Trial Search Results

Trastuzumab Deruxtecan for the Treatment of HER2+ Newly Diagnosed or Recurrent Osteosarcoma

This phase II trial studies the effects of trastuzumab deruxtecan in treating patients with HER2 positive osteosarcoma that is newly diagnosed or has come back (recurrent). Trastuzumab deruxtecan is a monoclonal antibody, called trastuzumab, linked to a chemotherapy drug called deruxtecan. Trastuzumab attaches to HER2 positive cancer cells in a targeted way and delivers deruxtecan to kill them.

Stanford is currently accepting patients for this trial.

Lead Sponsor:

National Cancer Institute (NCI)

Stanford Investigator(s):

Intervention(s):

  • Biological: Trastuzumab Deruxtecan

Phase:

Phase 2

Eligibility


Inclusion Criteria:

   - Patients must be > 12 years and =< 39 years of age at the time of study enrollment

   - Patients must have had histologic verification of osteosarcoma at original diagnosis
   or relapse

      - Patients with diagnoses of osteosarcoma and confirmed HER2 expression of > 10% of
      osteosarcoma cells are eligible for the intervention

         - Note: There is a mandatory tissue submission for HER2 staining during the
         Step 0 Eligibility Screening process. Metastatic tissue, when possible from
         the most recent relapse, is strongly preferred for HER2 staining over
         archival tissue from primary resection or diagnostic biopsy. The evaluation
         period for HER2 staining to determine eligibility for therapy will be less
         than 4 weeks from screening enrollment

   - Patients must have measurable disease according to Response Evaluation Criteria in
   Solid Tumors (RECIST) 1.1. Patients with clinically inactive brain metastases may be
   included in the study. Patients with treated brain metastases that are no longer
   symptomatic and who require no treatment with corticosteroids or anticonvulsants may
   be included in the study if they have recovered from the acute toxic effect of
   radiotherapy. Lastly, patient must have unresectable lesions or lesions with no
   intention to surgically remove in the 6 months following enrollment

   - Patient's current disease state must be one for which they have received at least
   standard initial therapy, defined as systemic therapy combined with either radiation
   or surgery for local control of the primary tumor at diagnosis. Prior therapy after
   relapse is not required

   - Patients must have a performance status corresponding to Eastern Cooperative Oncology
   Group (ECOG) scores of 0 or 1. Use Karnofsky for patients > 16 years of age and Lansky
   for patients =< 16 years of age. Patients who are non-ambulatory as a result of prior
   surgical treatment for osteosarcoma should be considered ambulatory for the purposes
   of assessing performance status

   - Patients must have recovered from the acute toxic effects of all prior anti-cancer
   therapy and must meet the following minimum duration from prior anti-cancer directed
   therapy prior to enrollment. If after the required timeframe, the numerical
   eligibility criteria are met, e.g., blood count criteria, the patient is considered to
   have recovered adequately

      - Cytotoxic chemotherapy or other anti-cancer agents known to be myelosuppressive:
      For agents not listed, the duration of this interval must be discussed with the
      study chair and the study-assigned Research Coordinator prior to enrollment

         - >= 21 days after the last dose of myelosuppressive chemotherapy (42 days if
         prior nitrosourea)

      - Anti-cancer agents not known to be myelosuppressive (e.g., not associated with
      reduced platelet or absolute neutrophil count [ANC] counts): >= 7 days after the
      last dose of agent

      - Antibodies: >= 4 weeks (28 days) must have elapsed from infusion of last dose of
      antibody, and toxicity related to prior antibody therapy must be recovered to
      grade =< 1

      - Corticosteroids

      - Hematopoietic growth factors: >= 14 days after the last dose of a long-acting
      growth factor (e.g. pegfilgrastim) or 7 days for short-acting growth factor. For
      agents that have known adverse events occurring beyond 7 days after
      administration, this period must be extended beyond the time during which adverse
      events are known to occur

      - Interleukins, interferons and cytokines (other than hematopoietic growth
      factors): >= 21 days after the completion of interleukins, interferon or
      cytokines (other than hematopoietic growth factors)

      - Stem cell Infusions (with or without total body irradiation [TBI]):

         - Allogeneic (non-autologous) bone marrow or stem cell transplant, or any stem
         cell infusion including donor lymphocyte infusion (DLI) or boost infusion:
         >= 84 days after infusion and no evidence of graft versus host disease
         (GVHD)

         - Autologous stem cell infusion including boost infusion: >= 30 days

      - Vellular therapy: >= 30 days after the completion of any type of cellular therapy
      (e.g., modified T cells, natural killer [NK] cells, dendritic cells, etc.)

      - Radiation therapy (XRT)/external beam irradiation including protons: >= 4 weeks
      (28 days) including palliative radiation therapy to the chest. >= 14 days after
      palliative local XRT to areas other than the chest or for whole brain
      radiotherapy

      - Radiopharmaceutical therapy (e.g., radiolabeled antibody, samarium): >= 42 days
      after systemically administered radiopharmaceutical therapy

      - Patients must not have received prior HER2 therapies including antibody drug
      conjugates (e.g. TDM-1 or DS-8201a), HER2 directed cellular therapies, HER2
      receptor therapy (e.g. trastuzumab, pertuzumab) or small molecule antagonists of
      HER2 (e.g lapatinib or neratinib)

   - Patients must be at least 7 days from the date of last surgery

   - Peripheral absolute neutrophil count (ANC) >= 1000/mm^3, (granulocyte
   colony-stimulating factor [G-CSF] administration is not allowed within 1 week prior to
   Step 1 screening assessment) (for patients with solid tumors without known bone marrow
   involvement)

   - Platelet count >= 100,000/mm^3 (transfusion independent, defined as not receiving
   platelet transfusions for at least 7 days prior to enrollment) (for patients with
   solid tumors without known bone marrow involvement)

   - Hemoglobin >= 8.0 g/dL at baseline (Red Blood Cell transfusion is not allowed within 1
   week prior to screening assessment) (for patients with solid tumors without known bone
   marrow involvement)

   - Creatinine clearance or radioisotope glomerular filtration rate (GFR) >= 60
   mL/min/1.73 m^2 or a serum creatinine based on age/gender as follows:

      - Age: 12 to < 13 years; Maximum serum creatinine (mg/dL): 1.2 (male); 1.2 (female)

      - Age: 13 to < 16 years; Maximum serum creatinine (mg/dL): 1.5 (male); 1.4 (female)

      - Age: >= 16 years; Maximum serum creatinine (mg/dL): 1.7 (male); 1.4 (female)

         - For participants less than 18 years of age that screen fail only based on
         creatinine, a 24 hour urine collection may be used instead to confirm
         eligibility. A calculated GFR > 60 mL/min/1.73 m^2 using a 24 hour
         collection will meet criteria for inclusion on this trial

   - Bilirubin (sum of conjugated + unconjugated or total) =< 1.5 x upper limit of normal
   (ULN) for age. For patients with documented Gilbert's syndrome (unconjugated
   hyperbilirubinemia) bilirubin must be < 3 x ULN for age (patients with solid tumors)

   - Serum glutamate pyruvate transaminase (SGPT) (alanine aminotransferase [ALT]) and
   serum glutamic-oxaloacetic transaminase (SGOT) (aspartate aminotransferase [AST]) =< 3
   x ULN. (if liver metastases present =< 5 x ULN). For the purpose of this study, the
   ULN for ALT is 45 U/L regardless of baseline and the ULN for AST is 50 U/L regardless
   of baseline (patients with solid tumors)

   - Serum albumin >= 2.5 g/dL (patients with solid tumors)

   - International normalized ratio (INR)/prothrombin time (PT) and either partial
   thromboplastin or activated partial thromboplastin time (aPTT) =< 1.5 x ULN (patients
   with solid tumors)

   - Shortening fraction of >= 27% by echocardiogram, or ejection fraction of >= 50% by
   either an echocardiogram (ECHO) or multigated acquisition (MUGA) scan within 28 days
   before Step 1 enrollment

   - Corrected QT interval (QTc) prolongation to < 470 ms (females) or < 450 ms (males)
   based on average triplicate 12-lead electrocardiogram (ECG)

   - Pulse oximetry > 93% on room air

   - Patients with seizure disorder may be enrolled if on anticonvulsants and well
   controlled as evidenced by no increase in seizure frequency in the prior 7 days

   - Nervous system disorders (Common Terminology Criteria for Adverse Events [CTCAE]
   version [v]5) resulting from prior chemotherapy, surgery, and/or radiation must be =<
   grade 2, with the exception of decreased tendon reflex (DTR). Any grade of DTR is
   eligible

   - All patients and/or their parents or legally authorized representatives must sign a
   written informed consent. Assent, when appropriate, will be obtained according to
   institutional guidelines

Exclusion Criteria:

   - Pregnant, planning to become pregnant, or breast-feeding women will not be entered on
   this study because there is yet no available information regarding human fetal or
   teratogenic toxicities. Pregnancy tests must be obtained in girls who are
   post-menarchal. Males or females of reproductive potential may not participate unless
   they have agreed to use two effective methods of birth control, including a medically
   accepted barrier or contraceptive method (e.g., male or female condom) for the
   duration of the study and upon completion of the study and for at least 7 months for
   females and 4 months for males after the last dose of study drug. Abstinence is an
   acceptable method of birth control

      - Methods considered as highly effective methods of contraception include:

         - Combined (estrogen and progestogen containing) hormonal contraception
         associated with inhibition of ovulation:

            - Oral

            - Intravaginal

            - Transdermal

         - Progestogen-only hormonal contraception associated with inhibition of
         ovulation:

            - Oral

            - Injectable

            - Implantable

         - Intrauterine device (IUD)

         - Intrauterine hormone-releasing system (IUS)

         - Bilateral tubal occlusion

         - Vasectomized partner

         - Complete sexual abstinence defined as refraining from heterosexual
         intercourse. Periodic abstinence (calendar, symptothermal, post-ovulation
         methods) is not an acceptable method of contraception

   - Non-child-bearing potential defined as pre-menopausal females with a documented tubal
   ligation or hysterectomy; or postmenopausal defined as 12 months of spontaneous
   amenorrhea (in questionable cases, a blood sample with simultaneous
   follicle-stimulating hormone [FSH] > 40 mIU/mL and estradiol < 40 pg/mL [< 147 pmol/L]
   is confirmatory). Females on hormone replacement therapy (HRT) and whose menopausal
   status is in doubt will be required to use one of the contraception methods outlined
   for women of child-bearing potential if they wish to continue their HRT during the
   study. Otherwise, they must discontinue HRT to allow confirmation of post-menopausal
   status prior to study enrollment. For most forms of HRT, at least 2-4 weeks will
   elapse between the cessation of therapy and the blood draw; this interval depends on
   the type and dosage of HRT. Following confirmation of their post-menopausal status,
   they can resume use of HRT during the study without use of a contraceptive method

   - Male subjects must not freeze or donate sperm starting at Screening and throughout the
   study period, and at least 4 months after the final study drug administration.
   Preservation of sperm should be considered prior to enrolment in this study

   - Female subjects must not donate, or retrieve for their own use, ova from the time of
   Screening and throughout the study treatment period, and for at least 7 months after
   the final study drug administration

   - Patients receiving corticosteroids who have not been on a stable or decreasing dose of
   corticosteroid for at least 7 days prior to enrollment are not eligible. If used to
   modify immune adverse events related to prior therapy, >= 14 days must have elapsed
   since last dose of corticosteroid

   - Patients who are currently receiving another investigational drug are not eligible

   - Patients who are currently receiving other anti-cancer agents are not eligible

   - Patients who are receiving cyclosporine, tacrolimus or other agents to prevent
   graft-versus-host disease post bone marrow transplant are not eligible for this trial

   - Patients who are receiving chloroquine or hydroxychloroquine within 14 days are not
   eligible for this trial

   - Patients who have received a prior solid organ transplantation are not eligible

   - Patients with a medical history of myocardial infarction within 180 days before
   enrollment, symptomatic congestive heart failure (CHF) (New York Heart Association
   Class II to IV) or troponin levels consistent with myocardial infarction as defined
   according to the manufacturer 28 days prior to enrollment are not eligible

   - Patients who have a pleural effusion, ascites or pericardial effusion that requires
   drainage, peritoneal shunt, or Cell-free and Concentrated Ascites Reinfusion Therapy
   (CART) are not eligible

   - Patients who have spinal cord compression or clinically active central nervous system
   metastases, defined as untreated and symptomatic, or requiring therapy with
   corticosteroids or anticonvulsants to control associated symptoms are not eligible

   - Patients with a known history of severe hypersensitivity to DS-8201a or any excipient
   contained in the DS-8201a drug formulation are not eligible

   - Patients who have an uncontrolled infection or non-healing surgical site are not
   eligible

   - Patients with a known history of substance abuse or any other clinically significant
   medical conditions (i.e. psychological conditions) that may, in the opinion of the
   investigator, interfere with the patient's participation in the clinical study or
   evaluation of the clinical study results are not eligible

   - Patients who have pulmonary compromise, ex hypoxia, resulting from intercurrent
   pulmonary illnesses including, but not limited to, any underlying pulmonary disorder
   (i.e. pulmonary emboli within three months of the study enrollment, severe asthma,
   severe chronic obstructive pulmonary disease (COPD), restrictive lung disease, pleural
   effusion etc.), or prior pneumonectomy are not eligible

   - Patients who have a history of (non-infectious) ILD (interstitial lung
   disease)/pneumonitis that required steroids, has current ILD/pneumonitis, or where
   suspected ILD/pneumonitis cannot be ruled out by imaging at screening are not eligible

   - Patients who have a pleural effusion, ascites or pericardial effusion that requires
   drainage, peritoneal shunt, or cell-free and concentrated ascites reinfusion therapy
   (CART) are not eligible. (Drainage and CART are not allowed within 2 weeks prior to
   screening assessment)

   - Patients who, in the opinion of the investigator, may not be able to comply with the
   safety monitoring requirements of the study are not eligible

Ages Eligible for Study

12 Years - 39 Years

Genders Eligible for Study

All

Now accepting new patients

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Nancy Sweeters
+1 650-721-4074
Recruiting