{
"info": {
"nct_id": "NCT01604031",
"official_title": "Treatment of B-CLL With Autologous IL2 and CD40 Ligand-Expressing Tumor Cells + Lenalidomide",
"inclusion_criteria": "ELIGIBILITY FOR BLAST COLLECTION (procurement):\n\n* Patients with B-CLL (not in Richter's transformation) with measurable disease.\n* Procurement consent signed and faxed to Research Coordinator\n* HIV negative (can be pending at this time)\n\nELIGIBILITY FOR VACCINE AND LENALIDOMIDE ADMINISTRATION (protocol entry):\n\n* Manipulated B-CLL cells available (at least 6 injections)\n* Patients with B-CLL (not in Richter's transformation) with measurable disease\n* Patients must have a life expectancy of at least 10 weeks.\n* Patients must be less than 75 years old\n* Patients must have ECOG performance status of 0-2.\n* Patients must have recovered from the toxic effects of all prior chemotherapy before entering this study:\n* Absolute neutrophil count (ANC) of greater than or equal to 500/microL\n* Absolute lymphocyte count (ALC) greater than or equal 200/microL,\n* Hemoglobin greater than or equal 8 g/dL\n* Platelet count greater than or equal 50,000/microL.\n* Patients must be willing to practice appropriate birth control methods during the study and for 28 days after their participation in the treatment portion of the study is concluded.\n* Patients must have adequate liver function:\n* Total bilirubin less than or equal to 1.5 mg/dl, SGOT less than or equal to 3 times normal\n* Normal prothrombin time\n* Patients must have adequate renal function (creatinine clearance greater than 50 ml/min).\n* Patients provide informed consent.\n* Patient must not have received treatment with other investigational agents within the last 4 weeks.\n* All study participants (treatment) must be registered in the REMS® Program and be willing to comply with the requirements of REMS® .\n\nNote: A female of childbearing potential is a sexually mature female who: 1) has not undergone a hysterectomy or bilateral oophorectomy; or 2) has not been naturally postmenopausal (amenorrhea following cancer therapy does not rule out childbearing potential) for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months).\nHealthy volunteers allowed\nMust have minimum age of 18 Years\nMust have maximum age of 75 Years",
"exclusion_criteria": "EXCLUSION CRITERIA FOR VACCINE ADMINISTRATION (protocol entry):\n\n* Infected at time of protocol entry, or receiving antibiotics (other than prophylactic trimethoprim sulfamethoxazole).\n* Pregnant or lactating\n* Suffering from an autoimmune disease (including refractory immune thrombocytopenia-ITP or refractory autoimmune hemolytic anemia-AIHA)\n* Receiving immunosuppressive drugs.\n* Received systemic steroids within 30 days of study enrollment\n* Autologous hematopoietic stem cell transplant or fludarabine chemotherapy within 6 months of study enrollment\n* History of allogeneic stem cell transplant\n* Patients with congestive heart failure or significant arrhythmia\n* Known hypersensitivity to thalidomide or lenalidomide.",
"miscellaneous_criteria": ""
},
"inclusion_lines": [
{
"identified_line": {
"line": "ELIGIBILITY FOR BLAST COLLECTION (procurement):",
"criterions": [
{
"exact_snippets": "ELIGIBILITY FOR BLAST COLLECTION (procurement)",
"criterion": "blast collection eligibility",
"requirement": {
"requirement_type": "eligibility",
"expected_value": true
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"exact_snippets": "ELIGIBILITY FOR BLAST COLLECTION (procurement)",
"criterion": "blast collection eligibility",
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"expected_value": true
}
}
]
}
},
{
"identified_line": {
"line": "* Procurement consent signed and faxed to Research Coordinator",
"criterions": [
{
"exact_snippets": "Procurement consent signed",
"criterion": "procurement consent",
"requirement": {
"requirement_type": "signed",
"expected_value": true
}
},
{
"exact_snippets": "faxed to Research Coordinator",
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"requirement": {
"requirement_type": "faxed",
"expected_value": true
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"exact_snippets": "Procurement consent signed",
"criterion": "procurement consent",
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"requirement_type": "signed",
"expected_value": true
}
},
{
"exact_snippets": "faxed to Research Coordinator",
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"requirement": {
"requirement_type": "faxed",
"expected_value": true
}
}
]
}
},
{
"identified_line": {
"line": "* HIV negative (can be pending at this time)",
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{
"exact_snippets": "HIV negative",
"criterion": "HIV status",
"requirement": {
"requirement_type": "status",
"expected_value": "negative"
}
}
]
},
"logical_structure": {
"and_criteria": [
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"exact_snippets": "HIV negative",
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}
}
]
}
},
{
"identified_line": {
"line": "ELIGIBILITY FOR VACCINE AND LENALIDOMIDE ADMINISTRATION (protocol entry):",
"criterions": [
{
"exact_snippets": "ELIGIBILITY FOR VACCINE",
"criterion": "vaccine eligibility",
"requirement": {
"requirement_type": "eligibility",
"expected_value": true
}
},
{
"exact_snippets": "ELIGIBILITY FOR ... LENALIDOMIDE ADMINISTRATION",
"criterion": "lenalidomide administration eligibility",
"requirement": {
"requirement_type": "eligibility",
"expected_value": true
}
}
]
},
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"exact_snippets": "ELIGIBILITY FOR VACCINE",
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"expected_value": true
}
},
{
"exact_snippets": "ELIGIBILITY FOR ... LENALIDOMIDE ADMINISTRATION",
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"expected_value": true
}
}
]
}
},
{
"identified_line": {
"line": "* Manipulated B-CLL cells available (at least 6 injections)",
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{
"exact_snippets": "Manipulated B-CLL cells available",
"criterion": "manipulated B-CLL cells",
"requirement": {
"requirement_type": "availability",
"expected_value": true
}
},
{
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"criterion": "injections",
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"expected_value": {
"operator": ">=",
"value": 6,
"unit": "injections"
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}
}
]
},
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"expected_value": true
}
},
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"operator": ">=",
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"unit": "injections"
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}
}
]
}
},
{
"identified_line": {
"line": "* Patients must have a life expectancy of at least 10 weeks.",
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{
"exact_snippets": "life expectancy of at least 10 weeks",
"criterion": "life expectancy",
"requirement": {
"requirement_type": "duration",
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"operator": ">=",
"value": 10,
"unit": "weeks"
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}
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"operator": ">=",
"value": 10,
"unit": "weeks"
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}
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}
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{
"identified_line": {
"line": "* Patients must be less than 75 years old",
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{
"exact_snippets": "less than 75 years old",
"criterion": "age",
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"expected_value": {
"operator": "<",
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"unit": "years"
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}
}
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"operator": "<",
"value": 75,
"unit": "years"
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}
}
]
}
},
{
"identified_line": {
"line": "* Patients must have ECOG performance status of 0-2.",
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{
"exact_snippets": "ECOG performance status of 0-2",
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"requirement": {
"requirement_type": "range",
"expected_value": {
"comparisons": [
{
"operator": ">=",
"value": 0,
"unit": "N/A"
},
{
"operator": "<=",
"value": 2,
"unit": "N/A"
}
]
}
}
}
]
},
"logical_structure": {
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{
"exact_snippets": "ECOG performance status of 0-2",
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"comparisons": [
{
"operator": ">=",
"value": 0,
"unit": "N/A"
},
{
"operator": "<=",
"value": 2,
"unit": "N/A"
}
]
}
}
}
]
}
},
{
"identified_line": {
"line": "* Patients must have recovered from the toxic effects of all prior chemotherapy before entering this study:",
"criterions": [
{
"exact_snippets": "recovered from the toxic effects of all prior chemotherapy",
"criterion": "recovery from prior chemotherapy toxicity",
"requirement": {
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"expected_value": "recovered"
}
}
]
},
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"exact_snippets": "recovered from the toxic effects of all prior chemotherapy",
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}
}
]
}
},
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"identified_line": {
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{
"exact_snippets": "Absolute neutrophil count (ANC) of greater than or equal to 500/microL",
"criterion": "absolute neutrophil count (ANC)",
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"operator": ">=",
"value": 500,
"unit": "microL"
}
}
}
]
},
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"exact_snippets": "Absolute neutrophil count (ANC) of greater than or equal to 500/microL",
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"unit": "microL"
}
}
}
]
}
},
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"identified_line": {
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{
"exact_snippets": "Absolute lymphocyte count (ALC) greater than or equal 200/microL",
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"operator": ">=",
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"unit": "microL"
}
}
}
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"unit": "microL"
}
}
}
]
}
},
{
"identified_line": {
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{
"exact_snippets": "Hemoglobin greater than or equal 8 g/dL",
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"operator": ">=",
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"unit": "g/dL"
}
}
}
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}
}
}
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"operator": ">=",
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}
}
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"operator": ">=",
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"unit": "microL"
}
}
}
]
}
},
{
"identified_line": {
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}
},
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"exact_snippets": "during the study and for 28 days after their participation in the treatment portion of the study is concluded",
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}
}
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},
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{
"exact_snippets": "Total bilirubin less than or equal to 1.5 mg/dl",
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"operator": "<=",
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"unit": "mg/dl"
}
}
},
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}
}
}
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"exact_snippets": "Total bilirubin less than or equal to 1.5 mg/dl",
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}
}
},
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"exact_snippets": "SGOT less than or equal to 3 times normal",
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}
}
}
]
}
},
{
"identified_line": {
"line": "* Normal prothrombin time",
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"exact_snippets": "Normal prothrombin time",
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}
}
]
},
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"exact_snippets": "Normal prothrombin time",
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}
}
]
}
},
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"identified_line": {
"line": "* Patients must have adequate renal function (creatinine clearance greater than 50 ml/min).",
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{
"exact_snippets": "adequate renal function (creatinine clearance greater than 50 ml/min)",
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"operator": ">",
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}
}
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]
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"exact_snippets": "adequate renal function (creatinine clearance greater than 50 ml/min)",
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}
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{
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"identified_line": {
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"exact_snippets": "Patient must not have received treatment with other investigational agents within the last 4 weeks.",
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"operator": ">=",
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"unit": "weeks"
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}
}
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}
}
}
},
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"identified_line": {
"line": "* All study participants (treatment) must be registered in the REMS® Program and be willing to comply with the requirements of REMS® .",
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}
},
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"exact_snippets": "be willing to comply with the requirements of REMS®",
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}
},
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{
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}
}
]
},
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}
}
}
},
{
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}
},
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}
},
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}
}
]
}
]
}
},
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"identified_line": {
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{
"exact_snippets": "Suffering from an autoimmune disease",
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"requirement_type": "presence",
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}
},
{
"exact_snippets": "refractory immune thrombocytopenia-ITP",
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"requirement_type": "presence",
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}
},
{
"exact_snippets": "refractory autoimmune hemolytic anemia-AIHA",
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"requirement_type": "presence",
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}
}
]
},
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{
"and_criteria": [
{
"exact_snippets": "Suffering from an autoimmune disease",
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}
},
{
"exact_snippets": "refractory immune thrombocytopenia-ITP",
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"requirement_type": "presence",
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}
}
]
},
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},
{
"exact_snippets": "refractory autoimmune hemolytic anemia-AIHA",
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"requirement_type": "presence",
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}
}
]
}
]
}
},
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"identified_line": {
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"exact_snippets": "Receiving immunosuppressive drugs",
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"requirement_type": "presence",
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}
}
]
},
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"exact_snippets": "Receiving immunosuppressive drugs",
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"requirement_type": "presence",
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}
}
}
},
{
"identified_line": {
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{
"exact_snippets": "Received systemic steroids within 30 days of study enrollment",
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"requirement_type": "time frame",
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"operator": "<=",
"value": 30,
"unit": "days"
}
}
}
]
},
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"exact_snippets": "Received systemic steroids within 30 days of study enrollment",
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"requirement_type": "time frame",
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"operator": "<=",
"value": 30,
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}
}
}
}
},
{
"identified_line": {
"line": "* Autologous hematopoietic stem cell transplant or fludarabine chemotherapy within 6 months of study enrollment",
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{
"exact_snippets": "Autologous hematopoietic stem cell transplant ... within 6 months of study enrollment",
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"requirement_type": "time since procedure",
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"operator": "<=",
"value": 6,
"unit": "months"
}
}
},
{
"exact_snippets": "fludarabine chemotherapy within 6 months of study enrollment",
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"requirement_type": "time since procedure",
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"operator": "<=",
"value": 6,
"unit": "months"
}
}
}
]
},
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{
"and_criteria": [
{
"exact_snippets": "Autologous hematopoietic stem cell transplant ... within 6 months of study enrollment",
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"requirement_type": "time since procedure",
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"operator": "<=",
"value": 6,
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}
}
}
]
},
{
"and_criteria": [
{
"exact_snippets": "fludarabine chemotherapy within 6 months of study enrollment",
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"requirement_type": "time since procedure",
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"operator": "<=",
"value": 6,
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}
}
}
]
}
]
}
},
{
"identified_line": {
"line": "* History of allogeneic stem cell transplant",
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{
"exact_snippets": "History of allogeneic stem cell transplant",
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"requirement": {
"requirement_type": "history",
"expected_value": true
}
}
]
},
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"exact_snippets": "History of allogeneic stem cell transplant",
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"requirement_type": "history",
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}
}
}
},
{
"identified_line": {
"line": "* Patients with congestive heart failure or significant arrhythmia",
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{
"exact_snippets": "Patients with congestive heart failure",
"criterion": "congestive heart failure",
"requirement": {
"requirement_type": "presence",
"expected_value": false
}
},
{
"exact_snippets": "significant arrhythmia",
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"requirement_type": "severity",
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}
]
},
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{
"exact_snippets": "Patients with congestive heart failure",
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"requirement_type": "presence",
"expected_value": false
}
},
{
"exact_snippets": "significant arrhythmia",
"criterion": "arrhythmia",
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"requirement_type": "severity",
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}
}
]
}
},
{
"identified_line": {
"line": "* Known hypersensitivity to thalidomide or lenalidomide.",
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{
"exact_snippets": "Known hypersensitivity to thalidomide",
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"requirement_type": "presence",
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}
},
{
"exact_snippets": "Known hypersensitivity to ... lenalidomide",
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"requirement_type": "presence",
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}
]
},
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"exact_snippets": "Known hypersensitivity to thalidomide",
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"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "Known hypersensitivity to ... lenalidomide",
"criterion": "hypersensitivity to lenalidomide",
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"requirement_type": "presence",
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}
]
}
}
],
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{
"identified_line": {
"line": "* Patients with B-CLL (not in Richter's transformation) with measurable disease.",
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{
"exact_snippets": "Patients with B-CLL",
"criterion": "B-CLL",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "not in Richter's transformation",
"criterion": "Richter's transformation",
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"requirement_type": "presence",
"expected_value": false
}
},
{
"exact_snippets": "measurable disease",
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"requirement_type": "measurability",
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}
]
},
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"and_criteria": [
{
"and_criteria": [
{
"exact_snippets": "Patients with B-CLL",
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}
},
{
"not_criteria": {
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"requirement_type": "presence",
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}
}
}
]
},
{
"exact_snippets": "measurable disease",
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]
}
},
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}
},
{
"exact_snippets": "not in Richter's transformation",
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"requirement_type": "presence",
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}
},
{
"exact_snippets": "measurable disease",
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},
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"and_criteria": [
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"exact_snippets": "Patients with B-CLL",
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{
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]
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]
}
},
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"identified_line": {
"line": "Note: A female of childbearing potential is a sexually mature female who: 1) has not undergone a hysterectomy or bilateral oophorectomy; or 2) has not been naturally postmenopausal (amenorrhea following cancer therapy does not rule out childbearing potential) for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months).",
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}
},
{
"exact_snippets": "bilateral oophorectomy",
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"requirement_type": "presence",
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}
},
{
"exact_snippets": "has not been naturally postmenopausal",
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"requirement_type": "status",
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}
},
{
"exact_snippets": "amenorrhea following cancer therapy does not rule out childbearing potential",
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"requirement_type": "impact on childbearing potential",
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}
},
{
"exact_snippets": "for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months)",
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"requirement_type": "occurrence",
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{
"operator": "<",
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"unit": "months"
}
]
}
}
}
]
},
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"requirement_type": "presence",
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},
{
"exact_snippets": "bilateral oophorectomy",
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}
}
]
},
{
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}
},
{
"exact_snippets": "for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months)",
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{
"operator": "<",
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]
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]
}
}
],
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{
"identified_line": {
"line": "* Pregnant or lactating",
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{
"exact_snippets": "Pregnant",
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"requirement_type": "presence",
"expected_value": false
}
},
{
"exact_snippets": "lactating",
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"requirement_type": "presence",
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}
}
]
},
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"exact_snippets": "Pregnant",
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}
},
{
"exact_snippets": "lactating",
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}
}
]
}
}
],
"failed_miscellaneous": []
}