ANC / Platelet Recovery

Getting Started
- Manual Reference Diagram
- Providing Feedback
- Historical Manual Updates
General Instructions
- Introduction
- Key Fields & Signature Lines
- General Guidelines for Completing Forms
Recipient Assignment, Indication, and Information Manuals
- 2804: CIBMTR Research ID Assignment Form
- 2807: Race, Ethnicity and Ancestry (REA)
  - Q1 – 2: Geographic Ancestry
- 2814: Indication for CIBMTR Data Reporting
- 2820: Recipient Contact Information
Transplant Essential Data (TED) Manuals
- 2400: Pre-TED
- 2402: Disease Classification
- 2450: Post-TED
Comprehensive Baseline & Follow-up Manuals
- 2000: Recipient Baseline
- 2004: Infectious Disease Markers
  - Q1: Donor / Cord Blood Unit Identification
  - Q2 – 28: Infectious Disease Markers
- 2005: Confirmation of HLA Typing
- 2006: Hematopoietic Stem Cell Transplant (HCT) Infusion
- 2100: Post-Infusion Follow-Up
Comprehensive Disease-Specific Manuals
- 2010/2110: Acute Myelogenous Leukemia (AML)
  - AML Response Criteria
  - 2010: AML Pre-Infusion
  - 2110: AML Post-Infusion
- 2011/2111: Acute Lymphoblastic Leukemia (ALL)
  - ALL Response Criteria
  - 2011: ALL Pre-Infusion
  - 2111: ALL Post-Infusion
- 2012/2112: Chronic Myeloid Leukemia (CML)
  - CML Response Criteria
  - 2012: CML Pre-Infusion Data
  - 2112: CML Post-Infusion Data
- 2013/2113: Chronic Lymphocytic Leukemia (CLL)
  - CLL Response Criteria
  - 2013: CLL Pre-Infusion
  - 2113: CLL Post-Infusion
- 2014/2114: Myelodysplastic Syndrome (MDS)
  - MDS Response Criteria
  - 2014: Myelodysplastic Syndrome (MDS) Pre-Infusion
  - 2114: Myelodysplastic Syndrome (MDS) Post-Infusion
- 2015/2115: Juvenile Myelomonocytic Leukemia (JMML)
  - JMML Response Criteria
  - 2015: JMML Pre-HCT
  - 2115: JMML Post HCT
- 2016/2116: Plasma Cell Disorders (PCD)
  - Multiple Myeloma Response Criteria
  - Plasma Cell Leukemia Response Criteria
  - POEMS Response Criteria
  - Amyloidosis Response Criteria
    - New York Heart Association Function Classifications
  - 2016: PCD Pre-Infusion
  - 2116: PCD Post-Infusion
- 2018/2118: Hodgkin and Non-Hodgkin Lymphoma
  - Lymphoma Response Criteria
  - 2018: LYM Pre-Infusion
  - 2118: LYM Post-Infusion
- 2019/2119: Waldenström’s Macroglobulinemia (WM)
  - Waldenstrom’s Macroglobulinemia Response Criteria
  - 2019: WM Pre-HCT
  - 2119: WM Post-HCT
- 2026/2126: Neuroblastoma
  - Neuroblastoma Response Criteria
  - 2026: Neuroblastoma Pre-Infusion
  - 2126: Neuroblastoma Post-Infusion
    - Q1 – 159: Disease Assessments at Time of Best Response to HSCT
- 2028/2128: Aplastic Anemia
  - 2028: Aplastic Anemia Pre-Infusion
  - 2128: Aplastic Anemia Post-HCT
    - Q1-25: Disease Assessment at the Time of Assessment for This Reporting Period
- 2029/2129: Fanconi Anemia / Constitutional Anemia
  - 2029: Fanconi Anemia / Constitutional Anemia Pre-HCT
  - 2129: Fanconi Anemia / Constitutional Anemia Post-HCT
    - Q1 – 6: Current Hematologic Parameters
- 2030/2130: Sickle Cell Disease (SCD)
  - 2030: SCD Pre-Infusion
  - 2130: SCD Post-Infusion
- 2031/2131: Immune Deficiencies (ID)
  - 2031: ID Pre-HCT
  - 2131: ID Post-HCT
- 2033/2133: Wiskott-Aldrich Syndome (WAS)
  - 2033: WAS Pre-HCT
  - 2133: WAS Post-HCT
- 2034/2134: X-Linked Lymphoproliferative Sydrome (XLP)
  - 2034: XLP Pre-HCT
  - 2134: XLP Post-HCT
- 2037 / 2137 Leukodystrophies
  - 2037: Leukodystrophies Pre-Infusion
  - 2137: Leukodystrophies Post-Infusion
- 2039/2139: Hemophagocytic Lymphohistiocytosis (HLH)
  - 2039: HLH Pre-HCT
  - 2139: HLH Post-HCT
    - Q1-32: Disease Assessment Since the Date of Last Report
- 2057/2157 Myeloproliferative Neoplasms (MPN)
  - MPN Response Criteria
  - 2057: Myeloproliferative Neoplasm (MPN) Pre-Infusion
  - 2157: Myeloproliferative Neoplasm (MPN) Post-Infusion
- 2058/2158: Thalassemia
  - 2058: Thalassemia Pre-Infusion
  - 2158: Thalassemia Post-Infusion
- 2059/3507: Solid Tumor
  - RECIST criteria
  - 2059: Solid Tumor Pre-Infusion
  - 3507: Solid Tumor Response
Cellular Therapy Manuals
- 4000: Cellular Therapy Essential Data Pre-Infusion
- 4001: Pre-Cellular Therapy Baseline Data
- 4003: Cellular Therapy Product
- 4006: Cellular Therapy Infusion
  - Q1-31: Product Identification
  - Q32-35: Concomitant Therapy
- 4100: Cellular Therapy Essential Data Follow-Up
- 4101: Post-Cellular Therapy Follow-Up
Gene Therapy Manuals
- 2003: Gene Therapy Product
- 2103: Persistence of Gene Therapy Product
  - Q1 – 18: Persistence of Gene Therapy Product
Infection & Miscellaneous Manuals
- 2046 / 2146: Fungal Infection
  - 2046: Fungal Infection Pre-Infusion Data
    - Q1-25: Infection Episode
    - Q26-31: Treatment of Infection
  - 2146: Fungal Infection Post-Infusion Data
- 2047 / 2147: Hepatitis Serology
  - 2047: Hepatitis Serology Pre-HCT
  - 2147: Hepatitis Serology Post-HCT
- 2149: Respiratory Virus Post-Infusion Data
- 2150: Viral Infection Diagnosis and Treatment Form
- 2199: Donor Cellular Infusion
  - Q1 – 4: Donor Information
  - Q5 – 39: Donor Cellular Infusion (DCI)
- 2451: Chimerism Essential Data
  - Q1 – 3: Chimerism Studies
- 2553: VOD/SOS
- 2900: Recipient Death
- 3500: Subsequent Neoplasms
  - Q1 – 11: New Malignancy, Lymphoproliferative or Myeloproliferative Disease / Disorder
  - Q12 – 22: Post-Transplant Lymphoproliferative Disorder
- 3501: Pregnancy Form
  - Q1-8: Functional Status
- 3502: Laboratory Studies
- 3503: Neurocognitive Assessment
  - Q1 – 69: Clinical Status Prior to Mobilization
- 3505: Transfusions
  - Q1 – 9: Transfusions
- 3506: Marrow Surveillance
  - Q1 – 18: Marrow Evaluation
Study-Specific Manuals
- 2540: Tepadina® Supplemental Data
- 2541: Inotuzumab Ozogamacin (Besponsa™) Supplemental Data
  - Q1-17: Inotuzumab Ozogamicin (Besponsa™)
- 2542: Mogamulizumab Supplemental Data Collection
  - Q1 – 3: Complications of Interest
  - Q4 – 12: Post-Infusion Critical Illness
- 2543: Mylotarg™ Supplemental Data Collection
  - Gemtuzumab ozogamicin (Mylotarg™) Administration Pre – HCT / Pre-Infusion
- 2554: CMS Registration
  - Q1-8: Registration and Confirmation
- 2555: MF Eligibility
  - Q1-4: Inclusion Criteria
  - Q5-7: Exclusion Criteria
- 2565: Sanofi Mozobil Supplemental Data
- 2544: Betibeglogene Autotemcel (Zynteglo®) Pre-Infusion Supplemental Data
- 2545: Betibeglogene Autotemcel (Zynteglo®) Post-Infusion Supplemental Data
- 2546: Elivaldogene Autotemcel (Skysona®) Pre-Infusion Supplemental Data
- 2547: Elivaldogene Autotemcel (Skysona®) Post-Infusion Supplemental Data
  - Q1-10: Growth Factor and Cytokine Therapy
  - Q11-14 Clinical Status Post-Infusion
Appendices
- Appendix A: Abbreviations and Definitions
- Appendix B: Glossary of Terms
- Appendix C: Cytogenetics
- Appendix D: How to Distinguish Infusion Types
- Appendix E: Definition of a Product
- Appendix F: Response Evaluation Criteria in Solid Tumors (RECIST)
- Appendix G: Tracking Disease Status for Multiple Myeloma
- Appendix I: Race, Ethnicity and Ancestry (REA)
- Appendix J: Reporting Comorbidities
- Appendix L: Karnofsky / Lansky Performance Status
- Appendix N: Drug Classification
Reporting Instruction Overview
- ANC / Platelet Recovery
  - ANC Recovery
  - Platelet Recovery
- Contact Dates
  - Determining Contact Dates
  - Subsequent Infusions and Contact Dates
- GVHD
- Lines of Therapy

This section is intended to provide general guidance about reporting ANC and platelet recovery.

Manual Updates
Sections of the Forms Instruction Manual are frequently updated. The most recent updates to the manual can be found below. For additional information, select the manual section and review the updated text.

If you need to review the historical Manual Change History for this form, reference the retired manual section on the Retired Forms Manuals.

Date	Manual Section	Add/Remove/Modify	Description
10/24/2025	ANC / Platelet Recovery	Add	ANC / Platelet Recovery Reporting Instruction Overview added.

Last modified: Oct 27, 2025

Reporting Instruction Overview

ANC Recovery

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