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Cyproheptadine in Preventing Weight Loss in Children Receiving Chemotherapy for Cancer

Primary Purpose

Cancer

Status
Terminated
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
cyproheptadine hydrochloride
placebo
Sponsored by
University of South Florida
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Cancer focused on measuring cachexia, weight changes, nausea and vomiting, alveolar childhood rhabdomyosarcoma, anaplastic osteosarcoma, childhood alveolar soft-part sarcoma, childhood angiosarcoma, childhood epithelioid sarcoma, childhood fibrosarcoma, childhood gliosarcoma, childhood leiomyosarcoma, childhood liposarcoma, childhood neurofibrosarcoma, childhood synovial sarcoma, chondrosarcoma, chondrosarcomatous osteosarcoma, clear cell sarcoma of the kidney, embryonal childhood rhabdomyosarcoma, embryonal-botryoid childhood rhabdomyosarcoma, endometrial stromal sarcoma, extraosseous Ewing sarcoma, peripheral primitive neuroectodermal tumor, fibrosarcomatous osteosarcoma, localized Ewing sarcoma, localized osteosarcoma, mast cell sarcoma, metastatic childhood soft tissue sarcoma, metastatic Ewing sarcoma, metastatic osteosarcoma, mixed childhood rhabdomyosarcoma, mixed osteosarcoma, nonmetastatic childhood soft tissue sarcoma, osteoblastic osteosarcoma, ovarian carcinosarcoma, ovarian sarcoma, pleomorphic childhood rhabdomyosarcoma, previously treated childhood rhabdomyosarcoma, previously untreated childhood rhabdomyosarcoma, recurrent adult soft tissue sarcoma, recurrent childhood gliosarcoma, recurrent childhood rhabdomyosarcoma, recurrent childhood soft tissue sarcoma, recurrent Ewing sarcoma, recurrent osteosarcoma, recurrent uterine sarcoma, small intestine leiomyosarcoma, stage I uterine sarcoma, stage II uterine sarcoma, stage III uterine sarcoma, stage IV uterine sarcoma, telangiectatic osteosarcoma, untreated childhood gliosarcoma, uterine carcinosarcoma, uterine leiomyosarcoma, localized resectable neuroblastoma, localized unresectable neuroblastoma, recurrent neuroblastoma, regional neuroblastoma, stage 4S neuroblastoma, recurrent Wilms tumor, childhood kidney tumors, stage III Wilms tumor, stage IV Wilms tumor, childhood hepatoblastoma, childhood extracranial germ cell tumor, childhood extragonadal germ cell tumor, childhood gonadal germ cell tumor, childhood malignant ovarian germ cell tumor, childhood malignant testicular germ cell tumor, recurrent childhood malignant germ cell tumor, recurrent extragonadal germ cell tumor, recurrent extragonadal non-seminomatous germ cell tumor, recurrent malignant testicular germ cell tumor, recurrent ovarian germ cell tumor, stage III extragonadal non-seminomatous germ cell tumor, stage III malignant testicular germ cell tumor, stage IIIA ovarian germ cell tumor, stage IIIB ovarian germ cell tumor, stage IIIC ovarian germ cell tumor, stage IV extragonadal non-seminomatous germ cell tumor, stage IV ovarian germ cell tumor, recurrent childhood medulloblastoma, untreated childhood medulloblastoma, childhood ependymoblastoma, childhood infratentorial ependymoma, newly diagnosed childhood ependymoma, recurrent childhood ependymoma, recurrent childhood subependymal giant cell astrocytoma, untreated childhood subependymal giant cell astrocytoma, peripheral primitive neuroectodermal tumor of the kidney, childhood supratentorial primitive neuroectodermal tumor, recurrent childhood brain stem glioma, recurrent childhood brain tumor, untreated childhood brain stem glioma, recurrent childhood anaplastic astrocytoma, recurrent childhood anaplastic oligoastrocytoma, recurrent childhood anaplastic oligodendroglioma, stage I childhood anaplastic large cell lymphoma, stage II childhood anaplastic large cell lymphoma, stage III childhood anaplastic large cell lymphoma, stage IV childhood anaplastic large cell lymphoma, untreated childhood anaplastic astrocytoma, untreated childhood anaplastic oligoastrocytoma, untreated childhood anaplastic oligodendroglioma, childhood high-grade cerebellar astrocytoma, childhood low-grade cerebellar astrocytoma, recurrent childhood astrocytoma, other tumor of glial origin, recurrent childhood cerebellar astrocytoma, recurrent childhood cerebral astrocytoma, recurrent childhood diffuse astrocytoma, recurrent childhood fibrillary astrocytoma, recurrent childhood gemistocytic astrocytoma, recurrent childhood oligoastrocytoma, recurrent childhood pilocytic astrocytoma, recurrent childhood pilomyxoid astrocytoma, recurrent childhood pleomorphic xanthoastrocytoma, recurrent childhood protoplasmic astrocytoma, untreated childhood cerebellar astrocytoma, untreated childhood cerebral astrocytoma, untreated childhood diffuse astrocytoma, untreated childhood fibrillary astrocytoma, untreated childhood gemistocytic astrocytoma, untreated childhood oligoastrocytoma, untreated childhood pilocytic astrocytoma, untreated childhood pilomyxoid astrocytoma, untreated childhood pleomorphic xanthoastrocytoma, untreated childhood protoplasmic astrocytoma, recurrent childhood gliomatosis cerebri, recurrent childhood oligodendroglioma, recurrent childhood visual pathway, hypothalamic glioma, recurrent childhood visual pathway glioma, untreated childhood gliomatosis cerebri, untreated childhood oligodendroglioma, untreated childhood visual pathway, untreated childhood visual pathway glioma, recurrent childhood giant cell glioblastoma, recurrent childhood glioblastoma, untreated childhood giant cell glioblastoma, untreated childhood glioblastoma, childhood choroid plexus tumor, childhood grade I meningioma, childhood grade II meningioma, childhood grade III meningioma, minimally differentiated myeloid leukemia (M0), myeloblastic leukemia with maturation (M2), myeloblastic leukemia without maturation (M1), childhood acute myelomonocytic leukemia (M4), childhood acute promyelocytic leukemia (M3), recurrent childhood acute myeloid leukemia, untreated childhood acute myeloid leukemia, other myeloid malignancies, childhood acute monoblastic leukemia (M5a), childhood acute monocytic leukemia (M5b), childhood acute erythroleukemia (M6), childhood acute megakaryocytic leukemia (M7), unspecified childhood solid tumor

Eligibility Criteria

2 Years - 21 Years (Child, Adult)All SexesDoes not accept healthy volunteers

INCLUSION CRITERIA:

  • ≥ 2 years and ≤ 21 years of age at the time of study entry
  • Scheduled to receive chemotherapy for:
  • Newly diagnosed:
  • Non-rhabdo soft tissue sarcomas, scheduled to receive chemotherapy, as well as intermediate or high-risk rhabdomyosarcoma, any stage osteosarcoma and any stage Ewing's sarcoma
  • Intermediate or high-risk neuroblastoma
  • Wilms' tumor (Stage III/IV)
  • Hepatoblastoma (Stage III/IV)
  • Germ cell tumors (Stage III/IV)
  • Brain tumors, including medulloblastoma, PNET and ependymomas
  • AML
  • Relapsed/recurrent disease (any patient)
  • Able to register and randomize within 28 days of starting chemotherapy (registration /randomization and start of study agent may occur at anytime up to and including Day 28 after the initiation of chemotherapy)

EXCLUSION CRITERIA:

  • ≥ 29 days after starting chemotherapy
  • Documented history of unintended weight loss ≥ 5% presumed secondary to cancer within 3 months of study entry
  • Currently taking cyproheptadine HCl (or have taken cyproheptadine HCl within 3 weeks of study registration)
  • History of anorexia nervosa or bulimia
  • Taking other appetite-stimulating medications, i.e. dronabinol (Marinol) during the past three weeks.
  • Initiation of other appetite enhancing agents, including steroids prescribed for the intent of weight gain, i.e. Megace. Note: Other forms of nutrition therapies, e.g. appetite-stimulating medications, TPN or enteral tube feedings are not allowed during this study.
  • Children receiving steroids for >7 days as part of their cancer treatment regimen are excluded from participation. However, intermittent steroid use in an antiemetic regimen is allowed during the study
  • Receiving monoamine oxidase (MAO) inhibitors, procarbazine, fluoxetine (Prozac), or paroxetine (Paxil)
  • Diagnosed with glaucoma, cystic fibrosis, inflammatory bowel disease, or GI/GU obstruction
  • Allergy to cyproheptadine HCl
  • Females of childbearing age must not be pregnant.
  • Female patients who are lactating must agree to stop breast-feeding.

Sites / Locations

  • Miller Children's Hospital
  • Connecticut Children's Medical Center
  • A.I. duPont Hospital for Children
  • Children's National Medical Center
  • Children's Hospital of Southwest Florida at Lee Memorial
  • Nemours Children's Clinic - Jacksonville
  • Arnold Palmer Hospital for Children
  • Nemours Children's Clinic - Orlando
  • Nemours Children's Hospital Pensacola
  • Kapiolani Medical Center for Women and Children
  • Ochsner Clinic Foundation
  • Columbia University Medical Center
  • CHRISTUS Santa Rosa Children's Hospital
  • Children's Hospital of The King's Daughters

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Arm I cyproheptadine hydrochloride

Arm II placebo

Arm Description

Patients receive oral cyproheptadine hydrochloride twice daily for 8 weeks.

Patients receive an oral placebo twice daily for 8 weeks.

Outcomes

Primary Outcome Measures

Participant With Weight Loss ≥ 5% at the 8- Week Assessment When Compared to Baseline
Severity of Weight Loss
Change from Baseline in Weight Z score

Secondary Outcome Measures

Pattern of Weight in the Study Population
Change from Baseline in Weight

Full Information

First Posted
May 26, 2010
Last Updated
June 4, 2015
Sponsor
University of South Florida
Collaborators
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT01132547
Brief Title
Cyproheptadine in Preventing Weight Loss in Children Receiving Chemotherapy for Cancer
Official Title
Prevention of Cancer/Treatment-Related Weight Loss in Children at High Nutritional Risk
Study Type
Interventional

2. Study Status

Record Verification Date
June 2015
Overall Recruitment Status
Terminated
Why Stopped
The study was terminated due to slow accrual.
Study Start Date
June 2010 (undefined)
Primary Completion Date
January 2014 (Actual)
Study Completion Date
January 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of South Florida
Collaborators
National Cancer Institute (NCI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
RATIONALE: Cyproheptadine hydrochloride may prevent weight loss caused by cancer or cancer treatment. It is not yet known whether cyproheptadine is more effective than a placebo in preventing weight loss in young patients receiving chemotherapy for cancer. PURPOSE: This randomized phase III trial is studying cyproheptadine hydrochloride to see how well it works in preventing weight loss in young patients receiving chemotherapy for cancer.
Detailed Description
OBJECTIVES: Primary To determine the effect of cyproheptadine hydrochloride in the prevention of cancer- or treatment-related weight loss (defined as ≥ 5% reduction in weight from baseline measurement) in children who are initiating a course of moderately or highly emetic chemotherapy. Secondary To investigate the effect of cyproheptadine HCl on the change in weight for age scores after 8 weeks of study drug administration in comparison to placebo. Investigate the relationship between the secondary outcome variables (prealbumin, triceps skin fold, mid-upper arm circumference, and weight loss)from baseline to end of treatment in each group (treatment and placebo) separately. OUTLINE: This is a multicenter study. Patients are stratified according to enrolling center and steroid use with cancer treatment (yes vs no). Study agent can start anytime up to and including day 28 after the first dose of chemotherapy. Arm I: Patients receive oral cyproheptadine hydrochloride twice daily for 8 weeks. Arm II: Patients receive an oral placebo twice daily for 8 weeks. Patients undergo weight and height measurements at baseline and at each follow-up visit in weeks 4 and 8 to evaluate the effect of cyproheptadine hydrochloride and duration of response. Patients or parents complete medicine logs at each follow-up visit in weeks 4 and 8 to evaluate drug compliance and tolerance. Patients also undergo measures of nutrition; and measures of body composition, lean body mass, and fat percentage using standardized equipment and procedures for measuring triceps skin fold and mid-arm muscle circumference at baseline and at the end of the study. Patients undergo blood sample collection at baseline and at the end of the study for biomarker studies. Samples are analyzed for pre-albumin levels.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer
Keywords
cachexia, weight changes, nausea and vomiting, alveolar childhood rhabdomyosarcoma, anaplastic osteosarcoma, childhood alveolar soft-part sarcoma, childhood angiosarcoma, childhood epithelioid sarcoma, childhood fibrosarcoma, childhood gliosarcoma, childhood leiomyosarcoma, childhood liposarcoma, childhood neurofibrosarcoma, childhood synovial sarcoma, chondrosarcoma, chondrosarcomatous osteosarcoma, clear cell sarcoma of the kidney, embryonal childhood rhabdomyosarcoma, embryonal-botryoid childhood rhabdomyosarcoma, endometrial stromal sarcoma, extraosseous Ewing sarcoma, peripheral primitive neuroectodermal tumor, fibrosarcomatous osteosarcoma, localized Ewing sarcoma, localized osteosarcoma, mast cell sarcoma, metastatic childhood soft tissue sarcoma, metastatic Ewing sarcoma, metastatic osteosarcoma, mixed childhood rhabdomyosarcoma, mixed osteosarcoma, nonmetastatic childhood soft tissue sarcoma, osteoblastic osteosarcoma, ovarian carcinosarcoma, ovarian sarcoma, pleomorphic childhood rhabdomyosarcoma, previously treated childhood rhabdomyosarcoma, previously untreated childhood rhabdomyosarcoma, recurrent adult soft tissue sarcoma, recurrent childhood gliosarcoma, recurrent childhood rhabdomyosarcoma, recurrent childhood soft tissue sarcoma, recurrent Ewing sarcoma, recurrent osteosarcoma, recurrent uterine sarcoma, small intestine leiomyosarcoma, stage I uterine sarcoma, stage II uterine sarcoma, stage III uterine sarcoma, stage IV uterine sarcoma, telangiectatic osteosarcoma, untreated childhood gliosarcoma, uterine carcinosarcoma, uterine leiomyosarcoma, localized resectable neuroblastoma, localized unresectable neuroblastoma, recurrent neuroblastoma, regional neuroblastoma, stage 4S neuroblastoma, recurrent Wilms tumor, childhood kidney tumors, stage III Wilms tumor, stage IV Wilms tumor, childhood hepatoblastoma, childhood extracranial germ cell tumor, childhood extragonadal germ cell tumor, childhood gonadal germ cell tumor, childhood malignant ovarian germ cell tumor, childhood malignant testicular germ cell tumor, recurrent childhood malignant germ cell tumor, recurrent extragonadal germ cell tumor, recurrent extragonadal non-seminomatous germ cell tumor, recurrent malignant testicular germ cell tumor, recurrent ovarian germ cell tumor, stage III extragonadal non-seminomatous germ cell tumor, stage III malignant testicular germ cell tumor, stage IIIA ovarian germ cell tumor, stage IIIB ovarian germ cell tumor, stage IIIC ovarian germ cell tumor, stage IV extragonadal non-seminomatous germ cell tumor, stage IV ovarian germ cell tumor, recurrent childhood medulloblastoma, untreated childhood medulloblastoma, childhood ependymoblastoma, childhood infratentorial ependymoma, newly diagnosed childhood ependymoma, recurrent childhood ependymoma, recurrent childhood subependymal giant cell astrocytoma, untreated childhood subependymal giant cell astrocytoma, peripheral primitive neuroectodermal tumor of the kidney, childhood supratentorial primitive neuroectodermal tumor, recurrent childhood brain stem glioma, recurrent childhood brain tumor, untreated childhood brain stem glioma, recurrent childhood anaplastic astrocytoma, recurrent childhood anaplastic oligoastrocytoma, recurrent childhood anaplastic oligodendroglioma, stage I childhood anaplastic large cell lymphoma, stage II childhood anaplastic large cell lymphoma, stage III childhood anaplastic large cell lymphoma, stage IV childhood anaplastic large cell lymphoma, untreated childhood anaplastic astrocytoma, untreated childhood anaplastic oligoastrocytoma, untreated childhood anaplastic oligodendroglioma, childhood high-grade cerebellar astrocytoma, childhood low-grade cerebellar astrocytoma, recurrent childhood astrocytoma, other tumor of glial origin, recurrent childhood cerebellar astrocytoma, recurrent childhood cerebral astrocytoma, recurrent childhood diffuse astrocytoma, recurrent childhood fibrillary astrocytoma, recurrent childhood gemistocytic astrocytoma, recurrent childhood oligoastrocytoma, recurrent childhood pilocytic astrocytoma, recurrent childhood pilomyxoid astrocytoma, recurrent childhood pleomorphic xanthoastrocytoma, recurrent childhood protoplasmic astrocytoma, untreated childhood cerebellar astrocytoma, untreated childhood cerebral astrocytoma, untreated childhood diffuse astrocytoma, untreated childhood fibrillary astrocytoma, untreated childhood gemistocytic astrocytoma, untreated childhood oligoastrocytoma, untreated childhood pilocytic astrocytoma, untreated childhood pilomyxoid astrocytoma, untreated childhood pleomorphic xanthoastrocytoma, untreated childhood protoplasmic astrocytoma, recurrent childhood gliomatosis cerebri, recurrent childhood oligodendroglioma, recurrent childhood visual pathway, hypothalamic glioma, recurrent childhood visual pathway glioma, untreated childhood gliomatosis cerebri, untreated childhood oligodendroglioma, untreated childhood visual pathway, untreated childhood visual pathway glioma, recurrent childhood giant cell glioblastoma, recurrent childhood glioblastoma, untreated childhood giant cell glioblastoma, untreated childhood glioblastoma, childhood choroid plexus tumor, childhood grade I meningioma, childhood grade II meningioma, childhood grade III meningioma, minimally differentiated myeloid leukemia (M0), myeloblastic leukemia with maturation (M2), myeloblastic leukemia without maturation (M1), childhood acute myelomonocytic leukemia (M4), childhood acute promyelocytic leukemia (M3), recurrent childhood acute myeloid leukemia, untreated childhood acute myeloid leukemia, other myeloid malignancies, childhood acute monoblastic leukemia (M5a), childhood acute monocytic leukemia (M5b), childhood acute erythroleukemia (M6), childhood acute megakaryocytic leukemia (M7), unspecified childhood solid tumor

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
22 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm I cyproheptadine hydrochloride
Arm Type
Experimental
Arm Description
Patients receive oral cyproheptadine hydrochloride twice daily for 8 weeks.
Arm Title
Arm II placebo
Arm Type
Placebo Comparator
Arm Description
Patients receive an oral placebo twice daily for 8 weeks.
Intervention Type
Drug
Intervention Name(s)
cyproheptadine hydrochloride
Other Intervention Name(s)
cyproheptadine HCl
Intervention Description
Given orally
Intervention Type
Other
Intervention Name(s)
placebo
Intervention Description
Given orally
Primary Outcome Measure Information:
Title
Participant With Weight Loss ≥ 5% at the 8- Week Assessment When Compared to Baseline
Time Frame
8 weeks
Title
Severity of Weight Loss
Description
Change from Baseline in Weight Z score
Time Frame
Baseline and 8 weeks
Secondary Outcome Measure Information:
Title
Pattern of Weight in the Study Population
Description
Change from Baseline in Weight
Time Frame
Baseline and 8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION CRITERIA: ≥ 2 years and ≤ 21 years of age at the time of study entry Scheduled to receive chemotherapy for: Newly diagnosed: Non-rhabdo soft tissue sarcomas, scheduled to receive chemotherapy, as well as intermediate or high-risk rhabdomyosarcoma, any stage osteosarcoma and any stage Ewing's sarcoma Intermediate or high-risk neuroblastoma Wilms' tumor (Stage III/IV) Hepatoblastoma (Stage III/IV) Germ cell tumors (Stage III/IV) Brain tumors, including medulloblastoma, PNET and ependymomas AML Relapsed/recurrent disease (any patient) Able to register and randomize within 28 days of starting chemotherapy (registration /randomization and start of study agent may occur at anytime up to and including Day 28 after the initiation of chemotherapy) EXCLUSION CRITERIA: ≥ 29 days after starting chemotherapy Documented history of unintended weight loss ≥ 5% presumed secondary to cancer within 3 months of study entry Currently taking cyproheptadine HCl (or have taken cyproheptadine HCl within 3 weeks of study registration) History of anorexia nervosa or bulimia Taking other appetite-stimulating medications, i.e. dronabinol (Marinol) during the past three weeks. Initiation of other appetite enhancing agents, including steroids prescribed for the intent of weight gain, i.e. Megace. Note: Other forms of nutrition therapies, e.g. appetite-stimulating medications, TPN or enteral tube feedings are not allowed during this study. Children receiving steroids for >7 days as part of their cancer treatment regimen are excluded from participation. However, intermittent steroid use in an antiemetic regimen is allowed during the study Receiving monoamine oxidase (MAO) inhibitors, procarbazine, fluoxetine (Prozac), or paroxetine (Paxil) Diagnosed with glaucoma, cystic fibrosis, inflammatory bowel disease, or GI/GU obstruction Allergy to cyproheptadine HCl Females of childbearing age must not be pregnant. Female patients who are lactating must agree to stop breast-feeding.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey P. Krischer, PhD
Organizational Affiliation
University of South Florida
Official's Role
Principal Investigator
Facility Information:
Facility Name
Miller Children's Hospital
City
Long Beach
State/Province
California
ZIP/Postal Code
90806
Country
United States
Facility Name
Connecticut Children's Medical Center
City
Hartford
State/Province
Connecticut
ZIP/Postal Code
06106
Country
United States
Facility Name
A.I. duPont Hospital for Children
City
Wilmington
State/Province
Delaware
ZIP/Postal Code
19803
Country
United States
Facility Name
Children's National Medical Center
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20010
Country
United States
Facility Name
Children's Hospital of Southwest Florida at Lee Memorial
City
Fort Myers
State/Province
Florida
ZIP/Postal Code
33908
Country
United States
Facility Name
Nemours Children's Clinic - Jacksonville
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32207-8482
Country
United States
Facility Name
Arnold Palmer Hospital for Children
City
Orlando
State/Province
Florida
ZIP/Postal Code
32806
Country
United States
Facility Name
Nemours Children's Clinic - Orlando
City
Orlando
State/Province
Florida
ZIP/Postal Code
32806
Country
United States
Facility Name
Nemours Children's Hospital Pensacola
City
Pensacola
State/Province
Florida
ZIP/Postal Code
32504
Country
United States
Facility Name
Kapiolani Medical Center for Women and Children
City
Honolulu
State/Province
Hawaii
ZIP/Postal Code
96826
Country
United States
Facility Name
Ochsner Clinic Foundation
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70121
Country
United States
Facility Name
Columbia University Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Facility Name
CHRISTUS Santa Rosa Children's Hospital
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78207
Country
United States
Facility Name
Children's Hospital of The King's Daughters
City
Norfolk
State/Province
Virginia
ZIP/Postal Code
23507
Country
United States

12. IPD Sharing Statement

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Cyproheptadine in Preventing Weight Loss in Children Receiving Chemotherapy for Cancer

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