civil capacity.

29. Any other reasons judged by the leading investigator to prevent the subject from
participating in this study.